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WORKERS. THE VALUE OBTAINED WERE IN THE RANGE OF 0.14-7.00 PPM. THEEXCRETION OF THIODIGYLCOLIC ACID, MEASURED BY GC-MS ANALYSIS, AMOUNTED TO0.3-4.0 MG/L. [MUELLER G ET AL; INT ARCH OCCUP ENVIRON HEALTH 41 (3): 199(1978)]**PEER REVIEWED**The first step in biotransformation <strong>of</strong> ... vinyl chloride ... has beenproposed to involve microsomal oxidation leading to epoxide formationacross <strong>the</strong> double bond. ... /It has been/ suggested that <strong>the</strong> resultingoxiranes are highly reactive and <strong>the</strong>refore can covalently bind to nucleicacids with <strong>the</strong> eventual end result <strong>of</strong> mutations and cancer. [Klaassen,C.D., M.O. Amdur, Doull J. (eds.). Casarett and Doull's Toxicology. TheBasic Science <strong>of</strong> Poisons. 5th ed. New York, NY: McGraw-Hill,1995.750]**PEER REVIEWED**The metab &amp; pharmacokinetics <strong>of</strong> vinyl chloride (VC) have beenextensively studied in rodents &amp; humans, but <strong>the</strong> max velocity (Vmax)&amp; Michaelis constant (K(m)) for <strong>the</strong> activation <strong>of</strong> VC by microsomalmonooxygenases in vitro have not yet been determined. ... The epoxidation<strong>of</strong> VC by rat liver microsomes (adult Sprague-Dawley) at concns from 1 ppmto 10(6) ppm in <strong>the</strong> gas phase was measured. In <strong>the</strong> assay, <strong>the</strong> reactive VCmetabolites chloroethylene oxide &amp; 2-chloroacetaldehyde were trappedwith excess cAMP, yielding, 1,N6-e<strong>the</strong>no-cAMP (epsilon cAMP) ... . ...Activation <strong>of</strong> VC by rat liver microsomes followed Michaelis-Mentenkinetics with K(m) = 7.42 +/- 0.37 (+/- SD) microM &amp; Vmax = 4674 +/-46 pmol.mg protein-1.min-1. Inhibitor studies &amp; immunoinhibitionassays showed that VC was activated by cytochrome P450 (CYP) 2E1 down to 1ppm in <strong>the</strong> air phase. [el Ghissassi F et al; Biochem Pharmacol 55 (9):1445-1452 (1998)]**PEER REVIEWED**ABSORPTION, DISTRIBUTION & EXCRETION:FOLLOWING EXPOSURE OF MALE RATS BY INHALATION TO 10 PPM (14)C VINYLCHLORIDE FOR 6 HOURS, URINARY (14)C ACTIVITY AND EXPIRED VINYL CHLORIDECOMPRISED 68 AND 2%, RESPECTIVELY, OF THE RECOVERED RADIOACTIVITY; AFTEREXPOSURE TO 1000 PPM (14)C VINYL CHLORIDE, THE PROPORTION OF RADIOACTIVITYIN THE URINE WAS LOWER AND THAT EXPIRED AS VINYL CHLORIDE HIGHER,REPRESENTING 56 AND 12%, RESPECTIVELY ... . [IARC. Monographs on <strong>the</strong>Evaluation <strong>of</strong> <strong>the</strong> Carcinogenic Risk <strong>of</strong> Chemicals to Man. Geneva: WorldHealth Organization, International Agency for Research on Cancer,1972-PRESENT. (Multivolume work).V19 392 (1979)]**PEER REVIEWED**Male Sprague-Dawley rats were given single oral doses (gavage) <strong>of</strong> (14)Cvinyl chloride at 0.05, 1.0 or 100 mg/kg, ... routes and rates <strong>of</strong>elimination <strong>of</strong> (14)C activity were followed for 72 hr. ... Of <strong>the</strong> samplesexamined (liver, skin, plasma, muscle, lung, fat, and carcass), liverretained <strong>the</strong> greatest percentage <strong>of</strong> admin radioactivity at all doses.[Watanabe PG et al; Toxicol Appl Pharmacol 36: 339-52 (1976) as cited inUSEPA; Office <strong>of</strong> Drinking Water; Criteria Document (Draft): Vinyl Chloridep.IX-3 (1983)]**PEER REVIEWED**Experiments with volunteers showed that 42% <strong>of</strong> an inhaled dose <strong>of</strong> vinylchloride ... was retained in <strong>the</strong> lung. This value was independent <strong>of</strong> <strong>the</strong>concn <strong>of</strong> vinyl chloride in <strong>the</strong> air. Elim <strong>of</strong> vinyl chloride through <strong>the</strong>lung was negligible since its concn in expired air decreased immediatelyafter cessation <strong>of</strong> exposure. [Krajewski J et al; Br J Ind Med 37 (4):373-4 (1980)]**PEER REVIEWED**ORAL DOSES OF 0.05-1.0 MG/KG IN RATS ... PULMONARY EXCRETION WAS

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