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男性志愿者中毒莠定的药代动力学

Pharmacokinetics of picloram in male volunteers.

作者信息

Nolan R J, Freshour N L, Kastl P E, Saunders J H

出版信息

Toxicol Appl Pharmacol. 1984 Nov;76(2):264-9. doi: 10.1016/0041-008x(84)90007-3.

Abstract

The fate of picloram (4-amino-3,5,6-trichloropicolinic acid), an active ingredient in TORDON brand herbicides, was defined in 6 healthy male volunteers following single po doses of 5.0 and 0.5 mg/kg, and a dermal dose of 2.0 mg/kg. Picloram was administered orally as the sodium salt in grape juice. The dermal dose was applied to the volunteers' backs as the free acid dissolved in ethanol. The data indicate picloram was rapidly absorbed from the gastrointestinal tract (t1/2 = 20 min) and rapidly excreted unchanged in the urine. Over 90% of the po dose was recovered as unchanged picloram in the urine excreted through 72 hr; most of the dose (greater than 75%) was excreted within 6 hr and the remainder was excreted with an average half-life of 27 hr. By comparison picloram was slowly absorbed through the skin (t1/2 = 12 hr) and, based on the quantity of picloram excreted in the urine, only a small fraction (0.2%) of the picloram applied to the skin was absorbed. These data indicate that picloram because of its rapid excretion has a low potential to accumulate in man during repeated or prolonged exposures. In addition, picloram was poorly absorbed through human skin and it is unlikely that acutely toxic quantities will be absorbed by this route.

摘要

毒莠定(4-氨基-3,5,6-三氯吡啶甲酸)是TORDON牌除草剂中的活性成分,对6名健康男性志愿者进行单剂量口服5.0毫克/千克和0.5毫克/千克以及经皮给予2.0毫克/千克剂量后,确定了其代谢情况。毒莠定以钠盐形式混于葡萄汁中口服给药。经皮剂量是以溶解于乙醇中的游离酸形式涂抹在志愿者背部。数据表明毒莠定可迅速从胃肠道吸收(t1/2 = 20分钟),并迅速以原形经尿液排出。口服剂量的90%以上在72小时内以原形毒莠定形式从尿液中回收;大部分剂量(超过75%)在6小时内排出,其余部分以平均半衰期27小时排出。相比之下,毒莠定经皮肤吸收缓慢(t1/2 = 12小时),根据尿液中排出的毒莠定数量,涂抹在皮肤上的毒莠定只有一小部分(0.2%)被吸收。这些数据表明,由于毒莠定排泄迅速,在反复或长期接触期间在人体内蓄积的可能性较低。此外,毒莠定经人体皮肤吸收较差,不太可能通过该途径吸收到急性中毒量。

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