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美沙酮血浆蛋白结合:癌症中的改变及从α1-酸性糖蛋白上的置换

Methadone plasma protein binding: alterations in cancer and displacement from alpha 1-acid glycoprotein.

作者信息

Abramson F P

出版信息

Clin Pharmacol Ther. 1982 Nov;32(5):652-8. doi: 10.1038/clpt.1982.217.

Abstract

Because of their elevated concentrations of plasma alpha 1-acid glycoprotein (AAG), cancer patients had a lower free fraction of methadone in plasma than did members of a control group. This difference was not great (-20%), but there was a fourfold variation in free fraction among a group of 13 patients (0.064 to 0.23). The bound/free methadone concentration ratio correlated linearly with plasma AAG. The binding of methadone to AAG was characterized by two classes of binding sites, the more avid having an association constant of 4 X 10(5)M-1 and an N of 0.38. Methadone could be displaced from AAG binding sites by a number of drugs: propranolol, chlorpromazine, prochlorperazine, thioridazine, and imipramine. The concentrations required for significant displacement (27 microM), as well as the relatively low Ka for methadone, suggest that the free fraction of methadone will not be significantly affected by elevated methadone concentrations or through displacement by other drugs that also bind to AAG.

摘要

由于癌症患者血浆α1-酸性糖蛋白(AAG)浓度升高,其血浆中美沙酮的游离分数低于对照组成员。这种差异不大(-20%),但在一组13名患者中,游离分数存在四倍的差异(0.064至0.23)。美沙酮的结合/游离浓度比与血浆AAG呈线性相关。美沙酮与AAG的结合具有两类结合位点,亲和力较高的一类结合常数为4×10⁵M⁻¹,N值为0.38。美沙酮可被多种药物从AAG结合位点上置换下来:普萘洛尔、氯丙嗪、丙氯拉嗪、硫利达嗪和丙咪嗪。显著置换所需的浓度(27μM)以及美沙酮相对较低的解离常数表明,美沙酮的游离分数不会因美沙酮浓度升高或被其他也与AAG结合的药物置换而受到显著影响。

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