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化学发光法测定药物制剂中的链霉素及其在流动注射分析装置中的药代动力学研究中的应用。

Chemiluminescence determination of streptomycin in pharmaceutical preparation and its application to pharmacokinetic study by a flow injection analysis assembly.

机构信息

School of Pharmaceutical Science, Zhengzhou University, Zhengzhou 450001, China.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2013 Nov;115:823-8. doi: 10.1016/j.saa.2013.07.007. Epub 2013 Jul 11.

DOI:10.1016/j.saa.2013.07.007
PMID:23892344
Abstract

A novel and rapid method for the determination of streptomycin has been established by chemiluminescence (CL) based on significant intensity enhancement of streptomycin on the weak CL of N-bromosuccinimide (NBS) and eosin in alkaline medium. The method is simple, rapid and effective to determine streptomycin in the range of 8.0×10(-9)-1.0×10(-6)gmL(-1) with a determination limit of 2.25×10(-9)gmL(-1). The relative standard deviation is 1.95% for the determination of 2.0×10(-7)gmL(-1) streptomycin (n=11). The pharmacokinetics of streptomycin in plasma of rat coincides with the two-compartment open model. The T1/2α, T1/2β, CL/F, AUC(0-t), MRT, Tmax and Cmax were 18.83±1.24min, 82.14±3.07min, 0.0026±0.0011Lkg(-1)min(-1), 36044.50±105.02mgmin(-1)L(-1), 92.29±8.21min, 21.63±1.26min and 375.61±8.50μgmL(-1), respectively. There was no significant difference between the results obtained by CL and HPLC. The FI-CL method can be used to determine streptomycin in pharmaceutical preparation and biological samples. The established method is simple, rapid and sensitive without expensive instruments. The possible enhancement mechanism was also investigated.

摘要

建立了一种基于 N-溴代丁二酰亚胺(NBS)和曙红在碱性介质中微弱化学发光(CL)强度增强的新的快速测定链霉素的方法。该方法简单、快速、有效,可在 8.0×10(-9)-1.0×10(-6)gmL(-1)范围内测定链霉素,测定下限为 2.25×10(-9)gmL(-1)。对于 2.0×10(-7)gmL(-1)链霉素(n=11)的测定,相对标准偏差为 1.95%。链霉素在大鼠血浆中的药代动力学符合二室开放模型。T1/2α、T1/2β、CL/F、AUC(0-t)、MRT、Tmax和 Cmax 分别为 18.83±1.24min、82.14±3.07min、0.0026±0.0011Lkg(-1)min(-1)、36044.50±105.02mgmin(-1)L(-1)、92.29±8.21min、21.63±1.26min 和 375.61±8.50μgmL(-1)。CL 和 HPLC 两种方法的测定结果无显著性差异。FI-CL 法可用于测定药物制剂和生物样品中的链霉素。该方法简单、快速、灵敏,无需昂贵的仪器。还探讨了可能的增强机制。

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