2,4,5-三氯苯氧乙酸(2,4,5- t)在妊娠小鼠体内的代谢和分布。

R P Koshakji, M T Bush, R D Harbison
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引用次数: 0

摘要

孕鼠单次口服[羧基- 14c]2,4,5- t (100 mg/kg;1.22 μ Ci/mg),于妊娠第12天处死,0.25、0.5、2、24小时处死。采用溶剂萃取法、薄层色谱法和逆流分布法对母血、胚胎、胎盘和卵黄囊进行分析。以给药剂量/g组织的百分比表示,在母体血液、胎盘、卵黄囊和胚胎中发现的不变的2,4,5- t在0.25小时后分别为3,0.5,0.5和0.2%,在24小时后分别为4,2,2和0.5%。未检测到2,4,5- t的主要代谢物。尿液和粪便也被收集和分析。在7天内,尿液中的放射性基本消除,占给药剂量的69-78%。粪便中含有5-9%的剂量。在尿液中,2,4,5- t占剂量的35-44%,22-23%为极极性物质。粪便中不变的2、4、5-T为极性物质的3-5%和1-2%。给妊娠小鼠的2,4,5- t主要以2,4,5- t和极极性物质的形式分布和消除。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Metabolism and distribution of 2,4,5-trichlorophenoxyacetic acid (2,4,5-T) in pregnant mice.

Pregnant mice were treated with a single oral dose of [carboxy-14C]2,4,5-T (100 mg/kg; 1.22 mu Ci/mg) on day 12 of gestation and sacrificed after 0.25, 0.5, 2 and 24 hours. Maternal blood, embryos, placentas and yolk sacs were analyzed by solvent extraction, TLC, and countercurrent distribution. Expressed as percentage of the administered dose/g tissue, the unchanged 2,4,5-T found in maternal blood, placentas, yolk sacs, and embryos was 3, 0.5, 0.5, and 0.2%, respectively, after 0.25 hours, and 4, 2, 2, and 0.5%, respectively, after 24 hours. No major metabolites of 2,4,5-T were detected. Urine and feces were also collected and analyzed. Radioactivity was largely eliminated in the urine, 69-78% of the administered dose in 7 days. Feces contained 5-9% of the dose. In the urine unchanged 2,4,5-T accounted for 35-44% of the dose, and 22-23% as very polar material. Unchanged 2,4,5-T in the feces was 3-5% and 1-2% as polar material. 2,4,5-T administered to pregnant mice is largely distributed and eliminated as 2,4,5-T and very polar material.

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