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荧光薄层色谱法测定人血浆和尿液中游离及结合的普萘洛尔、萘氧乳酸和对羟基普萘洛尔

Fluorometric TLC determination of free and conjugated propranolol, naphthoxylactic acid, and p-hydroxypropranolol in human plasma and urine.

作者信息

Garceau Y, Davis I, Hasegawa J

出版信息

J Pharm Sci. 1978 Jun;67(6):826-31. doi: 10.1002/jps.2600670626.

Abstract

Sensitive, specific, and reproducible TLC methods are described for the determination of propranolol and its major metabolites in humans, conjugated propranolol, free and conjugated naphthoxylactic acid, and free and conjugated p-hydroxypropranolol. The drug or metabolites are extracted from plasma or urine with ether and applied to TLC plates of silica gel or microcrystalline cellulose. After development, the plates are scanned in a spectrodensitometer equipped to measure fluorescence in the UV and blue regions of the light spectrum. Quantitation is achieved by comparing the areas under the peaks obtained from the unknowns to those obtained from standards applied to the same plate. Limits of quantitation in plasma are: free propranolol, 2 ng/ml; free p-hydroxypropranolol, 10 ng/ml; conjugated propranolol, 15 ng/ml; total (free and conjugated) naphthoxylactic acid, 25 ng/ml; and conjugated p-hydroxypropranolol, 50 ng/ml. These methods were used to obtain plasma level data in a volunteer after one single dose of propranolol and in patients under propranolol therapy. The Rf values of some known metabolites of propranolol obtained in various TLC developing systems are also presented.

摘要

本文描述了灵敏、特异且可重复的薄层色谱(TLC)方法,用于测定人体中的普萘洛尔及其主要代谢物、结合型普萘洛尔、游离及结合型萘氧乳酸以及游离及结合型对羟基普萘洛尔。药物或代谢物用乙醚从血浆或尿液中提取,然后点样于硅胶或微晶纤维素TLC板上。展开后,将薄板在配备可测量光谱紫外和蓝光区域荧光的分光密度计中扫描。通过比较未知样品峰面积与同一薄板上标准品峰面积来进行定量。血浆中的定量限为:游离普萘洛尔2 ng/ml;游离对羟基普萘洛尔10 ng/ml;结合型普萘洛尔15 ng/ml;总(游离及结合)萘氧乳酸25 ng/ml;结合型对羟基普萘洛尔50 ng/ml。这些方法用于在一名志愿者单次服用普萘洛尔后以及在接受普萘洛尔治疗的患者中获取血浆水平数据。还给出了在各种TLC展开系统中获得的普萘洛尔一些已知代谢物的比移值(Rƒ值)。

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