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Quantifying cartinina levels in dialysis patients.

机译:量化透析患者中​​的软骨素水平。

摘要

A method for quantifying the levels of concentration of free carnitine, total acylcarnitines and total carnitine in plasma samples of dialysis patients, using mass spectrometry cascade, said method comprising: obtaining a plurality of samples of calibration curve containing dialyzed plasma having mixed therein known concentrations of free carnitine; preparing a plurality of patient samples containing plasma collected from a patient and said samples of calibration curve for analysis, which comprises extracting the patient samples and samples of calibration curve with an alcohol solution containing labeled internal standards; analyzing said patient samples to quantify concentrations of free and acylcarnitine carnitine relative to internal to produce patient data patterns and analyzing said samples calibration curve to quantify free carnitine and acylcarnitines in relation to patterns internal to produce calibration curve data; comparing said patient data to said calibration curve data to obtain carnitine concentration data, said data including carnitine concentration free carnitine concentration, acetylcarnitine concentration and total acylcarnitines concentration for each patient sample; and correcting said free carnitine concentration and said acetylcarnitine concentration to obtain the concentration of free carnitine quantized concentration quantified total acylcarnitine, and concentration of total carnitine quantified for each patient sample, in which the correct concentration of free carnitine It takes into account the hydrolysis of acylcarnitines into free carnitine and the correcting acetylcarnitine concentration takes into account the interference of glutamic acid, and wherein the concentration quantified total carnitine is determined by adding said concentration quantified total acylcarnitines and the concentration of quantified free carnitine.
机译:一种使用质谱级联法定量分析透析患者血浆样品中游离肉碱,总酰基肉碱和总肉碱浓度水平的方法,所述方法包括:获得多个校准曲线样品,所述校准曲线样品中混合有已知浓度的透析血浆。游离肉碱;制备多个包含从患者体内收集的血浆的患者样品和所述校准曲线样品以进行分析,该方法包括:用含有标记的内标物的酒精溶液提取患者样品和校准曲线样品;分析所述患者样品以定量相对于内部的游离肉碱和酰基肉碱的浓度以产生患者数据模式,并且分析所述样品校准曲线以定量与内部模式相关的游离肉碱和酰基肉碱的浓度以产生校准曲线数据;比较所述患者数据与所述校准曲线数据以获得肉碱浓度数据,所述数据包括每个患者样品的肉碱浓度,游离肉碱浓度,乙酰肉碱浓度和总酰基肉碱浓度;并校正所述游离肉碱浓度和所述乙酰肉碱浓度,以获得游离肉碱的浓度,定量总酰基肉碱的定量浓度以及每个患者样品中定量的总肉碱浓度,其中游离肉碱的正确浓度考虑了酰基肉碱的水解加入游离肉碱,校正乙酰肉碱的浓度考虑了谷氨酸的干扰,其中定量总肉碱的浓度是通过将所述定量酰基总肉碱的浓度和定量游离肉碱的浓度相加而确定的。

著录项

  • 公开/公告号ES2336787T3

    专利类型

  • 公开/公告日2010-04-16

    原文格式PDF

  • 申请/专利权人 SIGMA-TAU PHARMACEUTICALS INC.;

    申请/专利号ES20030770386T

  • 发明设计人 CHACE DONALD H.;FORNASINI GIANFRANCO;

    申请日2003-09-23

  • 分类号G01N33/68;A61B;A61B1;G01N24;G01N33/92;

  • 国家 ES

  • 入库时间 2022-08-21 18:43:09

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