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伏安法对抗生素药物头孢哌酮的定量研究及药代动力学研究。

Voltammetric studies on the antibiotic drug cefoperazone quantification and pharmacokinetic studies.

作者信息

Hammam E, El-Attar M A, Beltagi A M

机构信息

Chemistry Department, Faculty of Science, Tanta University, 31527 Tanta, Egypt.

出版信息

J Pharm Biomed Anal. 2006 Oct 11;42(4):523-7. doi: 10.1016/j.jpba.2006.05.002. Epub 2006 Jun 19.

Abstract

A fully validated simple, sensitive and selective square-wave stripping voltammetry procedure was described for the trace quantification of cefoperazone in bulk form, formulations and human serum/plasma. The procedure was based on reduction of the adsorbed drug onto a hanging mercury drop electrode. The procedural conditions were optimized as: frequency=60Hz, scan increment=8mV, pulse amplitude=25mV, preconcentration potential=-0.3V (versus Ag/Ag/KCl(s)), preconcentration duration=60-150s and an acetate buffer of pH 4.2 as a supporting electrolyte. A limit of detection of 4.5x10(-10)M and a limit of quantitation of 1.5x10(-9)M bulk cefoperazone were achieved following preconcentration of the drug onto the hanging mercury drop electrode for 150s. The proposed square-wave adsorptive cathodic stripping voltammetric procedure was successfully applied for trace quantification of cefoperazone in human serum and plasma. The achieved limits of detection and quantitation of the drug in human serum were 6x10(-10)M (0.375ngml(-1)) and 2x10(-9)M (1.250ngml(-1)), respectively. The pharmacokinetic parameters of cefoperazone in plasma of hospitalized volunteers were successfully estimated.

摘要

本文描述了一种经过充分验证的简单、灵敏且具选择性的方波溶出伏安法,用于头孢哌酮原料药、制剂及人血清/血浆中痕量定量分析。该方法基于将吸附在悬汞滴电极上的药物进行还原。优化后的实验条件为:频率 = 60Hz,扫描增量 = 8mV,脉冲幅度 = 25mV,预富集电位 = -0.3V(相对于Ag/Ag/KCl(s)),预富集时间 = 60 - 150s,以pH 4.2的醋酸盐缓冲液作为支持电解质。将药物在悬汞滴电极上预富集150s后,头孢哌酮原料药的检测限为4.5×10⁻¹⁰M,定量限为1.5×10⁻⁹M。所提出的方波吸附阴极溶出伏安法成功应用于人血清和血浆中头孢哌酮的痕量定量分析。该药物在人血清中的检测限和定量限分别为6×10⁻¹⁰M(0.375ng/ml⁻¹)和2×10⁻⁹M(1.250ng/ml⁻¹)。成功估算了住院志愿者血浆中头孢哌酮的药代动力学参数。

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