Mena-Bravo A, Priego-Capote F, Luque de Castro M D
Department of Analytical Chemistry, Annex Marie Curie Building, Campus of Rabanales, University of Córdoba, Córdoba, Spain; Agroalimentary Excellence Campus, ceiA3, University of Córdoba, Córdoba, Spain; Maimónides Institute of Biomedical Research (IMIBIC), Reina Sofía University Hospital, University of Córdoba, Córdoba, Spain.
Department of Analytical Chemistry, Annex Marie Curie Building, Campus of Rabanales, University of Córdoba, Córdoba, Spain; Agroalimentary Excellence Campus, ceiA3, University of Córdoba, Córdoba, Spain; Maimónides Institute of Biomedical Research (IMIBIC), Reina Sofía University Hospital, University of Córdoba, Córdoba, Spain.
Anal Chim Acta. 2015 Jun 16;879:69-76. doi: 10.1016/j.aca.2015.03.012. Epub 2015 Mar 10.
The analysis of vitamin D status, with special emphasis on 25-hydroxyvitamin D and 1,25-dihydroxyvitamin D, is gaining interest in clinical studies due to the classical and non-classical effects attributed to this prohormone. In this research, the influence of the two steps preceding determination (viz. sample collection and preparation) on the quantitative analysis of vitamin D and its more important metabolites has been studied. Two preparation approaches, deproteination and solid-phase extraction (SPE), have been evaluated in terms of sensitivity to delimit their application, thus establishing that detection of 1,25-dihydroxyvitamin D cannot be addressed by protein precipitation. Concerning sample collection, serum and plasma reported high accuracy (above 83.3%) for vitamin D and metabolites, while precision, expressed as relative standard deviation, was below 12.9% for all analytes in both samples. Statistical analysis revealed that serum and plasma provided similar physiological levels for vitamin D3, 24,25-dihydroxyvitamin D3 and 25-hydroxyvitamin D3, while significantly different levels were obtained for 1,25-dihydroxyvitamin D3, always higher in plasma than in serum. Sample collection and treatment have proved to be significant in the analysis of vitamin D and its relevant metabolites.
由于这种激素原具有经典和非经典作用,对维生素D状态的分析,尤其是对25-羟基维生素D和1,25-二羟基维生素D的分析,在临床研究中越来越受到关注。在本研究中,研究了测定前的两个步骤(即样品采集和制备)对维生素D及其更重要代谢物定量分析的影响。已根据灵敏度评估了两种制备方法,即脱蛋白和固相萃取(SPE),以确定它们的应用范围,从而确定蛋白质沉淀法无法用于检测1,25-二羟基维生素D。关于样品采集,血清和血浆对维生素D及其代谢物的检测具有较高的准确度(高于83.3%),而以相对标准偏差表示的精密度在两种样品的所有分析物中均低于12.9%。统计分析表明,血清和血浆中维生素D3、24,25-二羟基维生素D3和25-羟基维生素D3的生理水平相似,而1,25-二羟基维生素D3的水平存在显著差异,血浆中的水平始终高于血清。事实证明,样品采集和处理在维生素D及其相关代谢物的分析中具有重要意义。