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Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1 (2000)

Chapter: Arsine: Acute Exposure Guideline Levels

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Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
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2

Arsine1
Acute Exposure Guideline Levels

SUMMARY

ARSINE is a colorless gas used in the semiconductor industry. Arsine also is used in mining and manufacturing processes involving arsenicals and paints and herbicides containing arsenicals.

Arsine is extremely toxic and a potent hemolytic agent, ultimately causing death via renal failure. Numerous human case reports are available, but these reports lack definitive quantitative exposure data. The reports, however, affirm the extreme toxicity and latency period for the toxic effects of arsine in humans.

Exposure-response data from animal studies were used to derive acute exposure guideline level (AEGL) values for arsine. AEGL values derived with animal data which had complete exposure data were more scientifically valid than AEGLs estimated from limited anecdotal human data. The greater conser

1  

This document was prepared by AEGL Development Team member Richard Thomas of the National Advisory Committee on Acute Exposure Guideline Levels for Hazardous Substances (NAC) and Robert Young of the Oak Ridge National Laboratory. The NAC reviewed and revised the document, which was then reviewed by the National Research Council (NRC) Subcommittee on Acute Exposure Guideline Levels. The NRC subcommittee concludes that the AEGLs developed in this document are scientifically valid conclusions based on the data reviewed by the NAC and are consistent with the NRC guidelines reports (NRC 1993; NRC in press).

Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×

vatism afforded by the animal data is justified by the incomplete and often equivocal data for human exposures, the documented extreme toxicity of arsine, and the known latency involved in arsine-induced lethality. The AEGL values for the various exposure periods of concern (0.5, 1, 4, and 8 h) were scaled from the experimental exposure duration using exponential scaling (Cn×t=k, where C=exposure concentration, t=exposure duration, and k=a constant). Data were unavailable to empirically derive a scaling factor (n) for arsine. The concentration-exposure time relationship for many irritant and systemically acting vapors and gases may be described by Cn×t=k, where the exponent n ranges from 0.8 to 3.5 (ten Berge et al. 1986). In the absence of an empirically derived exponent (n), temporal scaling was performed using n=3, when extrapolating to shorter time points and n=1 when extrapolating to longer time points using the Cn×t=k equation.

Based upon the available data, derivation of AEGL-1 values was considered inappropriate. The continuum of arsine-induced toxicity does not appear to include effects consistent with the AEGL-1 definition. The available human and animal data affirm that there is a very narrow margin between exposures that result in little or no signs or symptoms of toxicity and those that result in lethality. The mechanism of arsine toxicity (hemolysis that results in renal failure and death), and the fact that toxicity in humans and animals has been reported at concentrations at or below odor detection levels (−0.5 parts per million (ppm)) also support such a conclusion. The use of analytical detection limits (0.01 to 0.05 ppm) was considered as a basis for AEGL-1 values but was considered to be inconsistent with the AEGL-1 definition.

The AEGL-2 values were based upon exposures that did not result in significant alterations in hematologic parameters in mice exposed to arsine for 1 h (Peterson and Bhattacharyya 1985). Uncertainty factor application included 10-fold interspecies variability because of uncertainties regarding species-specific sensitivity to arsine-induced hemolysis. The 10-min LC50 (lethal concentration for 50% of the animals) value for the monkey was approximately 60% of the rat value and one-third the rabbit value. A less sensitive species, the rat, was used to calculate the AEGL levels because the data exhibited clear exposure-response relationships and the reduced hematocrit can be considered a sensitive indicator of arsine toxicity. Uncertainty regarding intraspecies variability was limited to a factor of 3-fold, because the hemolytic response is likely to occur to a similar extent and with similar susceptibility in most individuals. This was based on the assumption that physiologic parameters (such as absorption, distribution and metabolism of arsine, as well as renal responses and the structure of the erythrocyte and its response to arsine) would not vary among individuals of the same species by an order of magnitude. Additionally, individual variability (i.e.,

Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×

variability in erythrocyte structure/function or response of the kidney to hemolysis) is not likely to have a significant impact on any of the proposed subcellular mechanisms of arsine toxicity. The steep exposure-response curves from animal data also affirm the limited variability in response. Furthermore, the AEGL-2 values were developed using an exposure resulting in no significant hemolysis in mice exposed to arsine at 5 ppm for 1 h, and, therefore, additional reduction of the values was unwarranted.

Arsine data were not available to determine a concentration-exposure time relationship. The concentration-exposure time relationship for many irritant and systemically acting vapors may be described by Cn×t=k, where the exponent n ranges from 0.8 to 3.5 (ten Berge et al. 1986). In the absence of chemical-specific data, temporal scaling was performed using n=3 when extrapolating to shorter time points and n=1 when extrapolating to longer time points using the Cn×t=k equation.

The AEGL-3 values were based upon lethality and hemolysis in mice exposed to arsine for 1 h (Peterson and Bhattacharyya 1985). A 1-h exposure at 15 ppm resulted in significant hemolysis, and a 1-h exposure at 26 ppm produced 100% lethality. A total uncertainty factor of 30 was applied, as was done for AEGL-2 values using identical rationale. Because the AEGL-3 values were developed based upon an exposure producing hemolysis but no lethality in mice, no further reduction in the values was warranted. The derivation of AEGL-3 values using limited data in monkeys affirmed the values derived based upon the mouse data. Although the human experience was of qualitative value, the absence of definitive verifiable exposure terms severely limited its utility as a valid quantitative measure for AEGL-3 development.

Time scaling for AEGL-3 development was performed as previously described for the AEGL-2 tier.

The three AEGL exposure levels reflect the narrow range between exposures resulting in minor effects and those producing lethality. The approach used in the development of AEGLs for arsine was justified by the confirmed steep dose-response curve, the induction of hemolysis by arsine at extremely low concentrations, and the potential of hemolysis to progress to life-threatening renal failure. It is also noted that all of the AEGL values are near or below the odor threshold for arsine. A summary of AEGL values for arsine is shown in Table 2–1.

Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×

TABLE 2–1 Summary of AEGL Values for Arsine

Classification

30 min

1 h

4 h

8 h

Endpoint (Reference)

AEGL-1 (Non-disabling)

NRa

NR

NR

NR

Not recommended due to steep dose-response relationship, mechanism of toxicity, and because toxicity occurs at or below the odor threshold

AEGL-2 (Disabling)

0.21 ppm

0.7 mg/m3

0.17 ppm

0.5 mg/m3

0.04 ppm

0.1 mg/m3

0.02 ppm

0.06 mg/m3

Absence of significant hematologic alterations in mice consistent with the known continuum of arsine toxicity (Peterson and Bhattacharyya 1985)

AEGL-3 (Lethal)

0.63 ppm

2.0 mg/m3

0.50 ppm

1.6 mg/m3

0.13 ppm

0.4 mg/m3

0.06 ppm

0.2 mg/m3

Estimated threshold for lethality in mice (Peterson and Bhattacharyya 1985)

Numeric values for AEGL-1 are not recommended because (1) data are not available, (2) an inadequate margin of safety exists between the derived AEGL-1 and the AEGL-2, or (3) the derived AEGL-1 is greater than the AEGL-2. Absence of an AEGL-1 does not imply that exposure below the AEGL-2 is without adverse effects.

Abbreviations: NR, not recommended, ppm, parts per million; mg/m3, milligrams per cubic meter.

Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×

TABLE 2–2 Chemical and Physical Data

Parameter

Value

Reference

Synonyms

arsenic trihydride; hydrogen arsenide; arsenious trihydride; arsenic hydride; arsenic hydrid; arsineuretted hydrogen

Budavari et al. 1989;

AIHA 1993;

Hesdorffer et al.

1986

Chemical formula

AsH3

Budavari et al. 1989

Molecular weight

77.93

Budavari et al. 1989

CAS Registry No.

7784–42–1

Budavari et al. 1989

Physical state

gas

Budavari et al. 1989

Solubility in water

20% at 20°C

AIHA 1993

Vapor pressure

14.95 atm @ 21.1°C

Braker and Mossman 1980

Density

2.695 g/cm3

USAF 1990

Melting/boiling/flash point

−117°/−55°C/ND

Budavari et al. 1989

Odor threshold

0.5 ppm; garlic-like odor

NAPCA 1969

Conversion factors in air

1 mg/m3=0.31 ppm 1 ppm=3.19 mg/m3

AIHA 1993

1. INTRODUCTION

Arsine is an extremely toxic, colorless gas used extensively in the semiconductor industry. Arsine also is used in mining and manufacturing processes involving arsenicals and in paints and herbicides containing arsenicals (Risk and Fuortes 1991). Annual production has been estimated at over 10,000 pounds and is likely increasing with greater use in the semiconductor industry (U.S. EPA 1980). The physical and chemical data for arsine are shown in Table 2–2.

2. HUMAN TOXICITY DATA

Human data for arsine are compromised by deficiencies in exposure concentration and duration data and by concurrent exposures to other materials. It has been reported that exposure to 3–100 ppm for several hours may result in slight symptoms, and exposure to 16–30 ppm arsine for 0.5–1 h is dangerous (Coles

Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×

et al. 1969). These estimates, however, reflect uncertainties in the human data and are not necessarily consistent with all the available data. The odor threshold for arsine ranges from 0.5 to 1 ppm. The clinical aspects of arsine poisoning have been reviewed by Fowler and Weissberg (1974) and Dreisbach (1983).

2.1. Acute Lethality

Human LClo values of 25 ppm (30 min) and 300 ppm (5 min) have been reported (RTECS 1986). Henderson and Haggard (1943) (as cited in AIHA 1993) noted that exposure of humans to arsine at 250 ppm for 30 min was fatal.

Early reports, summarized by Flury and Zernik (1931), provided the following anecdotal information regarding human responses to arsine exposure: immediately fatal following exposure at 1,530 ppm (no duration specified), fatal within 30 min following exposure at 250 ppm, immediately fatal following exposure at 15.5 ppm for 30–60 min, dangerous to life following exposure at 6.25 ppm for 30–60 min. Contrary to the above estimates, the following were also reported in Flury and Zernik (1931): no immediate or delayed effects following exposure at 6.25 ppm for 30–60 min, no symptoms following 6-h exposure at 3.1 ppm.

2.1.1. Case Reports

Case reports are available regarding lethal effects of acute exposure to arsine (Pinto et al. 1950; Morse and Setterlind 1950; Hesdorffer et al. 1986). However, no definitive quantitative exposure data accompany these reports. Signs and symptoms varied depending on the exposure situation but usually included abdominal and muscle pain, nausea and diarrhea, hematuria, and oliguria. Delayed lethality, common in arsine poisoning, varied considerably.

Levinsky et al. (1970) reported on three men exposed to an unknown concentration of arsine for an estimated, 2, 3, and 15 min. Signs and symptoms of exposure (malaise, headache, abdominal pain, chills, nausea, vomiting, oliguria/ anuria, hematuria, bronze skin color) developed within 1–2 h. All three individuals required extensive medical intervention to save their lives. Clinical findings were indicative of massive hemolysis and repeated blood exchange transfusions were necessary for the survival of these individuals.

Pinto (1976) also reported similar characteristics regarding acute arsine poisoning. Although, an exposure concentration was unavailable, exposure to newly formed arsine for less than 1 h resulted in severe (likely fatal without medical intervention of exchange transfusion) signs and symptoms, including

Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×

abdominal pain, chest pain, and hematuria within hours of exposure. A successive reduction in hematocrit (42.2 to 27.7) and hemoglobin (14.1 to 9.6 g %) occurred within 3 d. Cardiac involvement indicative of left ventricular ischemia was detected within 1 d of exposure.

2.2. Nonlethal Toxicity

Human TClo values of 3 ppm (no duration specified) and 325 micrograms per cubic meter (µg/m3) (0.1 ppm) (no duration specified) have been reported (RTECS 1987). Henderson and Haggard (1943) (as cited in AIHA1993) noted that exposure of humans to arsine at 3–10 ppm for a few hours may result in signs and symptoms of poisoning. Similar to the data set for acute lethality, most information on nonlethal effects of arsine exposure in humans are case reports representing exposure estimates.

2.2.1. Case Reports

Numerous cases of arsine poisoning have been reported (Elkins and Fahy 1967; DePalma 1969). However, these reports lack definitive exposure concentration data and usually lack exposure duration data as well. Some of the more recent and complete reports involving nonlethal consequences are described in the following section. These reports do not provide quantitative data suitable for AEGL derivations, but they do provide valuable insight into the nature and progression of arsine poisoning in humans. In most cases, the severity of the effects was usually sufficient to necessitate medical intervention to prevent lethality. Some of the more prominent reports and those with the best descriptive data have been summarized, but the overview is by no means exhaustive.

Three cases of arsine poisoning were reported by DePalma (1969). One day after exposure, the blood arsenic levels were 0.66, 0.25 and 2.2 milligram per liter (mg/L). Hemoglobin levels at 1 d after exposure were 5.9, 7.8, and 11.7 grams per deciliter (g/dL) but tended to fluctuate considerably over several weeks. Although no quantitative exposure data were provided, the case reports serve to identify the hemolysis, abdominal pain and tenderness, hematuria, nausea and vomiting that appears to be characteristic signs and symptoms of acute arsine poisoning. Additionally, the case reports attest to the prolonged nature of arsine-induced toxicity; recovery frequently requires many weeks even with medical intervention.

A case of oliguric renal failure following acute exposure to arsine was reported by Uldall et al. (1970). The concentration of arsine was not available,

Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×

but the duration of exposure was approximately 7 h. Within hours of the exposure, the subject experienced episodic hot and cold sensation, abdominal pain and cramping, hematuria, and confusion. On admission to the hospital (3 d post-exposure), the subject was disoriented, abdominal pain had increased, and his skin was discolored (yellowish-brown), and mucous membranes were pale. Hemoglobin was 6.1 g/dL, hematocrit was 18%, and urine samples contained protein and erythrocytes and erythrocyte casts. The victim required peritoneal dialysis and considerable medical intervention prior to a long-term moderate recovery. Two additional workers were also exposed in a similar fashion but for only 1 h. Hemoglobin values for these individuals (admitted to the hospital 3 and 4 d post-exposure) was 8.9 and 12 g/dL, respectively, and hematocrit was 27% and 36%, respectively. Both exhibited hematuria and mild proteinuria, and both recovered without sequelae.

A case report of acute arsine poisoning in which a 27-y-old man was exposed to arsine during chemical manufacturing was reported by Pinto (1976). The subject was exposed to arsine as a result of arsine production via a reaction between a galvanized bucket and an arsenic-containing sulfuric acid solution. The exposure (duration not specified) produced toxic effects characterized by abdominal cramping, thoracic discomfort, and hematuria. Over the next week, the patient’s hematocrit declined from 42.5 to 27.1 and hemoglobin dropped from 14.1 to 9.5 g/dL even with medical intervention (blood transfusions and mannitol diuresis). Nine hours after exposure, blood arsenic was 159 µg/dL and urinary arsenic was 1862 µg/L.

Kleinfeld (1980) reported a case of arsine poisoning in a 31-y-old man. The exposure to arsine occurred from a leaking canister thought to be empty. The exposure duration was estimated to be 1–2 min, but no actual or estimated arsine concentrations were available. The victim presented with hematuria. On hospital admission, no intact erythrocytes were present in the urine, hematocrit was 43%, and hemoglobin was 9.8 g/dL. The hematocrit dropped to as low as 18%, the correction of which required one unit of packed cells. Based upon the exposure history and the subject's note of a "garlicky" odor, the diagnosis was arsine-induced hemolytic anemia. Urinary arsenic was 7.2 mg/L on admission and 0.1 mg/L 4 d later. The patient was subsequently discharged.

The occupational exposure of five workers to arsine was reported by Phoon et al. (1984). All cases involved hematuria and, except for one patient, abdominal pain and jaundice. One worker was exposed for approximately 1 3/4 h, while the others were exposed for approximately 2 1/4 h. The latency in appearance of toxic effects was unusually short (≈3 h). The following day, the arsine level in the workers’ breathing zone was 0.055 mg/m3 (0.017 ppm), although no processing of arsenic-containing material was taking place at the time of measurement. It was hypothesized by the report authors that the arsine

Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×

concentration at the time of exposure was much higher, thus accounting for the very short latency period.

Mora et al. (1992) reported on two cases of acute arsine poisoning in workers shoveling scories at a ferrous metal foundry. One case involved acute hemolysis followed by acute renal failure requiring dialysis, and the other involved acute hemolysis and cytolytic hepatitis; a definitive etiology for the hepatitis was not found but was thought to be possibly related to the arsine exposure. Arsine levels were subsequently found to be at or below the ACGIH Threshold Limit Value (TLV) (0.05 ppm) during dry conditions but increased to 60 ppm when water was added to the scories. It was not known if the exposures occurred during wet or dry conditions.

Data from case reports indicated that there is usually a 1- to 24-h delay between exposure and onset of signs and symptoms of poisoning. Additionally, hematologic parameters (e.g., hemoglobin, hematocrit levels) appear to be progressively affected for several days after the exposure. Hence although the exposure is acute, the most serious adverse effect may be delayed by several hours or days.

Bulmer et al. (1940) (as cited in Elkins 1959) reported on eight workers in a gold extraction plant who were exposed to arsine for up to 8 mon. During this period, major medical findings were jaundice and anemia. Based upon urinary arsine levels (0.7–4 mg/L), a 50% absorption factor, and an inhalation rate of 5 m3/8 h, the arsine concentration was estimated at 0.12 ppm. It was suggested that a maximum allowable concentration of 0.05 ppm would not be unreasonable. The estimation of exposure levels provides some insight into arsine toxicity in humans but it is unclear if the effects observed were the result of long-term, repeated exposure or would have been observed after a single exposure.

2.2.2. Epidemiologic Studies

Landrigan et al. (1982) conducted an epidemiologic survey to evaluate occupational exposure to arsine in a lead-acid battery manufacturing plant. Arsine concentrations ranged from nondetectable to 49 µg/m3 (≈0.02 ppm) in 177 breathing zone samples. A high correlation was found between urinary arsenic concentration and arsine exposure (r=0.84; p=0.0001 for an n of 47). Additionally, arsine levels above 15.6 µg/m3 (≈0.005 ppm) were associated with urinary arsenic concentrations in excess of 50 µg/L. The investigators concluded that exposure to a 200 µg/m3 arsine exposure standard would not prevent chronic increased absorption of trivalent arsenic.

Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×
2.3. Developmental and Reproductive Toxicity

No definitive, quantitative data were available regarding the potential reproductive and developmental toxicity of arsine in humans.

2.4. Genotoxicity

Genotoxicity data relevant to the derivation of AEGLs for arsine were not available.

2.5. Carcinogenicity

Although some forms of inorganic arsenic are considered known human carcinogens, there are no data available regarding the carcinogenic potential of arsine or its conversion to carcinogenic forms. The extreme acute toxicity of arsine gas precludes the relevance of carcinogenic potential for acute exposures. Therefore, a carcinogenicity assessment based upon elemental equivalence has not been carried out.

2.6. Summary

Numerous case reports are available regarding the lethal and nonlethal toxicity of arsine in humans, but definitive exposure concentration or duration data are lacking. Although the case reports are of limited use for quantitative estimates of exposure limits, they do provide qualitative information about the nature of arsine poisoning in humans. Some estimated human toxicity values are available and are summarized in Table 2–3.

3. ANIMAL TOXICITY DATA

3.1. Acute Lethality

Acute lethality data for several laboratory species are summarized in the following sections. Lethal concentrations for various species are shown in Table 2–4. Cumulative exposures (C×t) exhibit notable variability even within species.

Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×

TABLE 2–3 Acute Toxicity Values for Arsine Poisoning in Humans

Estimated Toxicity Value

C×t (ppm·min)

Comments

Reference

30-min LClo: 25 ppm

750

Fatal within 30 min

RTECS 1987

5-min LClo: 300 ppm

1,500

RTECS 1987

30-min LClo: 250 ppm

7,500

Henderson and Haggard 1943 (as cited in AIHA 1993)

30-min LClo: 250 ppm

7,500

Flury and Zernik 1931

30 to 60-min LClo: 15.5 ppm

465–930

Flury and Zernik 1931

30 to 60-min LClo: 6.25 ppm

188–375

"Dangerous to life"a

Flury and Zernik 1931

6-h NOAEL: 3.1 ppm

19

No symptoms reported following this 6-h exposure

Flury and Zernik 1931

aFlury and Zernik (1931) also reported no immediate or delayed effects in a human exposed at 6.25 ppm for 30–60 min.

Abbreviation: NOAEL, no-observed-adverse-effect level.

3.1.1. Nonhuman Primates

A 30-min LC50 of 250 mg/m3 for monkeys was reported by RTECS (1987). Effects included hemolysis without anemia and abnormal erythrocytes.

Kensler et al. (1946) exposed three monkeys (species not specified) to arsine at a concentration of 0.45 mg/L (450 mg/m3 or 140 ppm) for 15 min. One monkey died in 24 h and exhibited marked intravascular hemolysis and hematuria.

Delayed lethality (3 d post-exposure) in a monkey exposed to arsine at approximately 190,000 ppm for 1 h was reported by Joachimoglu (1924) (as cited in Flury and Zernik 1931). Four hours after the exposure, the monkey was vomiting and hematuria was evident.

3.1.2. Dogs

Dubitski (1911) (as cited in Flury and Zernik 1931) noted that the dog was similar to the cat regarding arsine toxicity. Exposure to 10 ppm was without

Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×

TABLE 2–4 Acute Lethality of Arsine in Laboratory Species

Species

Lethal Concentration in ppm [mg/m3]

C×T (ppm·min)

Reference

Monkey

10-min LC50: 78 [250]

780

RTECS 1987

Monkey

15-min LClo: 140 [450]

2,100

Kensler et al. 1946

Rat

30-min LC50: 250 [798]

7,500

IRDC 1985

Rat

1-h LC50: 178 [568]

10,680

IRDC 1985

Rat

4-h LC50: 45 [144]

10,800

IRDC 1985

Rat

10-min LC50 121 [390]

1,210

RTECS 1987

Rat

4-h LC50 42.6 [135]

10,224

Craig and Frye 1988

Rat

10-min LC50: 202 [650]

2,020

RTECS 1987

Mouse

1-h: 26 ppm [83]; 100% mortality

1,560

Peterson and Bhattacharyya 1985

Rabbit

10-min LC50: 202 [650]

2,020

RTECS 1987

Dog

10-min LC50: 109 [350]

1,090

RTECS 1987

Mouse

50-min LC50: 31 [100]

5,450

Levvy 1948

Mouse

24-h LC50: 8 [25]

11,520

Levvy 1948

observable effects but exposure to 100 ppm was noted as being "quickly dangerous." Exposure durations were not specified but were assumed to be 1 h as for the cat experiments (Section 3.1.3).

3.1.3. Cats

Dubitski (1911) (as cited in Flury and Zernik 1931) provided data on the acute lethality of arsine in cats, noting the following for 1-h exposures: no observable signs of toxicity following exposure to 43–50 ppm, sick with recovery following exposure to 50–100 ppm, and death (12–40 h post-exposure) following exposure to 120–290 ppm.

3.1.4 Rats

Several LC50 values for arsine are listed in RTECS (1987) for rats (Table 2–4 ). Several inhalation studies evaluating lethality are also available and are summarized in the following paragraphs.

Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×

Fowler et al. (1989) reported a 100% mortality in male and female Fischer 344 (F344) rats exposed to arsine at concentrations above 10 ppm, 6 h/d over 4 d. However, rats survived 28-d (6 h/d) exposures to 5 ppm and exhibited no mortality or overt signs of toxicity. The study authors noted the sharp threshold between tolerated and lethal exposures to arsine.

Craig and Frye (1988) reported a 4-h LC50 values for Sprague-Dawley rats. The 4-h LC50 for males, females, and both sexes combined were 46.8 ppm, 38.9 ppm, and 42.6 ppm, respectively. Groups of five male and five female rats were exposed to concentrations of 25.2, 35.1, 44, 54.4, or 63.5 ppm. At 54.4 ppm four of five males and five of five females died. At 63.5 ppm, all rats of both sexes died. At 25.2 ppm there was no mortality. At 35.1 ppm mortality was 2/5 in females and 0/5 in males.

The International Research and Development Corporation (IRDC 1985) also conducted acute lethality studies on male and female Sprague-Dawley rats to determine 0.5-h, 1.0-h, and 4.0-h LC50 values. For all experiments, groups of 10 male and 10 female rats were used, and there was a 14-d post-exposure observation period. For determining the 0.5-h LC50, rats were exposed to concentrations of 97, 170, 200, 260 (two groups), 350, or 400 ppm. The 0.5-h LC50 (sexes combined) was 250 ppm. There were no deaths in male rats exposed at 97, 170, or 200 ppm and no deaths in females exposed at 97 ppm. All male rats exposed at 400 ppm died and all female rats exposed at 350 or 400 ppm died. In the 1-h LC50 experiments, rats were exposed to arsine concentrations of 120, 160, 190, or 220 (two groups) ppm. The 1-h LC50 was 178 ppm (sexes combined). No males and two females died at the lowest exposure, although rats in all exposure groups exhibited pale ears, and red/brown material around the nose. A 60% and 70% mortality occurred in each group of males exposed to the highest concentration (220 ppm); the mortality in females exposed at 220 ppm was 90% and 100%. In the 4-h exposure studies, rats were exposed to arsine at concentrations of 24, 27, 36, 46, 56, or 110 ppm. The 4-h LC50 (sexes combined) was 45 ppm. No males died at 24, 27, or 36 ppm, but mortality was 100% at 110 ppm. For female rats, there was no mortality at 24 or 27 ppm, but mortality at 46, 56, or 110 ppm was 100%, 90%, and 100%, respectively. Rats in most exposure groups exhibited pale ears. Additional signs included pale feet and eyes, especially in exposures ≥37 ppm, although these signs were noted for female rats in the lowest exposure groups.

3.1.5. Mice

Early studies in mice indicated that the following exposure conditions resulted in lethality: 900 ppm for 20–30 min, 400 ppm for 45 min, 300 ppm for

Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×

15 min (2 h post-exposure), 150–300 ppm for 1 h, 100 ppm for 15 min (7 h post-exposure), and 30–60 ppm for 2–4 h (Flury and Zernik 1931).

Levvy (1948) studied acute arsine toxicity in mice. In this study, groups of 30 inbred mice (15 males and 15 females; 25–30 g) were exposed by inhalation (whole-body) to arsine at concentrations of 2.5, 1.0, 0.50, 0.25, 0.10, or 0.025 mg/L (six mice only) for periods ranging from 0.33 min to 30 h. The results of this experiment are shown in Table 2–5. The average time-to-death was 4 d. Hemoglobinemia was noted for many of the mice exposed at 8 ppm (0.025 mg/L), indicating that even at the lowest exposure, effects characteristic of arsine poisoning were observed. It was not specified whether an assessment of this effect was made for mice in the other exposure groups. It was noted that, for concentrations at or below 155 ppm, the relationship between arsine concentration and duration of exposure for 50% mortality was consistent with C2×t =k.

The effects of acute inhalation exposure of mice (B6C3F1/Anl) to arsine were reported by Peterson and Bhattacharyya (1985). Although the study focused on assessing hematologic responses, specifically hematocrit, numbers of erythrocytes, leukocytes and reticulocytes, and erythrocyte fragility, lethality occurred in the high-exposure group. A 100% mortality was noted for groups of eight female B6C3F1 mice exposed to arsine for 1 h at a concentration of 26 ppm (three died immediately following exposure, and the remaining five died within 4 d. At 24 h post-exposure, there was a significant exposure-related decrease (21.7% relative to sham-exposed controls) in hematocrit values of the 26-ppm exposure group. Mice in this group subsequently died within 4 d following exposure.

Similar to the results of studies in rats, female B6C3F1 mice exposed to arsine at concentrations above 10 ppm, 6 h/d over 4 d exhibited a 100% mortality (Fowler et al. 1989).

3.2. Nonlethal Toxicity
3.2.1. Nonhuman Primates

In a study by Kensler et al. (1946), three monkeys were exposed by inhalation to arsine at a concentration of 0.45 mg/L (450 mg/m3 or 140 ppm) for 15 min. Although one monkey died in 24 h, one remaining monkey survived without treatment; another was treated with 2,3-dimercaptopropyl ethyl ether. The surviving monkey that was not treated could "scarcely raise himself from the floor of his cage from the 2nd to the 7th days." The erythrocyte count of this monkey decreased to 65% of pre-treatment level in 24 h, and by d 3–4 decreased to approximately 20% prior to recovery. The monkey treated with

Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×

TABLE 2–5 Acute Inhalation Toxicity in Mice Exposed to Arsine (Levvy 1948)

Concentration

Exposure Duration (min)

C×T (ppm·min)

Mortality

Estimated Duration (min) for 50% Mortality

mg/L

mg/m3

ppm

2.5

2,500

775

0.50

388

93

0.40

 

0.33

257

20

 

1.0

1,000

310

1.25

388

57

1.18

 

0.83

257

13

 

0.50

500

155

10

1,550

100

2.4

 

5

775

93

 

 

2.5

388

57

 

 

1.7

264

0

 

0.25

250

78

15

1,170

70

12

 

9

702

33

 

0.10

100

31

70

2,170

100

50

 

50

1,550

50

 

0.025

25

8

900

7,200

0

1,440

 

1,080

8,640

0

 

 

1,260

10,000

50

 

 

1,440

11,520

50

 

 

1,620

12,960

50

 

 

1,800

14,400

100

 

2,3-dimercaptopropyl ethyl ether did not exhibit the rate or magnitude of erythrocyte reduction observed in the untreated monkey.

3.2.2. Rats

Blair et al. (1990a) conducted experiments to evaluate interspecies variability in the toxic effects of arsine. In addition to hamsters and mice, this study assessed the toxic effects of subchronic exposure (14, 28, or 90 d) of F344 rats to arsine. Rats were exposed 6 h/d for 14 or 28 consecutive days, or for 6 h/d for 5 consecutive days per week for 13 w. Exposure concentrations were 0.5, 2.5, or 5.0 ppm for the 14- and 28-d exposures and 0.025, 0.5, or 2.5 ppm for the 90-d exposure. Rats exposed at the two highest concentrations exhibited significant increases in relative liver weight and relative spleen weight. Relative spleen weight was also significantly increased in the 0.5-ppm group (except 14-d females). Packed cell volume also was significantly decreased in the 0.5-, 2.5-, and 5.0-ppm groups (except 14-d females). Some alterations in hemato-

Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×

logic values were observed but only for rats in the 90-d exposure group. This report focuses on arsine-induced effects following 14-, 28-, and 90-d exposures, the duration of which would not allow for valid extrapolation to durations relevant to AEGLs.

Male and female F344 rats exposed to arsine at 5 ppm, 6 h/d for 28 d exhibited no mortality or overt signs of toxicity (Fowler et al. 1989). However, there was a 100% mortality within 4 d of exposure to 10 ppm, thereby demonstrating a sharp delimitation and very narrow margin between lethal and nonlethal exposure concentrations.

3.2.3. Mice

The results of nonlethal effects in mice following acute inhalation exposure to arsine were reported by Peterson and Bhattacharyya (1985). The study focused on assessing hematologic responses, specifically hematocrit levels, numbers of erythrocytes, leukocytes and reticulocytes, and erythrocyte fragility. In this study, groups of eight female B6C3F1 mice were exposed to arsine for 1 h at concentrations of 0, 5, 9, 11, 15, or 26 ppm. Exposure to 26 ppm resulted in the death of three of eight mice shortly after the exposure. The remaining five mice died within 4 d. Blood samples were taken from mice of the other exposure groups at 1, 5, and 11 d following the 1-h exposure. At 24 h post-exposure, there was a significant exposure-related decrease in hematocrit values following exposure to ≥9 ppm; 80.2%, 79.7%, 61.4%, and 21.7% of sham-exposed controls for the 5-, 9-, 11-, 15-, and 26-ppm groups, respectively. At 5 d post-exposure, hematocrit values for the 9-, 11-, and 15-ppm groups had increased but were still significantly lower than those for controls. The number of erythrocytes was also significantly decreased relative to sham-exposed controls (7.8×106/mm3) at 1 d following exposure to arsine at 9 ppm (6.1× 106), 11 ppm (6.2×106/mm3), 15-ppm (4.0×106/mm3), or 15 ppm (2.2× 106/mm3). By 11 d post-exposure, erythrocyte numbers exhibited notable recovery to near normal values. At 5 d post-exposure, significant reticulocytosis was observed in mice exposed to arsine at ≥9 ppm. This condition was ameliorated by 11 d post-exposure. Transient leukocytosis was noted for 9- and 15-ppm groups 1 d after exposure, and erythrocyte osmotic fragility was altered in the 15- and 26-ppm groups 1 d after exposure. Generally, this study showed that a hemolytic response occurs rapidly in mice exposed to arsine at concentrations ≥9 ppm and that the margin between the no-effect level (5 ppm) and a lethal concentration (26 ppm) is less than 10-fold in mice.

Female B6C3F1 mice exposed to arsine at 5 ppm, 6 h/d for 28 d exhibited no mortality or overt signs of toxicity (Fowler et al. 1989). However, there was a 100% mortality within 4 d of exposure to 10 ppm, thereby demonstrating a sharp threshold between lethal and nonlethal exposures.

Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×

As part of the aforementioned short-term exposure study by Fowler et al. (1989), an assessment of immune function was also conducted (Rosenthal et al. 1989). In the Rosenthal et al. (1989) study, female B6C3F1 mice (18–22 g, 6–8 w of age) were exposed to arsine at 0.5, 2.5, or 5.0 ppm, 6 h/d for 14 d; controls were exposed to clean air. All mice survived through the exposure period. Briefly, alterations in splenic cell populations (i.e., increase in rubricytes and decrease in percentage of lymphocytes) suggested the spleen as a target for short-term arsine exposure. These cell population changes were considered to be the result of the hemolytic effects of arsine. An impairment of immune function, possibly the result of cellular redistribution, was noted. The relevance of these findings to human exposure is that they occurred at concentrations only 10-fold higher than the current TLV of 0.05 ppm (see Table 2–11).

The hematopoietic effects of arsine exposure in mice was investigated by Hong et al. (1989). In this study, female B6C3F1 mice (12/group) were exposed to arsine at concentrations of 0, 0.5, 2.5, or 5.0 ppm, 6 h/d for 14 d. Additional groups of mice were also exposed at 0, 0.025, 0.5, or 2.5 ppm, 6 h/d, 5 d/w for 12 w. Following the 14-d exposure, there was a significant exposure concentration-related decrease in erythrocyte count, hemoglobin, and hematocrit levels. These alterations returned to normal by 3 w after exposure. At 2 d post-exposure, there was a significant increase in absolute spleen weight (35%, 102%, and 236%, for the 0.5-, 2.5-, and 5.0-ppm groups, respectively) and relative spleen weight (38%, 97%, and 236% for the 0.5-, 2.5-, and 5.0-ppm groups, respectively) in the arsine-exposed mice. At 24 d post-exposure, the absolute spleen weight returned to normal in the 0.5-ppm group only, and the relative spleen weight remained significantly elevated.

As previously described in Section 3.2.2, Blair et al. (1990a) conducted experiments to evaluate interspecies variability in the toxic effects of arsine. In addition to subchronic exposure studies in rats and hamsters, this study assessed the toxic effects on female B6C3F1 mice following exposure to arsine (0.025, 0.5, 2.5, or 5.0 ppm) for 6 h/d for 1 d or 14 consecutive days, or for 6 h/day, 5 consecutive days per week for 13 w. Relative spleen weight and packed cell volume were assessed at termination of exposure and after 1, 2, 4, and 7 d of recovery. At 2, 4, and 7 d post-exposure, the 5.0-ppm arsine exposure group exhibited significantly increased relative spleen weight relative to sham-exposed controls. Packed cell volume was also significantly decreased in the 2.5-ppm group at 2, 4, and 7 d of recovery and in the 5.0-ppm group throughout the 7-d recovery period. Experiments were also conducted wherein mice were exposed for 14 or 90 d. It is significant that the results of this study suggest that a single exposure (0.5 ppm) to 10 times the ACGIH TLV (0.05 ppm) resulted in no significant hematopoietic damage but that repeated exposure to one-half the TLV for 13 w produced significant hematopoietic effects.

Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×
3.2.4. Hamsters

Groups of 16 male and 16 female Syrian golden hamsters were exposed to arsine at 0, 0.5, 2.5, or 5.0 ppm, 6 h/d, 5 d/w for 28 d (Blair et al. 1990a). Relative liver weight, relative spleen weight, packed cell volume, and whole-blood aminolevulinic acid dehydratase (ALAD) activity were examined at 3 and 4 d post-exposure. Minor changes in relative liver weight occurred, and significant increases in relative spleen weight were observed for the 2.5- and 5.0-ppm groups. Minor decreases in packed cell volumes were noted for the 5.0-ppm group at both post-exposure times. ALAD activity was significantly increased at 3 d post-exposure. The increased ALAD activity is indicative of a red-blood-cell (RBC) regenerative process and is considered a compensatory response.

3.3. Developmental/Reproductive Toxicity
3.3.1. Rats

The developmental toxicity of arsine in rats was investigated by Morrissey et al. (1990). Groups (28–29) of pregnant F344 rats were exposed (whole-body exposure) to arsine at concentrations of 0, 0.025, 0.5, or 2.5 ppm (0, 0.08, 1.6, or 8 mg/m3) for 6 h/d on gestation d 6 through 15. Measures were assessed for all litters (number of corpora lutea per litter, percent pre-implantation, and percent post-implantation) and live litters (number of live fetuses per litter, average fetal body weight per litter, and percent fetuses malformed per litter). With the exception of an increase in average fetal body weight in the highest exposure group, no significant treatment-related effects were detected. High-dose dams exhibited significant decreases in RBC count, hemoglobin content, hematocrit level, and mean corpuscular hemoglobin concentration, and significant increases in white-blood-cell count, mean corpuscular volume, mean corpuscular hemoglobin, and platelet counts. At 2.5 ppm, maternal spleen size was increased and an exposure-related increase in anemia was noted. In conclusion, there were no significant arsine-related development effects in the presence of mild maternal toxicity.

3.3.2. Mice

Morrissey et al. (1990) also conducted experiments to assess the developmental toxicity of arsine in mice. Groups (24–25) of pregnant Swiss (CD-1) mice were exposed to arsine at concentrations of 0, 0.025, 0.5, or 2.5 ppm (0, 0.08, 1.6, or 8 mg/m3) for 6 h/d on gestation d 6 through 15. Developmental

Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×

measures for all litters included number of implantation sites per litter, percent resorptions per litter, and percent litters with resorptions. Assessments for live litters included the number of live fetuses per litter, average fetal body weight per litter, and percent fetuses malformed per litter. Maternal spleen weights (relative and absolute) were significantly increased in the 2.5-ppm group. No treatment-related developmental effects were observed.

3.4. Genotoxicity

No data regarding the genotoxicity of arsine in animals were available.

3.5. Carcinogenicity

There are no data suggesting a carcinogenic potential for arsine in animals. Inorganic arsenic has been associated with skin and pulmonary tumors (IARC 1987; U.S. EPA 1987). The National Institute for Occupational Safety and Health (NIOSH) has recommended that all inorganic arsenicals, including arsine, be considered a potential human carcinogen. However, the extreme acute toxicity of arsine and the absence of carcinogenicity and genotoxicity data for arsine would preclude these endpoints as valid for AEGL consideration.

3.6. Summary

The nonlethal effects of acute exposure of laboratory species to arsine are summarized in Table 2–6. Many of the effects observed appear to occur from one to several days following cessation of exposure and, to some extent, increase in severity as post-exposure time increases. This is consistent with clinical observations for human poisonings with arsine.

4. SPECIAL CONSIDERATIONS

4.1. Metabolism and Disposition

There are no definitive data regarding the metabolism of arsine. Based upon proposed mechanisms of action and the known interaction with RBCs and hemoglobin, metabolism per se may of limited importance relative to acute exposures to arsine. Delayed toxicity and lethality are observed in both humans and animals following acute exposure to arsine, and it is known that increased

Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×

TABLE 2–6 Nonlethal Effects of Acute Arsine Exposure in Animals

Species

Exposure (ppm) Duration (hr)

C×t (ppm·min)

Effecta

Reference

Monkey

140 (15 min)

2,100

Extreme disability (inability to maintain normal posture) at 2– 7 d post-exposure

Kensler et al. 1946

Mouse

0.5 (6 h)

180

No effect on spleen weight or packed cell volume

Blair et al. 1990a

Mouse

2.5 (6 h)

900

Slight decrease in packed cell volume (females only)

Blair et al. 1990a

Mouse

5.0 (6 h)

1,800

Statistically significant increase in relative spleen weight and decrease in packed cell volume

Blair et al. 1990a

Mouse

5 (1 h)

300

Minor hematologic alterations (reduced erythrocyte count)

Peterson and Bhattacharyya 1985

Mouse

9 (1 h)

540

Minor hematologic alterations (reduced erythrocyte count, decreased hematocrit, increased reticulocyte count)

Peterson and Bhattacharyya 1985

Mouse

11 (1 h)

660

Significant reduction (20% of control) in erythrocytes and hematocrit, significant increase in reticulocytes and leukocytes

Peterson and Bhattacharyya 1985

Mouse

15 (1 h)

900

Significant reduction (40–50% of control) in erythrocytes and hematocrit, significant increase in reticulocytes and leukocytes

Peterson and Bhattacharyya 1985

Mouse

26 (1 h)

1,560

Significant reduction (20–30% of control) in erythrocytes and hematocrit, significant increase in reticulocytes and leukocytesb

Peterson and Bhattacharyya 1985

aSome effects observed at post-exposure periods of varying duration, see text for details.

bData from five surviving mice (38% mortality) all of which died within days after exposure.

Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×

damage occurs even after cessation of exposure. It is not known if such damage is a function of arsine metabolites or a continuation of sequential subcellular processes resulting in increased hematologic effects and renal failure.

Urinary arsenic is routinely evaluated in victims of arsine poisoning. Urine arsenic in unexposed people is <50 µg/L (Landrigan et al. 1982). These authors reported that 15.6 µg of arsine/m3 is associated with urinary arsenic of 50 µg/L. Other studies of urinary arsenic levels have also been reported, but the post-exposure time of measurement varies considerably, and there are no corresponding exposure correlates. Urinary arsenic levels in humans poisoned by arsine include 3.08 mg/L (Spolyar and Harger 1950), 1.14 mg/L, and 2.25 mg As/L (Elkins and Fahy 1967); 20 mg/L, 220 mg/L (24 h post-exposure) (Uldall et al. 1970), 130 mg/L, 175 mg/L (Uldall et al. 1970), and 0.43 mg As/L (24 h post-exposure) (De Palma 1969)

Blood arsenic levels are also routinely evaluated but also lack exposure correlates and vary as to post-exposure assessment: 0.6 mg/L (2 d post-exposure; Hesdorffer et al. 1986), 0.66 mg/L, 0.25 mg/L, and 2.2 mg/L (1 d post-exposure, De Palma 1969).

4.2. Mechanism of Toxicity

It is well documented that exposure to arsine causes intravascular hemolysis resulting in anemia and acute oliguric renal failure (Fowler and Weissberg 1974; Landrigan et al. 1982). However, the underlying mechanism by which arsine causes these effects is not fully understood. Several investigators have noted that hemoglobin is a primary subcellular target for arsine (Klimecki and Carter 1995; Hatlelid et al. 1996), and several mechanisms of arsine-induced hemolysis have also been proposed: (1) formation of colloidal arsenic within the erythrocyte (Labes 1926; Heubner 1935), (2) arsine-induced formation of hydrogen peroxide (Jung 1947), (3) inhibition of catalase (Lasch 1958), and (4) inhibition of NA+/K+ -ATPase (Levinsky et al. 1970). More recently, Blair et al. (1990b) noted increased levels of circulating methemoglobin and decreased reduced glutathione levels in erythrocytes of mice exposed to arsine, and hypothesized that oxidative stress may be a key mechanism in arsine toxicity.

The hemolytic potential of arsine is considerable. Arsine at 0.1–0.5 mM may cause significant hemolysis (Hatelid et al. 1995; Pernis and Magistretti 1960). Inhalation exposure of mice to arsine at 9 ppm for only 1 h resulted in a statistically significant decrease in hematocrit levels at 24 h to 11 d after exposure (Peterson and Bhattacharyya 1985). The practical significance of this finding is demonstrated by a simple calculation provided by Klimecki and Carter (1995) showing an arsine concentration of 0.26 mM resulting from a 4-h exposure to arsine at a concentration of 30 ppm. This calculation assumed a minute alveolar

Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×

volume of 5.25 L/min, a circulatory volume of 5 L, and an arsine density and molecular weight of 2.696 g/L and 77.95, respectively.

Of additional concern regarding acute exposures to arsine is the fact that human case reports indicate that serious health effects (e.g., renal failure) resulting from arsine exposure may be delayed for several hours or several days. Legge (1916) noted an interval of 6–36 h between the arsine exposure and the appearance of RBC destruction. Latency is also indicated by data from laboratory species that show hematopoietic effects of arsine persisting after exposure has ceased (Hong et al. 1989; Blair et al. 1990a). Based upon clinical chemistry and hematologic parameters, effects of severe arsine poisoning may last for weeks and months after exposure even following medical intervention (Levinsky et al. 1970).

4.3. Structure-Activity Relationships

There are no structure-activity relationships applicable to estimating acute exposure limits for arsine. The nature and rapidity of its toxicity are notably different from other inorganic arsenic compounds.

4.4. Other Relevant Information

Delayed neurologic and psychiatric disorders following acute arsine exposures have been reported (Frank 1976). Exposure concentrations were not provided, but duration of exposure ranged from 10 to 90 min. Within hours after the exposures, characteristic signs of arsine poisoning (e.g., hemolysis and hematuria) were observed. Polyneuropathies and neuropsychiatric syndromes were detected at 1–36 mon after the acute exposures to arsine.

4.4.1. Species Variability

No significant differences in arsine-induced toxicity were observed among F344 rats, B6C3F1 mice, and Syrian golden hamsters subjected to various exposure regimens (Blair et al. 1990a). In this inhalation study, mice were exposed to arsine for 6 h/d for 1 d or 4 consecutive days or for 6 h/d, 5 consecutive days per week for 13 w. Rats were exposed 6 h/d for 14 or 28 consecutive days, or for 6 h/d for 5 consecutive days per week for 13 w. Hamsters were exposed 6 h/d for 5 consecutive days each week for 4 w. Exposure concentrations were 0.5, 2.5, or 5.0 ppm except for the 13-w exposures where concentrations were reduced to 0.025, 0.5, or 2.5 ppm. The investigators assessed

Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×

alterations in various parameters of the hematopoietic system (e.g., spleen weight, extramedullary splenic hematopoiesis, hematocrit, hematology profiles, etc.) and found the effects to be similar among the species tested. In comparing the effects resulting from the various exposure regimens, it was noted that the 1-d 0.5 ppm (10 times the ACGIH TLV) exposure failed to produce significant effects on the hematopoietic system but that repeated exposure to 0.025 ppm (1/2 the ACGIH TLV) caused significant anemia.

4.4.2. Unique Physicochemical Properties

The uniqueness of arsine revolves primarily around its accidental formation (need for nascent hydrogen) resulting in relatively unexpected exposures.

4.4.3. Concurrent Exposure Issues

Exposure to arsine usually occurs in occupational settings that often involve concurrent exposures to other metal vapors and solvents. It is assumed that concurrent exposure with other chemicals, the toxicity of which targets the erythrocyte or renal function, would increase the severity of the response to arsine.

5. DATA ANALYSIS AND PROPOSED AEGL-1

5.1. Summary of Human Data Relevant to AEGL-1

For derivation of an AEGL-1, human data are limited to equivocal anecdotal information reported by Flury and Zernik (1931) and Coles et al. (1969). These include a 6-h NOAEL of 3.1 ppm and a 1-h NOAEL of 6.25 ppm, equivalent to cumulative exposures of 1,116 and 375 ppm·min, respectively (Flury and Zernik 1931). Coles et al. (1969) estimated that humans could be exposed at 3– 100 ppm for several hours with the occurrence of only slight symptoms. However, these data are not consistent with similar or lower exposures resulting in lethality (see Table 2–3). Numerous case reports are available documenting effects of varying severity following acute exposures of humans to arsine, but these reports lack definitive exposure data. Although human data are considered to be inadequate for derivation of AEGL-1 values for arsine, the available data do provide valuable qualitative insight into the signs and symptoms of arsine-induced toxicity and the oftentimes delayed nature of this toxicity.

Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×
5.2. Summary of Animal Data Relevant to AEGL-1

Acute toxicity data are available for several animal species but earlier reports often lacked details regarding experimental protocol and results. Most studies involved longer-term exposures (e.g., 14 d to 12 w or longer) but some provided data for exposure durations within the scope of AEGL concern. Data showing relatively inconsequential effects of acute exposure to arsine were available for mice (Peterson and Bhattacharyya 1985; Blair et al. 1990a). Results of these studies showed that cumulative exposures of 180–540 ppm-min resulted in minor alterations in hematologic parameters (e.g., packed cell volume, hematocrit level, erythrocyte count; see Table 2–6). Slightly higher cumulative exposures (660–1,800 ppm·min) resulted in more severe changes in the same parameters. The parameters evaluated in these studies are appropriate endpoints for assessing arsine toxicity. Although some of the observed changes were statistically significant, they may be more appropriately considered compensatory responses (e.g., minor increase in spleen weight) and not necessarily indicative of a biologically significant toxic response (minor reduction in erythrocyte count or decreased hematocrit).

5.3. Derivation of AEGL-1

For comparative purposes, AEGL-1 values were initially derived using two data sets (Blair et al. 1990a; Flury and Zernick 1931). These included a 6-h NOAEL of 0.5 ppm for mice (Blair et al. 1990a) and the estimated 1-h NOAEL of 6.25 ppm for humans reported by Flury and Zernik (1931).

The values calculated using the data (6-h NOAEL of 0.5 ppm in mice) from Blair et al. (1990a) were initially selected to estimate the AEGL-1. For AEGL-1 derivation, an uncertainty factor of 30 was applied to this value to account for intraspecies variability and interspecies extrapolation. The uncertainty factor of 10 for interspecies variability was chosen to account for the uncertainties in distribution kinetics and susceptibility to subsequent renal failure among different species. The uncertainty factor of 3 for intraspecies variability was applied because of the extreme toxicity of arsine and because the mechanism of toxicity (hemolysis and subsequent renal failure) is not likely to vary greatly among individuals. The basis for this assumption was that physiologic parameters (e.g., absorption, distribution, metabolism, structure of the erythrocyte and its response to arsine, and renal responses) would not vary among individuals of the same species to such an extent that the response severity to arsine would be altered by an order of magnitude. It is unlikely that individual variability (i.e., variability in erythrocyte structure/function or response of the kidney to

Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×

hemolysis) would have a significant impact on any of the proposed subcellular mechanisms of arsine toxicity.

Exponential scaling (Cn×t=k; ten Berge et al. 1986) was used to derive the other exposure duration-specific values. The concentration exposure time relationship for many irritant and systemically acting vapors and gases may be described by Cn×t=k, where the exponent n ranges from 0.8 to 3.5 (ten Berge et al. 1986). In lieu of a definitive data set allowing empirical derivation of the exponent (n), temporal scaling was performed using n=3 when extrapolating to shorter time points and n=1 when extrapolating to longer time points using the Cn×t=k equation. The human data from the earlier reports appears to be equivocal and unverifiable. Although of some qualitative value, the human experience information was not considered of sufficient quality for quantitative applications.

The calculations for the AEGL-1 values initially derived are shown in Appendix A. However, because of the extreme toxicity of arsine and the steep dose-response indicated by the available data, the derivation of AEGL-1 values for arsine was considered inappropriate. The available human and animal toxicity data indicate that there is little margin between exposures that produce little or no toxicity and those that result in lethality and, therefore, do not justify the derivation of a safe exposure level that meets the AEGL-1 definition. This is further supported by reports of toxicity in humans and animals at concentrations similar to or below odor detection levels (~0.5 ppm) and where hemolysis, the mechanism of toxicity, may rapidly progress to renal failure. The decision also was based on the known toxicity of arsine, the latency in development and expression of toxicity even after removal from exposure, and the possible progression of hemolysis to life-threatening renal failure. The continuum of arsine-induced toxicity does not appear to include effects consistent with the AEGL-1 definition. The use of detection limits (0.01 to 0.05 ppm; (OSHA 1999)) was considered to be inconsistent with the AEGL-1 definition. The AEGL-1 values for arsine are shown in Table 2–7.

TABLE 2–7 AEGL-1 for Arsine

AEGL Level

30 min

1 h

4 h

8 h

AEGL-1

NR

NR

NR

NR

NR: Not recommended. Numeric values for AEGL-1 are not recommended, because (1) data are not available, (2) an inadequate margin of safety exists between the derived AEGL-1 and the AEGL-2, or (3) the derived AEGL-1 is greater than the AEGL-2. Absence of an AEGL-1 does not imply that exposure below the AEGL-2 is without adverse effects.

Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×

6. DATA ANALYSIS AND PROPOSED AEGL-2

6.1. Human Data Relevant to AEGL-2

Several reports identified nonlethal effects in humans acutely exposed to arsine. These reports, however, lacked definitive exposure data but verified hematologic disorders leading to renal failure as critical effects of arsine exposure. Bulmer et al. (1940) (as cited in Elkins 1959) reconstructed an exposure incident at a gold extraction facility and estimated that subchronic (up to 8 mon) exposure to 0.12 ppm arsine resulted in jaundice and anemia (see Section 2.2.1). The lack of definitive exposure data for humans necessitates the use of animal data for quantitative estimation of AEGL values. Derivation of AEGL-2 values based upon limited human data (Flury and Zernik 1931) was considered but rejected because the data were poorly documented and inconsistent with other data showing lethality at lower cumulative exposures.

6.2. Animal Data Relevant to AEGL-2

Consistent with the human responses to arsine exposure, observations in several animal species (rats, mice, and hamsters) indicated hematologic involvement. Cumulative exposures of 540–1,800 ppm·min produced decreases in hematocrit levels, RBC counts, packed cell volumes, and increases in absolute and relative spleen weights (consistent with erythrocyte damage). For acute exposures, the exposure-response curve is steep; generally less than a 10-fold difference between no-effect and lethality exposures.

6.3. Derivation of AEGL-2

Although several data sets were available to derive AEGL-2 values, the 1-h exposure data from the mouse study by Peterson and Bhattacharyya (1985) provided the most sound basis.

The 1-h no-observed-effect level (NOEL) of 5 ppm represented a no-effect exposure level for mice, and 11 ppm represented a lowest-observed-adverse-effect level (LOAEL) based upon altered hematologic parameters in mice that were reversible at 5 d post-exposure. At 15 ppm, the effects on hematocrit levels, packed cell volume, and RBC count were more severe but were approaching reversibility at 11 d. The use of what might appear to be a conservative NOEL in the derivation of AEGL-2 is justified by the documented latency in the expression of severe toxicity in humans even after removal from exposure

Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×

and the potential for hemolysis to rapidly progress to life-threatening renal failure. Furthermore, the steep exposure-response curve for arsine (1-h exposure of mice to 26 ppm resulted in 100% lethality within 4 d, but exposure to 15 ppm resulted in nothing more than severe but reversible hematologic changes (Peterson and Bhattacharyya 1985)) justifies the approach used for derivation of the AEGL-2.

Data from mice were used to calculate the AEGL levels because these data exhibited a good exposure response relationship, and the endpoint of decreased hematocrit levels can be considered a sensitive indicator of arsine toxicity. For AEGL-2 derivation, an uncertainty factor of 30 was applied to the 1-h NOAEL of 5.0 ppm to account for intraspecies variability and interspecies extrapolation. A factor of 10 was applied for interspecies variability. The 10-min LC50 value for the monkey was about 60% of the rat value and one-third the rabbit value, thereby demonstrating interspecies variability. Additionally, the human experience data lacked sufficient quantitative exposure terms to allow for a definitive assessment of the animal-to-human variability. An uncertainty factor of 3-fold was used to account for intraspecies variability. Since the hemolytic response is likely to occur to a similar extent and with similar susceptibility in most individuals following exposure to extremely low arsine concentrations. The physiologic parameters (e.g., absorption, distribution, metabolism, structure of the erythrocyte and its response to arsine, and renal responses) would not vary among individuals of the same species to such an extent that the severity in response to arsine would be altered by an order of magnitude. Also it is unlikely that individual variability (i.e., variability in erythrocyte structure/function or response of the kidney to hemolysis) would have a significant impact on any of the proposed subcellular mechanisms of arsine toxicity. Only a twofold reduction in dosage is used to account for variability in sensitivity to the hemolytic response to some antimalarial drugs such as primaquine (Kellermeyer et al., 1962; Webster 1985). The steep exposure-response curves from animal data also affirm the limited variability in response and would appear to argue for no further reduction in the AEGL values. Finally, the AEGL-2 values were developed using a conservative estimate of a toxic response (no significant indication of hemolysis in mice exposed to arsine at 5 ppm for 1 h) and additional reduction of the values would seem unwarranted. The AEGL-2 values are shown in Table 2–8 and their derivations shown in Appendix A.

Exponential scaling (Cn×t=k; ten Berge et al. 1986) was used to derive the other exposure duration-specific values. The concentration exposure time relationship for many irritant and systemically acting vapors and gases may be described by Cn×t=k, where the exponent n ranges from 0.8 to 3.5 (ten Berge et al. 1986). In lieu of a definitive data set allowing empirical derivation of the exponent n, temporal scaling was performed, using n=3 when extrapolating to

Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×

TABLE 2–8 AEGL-2 for Arsine

AEGL Level

30 min

1 h

4 h

8 h

AEGL-2

0.21 ppm

0.7 mg/m3

0.17 ppm

0.5 mg/m3

0.04 ppm

0.1 mg/m3

0.03 ppm

0.1 mg/m3

shorter time points and n=1 when extrapolating to longer time points using the Cn×t=k equation.

7. DATA ANALYSIS AND PROPOSED AEGL-3

7.1. Human Data Relevant to AEGL-3

There are numerous case reports of human lethality resulting from acute exposure to arsine. Although these reports verify the extreme toxicity of arsine, with the erythrocyte as the primary target, and the propensity for delayed lethality due to renal failure, valid exposure data are lacking. Human lethality has been documented for cumulative exposures ranging from 375 to 7,500 ppm·min. Although an AEGL-3 could be derived based upon the human experience (Flury and Zernick 1931; Henderson and Haggard 1943, as cited in AIHA 1993), the resulting values are higher than those using animal data and are compromised by uncertainties regarding validity of exposure terms. More important, however, is the fact that the human data appear to be equivocal and lack verification.

7.2. Summary of Animal Data Relevant to AEGL-3

Lethality data are available for several animal species including rats, mice, monkeys, dogs, and cats. Cumulative exposures producing lethality range from 525 to 11,520 ppm·min, with the highest value representing a 24-h exposure to only 8 ppm.

7.3. Derivation of AEGL-3

The most definitive data set for deriving AEGL-3 values is that of Peterson and Bhattacharyya (1985), which provides exposure response data for mice exposed to arsine for 1 h at concentrations of 0, 5, 9, 11, 15, or 26 ppm. Al-

Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×

though the 26-ppm exposure resulted in 100% mortality within 4 d post-exposure, the 15-ppm exposure produced significant, hematologic changes. Therefore, these data affirm the steep exposure-response curve for arsine and provide a basis for a lethality threshold.

Although several data sets could be used to derive AEGL-3 values, the 1-h exposure data from the mouse study by Peterson and Bhattacharyya (1985) provided the most sound basis and were selected to derive AEGL-3 values. Due to the steep concentration-response curve for arsine, the 15-ppm exposure (where there was no lethality) was considered an estimate of the lethality threshold. An uncertainty factor of 30-fold was applied to account for interspecies extrapolation (10-fold) and intraspecies variability (3-fold) (see Section 6.3).

As described in Section 6.3, exponential scaling (Cn×t=k; ten Berge et al. 1986) was used to derive exposure duration-specific values.

The AEGL-3 values are shown in Table 2–9 and their derivations shown in Appendix A.

8. SUMMARY OF PROPOSED AEGLS

8.1.

AEGL Values and Toxicity Endpoints

The data used to derive exposure values for the various AEGL tiers are consistent with respect to the known target (erythrocytes) and effects (hemolysis and alteration of hematologic parameters resulting in renal failure and death) of arsine. The relationship among the three tiers of proposed AEGLs reflects the steep exposure-response relationship and extreme toxicity documented for arsine. It is apparent from the AEGL values that it is difficult to quantitatively differentiate a lethal exposure from one that produces serious but nonlethal effects. This lack of quantitative discrimination is also reflected in the overall database for arsine where there does not appear to be a well-defined exposure threshold between irreversible, nonlethal effects and lethality. It must also be noted that the reported odor threshold (0.5 ppm) is above the proposed AEGL-2 values. The approach used in the selection of the exposure concentrations and

TABLE 2–9 AEGL-3 for Arsine

AEGL Level

30 min

1 h

4 h

8 h

AEGL-3

0.63 ppm

2.0 mg/m3

0.5 ppm

1.6 mg/m3

0.13 ppm

0.4 mg/m3

0.06 ppm

0.2 mg/m3

Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×

the respective determinants for AEGL-2 (absence of significant hemolysis) and AEGL-3 (absence of lethal response) along the continuum of arsine toxicity and the approach employed for time scaling are considered sufficient for AEGLs that are protective of human health. Selection of uncertainty factors (10-fold for interspecies variability and 3-fold for protection of sensitive populations) are also considered sufficient for protection of human health.

A relational comparison of AEGL values for arsine is made in Table 2–10.

8.2. Comparison with Other Standards and Criteria

All currently available standards and guidelines are shown in Table 2–11. Emergency exposure limits (EELs) and continuous exposure limits (CELs) were previously derived by the Committee on Toxicology (reported in NRC 1984). Additionally, ACGIH TLV values, emergency response planning guideline (ERPG) values, NIOSH immediately dangerous to life and health (IDLH) values, and Dutch maximum allowable concentration (MAC) values have been published. Currently, no German MAK values are available. The AEGL values are consistent with, albeit somewhat lower, than currently established guidelines. The absence of AEGL-1 values is also consistent with the AIHA ERPG decision not to recommend ERPG-1 values.

8.3. Data Adequacy and Research Needs

The human experience is defined by only qualitative data. These data, however, affirm the extreme toxicity of arsine and the characteristic latency

TABLE 2–10 Relational Comparison of AEGL Values for Arsine

Classification

30 min

1 h

4 h

8 h

AEGL-1 (Nondisabling)

NR

NR

NR

NR

AEGL-2 (Disabling)

0.21 ppm

0.17 ppm

0.04 ppm

0.02 ppm

AEGL-3 (Lethal)

0.63 ppm

0.50 ppm

0.13 ppm

0.06 ppm

NR: Not recommended. Numeric values for AEGL-1 are not recommended because (1) data are not available, (2) an inadequate margin of safety exists between the derived AEGL-1 and the AEGL-2, or (3) the derived AEGL-1 is greater than the AEGL-2. Absence of an AEGL-1 does not imply that exposure below the AEGL-2 is without adverse effects.

Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×

TABLE 2–11 Extant Standards and Guidelines for Arsine

Guideline

30 min

1 h

4 h

8 h

AEGL-1 (Nondisabling)

NR

NR

NR

NR

AEGL-2 (Disabling)

0.21 ppm

0.17 ppm

0.04 ppm

0.02 ppm

AEGL-3 (Lethal)

0.63 ppm

0.50 ppm

0.13 ppm

0.06 ppm

ERPG-1a

 

NR

 

ERPG-2a

 

0.5 ppm

 

ERPG-3a

 

1.5 ppm

 

NRC CELb

 

1 ppm

 

0.05 ppm

NRC EELb

 

1 ppm

 

NIOSHc

3 ppm

 

ACGIH TLV-TWAd

 

0.05 ppm

MAC (Netherlands)e

 

0.2 mg/m3 (0.06 ppm)

NR: Not recommended. Numeric values for AEGL-1 are not recommended because (1) data are not available, (2) an inadequate margin of safety exists between the derived AEGL-1 and the AEGL-2, or (3) the derived AEGL-1 is greater than the AEGL-2. Absence of an AEGL-1 does not imply that exposure below the AEGL-2 is without adverse effects.

aAIHA 1993.

bNRC 1984.

cNIOSH 1997, a 15-min recommended exposure limit (REL) of 0.002 mg/m3 (0.0006 ppm) is also listed.

dACGIH 1999, 8-h time-weighted average (TWA) (impending change to 0.002 ppm proposed).

eMinistry of Social Affairs and Employment 1999.

period prior to renal failure. Quantitative animal data are available from several well-conducted peer-reviewed studies that demonstrate a toxic response similar to that observed for humans. There are no exposure-response data consistent with AEGL-1 level effects. This is likely a function of the progression of arsine-induced toxicity from essentially no observable effects to those effects indicative of a lethal response, and the consequent steep exposure-response relationship.

The inappropriateness of AEGL-1 values is affirmed by the steep dose-response for arsine and the inability, based upon available data, to imply a safe

Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×

exposure level for this chemical. The validity of AEGL-2 values that are markedly different from AEGL-3 values would be questionable because of the steep exposure-response curve for arsine. Additional data would be useful in providing greater precision in identifying thresholds between nonlethal and lethal exposures that may cause immediate or delayed lethality. The relatively low values of the proposed AEGLs reflect the steep exposure-concentration response for arsine-induced toxicity. Although based upon animal data, the values appear to be consistent with limited human exposure information to the extent that they offer a margin of safety.

As for most chemical hazard evaluations, the greatest data deficiency is the lack of definitive human exposure values. The animal data are adequate for demonstrating the extreme toxicity of arsine and the fact that there is little margin between exposures resulting in mild, reversible effects and lethality. There are no exposure-response data consistent with AEGL-1 level effects. This is likely a function of the rapid progression of arsine-induced toxicity from essentially no observable effects to that of a lethal response and the consequent steep exposure-response relationship. Additionally, studies addressing exposure concentration-duration relationships would allow for more precise temporal extrapolation for the development of AEGL values of varying exposure time durations.

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Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
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Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×

Appendixes

Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
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Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
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APPENDIX A

DERIVATION OF AEGL VALUES

Derivation of AEGL-1

Key study:

Blair et al. (1990a). Male and female B6C3F1 mice exposed to arsine at 0.5 ppm for 6 h exhibited no change in relative spleen weights or hematologic parameters and exhibited no overt signs of toxicity.

Uncertainty factors:

An uncertainty factor of 10 was used for interspecies variability to account for possible variability in arsine-induced hemolysis and progression to renal effects.

An uncertainty factor of 3 was used for intraspecies variability assuming limited individual variability in hemolytic response (described more fully under AEGL-2 and AEGL-3).

Calculations:

0.5 ppm/30=0.0167 ppm

C3×t=k

(0.0167 ppm)3×30 min=0.00167 ppm3·min

Time scaling:

Cn×t=k; data were unavailable for empirical derivation of a scaling factor. The concentration-exposure time relationship for many irritant and systemically acting vapors and gases may be described by Cn×t=k, where the exponent n ranges from 0.8 to 3.5 (ten Berge et al. 1986). In the absence of chemical-specific data, temporal scaling was performed using n=3 when extrapolating to shorter time points and n=1 when extrapolating to longer time points using the Cn×t=k equation.

NOTE: The following analysis served as an initial estimate for the AEGL-1. However, it is believed that it is not appropriate to derive AEGL-1 values for arsine because of the steep dose-response and the inability of available data to justify an exposure that would result in little or no toxic effect.

30-min AEGL-1:

C3×30 min=0.00167 ppm3·min

C=0.04 ppm

Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×

1-h AEGL-1:

C3×60 min=0.00167 ppm3·min

C=0.03 ppm

4-h AEGL-1:

C3×240 min=0.00167 ppm3·min

C=0.02 ppm

8-h AEGL-1:

C3×480 min=0.00167 ppm3·min

C=0.01 ppm.

Derivation of AEGL-2

Key study:

Peterson and Bhattacharyya (1985). NOAEL of 5 ppm based upon absence of hematologic changes in mice following 1-h exposure. At 15 ppm, hematologic changes were significant, and at 26 ppm there was 100% mortality.

Uncertainty factors:

An uncertainty factor of 10 was used for interspecies variability to account for possible variability in arsine-induced hemolysis and progression to renal effects. Uncertainty regarding intraspecies variability was limited to 3, because the hemolytic response is likely to occur to a similar extent and with similar susceptibility in most individuals. This was based on the consideration that physiologic parameters (e.g., absorption, distribution, metabolism, structure of the erythrocyte and its response to arsine, and renal responses) are not likely to vary among individuals of the same species to such an extent that the response severity to arsine would be altered by an order of magnitude. Individual variability (i.e., variability in erythrocyte structure/function or response of the kidney to hemolysis) would not likely have a significant impact on any of the proposed subcellular mechanisms of arsine toxicity. The steep exposure-response relationships from animal data also affirm the limited variability in response. Because of the forgoing considerations and the fact that the AEGL-2 values were developed from a data point showing no significant indication of hemolysis in mice exposed for 1 h to arsine at 5 ppm, the additional reduction of the values would seem unwarranted.

Calculations:

5 ppm/30=0.167 ppm

C3×t=k

Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×

 

(0.167 ppm)3×60 min=0.278 ppm3·min

C1×t=k

0.167 ppm×60 min=10 ppm·min

Time scaling:

Cn×t=k; data were unavailable for empirical derivation of a scaling factor. The concentration-exposure time relationship for many irritant and systemically acting vapors and gases may be described by Cn×t=k, where the exponent n ranges from 0.8 to 3.5 (ten Berge et al. 1986). In the absence of chemical-specific data, temporal scaling was performed using n=3 when extrapolating to shorter time points and n=1 when extrapolating to longer time points using the Cn×t=k equation.

30-min AEGL-2:

C3×30 min=0.278 ppm3·min

C=0.21 ppm

1-h AEGL-2:

C3×60 min=0.278 ppm3·min

C=0.17 ppm

4-h AEGL-2:

C1×240 min=10 ppm·min

C=0.04 ppm

8-h AEGL-2:

C1×480 min=10 ppm·min

C=0.02 ppm.

Derivation of AEGL-3

Key study:

Peterson and Bhattacharyya (1985), based upon an estimate of a lethality threshold (15 ppm) in mice exposed for 1 h. Hematologic changes were significant at 15 ppm, and at 26 ppm there was 100% mortality.

Uncertainty factors:

An uncertainty factor of 10 was retained for interspecies variability to account for possible variability in arsine-induced hemolysis and progression to renal effects. An uncertainty factor for intraspecies variability of 3 was used, because the hemolytic response is likely to occur to a similar extent and with similar susceptibility in most individuals. This was based on the consideration that physiologic parameters (e.g., absorption, distribution, metabolism, structure of

Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×

 

the erythrocyte and its response to arsine, and renal responses) would not vary among individuals of the same species to such an extent that the response severity to arsine would be altered by an order of magnitude. Individual variability (i.e., variability in erythrocyte structure/function or response of the kidney to hemolysis) is not likely to have a significant impact on any of the proposed subcellular mechanisms of arsine toxicity. The steep exposure-response relationships from animal data also affirm the limited variability in response. Because of the aforementioned considerations and the fact that the AEGL-3 values were developed based on a nonlethal toxic response (hemolysis in the absence of lethality), any additional reduction of the values would seem unwarranted.

Calculations:

15 ppm/30=0.5 ppm

C3×t=k

(0.5 ppm)3×60 min=7.5 ppm3·min

C1×t=k

0.5 ppm×60 min=30 ppm·min

Time scaling:

Cn×t=k; data were unavailable for empirical derivation of a scaling factor. The concentration-exposure time relationship for many irritant and systemically acting vapors and gases may be described by Cn×t=k, where the exponent n ranges from 0.8 to 3.5 (ten Berge et al. 1986). In the absence of chemical-specific data, temporal scaling was performed using n=3 when extrapolating to shorter time points and n=1 when extrapolating to longer time points using the Cn×t=k equation.

30-min AEGL-3:

C3×30 min=7.5 ppm3·min

C=0.63 ppm

1-h AEGL-3:

C3×60 min=7.5 ppm3·min

C=0.50 ppm

4-h AEGL-3:

C1×240 min=30 ppm·min

C=0.13 ppm

8-h AEGL-3:

C1×480 min=30 ppm·min

C=0.06 ppm.

Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×

APPENDIX B

TIME SCALING CALCULATIONS FOR ARSINE

Data were unavailable to empirically derive a scaling factor (n) for arsine. The concentration-exposure time relationship for many irritant and systemically acting vapors and gases may be described by Cn×t=k, where the exponent n ranges from 0.8 to 3.5 (ten Berge et al. 1986). In the absence of an empirically derived exponent (n), and to obtain AEGL values, temporal scaling was performed using n=3 when extrapolating to shorter time points and n=1 when extrapolating to longer time points using the Cn×t=k equation.

Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×

APPENDIX C

DERIVATION SUMMARY FOR ACUTE EXPOSURE GUIDELINES FOR ARSINE (CAS No. 7784–42–1)

AEGL-1 Values-Arsine

30 min

1 h

4 h

8 h

Not

Not

Not

Not

recommended

recommended

recommended

recommended

Reference: The available human and animal data indicate that there is very little margin between seemingly inconsequential exposures and lethal exposures. The mechanism of arsine toxicity (hemolysis and subsequent renal failure) and the fact that toxicity has been demonstrated at or below the odor threshold justify the inappropriateness of AEGL-1 values for any exposure period.

Test Species/Strain/Number: Not applicable

Exposure Route/Concentrations/Durations: Not applicable

Effects: Not applicable

Endpoint/Concentration/Rationale: Not applicable

Uncertainty Factors/Rationale: Not applicable

Modifying Factor: Not applicable (1)

Animal to Human Dosimetric Adjustment: Not applicable

Time Scaling: Not applicable

Data Adequacy: Numeric values for AEGL-1 are not recommended, because (1) data are not available, (2) an inadequate margin of safety exists between the derived AEGL-1 and the AEGL-2, or (3) the derived AEGL-1 is greater than the AEGL-2. Absence of an AEGL-1 does not imply that exposure below the AEGL-2 is without adverse effects.

Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×

AEGL-2 Values-Arsine

30 min

1 h

4 h

8 h

0.21 ppm

0.17 ppm

0.04 ppm

0.02 ppm

Reference: Peterson, D.P., and M.H.Bhattacharyya. 1985. Hematological responses to arsine exposure: quantitation of exposure response in mice. Fundam. Appl. Toxicol. 5:499–505

Test Species/Strain/Sex/Number: Female B6C3F1 mice, 8/group

Exposure Route/Concentrations/Durations: Inhalation: 0, 5, 9, 11, 15, or 26 ppm for 1 h

Effects:

hematocrit level (as % of controls)

5 ppm

no significant effects (determinant for AEGL-2)

9 ppm

80.2%

11 ppm

79.7%

15 ppm

61.4%

26 ppm

21.7% (100% mortality at 4 d post-exposure)

Endpoint/Concentration/Rationale: 5 ppm for 1 h considered as a no-observed-effect level (NOEL) for decreased hematocrit levels. A NOEL was used because of an extremely steep dose-response curve and the fact that the ultimate toxic effect, renal failure, is delayed for several days.

Uncertainty Factors/Rationale: Total uncertainty factor: 30

Interspecies: 10—The 10-min LC50 value for the monkey was about 60% of the rat value and one-third the rabbit value. The mouse data were used to calculate the AEGL levels, because the data exhibited a good exposure-response relationship and the endpoint of decreased hematocrit levels can be considered a sensitive indicator of arsine toxicity. In addition, arsine has an extremely steep dose-response relationship, allowing little margin in exposure between no effects and lethality.

Intraspecies: 3—An uncertainty factor of 3-fold was used, because the hemolytic response is likely to occur to a similar extent and with similar susceptibility in most individuals. This was based on the consideration that physiologic parameters (e.g., absorption, distribution, metabolism, structure of the erythrocyte and its response to arsine, and renal responses) are not likely to vary among individuals of the same species to such an extent that the response severity to arsine would be altered by an order of magnitude. Individual variability (i.e., variability in erythrocyte structure/function or response of the kidney to hemolysis)

Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×

also is not likely have a significant impact on any of the proposed subcellular mechanisms of arsine toxicity. The steep exposure-response curves derived from animal data also affirm the limited variability in response. Because of these considerations and the fact that the AEGL-2 values were developed using a toxic response indicative of no significant hemolysis in mice exposed for 1 h to arsine at 5 ppm, an additional reduction of the values would seem unwarranted.

Modifying Factor: Not applicable

Animal to Human Dosimetric Adjustment: None applied, insufficient data

Time Scaling: Cn×t=k, where n=1 or 3. The concentration-exposure time relationship for many irritant and systemically acting vapors and gases may be described by Cn×t=k, where the exponent n ranges from 0.8 to 3.5 (ten Berge et al. 1986). Temporal scaling was performed using n=3 when extrapolating to shorter time points and n=1 when extrapolating to longer time points using the Cn×t=k equation.

Data Adequacy: The study was considered adequate for AEGL-2 derivation. It was carefully designed and performed, used adequate numbers of animals, used an appropriate exposure regimen, and identified an endpoint consistent with the AEGL-2 definition and with the known effects of arsine.

Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×

AEGL-3 Values-Arsine

30 min

1 h

4 h

8 h

0.63 ppm

0.50 ppm

0.13 ppm

0.06 ppm

Reference: Peterson, D.P., and M.H.Bhattacharyya. 1985. Hematological responses to arsine exposure: quantitation of exposure response in mice. Fundam. Appl. Toxicol. 5:499–505

Test Species/Strain/Sex/Number: Female B6C3F1 mice, 8/group

Exposure Route/Concentrations/Durations: Inhalation: 0, 5, 9, 11, 15, or 26 ppm for 1 h

Effects:

hematocrit level (as % of controls) and lethality

5 ppm

no significant effects

9 ppm

80.2 % (no mortality)

11 ppm

79.7% (no mortality)

15 ppm

61.4% (no mortality) (determinant for AEGL-3)

26 ppm

21.7% (3/8 immediately following exposures; 100% mortality at 4 d post-exposure)

Endpoint/Concentration/Rationale: 15 ppm for 1 h induced a significant decrease in hematocrit levels that may be approaching a degree of hemolysis that can lead to renal failure. Given the steepness of the dose-response relationship this is justified as an estimate of the lethality threshold. An exposure of 26 ppm for 1 h resulted in 100% lethality.

Uncertainty Factors/Rationale: Total uncertainty factor: 30

Interspecies: 10—The 10-min LC50 value for the monkey was about 60% of the rat value and one-third the rabbit value. The mouse data were used to calculate the AEGL levels, because the data exhibited a good exposure-response relationship curve, and the endpoint of decreased hematocrit levels can be considered a sensitive indicator of arsine toxicity. In addition, arsine has an extremely steep dose-response relationship giving little margin between no effects and lethality.

Intraspecies: 3—Uncertainty regarding intraspecies variability was limited to 3, because the hemolytic response is likely to occur to a similar extent and with similar susceptibility in most individuals. This was based on the consideration that physiologic parameters (e.g., absorption, distribution, metabolism, structure of the erythrocyte and its

Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×

response to arsine, and renal responses) are not likely to vary among individuals of the same species to such an extent that the response severity to arsine would be altered by an order of magnitude. Individual variability (i.e., variability in erythrocyte structure/function or response of the kidney to hemolysis) also is not likely to have a significant impact on any of the proposed subcellular mechanisms of arsine toxicity. The steep exposure-response curves derived from animal data also affirm the limited variability in response. Because of these considerations and the fact that the AEGL-2 values were developed using a toxic response indicative of no significant hemolysis in mice exposed for 1 h to arsine at 5 ppm, additional reduction of the values would seem unwarranted.

Modifying Factor: Not applicable

Animal to Human Dosimetric Adjustment: None applied, insufficient data

Time Scaling: Cn×t=k, where n=1 or 3. The concentration-exposure time relationship for many irritant and systemically acting vapors and gases may be described by Cn×t=k, where the exponent n ranges from 0.8 to 3.5 (ten Berge et al. 1986). Temporal scaling was performed using n=3 when extrapolating to shorter time points and n=1 when extrapolating to longer time points using the Cn×t=k equation.

Data Adequacy: The study was considered adequate for AEGL-3 derivation. It was carefully designed and performed, used adequate numbers of animals, used an appropriate exposure regimen, and identified an endpoint consistent with AEGL-3 definition and with the known effects of arsine. The available data indicate that the exposure-response relationship for arsine is very steep, thereby justifying the approach taken to derive the AEGL-3 values.

Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×
Page 65
Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×
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×
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×
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Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×
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×
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Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
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Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×
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Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×
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×
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Suggested Citation:"Arsine: Acute Exposure Guideline Levels." National Research Council. 2000. Acute Exposure Guideline Levels for Selected Airborne Chemicals: Volume 1. Washington, DC: The National Academies Press. doi: 10.17226/10043.
×
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In the Bhopal disaster of 1984, approximately 2,000 residents living near a chemical plant were killed and 20,000 more suffered irreversible damage to their eyes and lungs following the accidental release of methyl isocyanate. This tragedy served to focus international attention on the need for governments to identify hazardous substances and assist local communities in planning how to deal with emergency exposures. Since 1986, the U.S. Environmental Protection Agency has been tasked with identifying extremely hazardous substances and, in cooperation with the Federal Emergency Management Agency and the Department of Transportation, assist local emergency response planners. The National Advisory Committee on Acute Exposure Guideline Levels for Hazardous Substances was established in 1995 to develop acute exposure guideline levels (AEGLs) for high priority toxic chemicals that could be released into the air from accidents at chemical plants, storage sites, or during transportation. This book reviews toxicity documents on five chemicals—chlorine, hydrogen chloride, hydrogen fluoride, toluene, and uranium hexafluoride—for their scientific validity, comprehensives, internal consistency, and conformance to the 1993 guidelines report.

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