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高效液相色谱法测定血清中噻氯匹定的优化方法。

Optimised method for determination of ticlopidine in serum by high performance liquid chromatography.

作者信息

Furlan G, Malusà N, Strohmayer A, Klugmann F B, Decorti G, Candussio L, Klugmann S

机构信息

Laboratorio di Tossicologia, Istituto di Medicina Legale e delle Assicurazioni, Ospedale Maggiore, Trieste.

出版信息

Farmaco. 1996 Nov;51(11):747-51.

PMID:9035381
Abstract

In this study we verified whether high performance liquid chromatography with UV detection (HPLC-UV) could be optimised and hence become a useful method for measuring ticlopidine concentrations in patient blood. The extraction step was improved by adding isoamylic alcohol in the extraction mixture, resulting in a better recovery. Moreover, the extraction efficiency was consistently ameliorated by evaporation to dryness of the organic extract; we could therefore utilise a lower (213 nm) wavelength, corresponding to the maximum of absorption, achieving a better sensitivity. With these technical improvements, the limit of quantitation is 0.02 microgram/ml, and the limit of detection is 0.01 microgram/ml, hence comparable to levels obtained with gas-liquid chromatography with nitrogen detection (GC-NPD). In addition, HPLC method, if compared with GC-NPD, is simpler and can be easily used for routine determinations of a lot of serum samples.

摘要

在本研究中,我们验证了配备紫外检测的高效液相色谱法(HPLC-UV)是否能够得到优化,从而成为一种测定患者血液中噻氯匹定浓度的有用方法。通过在萃取混合物中添加异戊醇改进了萃取步骤,回收率更高。此外,通过将有机萃取物蒸发至干,萃取效率持续提高;因此,我们可以使用对应最大吸收值的较低波长(213 nm),从而获得更高的灵敏度。通过这些技术改进,定量限为0.02微克/毫升,检测限为0.01微克/毫升,与配备氮检测的气液色谱法(GC-NPD)所获得的水平相当。此外,与GC-NPD相比,HPLC方法更简单,可轻松用于大量血清样品的常规测定。

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