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一种使用Sep-Pak C18柱和单一高效液相色谱步骤测量血浆25-羟基维生素D2和25-羟基维生素D3的快速简便方法。

A rapid and simple method for the measurement of plasma 25-hydroxyvitamin D2 and 25-hydroxyvitamin D3 using Sep-Pak C18 cartridges and a single high-performance liquid chromatographic step.

作者信息

Turnbull H, Trafford D J, Makin H L

出版信息

Clin Chim Acta. 1982 Mar 26;120(1):65-76. doi: 10.1016/0009-8981(82)90078-x.

Abstract

A simple one step high-performance liquid chromatographic (HPLC) procedure for the analysis of plasma concentrations of 25-hydroxyvitamin D3 (25-OHD3) and 25-hydroxyvitamin D2 (25-OHD2) is described. Plasma (2-4 ml) was extracted with methyl cyanide which was passed through a Sep-Pak C18 cartridge, washed with methanol:water (70:30, v/v) and the 25-OHD fraction eluted with methyl cyanide. After isomerisation to their isotachysterol derivatives, the secosteroids were estimated using a straight-phase HPLC system, monitoring the eluent at 301 nm. Radioactive 25-OHD3, added to plasma at the start of the procedure, was used to correct for losses. Recovery of added 25-OHD3 was quantitative and values obtained using this method were similar to those obtained on the same plasma samples using a mass fragmentographic technique. Normal ranges were similar to those described by other workers and within- (5.8% for 25-OHD3) and between-(8.0% for 25-OHD3) batch reproducibilities were satisfactory.

摘要

本文描述了一种用于分析血浆中25-羟基维生素D3(25-OHD3)和25-羟基维生素D2(25-OHD2)浓度的简单高效液相色谱(HPLC)一步法。取2 - 4毫升血浆,用乙腈萃取,将萃取液通过Sep-Pak C18柱,先用甲醇:水(70:30,v/v)洗涤,然后用乙腈洗脱25-OHD部分。将这些甾醇类化合物异构化为它们的异速甾醇衍生物后,使用正相HPLC系统进行测定,在301 nm处监测洗脱液。在操作开始时向血浆中添加放射性25-OHD3,用于校正损失。添加的25-OHD3回收率是定量的,用该方法获得的值与使用质量碎片谱技术在相同血浆样品上获得的值相似。正常范围与其他研究者描述的相似,批内(25-OHD3为5.8%)和批间(25-OHD3为8.0%)重现性令人满意。

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