Pollock G A, Kilgore W
J Toxicol Environ Health. 1980 Jan;6(1):127-40. doi: 10.1080/15287398009529836.
The 7-d urinary and fecal excretions of [14C]toxaphene and two isolated [14C]toxaphene fractions (polar fraction 7 and nonpolar fraction 2) were determined in orally dosed rats. The urinary, fecal, and total excretions of toxaphene were, respectively, 22.5, 35.7, and 58.2% of the administered dose. The total excretions of fractions 2 and 7 were, respectively, 69.4 and 65.0%, and the overall order of excretion was fraction 2 greater than toxaphene greater than fraction 7. All three groups had low toxaphene levels (below 0.2 ppm) in all tissues analyzed except for fat, where significant levels were detected. Hexane and chloroform extracts of the urine revealed that the activity was more polar than the parent material for all three groups. Apparently, toxaphene must be metabolized before it can be excreted in the urine. When fat extracts were analyzed by thin-layer chromatography and autoradiography, differences were found between the parent material and the extracted activity. There was an increase in polar activity in the residue obtained from toxaphene-treated rats. The fat from the fraction 2 group contained fraction 2 and two additional more polar spots, which represented about 11% of the total activity. The fat from the fraction 7 group also contained two additional spots, but they were less polar than fraction 7. Apparently, the metabolism of fraction 7 results in some products that are less polar and, perhaps, more persistent.
通过给大鼠口服给药,测定了[14C]毒杀芬以及两种分离得到的[14C]毒杀芬组分(极性组分7和非极性组分2)的7天尿液和粪便排泄情况。毒杀芬的尿液、粪便和总排泄量分别为给药剂量的22.5%、35.7%和58.2%。组分2和7的总排泄量分别为69.4%和65.0%,排泄的总体顺序为组分2>毒杀芬>组分7。除脂肪组织中检测到显著水平外,所有三组在所有分析组织中的毒杀芬水平均较低(低于0.2 ppm)。尿液的己烷和氯仿提取物显示,所有三组的活性均比母体物质极性更强。显然,毒杀芬在通过尿液排泄之前必须先进行代谢。当通过薄层色谱法和放射自显影法分析脂肪提取物时,发现母体物质和提取物活性之间存在差异。经毒杀芬处理的大鼠所获残渣中的极性活性有所增加。组分2组的脂肪中含有组分2以及另外两个极性更强的斑点,约占总活性的11%。组分7组的脂肪中也含有另外两个斑点,但它们的极性比组分7弱。显然,组分7的代谢产生了一些极性较弱、或许更持久的产物。