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毛细管液相色谱和串联质谱法用于定量测定脑脊液中的脑啡肽。

Capillary liquid chromatography and tandem mass spectrometry for the quantification of enkephalins in cerebrospinal fluid.

作者信息

Sinnaeve Bart A, Storme Michael L, Van Bocxlaer Jan F

机构信息

Laboratorium voor Medische Biochemie en Klinische Analyse, Universiteit Gent, Gent, Belgium.

出版信息

J Sep Sci. 2005 Sep;28(14):1779-84. doi: 10.1002/jssc.200500114.

Abstract

A capillary LC-MS/MS system was evaluated for the absolute quantification of enkephalins in cerebrospinal fluid (CSF). On column focusing on a C18 trapping column, in-line with the analytical column, was used for preconcentration. Quantification was performed with a triple quadrupole instrument in the multiple reaction monitoring mode. Weighted linear regression analysis proves to be a good linearity in a dynamic range of two orders of magnitude. The method was validated, yielding calibration curves with correlation coefficients greater than 0.9914. Assay precision and accuracy were evaluated by direct injection of enkephalin fortified artificial CSF (aCSF) samples at three concentration levels. Mean accuracy of analysed concentrations was between 97.63 and 107.6%. LOD and LOQ were assessed at, respectively, 0.5 and 1 pmol/mL. Validation results show that it is feasible, with a capillary LC-MS/MS system, to quantify neuropeptides in the low femtomole range in aCSF. The obtained coefficients of variation, however, indicate that the use of appropriate isotopically labelled internal standards in neuropeptide quantification using narrow bore LC, combined with ESI-MS, may be highly beneficial.

摘要

对毛细管液相色谱-串联质谱(LC-MS/MS)系统进行了评估,以用于脑脊液(CSF)中脑啡肽的绝对定量分析。在与分析柱串联的C18捕集柱上进行柱上聚焦,用于预浓缩。使用三重四极杆仪器在多反应监测模式下进行定量分析。加权线性回归分析表明,在两个数量级的动态范围内具有良好的线性。该方法经过验证,得到的校准曲线相关系数大于0.9914。通过直接进样三个浓度水平的添加脑啡肽的人工脑脊液(aCSF)样品来评估分析的精密度和准确度。分析浓度的平均准确度在97.63%至107.6%之间。检测限(LOD)和定量限(LOQ)分别评估为0.5和1 pmol/mL。验证结果表明,使用毛细管LC-MS/MS系统在aCSF中对低飞摩尔范围内的神经肽进行定量分析是可行的。然而,所获得的变异系数表明,在使用窄径LC结合电喷雾电离质谱(ESI-MS)进行神经肽定量分析时,使用适当的同位素标记内标可能非常有益。

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