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一种用于定量测定大鼠血浆中地高辛的快速灵敏的液相色谱/串联质谱分析法。

A rapid and sensitive LC/MS/MS assay for quantitative determination of digoxin in rat plasma.

作者信息

Yao Ming, Zhang Hongjian, Chong Saeho, Zhu Mingshe, Morrison Richard A

机构信息

Department of Metabolism and Pharmacokinetics, Bristol-Myers Squibb Pharmaceutical Research Institute, F13-07, PO Box 4000, Princeton, NJ 08543, USA.

出版信息

J Pharm Biomed Anal. 2003 Aug 21;32(6):1189-97. doi: 10.1016/s0731-7085(03)00050-5.

Abstract

Digoxin is a cardiac glycoside that is widely used for the treatment of congestive heart failure. To evaluate pharmacokinetics of digoxin in rats, a sensitive LC/MS/MS assay was developed and validated for the determination of digoxin concentration in rat plasma. For detection, a Sciex API3000 LC/MS/MS with atmospheric pressure ionization (API) mass spectrometry turbo ion spray inlet in the positive ion-multiple reaction monitoring mode was used to monitor precursor-->product ions of m/z 798.6-->651.6 for digoxin and m/z 577.6-->433.3 for oleandrin, the internal standard (IS). The standard curve was linear (r(2)>or=0.999) over the digoxin concentration range of 0.1-100 ng/ml in plasma for digoxin. The mean predicted concentrations of the quality control samples deviated by <5.8% from the corresponding nominal values; the intra-assay and inter-assay precision of the assay were within 8.6% relative standard deviation. At the lower limit of quantitation (LLQ) of 0.1 ng/ml, the mean deviation of predicted concentrations from the nominal value was within 3.7%. The extraction recoveries of digoxin and internal standard were 82.7+/-3.9 and 105.9+/-2.3%, respectively. The present method was successfully applied to characterization of pharmacokinetic profiles of digoxin in rats after oral administration.

摘要

地高辛是一种强心苷,广泛用于治疗充血性心力衰竭。为评估地高辛在大鼠体内的药代动力学,开发并验证了一种灵敏的液相色谱-串联质谱(LC/MS/MS)分析法,用于测定大鼠血浆中的地高辛浓度。检测时,使用配备大气压电离(API)质谱涡轮离子喷雾进样口的Sciex API3000 LC/MS/MS,在正离子多反应监测模式下监测地高辛的m/z 798.6→651.6的前体离子→产物离子以及内标(IS)夹竹桃苷的m/z 577.6→433.3的前体离子→产物离子。地高辛在血浆中的浓度范围为0.1 - 100 ng/ml时,标准曲线呈线性(r(2)≥0.999)。质控样品的平均预测浓度与相应标称值的偏差<5.8%;该分析方法的批内和批间精密度在相对标准偏差8.6%以内。在定量下限(LLQ)为0.1 ng/ml时,预测浓度与标称值的平均偏差在3.7%以内。地高辛和内标的提取回收率分别为82.7±3.9%和105.9±2.3%。本方法成功应用于口服给药后大鼠体内地高辛药代动力学特征的表征。

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