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通过对酶促衍生异麦芽糖进行液相色谱-串联质谱分析,鉴定并定量测定人尿液中的血浆容量扩充剂右旋糖酐。

Identification and quantification of the plasma volume expander dextran in human urine by liquid chromatography-tandem mass spectrometry of enzymatically derived isomaltose.

作者信息

Guddat Sven, Thevis Mario, Schänzer Wilhelm

机构信息

Institute of Biochemistry, German Sport University, Cologne, Germany.

出版信息

Biomed Chromatogr. 2005 Dec;19(10):743-50. doi: 10.1002/bmc.509.

Abstract

Plasma volume expanders are used in sports in order to control haematological parameters and/or to mask erythropoietin (EPO) misuse. A reliable method based on liquid chromatography-tandem mass spectrometry (LC-MS/MS) was developed for doping control purposes, enabling the identification and quantification of the plasma volume expander dextran in human urine. The dextran polymer was enzymatically hydrolysed by alpha-1,6-glucosidase (dextranase) followed by acetylation of the generated isomaltose subunits, allowing the chromatographic separation of different disaccharides, such as lactose, saccharose and isomaltose, as well as the identification and quantification of the analyte in human urine. The method was used to determine the basal concentration of isomaltose resulting from the enzymatic hydrolysis of polymeric 1,6-linked glucose in 238 routine doping control samples. In addition the concentration of dextran measured as isomaltose was estimated in seven urine specimens obtained from patients treated with dextran. Calibration curves for dextran were linear and reproducible. The inter- and intra-assay coefficients of variation for dextran ranged from 4.9 to 7.3% at three concentration levels between 53 and 1186 microg/mL. Recovery ranged from 97 to 112% (mean 106.9%). The assay limit of detection was 3.8 microg/mL and the lower limit of quantification was 12.5 microg/mL. In 96% of the investigated doping control samples, the concentrations of isomaltose were below the LLOQ of 12.5 microg/mL. Even the highest concentrations were approximately 100-300-fold lower than concentrations found in urine samples of patients after intravenous application of dextran. The presented results demonstrate the capability and reliability of the developed LC-MS/MS method for the identification and quantification of dextran in human urine and can be regarded as a method revealing the misuse of dextran in sports.

摘要

血浆容量扩充剂被用于体育运动中,以控制血液学参数和/或掩盖促红细胞生成素(EPO)的滥用情况。为了进行兴奋剂检测,开发了一种基于液相色谱-串联质谱法(LC-MS/MS)的可靠方法,可对人尿中的血浆容量扩充剂右旋糖酐进行鉴定和定量。右旋糖酐聚合物经α-1,6-葡萄糖苷酶(右旋糖酐酶)酶解,随后对生成的异麦芽糖亚基进行乙酰化,从而实现不同二糖(如乳糖、蔗糖和异麦芽糖)的色谱分离,以及人尿中分析物的鉴定和定量。该方法用于测定238份常规兴奋剂检测样品中由聚合1,6-连接葡萄糖酶解产生的异麦芽糖的基础浓度。此外,还对7份来自接受右旋糖酐治疗患者的尿液标本中以异麦芽糖形式测得的右旋糖酐浓度进行了估算。右旋糖酐的校准曲线呈线性且具有可重复性。在53至1186微克/毫升的三个浓度水平下,右旋糖酐的批间和批内变异系数在4.9%至7.3%之间。回收率在97%至112%之间(平均为106.9%)。检测限为3.8微克/毫升,定量下限为12.5微克/毫升。在96%的受调查兴奋剂检测样品中,异麦芽糖浓度低于12.5微克/毫升的定量下限。即使是最高浓度也比静脉注射右旋糖酐后患者尿液样本中的浓度低约100至300倍。所呈现的结果证明了所开发的LC-MS/MS方法在鉴定和定量人尿中右旋糖酐方面的能力和可靠性,可被视为一种揭示体育运动中右旋糖酐滥用情况的方法。

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