Acrylonitrile biotransformation in rats, mice, and chinese hamsters as influenced by the route of administration and by phenobarbital, SKF 525-A, cysteine, dimercaprol, or thiosulfate-Reference-Cited by-同舟云学术

Acrylonitrile biotransformation in rats, mice, and chinese hamsters as influenced by the route of administration and by phenobarbital, SKF 525-A, cysteine, dimercaprol, or thiosulfate

Published:1975-06 Issue:2 Volume:33 Page:151-161
ISSN:0340-5761
Container-title:Archives of Toxicology
language:en
Short-container-title:Arch. Toxicol.

Author:

Gut I.,Nerudová J.,Kopecký J.,Holeček V.

Publisher

Springer Science and Business Media LLC

Subject

Health, Toxicology and Mutagenesis,Toxicology,General Medicine

Link

http://link.springer.com/content/pdf/10.1007/BF00353240.pdf

Reference13 articles.

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2. Bickel, M. H., Weder, H. J.: Demethylation of imipramine in the rat as influenced by SKF 525-A and by different routes of administration. Life Sci. 7, 1223–1230 (1968)

3. Brieger, H., Rieders, F., Hodes, W. A.: Acrylonitrile: Spectrophotometric determination, acute toxicity, and mechanism of action. Arch. industr. Hyg. 6, 128–140 (1952)

4. Czajkowska, T.: Acrylonitrile metabolites excretion following a single dose. Med. Pracy 22, 381–385 (1971)

5. Dollery, C. T., Davies, D. S., Conolly, M. E.: Differences in the metabolism of drugs, depending upon their routes of administration. Ann. N.Y. Acad. Sci. 179, 108–112 (1971)

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