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苯二氮䓬类药物:生物样品中其测定的样品制备及高效液相色谱法

Benzodiazepines: sample preparation and HPLC methods for their determination in biological samples.

作者信息

Samanidou Victoria F, Uddin Mohammad N, Papadoyannis Ioannis N

机构信息

Laboratory of Analytical Chemistry, Department of Chemistry, Aristotle University of Thessaloniki, Thessaloniki, GR-541 24, Greece.

出版信息

Bioanalysis. 2009 Jul;1(4):755-84. doi: 10.4155/bio.09.43.

Abstract

Benzodiazepines (BDZs) belong to a group of substances known for their sedative, antidepressive, muscle relaxant, tranquilizer, hypnotic and anticonvulsant properties. Their determination in biological fluids is essential in clinical assays as well as in forensics and toxicological studies. Researchers focus on the development of rapid, accurate, precise and sensitive methods for the determination of BDZs and their metabolites. A large number of analytical methods using different techniques have been reported, but none can be considered as the method of choice. BDZs are usually present at trace levels (microgram or nanogram per milliliter) in a complex biological matrix and the potentially interfering compounds must be isolated by various extraction techniques before analysis. An extended and comprehensive review is presented herein, focusing on sample preparation (pretreatment and extraction) and HPLC conditions applied by different authors. These methods enable bioanalysts to achieve detection limits down to 1-2 ng/ml using UV/diode array detection, readily available in most laboratories, and better than 1 ng/ml using electron capture detection, which is lower than that obtained using a nitrogen phosphorus detector. MS interfaced with electrospray ionization offered a similar sensitivity, while negative chemical ionization MS or sonic spray ionization MS provided sensitivity down to 0.1 ng/ml.

摘要

苯二氮䓬类药物(BDZs)属于一类以其镇静、抗抑郁、肌肉松弛、安定、催眠和抗惊厥特性而闻名的物质。在临床检测以及法医学和毒理学研究中,对其在生物体液中的测定至关重要。研究人员专注于开发快速、准确、精密和灵敏的方法来测定BDZs及其代谢物。已经报道了大量使用不同技术的分析方法,但没有一种可以被视为首选方法。BDZs通常以痕量水平(每毫升微克或纳克)存在于复杂的生物基质中,在分析之前,必须通过各种萃取技术分离潜在的干扰化合物。本文给出了一篇详尽全面的综述,重点关注不同作者所采用的样品制备(预处理和萃取)及高效液相色谱条件。这些方法使生物分析人员使用紫外/二极管阵列检测(大多数实验室都可轻易获得)能够达到低至1-2纳克/毫升的检测限,使用电子捕获检测则优于1纳克/毫升,该检测限低于使用氮磷检测器所获得的检测限。与电喷雾电离联用的质谱提供了类似的灵敏度,而负化学电离质谱或超声喷雾电离质谱的灵敏度低至0.1纳克/毫升。

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