LINEAR ALKYLBENZENE SULFONATE (LAS) - UNEP Chemicals
LINEAR ALKYLBENZENE SULFONATE (LAS) - UNEP Chemicals
LINEAR ALKYLBENZENE SULFONATE (LAS) - UNEP Chemicals
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OECD SIDS <strong>LINEAR</strong> <strong>ALKYLBENZENE</strong> <strong>SULFONATE</strong> (<strong>LAS</strong>)<br />
serum protein and degeneration of the renal tubes. The 0.2% group showed<br />
increased weight of the cecum and slight degeneration of the renal tubes, the<br />
0.07% group showed no adverse effects related to the administration of <strong>LAS</strong>.<br />
The intake of <strong>LAS</strong> in the 0.07% group was about 40 mg/kg bw d.<br />
GLP: Yes [ ] No [X] ? [ ]<br />
Test substance: C10-14 <strong>LAS</strong>, sodium salt (CAS #69669-44-9). C10 10.6%, C11 34.1%, C12<br />
27.7%, C13 19.0%, C14 8.7%; average alkyl chain length = C11.8; mean<br />
molecular weight: 345.8.<br />
Remarks: Information as cited in IPCS document. This is a key study for repeated dose<br />
toxicity because it represents the lowest LOAEL (see SIAR Table 6).<br />
Reference: 1) European Commission. 2000a. Benzenesulfonic acid, C10-13-alkyl derivs.,<br />
sodium salts. Year 2000 CD-ROM edition.<br />
2) Yoneyama, M. Fujii, T., Ikawa, M., Shiba, H., Sakamoto, Y., Yano, N.,<br />
Kobayashi, H., Ichikawa, H. and Hiraga, K. 1972. Studies on the toxicity of<br />
synthetic detergents. (II) Subacute toxicity of linear and branched alkyl<br />
benzene sulfonates in rats. Ann. Rep. Tokyo Metrap. Res. Lab. Public<br />
Health. 24:409-440. (In Japanese). cited in IPCS (1996); Environmental<br />
Health Criteria 169: Linear Alkylbenzene Sulfonates (<strong>LAS</strong>) and Related<br />
Compounds. WHO, Geneva, Switzerland.<br />
Reliability: 4 This study is assigned a reliability score of 4 because the original report<br />
was not available for review. However, the study was evaluated by IPCS<br />
prior to inclusion in their criteria document.<br />
(g)<br />
Species/strain: Rat<br />
Sex: Female [ ]; Male [ ]; Male/Female [X]; No data [ ]<br />
Administration: gavage<br />
Exposure period: 10 weeks<br />
Doses: 50, 100 or 250 mg/kg bw d<br />
Control: Yes [X]; No [ ]; No data [ ];Concurrent no treatment [X];<br />
Concurrent vehicle [ ]; Historical [ ]<br />
LOEL: 50 mg/kg bw d<br />
Results: Histopathology was evaluated in the females only. At the highest dose level,<br />
the kidneys showed mild degeneration and desquamation of the tubular<br />
epithelium and there was a moderate degree of fatty change in the liver as<br />
well as proteinaceous degeneration. Sections of the intestine did not exhibit<br />
any significant histologic variation. Adenosine triphosphatase activity was<br />
inhibited with increasing dose in both sexes while alkaline phosphatase and<br />
acid phosphatase activities were increased with increasing dose. The activity<br />
of lactate dehydrogenase was significantly inhibited at all dose levels in<br />
females but was not measured in males. SGOT and SGPT were significantly<br />
decreased in females at 100 and 250 mg/kg/day and SGPT was inhibited in<br />
males at 250 mg/kg/day.<br />
Method: Twenty four male (50+/-5g) and 36 female (40+/-5g) rats were given daily<br />
oral (cannula) doses of <strong>LAS</strong> detergent solution (0, 50, 100 and 250 mg/kg)<br />
by gavage for 10 weeks. Animals were maintained on standard pellet diets<br />
and drinking water ad libitum. After 10 weeks, animals were fasted for 24<br />
hours and sacrificed. Liver, kidney, heart, and intestine were removed<br />
immediately, weighed, and parts sectioned for histological examinational.<br />
The remaining parts of the liver and kidney homogenized in ice cold 0.25 M<br />
sucrose solution using Potter-Elvehjem type homogenizer and 10% w/v<br />
homogenates were prepared for histopathology and enzyme analysis. The<br />
activities of adenosine triphoshatase (ATPase), acid phosphatase (ACP),<br />
alkaline phosphatase (ALP), glutamic oxaloacetic transaminase (GOT), and<br />
glutamic pyruvic transaminase (GPT) were determined in the homogenates.<br />
GLP: Yes [ ] No [X] ? [ ]<br />
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