Shepard R M, Horst R L, Hamstra A J, DeLuca H F
Biochem J. 1979 Jul 15;182(1):55-69. doi: 10.1042/bj1820055.
A multiple assay capable of reliably determining vitamins D(2) and D(3) (ergocalciferol and cholecalciferol), 25(OH)D(2) (25-hydroxyvitamin D(2)) and 25(OH)D(3) (25-hydroxyvitamin D(3)), 24,25(OH)(2)D (24,25-dihydroxyvitamin D), 25,26(OH)(2)D (25,26-dihydroxyvitamin D) and 1,25(OH)(2)D (1,25-dihydroxyvitamin D) in a single 3-5ml sample of human plasma was developed. The procedure involves methanol/methylene chloride extraction of plasma lipids followed by separation of the metabolites and purification from interfering contaminants by batch elution chromatography on Sephadex LH-20 and Lipidex 5000 and by h.p.l.c. (high-pressure liquid chromatography). Vitamins D(2) and D(3) and 25(OH)D(2) and 25(OH)D(3) are quantified by h.p.l.c. by using u.v. detection, comparing their peak heights with those of standards. 24,25(OH)(2)D and 25,26(OH)(2)D are measured by competitive protein-binding assay with diluted plasma from vitamin D-deficient rats. 1,25(OH)(2)D is measured by competitive protein-binding assay with diluted cytosol from vitamin D-deficient chick intestine. Values in normal human plasma samples taken in February are: vitamin D 3.5+/-2.5ng/ml; 25(OH)D 31.6+/-9.3ng/ml; 24,25(OH)(2)D 3.5+/-1.4ng/ml; 25,26(OH)(2)D 0.7+/-0.5ng/ml; 1,25(OH)(2)D 31+/-9pg/ml (means+/-s.d.). Values in two normal human plasma samples taken in February after 1 week of high sun exposure are: vitamin D 27.1+/-7.9ng/ml; 25(OH)D 56.8+/-4.2ng/ml; 24,25(OH)(2)D 4.3+/-1.6ng/ml; 25,26(OH)(2)D 0.5+/-0.2ng/ml. Values in anephric-human plasma are: vitamin D 2.7+/-0.8ng/ml; 25(OH)D 36.4+/-16.5ng/ml; 24,25(OH)(2)D 1.9+/-1.3ng/ml; 25,26(OH)(2)D 0.6+/-0.3ng/ml; 1,25(OH)(2)D was undetectable.
开发了一种能在3 - 5毫升人血浆样本中可靠测定维生素D₂和D₃(麦角钙化醇和胆钙化醇)、25(OH)D₂(25 - 羟基维生素D₂)和25(OH)D₃(25 - 羟基维生素D₃)、24,25(OH)₂D(24,25 - 二羟基维生素D)、25,26(OH)₂D(25,26 - 二羟基维生素D)以及1,25(OH)₂D(1,25 - 二羟基维生素D)的多重检测方法。该程序包括用甲醇/二氯甲烷提取血浆脂质,然后通过在Sephadex LH - 20和Lipidex 5000上的分批洗脱色谱法以及高效液相色谱法(h.p.l.c.)从干扰污染物中分离代谢物并进行纯化。维生素D₂和D₃以及25(OH)D₂和25(OH)D₃通过高效液相色谱法使用紫外检测进行定量,将它们的峰高与标准品的峰高进行比较。24,25(OH)₂D和25,26(OH)₂D通过与维生素D缺乏大鼠的稀释血浆进行竞争性蛋白结合测定来测量。1,25(OH)₂D通过与维生素D缺乏鸡肠道的稀释胞质溶胶进行竞争性蛋白结合测定来测量。2月份采集的正常人类血浆样本中的值为:维生素D 3.5±2.5纳克/毫升;25(OH)D 31.6±9.3纳克/毫升;24,25(OH)₂D 3.5±1.4纳克/毫升;25,26(OH)₂D 0.7±0.5纳克/毫升;1,25(OH)₂D 31±9皮克/毫升(均值±标准差)。2月份经过1周强烈阳光照射后采集的两份正常人类血浆样本中的值为:维生素D 27.1±7.9纳克/毫升;25(OH)D 56.8±4.2纳克/毫升;24,25(OH)₂D 4.3±1.6纳克/毫升;25,26(OH)₂D 0.5±0.2纳克/毫升。无肾人类血浆中的值为:维生素D 2.7±0.8纳克/毫升;25(OH)D 36.4±16.5纳克/毫升;24,25(OH)₂D 1.9±1.3纳克/毫升;25,26(OH)₂D 0.6±0.3纳克/毫升;未检测到1,25(OH)₂D。