Savolainen K, Mäenpää P H, Alhava E M, Kettunen K
Med Biol. 1980 Feb;58(1):49-52.
A chromatographic assay procedure for the analysis of 25-hydroxyvitamin D3 [25(OH)D3] in human serum is described. The procedure involves methanol/chloroform extraction of serum lipids followed by separation of the vitamin D metabolites and purification from interfering contaminents by chromatography on Sephadex LH-20 and by high-pressure liquid chromatography. 25(OH)D3 is quantitated by uv detection, and its peak height compared with those of standards. Values in normal human serum samples taken in July-August and January-February are: 33.0 +/- 13.6 ng/ml (82.5 +/- 34.1 nmol/1) and 14.5 +/- 12.2 ng/ml (36.3 +/- 30.5 nmol/1) (means +/- SD), respectively (p less than 0.001). The summer values are somewhat lower in the elderly subjects as compared to younger ones, but a seasonal difference was observed in both groups. This difference may be due to a relatively low vitamin D intake and a limited sun exposure.
本文描述了一种用于分析人血清中25-羟基维生素D3 [25(OH)D3]的色谱分析方法。该方法包括用甲醇/氯仿提取血清脂质,然后通过在Sephadex LH-20上进行色谱分离以及高压液相色谱法分离维生素D代谢物并从干扰污染物中纯化。通过紫外检测对25(OH)D3进行定量,并将其峰高与标准品的峰高进行比较。7月至8月和1月至2月采集的正常人血清样本中的值分别为:33.0±13.6 ng/ml (82.5±34.1 nmol/1)和14.5±12.2 ng/ml (36.3±30.5 nmol/1)(均值±标准差),差异有统计学意义(p<0.001)。与年轻受试者相比,老年受试者的夏季值略低,但两组均观察到季节性差异。这种差异可能是由于维生素D摄入量相对较低和阳光照射有限所致。