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高效液相色谱法测定人母乳中的曲马多

HPLC determination of tramadol in human breast milk.

作者信息

Kmetec Vojko, Roskar Robert

机构信息

Department of Biopharmaceutics and Pharmacokinetics, Faculty of Pharmacy, Askerceva 7, 1000 Ljubljana, Slovenia.

出版信息

J Pharm Biomed Anal. 2003 Aug 8;32(4-5):1061-6. doi: 10.1016/s0731-7085(03)00209-7.

Abstract

Tramadol is a centrally acting analgesic used for prevention and treatment of moderate to severe pain. It is estimated that 0.1% of the administered dose passes into breast milk causing potentially unwanted effects in nursing babies. Pharmacokinetically, breast milk is supposed to be a separate compartment into which the drug is excreted-mainly by passive diffusion. Due to a complex composition of breast milk, a suitable sample preparation procedure is needed with a subsequent chromatographic analysis for drug determination. Among several sample cleanup procedures tested we chose the liquid-liquid extraction procedure using n-hexane as an organic phase with back extraction into aqueous phase since it was considered the most suitable and the most compatible with the subsequent HPLC analysis. The precision and the reproducibility of the method were improved approximately two times by using metoprolol as an internal standard thus making the method also more robust with regard to a variable composition of milk samples. These characteristics, together with low detection limit and short analysis time, proved that the developed method is suitable for monitoring of tramadol in human breast milk.

摘要

曲马多是一种中枢性镇痛药,用于预防和治疗中度至重度疼痛。据估计,给药剂量的0.1%会进入母乳,对哺乳期婴儿产生潜在不良影响。从药代动力学角度来看,母乳被认为是一个独立的隔室,药物主要通过被动扩散排泄到其中。由于母乳成分复杂,需要一个合适的样品制备程序,随后进行色谱分析以测定药物。在测试的几种样品净化程序中,我们选择了以正己烷为有机相的液-液萃取程序,并反萃取到水相中,因为它被认为是最合适的,并且与随后的高效液相色谱分析最兼容。通过使用美托洛尔作为内标,该方法的精密度和重现性提高了约两倍,从而使该方法在母乳样品成分可变的情况下也更稳健。这些特性,连同低检测限和短分析时间,证明所开发的方法适用于监测人母乳中的曲马多。

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