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An improved reference measurement procedure for triglycerides and total glycerides in human serum by isotope dilution gas chromatography-mass spectrometry

机译:同位素稀释气相色谱-质谱法测定人血清中甘油三酸酯和总甘油酯的参考方法改进

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Background: Triglycerides are widely tested in clinical laboratories using enzymatic methods for lipid profiling. As enzymatic methods can be affected by interferences from biological samples, this together with the non-specific nature of triglycerides measurement makes it necessary to verify the accuracy of the test results with a reference measurement procedure. Several such measurement procedures had been published. These procedures generally involved lengthy and laborious sample preparation steps. In this paper, an improved reference measurement procedure for triglycerides and total glycerides was reported which simplifies the sample preparation steps and greatly shortens the time taken. Methods: The procedure was based on isotope dilution gas chromatography-mass spectrometry (ID GC-MS) with tripalmitin as the calibration standard. Serum samples were first spiked with isotope-labeled tripalmitin. For the measurement of triglycerides, the serum samples were subjected to lipid extraction followed by separation of triglycerides from diglycerides and monoglycerides. Triglycerides were then hydrolyzed to glycerol, derivatized and injected into the GC-MS for quantification. For the measurement of total glycerides, the serum samples were hydrolyzed directly and derivatized before injection into the GC-MS for quantification. Results: All measurement results showed good precision with CV <. 1%. A certified reference material (CRM) of lipids in frozen human serum was used to verify the accuracy of the measurement. The obtained values for both triglycerides and total glycerides were well within the certified ranges of the CRM, with deviation <. 0.4% from the certified values. The relative expanded uncertainties were also comparable with the uncertainties associated with the certified values of the CRM. The validated procedure was used in an External Quality Assessment (EQA) Program organized by our laboratory to establish the assigned values for triglycerides and total glycerides.
机译:背景:甘油三酸酯已在临床实验室中使用酶促方法进行脂质谱分析得到了广泛测试。由于酶促方法可能会受到生物样品干扰的影响,因此,再加上甘油三酸酯测量的非特异性,使得有必要使用参考测量程序来验证测试结果的准确性。已经发布了几种这样的测量程序。这些程序通常涉及冗长而费力的样品制备步骤。本文报道了一种改进的甘油三酸酯和总甘油酯参考测量程序,该程序简化了样品制备步骤并大大缩短了时间。方法:该方法基于同位素稀释气相色谱-质谱法(ID GC-MS),以三棕榈精为标准品。血清样品首先用同位素标记的三棕榈精蛋白加标。为了测量甘油三酸酯,对血清样品进行脂质提取,然后从甘油二酸酯和甘油单酸酯中分离甘油三酸酯。然后将甘油三酸酯水解为甘油,进行衍生化,然后注入GC-MS中进行定量。为了测量总甘油酯,将血清样品直接水解并衍生化,然后注入GC-MS进行定量。结果:所有测量结果在CV <时均显示出良好的精度。 1%冷冻人血清中脂质的认证参考物质(CRM)用于验证测量的准确性。甘油三酸酯和总甘油酯的获得值均在CRM的认证范围内,偏差<。认证值的0.4%。相对扩展的不确定性也可以与CRM认证值相关的不确定性进行比较。经验证的程序用于我们实验室组织的外部质量评估(EQA)计划中,以建立甘油三酸酯和总甘油酯的分配值。

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