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高效液相色谱-负离子串联质谱法测定人血浆中的普伐他汀

High-performance liquid chromatography coupled with negative ion tandem mass spectrometry for determination of pravastatin in human plasma.

作者信息

Zhu Zhimeng, Neirinck Len

机构信息

Pharmascience, 6111 Royalmount Ave., Suite 100, Quebec, H4P 2T4, Montreal, Canada.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2003 Jan 5;783(1):133-40. doi: 10.1016/s1570-0232(02)00526-3.

DOI:10.1016/s1570-0232(02)00526-3
PMID:12450532
Abstract

A new method, using high-performance liquid chromatography/ion electrospray (negative ion) mass spectrometry, has been developed for the determination of a hydrophilic liver-specific inhibitor of the enzyme 3-hydroxy-3-methylglutaryl coenzyme A reductase, pravastatin in human plasma. In this method, plasma samples were prepared by a solid-phase extraction on C(18) Bond Elut cartridge. Chromatography was carried out with a Zorbax C(8) column. Simple isocratic chromatography conditions were used. The method has been validated in a linear range of 0.25-300 ng/ml with a coefficient of variation of 0.6-3.4%. The overall recovery was 90.5% for pravastatin and 90.8% for the internal standard beta-hydroxy-lovastatin. The method is simple and reliable with a total run time of less than 2 min.

摘要

已开发出一种采用高效液相色谱/离子电喷雾(负离子)质谱法测定人血浆中3-羟基-3-甲基戊二酰辅酶A还原酶的亲水性肝脏特异性抑制剂普伐他汀的新方法。在此方法中,血浆样品通过在C(18) Bond Elut柱上进行固相萃取来制备。色谱分离采用Zorbax C(8)柱进行。使用简单的等度色谱条件。该方法在0.25 - 300 ng/ml的线性范围内得到验证,变异系数为0.6 - 3.4%。普伐他汀的总回收率为90.5%,内标β-羟基洛伐他汀的总回收率为90.8%。该方法简单可靠,总运行时间不到2分钟。

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