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首页> 外文期刊>Bioanalysis >Development of a UHPLC-MS/MS (SRM) method for the quantitation of endogenous glucagon and dosed GLP-1 from human plasma
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Development of a UHPLC-MS/MS (SRM) method for the quantitation of endogenous glucagon and dosed GLP-1 from human plasma

机译:用于定量内源性胰高血糖素的UHPLC-MS / MS(SRM)方法和来自人血浆的含量GLP-1的方法

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Aim: The performance of glucagon and GLP-1 immunoassays is often poor, but few sensitive LC-MS/MS methods exist as alternatives. Experimental: A multiplexed LC-MS/MS method using a 2D extraction technique was developed. Results: The method was established for the quantitation of endogenous glucagon (LLOQ: 15 pg/ml) and dosed GLP-1 (LLOQ: 25 pg/ml) in human plasma, and is the first such method avoiding immunoenrichment. Specificity of endogenous glucagon quantitation was assured using a novel approach with a supercharging mobile phase additive to access a sensitive qualifier SRM. Endogenous glucagon concentrations were within the expected range, and showed good reproducibility after extended sample storage. A cross-validation against established immunoassays using physiological study samples demonstrated some similarities between methods. Conclusion: The LC-MS/MS method offers a viable alternative to immunoassays for quantitation of endogenous glucagon, dosed glucagon and/or dosed GLP-1.
机译:目的:胰高血糖素和GLP-1免疫测定的性能往往差,但很少有敏感的LC-MS / MS方法作为替代品。实验:开发了使用2D提取技术的多路复用LC-MS / MS方法。结果:建立了用于定量内源性胰高血糖素(LLOQ:15 pg / mL)的方法,并在人血浆中定量GLP-1(LLOQ:25pg / mL),是第一种避免免疫激素的方法。使用一种新方法通过具有增压移动相添加剂的新方法确保内源性胰高血糖素定量的特异性,以进入敏感的限定符SRM。内源性胰高血糖素浓度在预期范围内,并且在延长样品储存后显示出良好的再现性。使用生理学研究样品对已建立的免疫测定的交叉验证证明了方法之间存在一些相似之处。结论:LC-MS / MS方法提供了可行的免疫测定可用于定量内源性胰高血糖素,给药胰高血糖素和/或给药GLP-1的可行替代品。

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