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使用库克森型试剂衍生化后,采用液相色谱-质谱法测定人血浆中24,25-二羟基维生素D(3)

Determination of 24,25-dihydroxyvitamin D(3) in human plasma using liquid chromatography-mass spectrometry after derivatization with a Cookson-type reagent.

作者信息

Higashi T, Awada D, Shimada K

机构信息

Faculty of Pharmaceutical Sciences, Kanazawa University, 13-1 Takara-machi, Kanazawa 920-0934, Japan.

出版信息

Biomed Chromatogr. 2001 Apr;15(2):133-40. doi: 10.1002/bmc.43.

Abstract

A practical LC-MS method for determination of (24R)-24,25-dihydroxyvitamin D(3) [24,25(OH)(2)D(3)] in human plasma has been developed using derivatization with a Cookson-type reagent, 4-[4-(6-methoxy-2-benzoxazolyl)phenyl]-1,2,4-triazoline-3,5-dione (MBOTAD). The derivatization with MBOTAD significantly improved the ionization efficiency of the analyte with a detection limit of 18 fmol [equivalent to 7.5 pg of 24,25(OH)(2)D(3)] per injection. The method employed protein precipitation with acetonitrile, purification with OASIS HLB cartridge and silica gel column, derivatization with MBOTAD and atmospheric pressure chemical ionization MS detection. The mass spectrometer was operated in the positive-ion mode of mass chromatography and [26,26,26,27,27,27-(2)H(6)]-24,25(OH)(2)D(3) was used as an internal standard. The intra- and inter-assay coefficients of variation were below 3.4 and 2.5%, respectively, and the analytical recovery of 24,25(OH)(2)D(3) was quantitative. Assay linearity was obtained in the range of 0.05-1.2 ng per tube and the limit of quantitation was 0.23 ng/mL for a 0.3 mL plasma aliquot. The developed method was applied to plasma samples obtained from volunteers and gave satisfactory results.

摘要

已开发出一种实用的液相色谱-质谱法,用于测定人血浆中的(24R)-24,25-二羟基维生素D(3)[24,25(OH)(2)D(3)],该方法使用库克森型试剂4-[4-(6-甲氧基-2-苯并恶唑基)phenyl]-1,2,4-三唑啉-3,5-二酮(MBOTAD)进行衍生化。MBOTAD衍生化显著提高了分析物的电离效率,每次进样的检测限为18 fmol[相当于7.5 pg的24,25(OH)(2)D(3)]。该方法采用乙腈进行蛋白沉淀,通过OASIS HLB柱和硅胶柱进行纯化,用MBOTAD进行衍生化,并采用大气压化学电离质谱检测。质谱仪以质量色谱的正离子模式运行,[26,26,26,27,27,27-(2)H(6)]-24,25(OH)(2)D(3)用作内标。批内和批间变异系数分别低于3.4%和2.5%,24,25(OH)(2)D(3)的分析回收率为定量。在每管0.05-1.2 ng的范围内获得了分析线性,对于0.3 mL血浆等分试样,定量限为0.23 ng/mL。所开发的方法应用于从志愿者获得的血浆样本,结果令人满意。

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