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通过平衡透析法和脑脊液测量齐美利定和去甲齐美利定的蛋白结合率。

Zimelidine and norzimelidine protein binding measured by equilibrium dialysis and cerebrospinal fluid.

作者信息

Calil H M, Jostell K G, Cowdry R W, Potter W Z

出版信息

Clin Pharmacol Ther. 1982 Apr;31(4):522-7. doi: 10.1038/clpt.1982.70.

Abstract

Steady-state concentrations of a new antidepressant, zimelidine (ZIM), and its active metabolite, norzimelidine (NZIM), were measured in plasma and cerebrospinal fluid (CSF) in eight depressed patients. Free drug, as calculated from the ratio of CSF to plasma concentration, of ZIM was 8.4 +/- 1.8% and of NZIM was 18.3 +/- 2.8%. Equilibrium dialysis (ED) of plasma from the same patients on placebo yielded free fractions of 8.6 +/- 2.2% and 28.1 +/- 3.4% for the two compounds. alpha 1-Acid glycoprotein (alpha a-AG) was also measured in the same samples. Variation in free drug using either method was not great, but did modestly correlate with alpha 1-AG concentration in six of the eight patients in whom simultaneous placebo measures were available. Our results indicate that measurements in plasma or of free drug dependent on ED lead to erroneous conclusions regarding the proportion of free NZIM to ZIM. Considering the different potencies of the parent compound and active metabolite, this is an unusual problem.

摘要

在8名抑郁症患者中测量了新型抗抑郁药齐美利定(ZIM)及其活性代谢物去甲齐美利定(NZIM)在血浆和脑脊液(CSF)中的稳态浓度。根据脑脊液与血浆浓度之比计算得出,ZIM的游离药物比例为8.4±1.8%,NZIM为18.3±2.8%。对同一批患者服用安慰剂时的血浆进行平衡透析(ED),两种化合物的游离分数分别为8.6±2.2%和28.1±3.4%。同时还在相同样本中测量了α1-酸性糖蛋白(αa-AG)。使用两种方法测得的游离药物变化不大,但在有同时服用安慰剂测量数据的8名患者中的6名患者中,其与α1-AG浓度存在适度相关性。我们的结果表明,血浆测量或依赖平衡透析的游离药物测量会导致关于游离NZIM与ZIM比例的错误结论。考虑到母体化合物和活性代谢物的不同效力,这是一个不寻常的问题。

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