Shimizu M, Wang X, Yamada S
Division of Molecular Biology, Tokyo Medical and Dental University, Japan.
J Chromatogr B Biomed Sci Appl. 1997 Mar 7;690(1-2):15-23. doi: 10.1016/s0378-4347(96)00379-9.
The first fluorimetric method for assaying plasma 1 alpha,25-dihydroxyvitamin D3 [1,25-(OH)2D3] is described. Lipid extracts from human plasma were successively purified by a Bond Elut NH2 column and a normal-phase HPLC column, and the 1,25-(OH)2D3 fractions obtained were fluorescence-labelled with 4-[2-(6,7-dimethoxy-4-methtyl-3-oxo-3,4-dihydroquinoxalyl)et hyl]-1, 2,4-triazoline-3,5-dione (DMEQ-TAD). The fluorescent adducts of 1,25-(OH)2D3 were analyzed by HPLC on a reversed-phase column, after extensive elimination of the degradation products of excess reagents, by a Bond Elut PSA column followed by a normal-phase HPLC column. The intra- and inter-assay coefficients of variation were within 10% in both assays. The analytical recoveries of standard 1,25-(OH)2D3 added to plasma were quantitative. The present fluorimetric assay was compared with the established radioreceptor assay (RRA) used in measuring plasma 1,25-(OH)2D3 concentration. The regression analysis of the data afforded a relationship y = 1.049x - 2.657 and a correlation coefficient (r) of 0.900.
本文描述了第一种用于测定血浆1α,25-二羟基维生素D3 [1,25-(OH)2D3]的荧光分析法。人血浆的脂质提取物先后通过Bond Elut NH2柱和正相高效液相色谱柱进行纯化,所得的1,25-(OH)2D3馏分用4-[2-(6,7-二甲氧基-4-甲基-3-氧代-3,4-二氢喹喔啉基)乙基]-1,2,4-三唑啉-3,5-二酮(DMEQ-TAD)进行荧光标记。在通过Bond Elut PSA柱和正相高效液相色谱柱广泛去除过量试剂的降解产物后,1,25-(OH)2D3的荧光加合物在反相柱上通过高效液相色谱法进行分析。两种分析方法的批内和批间变异系数均在10%以内。添加到血浆中的标准1,25-(OH)2D3的分析回收率是定量的。将本荧光分析法与用于测量血浆1,25-(OH)2D3浓度的既定放射受体分析法(RRA)进行了比较。数据的回归分析得出y = 1.049x - 2.657的关系,相关系数(r)为0.900。