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[生物材料中促智药吡拉西坦的快速薄层光密度测定法]

[Fast thin-layer densitometric determination of the nootropic piracetam in biological material].

作者信息

Bockhard H, Oelschläger H, Pooth R

机构信息

Institut für Pharmazie, Friedrich-Schiller-Universität, Jena, Germany.

出版信息

Pharmazie. 1997 May;52(5):357-61.

PMID:9229717
Abstract

After oral doses of piracetam this drug is detectable in serum as well as in urine after formation of the red Fe(III)-hydroxamatecomplex by thin-layer densitometry. Detection in serum requires extraction with a mixture of dichloromethane/ methanol, while urine can be used directly after dilution. The limit of quantification in urine is 100 micrograms/ml and in serum 4.0 micrograms/ml. The new method was validated by HPLC. The coefficient of correlation was 0.9999% for determination in urine and 0.9986% for determination in serum.

摘要

口服吡拉西坦后,通过薄层光密度法形成红色Fe(III)-异羟肟酸络合物后,该药物在血清和尿液中均可检测到。血清检测需要用二氯甲烷/甲醇混合物萃取,而尿液稀释后可直接使用。尿液中的定量限为100微克/毫升,血清中的定量限为4.0微克/毫升。该新方法通过高效液相色谱法进行了验证。尿液测定的相关系数为0.9999%,血清测定的相关系数为0.9986%。

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引用本文的文献

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Development of new method for simultaneous analysis of piracetam and levetiracetam in pharmaceuticals and biological fluids: application in stability studies.药物及生物流体中吡拉西坦和左乙拉西坦同步分析新方法的开发:在稳定性研究中的应用
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Development and Validation of RP-LC Method for the Determination of Cinnarizine/Piracetam and Cinnarizine/Heptaminol Acefyllinate in Presence of Cinnarizine Reported Degradation Products.用于测定西桂嗪/吡拉西坦以及西桂嗪/海他明茶碱在存在西桂嗪报告降解产物的情况下的反相液相色谱法的开发与验证
Anal Chem Insights. 2013 Oct 7;8:99-106. doi: 10.4137/ACI.S12478. eCollection 2013.