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采用柱后三(2,2'-联吡啶)钌(III)化学发光检测法对新型红霉素衍生物EM523及其在人血浆和尿液中的主要代谢产物进行高灵敏度高效液相色谱测定方法。

Highly sensitive high-performance liquid chromatographic determination method for a new erythromycin derivative, EM523, and its major metabolites in human plasma and urine using post-column tris(2,2'-bipyridine) ruthenium(III) chemiluminescence detection.

作者信息

Monji H, Yamaguchi M, Aoki I, Ueno H

机构信息

Takeda Analytical Research Laboratories Ltd., Osaka, Japan.

出版信息

J Chromatogr B Biomed Sci Appl. 1997 Mar 7;690(1-2):305-13. doi: 10.1016/s0378-4347(96)00412-4.

DOI:10.1016/s0378-4347(96)00412-4
PMID:9106057
Abstract

A method for the simultaneous determination of de(N-methyl)-N-ethyl-8,9 -anhydroerythromycin A 6,9-hemiacetal (EM523, I) and its three metabolites in human plasma and urine has been developed using high-performance liquid chromatography (HPLC) with chemiluminescence (CL) detection. Plasma and urine samples spiked with erythromycin as an internal standard were extracted with a mixture of dichloromethane and diethyl ether under alkaline conditions. The organic layer was evaporated under a stream of nitrogen gas. The reconstituted sample was injected into an HPLC apparatus and separated on an ODS column using a gradient elution method. The eluate was reacted on-line with a mixture of tris(2,2'-bipyridine) ruthenium(II) and peroxodisulfate, and the generated CL intensity was detected. Optimization of the CL reaction conditions resulted in a sensitive and stable CL intensity for the determination of I and its metabolites. The recovery of each compound from human plasma and urine, and the sensitivity, linearity, accuracy and precision of the method were satisfactory. The lower limits of quantitation for each compound using 0.2 ml of plasma and 0.1 ml of urine were 1 and 10 ng/ml, respectively. This method has been used for the determination of 1 in samples from clinical trials.

摘要

已开发出一种使用高效液相色谱(HPLC)结合化学发光(CL)检测法同时测定人血浆和尿液中去(N - 甲基)-N - 乙基 - 8,9 - 脱水红霉素A 6,9 - 半缩醛(EM523,I)及其三种代谢物的方法。加入红霉素作为内标的血浆和尿液样品在碱性条件下用二氯甲烷和乙醚的混合物萃取。有机层在氮气流下蒸发。将重构后的样品注入HPLC仪器中,使用梯度洗脱法在ODS柱上进行分离。洗脱液与三(2,2'-联吡啶)钌(II)和过二硫酸盐的混合物进行在线反应,并检测产生的CL强度。CL反应条件的优化为测定I及其代谢物产生了灵敏且稳定的CL强度。各化合物在人血浆和尿液中的回收率以及该方法的灵敏度、线性、准确度和精密度均令人满意。使用0.2 ml血浆和0.1 ml尿液时,各化合物的定量下限分别为1和10 ng/ml。该方法已用于测定临床试验样品中的I。

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