Hollis B W
Clin Chem. 1986 Nov;32(11):2060-3.
By use of a single-cartridge system, 1,25-dihydroxyvitamin D [1,25(OH)2D] is extracted and purified from a plasma or serum sample. Proteins are removed and 1,25(OH)2D is liberated from the sample with acetonitrile. The acetonitrile extract is applied to the nonpolar octadecylsilanol silica cartridge, in which 1,25(OH)2D is retained while polar compounds are eluted. Then by "phase-switching" on the same cartridge, 1,25(OH)2D is sufficiently resolved from other vitamin D metabolites and extraneous lipophilic compounds to allow its quantification by radioreceptor assay according to an established procedure. Mean (and SD) values for 1,25(OH)2D in serum of 29 normal, 27 chronic renal failure, and nine pregnant subjects were 28.2 (11.3), 10.9 (5.2), and 47.3 (12.9) ng/L, respectively. Results compared well with those of an established radioreceptor procedure. This procedure offers the advantage of a single rapid purification step not involving "high-performance" liquid chromatography or evaporation, under nitrogen, of polar solvents such as acetonitrile or methanol.
通过使用单柱系统,从血浆或血清样本中提取并纯化1,25 - 二羟基维生素D [1,25(OH)₂D]。去除蛋白质,并用乙腈从样本中释放出1,25(OH)₂D。将乙腈提取物应用于非极性十八烷基硅烷醇硅胶柱,其中1,25(OH)₂D被保留,而极性化合物被洗脱。然后通过在同一柱上进行“相切换”,1,25(OH)₂D与其他维生素D代谢物和外来亲脂性化合物充分分离,从而能够根据既定程序通过放射受体测定法对其进行定量。29名正常受试者、27名慢性肾衰竭患者和9名孕妇血清中1,25(OH)₂D的平均值(及标准差)分别为28.2(11.3)、10.9(5.2)和47.3(12.9)ng/L。结果与既定放射受体程序的结果相比良好。该程序的优点是只需一个快速纯化步骤,不涉及“高效”液相色谱法或在氮气下蒸发乙腈或甲醇等极性溶剂。