首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >A validated procedure for detection and quantitation of salvinorin a in pericardial fluid, vitreous humor, whole blood and plasma using solid phase extraction and gas chromatography-mass spectrometry
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A validated procedure for detection and quantitation of salvinorin a in pericardial fluid, vitreous humor, whole blood and plasma using solid phase extraction and gas chromatography-mass spectrometry

机译:使用固相萃取和气相色谱-质谱法检测和定量心包液,玻璃体液,全血和血浆中salvinorin a的有效方法

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摘要

The use of vitreous humor and pericardial fluid as alternative matrices to blood and plasma in the field of forensic toxicology is described to quantitate low levels of Salvinorin A using ethion as internal standard. The method was optimized and fully validated using international accepted guidelines. The developed methodology utilizes a solid phase extraction procedure coupled to gas chromatography mass spectrometry operated in the selected ion monitoring mode. The method was linear in the range of 5.0-100. ng/mL with determination coefficients higher than 0.99 in 100. μL of vitreous humor and in 250. μL of each matrix pericardial fluid, whole blood and plasma. The limits of detection and quantitation were experimentally determined as 5.0. ng/mL, intra-day precision, intermediate precision and accuracy were in conformity with the criteria normally accepted in bioanalytical method validation. The sample cleanup step presented mean efficiencies between 80 and 106% in the different biological specimens analyzed. According to the low volumes of samples used, and the low limits achieved using a single quadrupole mass spectrometer, which is available in most laboratories, we can conclude that the validated methodology is sensitive and simple and is suitable for the application in forensic toxicology laboratories for the routine analysis of Salvinorin A in both conventional and unconventional biological samples.
机译:在法医毒理学领域,玻璃体液和心包积液用作血液和血浆的替代基质已被描述为使用乙硫磷作为内标物来定量测定低含量的SalvinorinA。该方法已经过优化,并使用国际公认的准则进行了充分验证。所开发的方法利用固相萃取程序与在选定离子监测模式下运行的气相色谱质谱联用。该方法在5.0-100范围内是线性的。 ng / mL,在100.μL玻璃体液和250.μL每种基质心包液,全血和血浆中的测定系数均高于0.99。实验确定的检出限和定量限为5.0。 ng / mL,日内精密度,中间精密度和准确度均符合生物分析方法验证中通常接受的标准。在分析的不同生物样品中,样品净化步骤的平均效率在80%至106%之间。根据大多数实验室中可用的样品量少和使用单四极杆质谱仪所达到的下限,我们可以得出结论,已验证的方法是灵敏且简单的,适合用于法医毒理学实验室常规和非常规生物样品中Salvinorin A的常规分析。

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