无毛豚鼠经皮吸收时苯佐卡因的代谢:乙酰苯佐卡因的形成和活性。

M E Kraeling, R J Lipicky, R L Bronaugh
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引用次数: 16

摘要

在体外无毛豚鼠体内研究了剂量和酶抑制对苯佐卡因经皮吸收代谢的影响。在2微克/平方厘米剂量水平下,苯佐卡因被乙酰转移酶迅速吸收并广泛代谢(80%)。当苯佐卡因剂量增加到40和200微克/平方厘米时,苯佐卡因的n -乙酰化率分别下降到44%和34%,表明乙酰转移酶系统饱和。应用苯佐卡因后的总14C吸收在对照组和酶抑制皮肤之间没有显著差异,因此似乎不受经皮渗透过程中苯佐卡因代谢程度的影响。对于经皮吸收的治疗剂量苯佐卡因,皮肤提供了显著的首过代谢效应,形成的初级代谢物乙酰苯佐卡因具有生物活性。
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Metabolism of benzocaine during percutaneous absorption in the hairless guinea pig: acetylbenzocaine formation and activity.
The effect of dose and enzymatic inhibition on the percutaneous absorption and metabolism of benzocaine was studied in vitro in the hairless guinea pig. At the dose level of 2 micrograms/cm2, benzocaine was rapidly absorbed and extensively metabolized (80%) by acetyltransferase. As the applied dose of benzocaine was increased to 40 and 200 micrograms/cm2, N-acetylation of benzocaine decreased to 44 and 34%, respectively, suggesting saturation of the acetyltransferase system. Total 14C absorption after benzocaine application was not significantly different between control and enzyme-inhibited skin and therefore does not appear to be affected by the extent of benzocaine metabolism during percutaneous penetration. Skin provides a significant first-pass metabolic effect for therapeutic doses of percutaneously absorbed benzocaine, and the primary metabolite formed, acetylbenzocaine, is biologically active.
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