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通过对其过苯甲酰衍生物进行高效液相色谱法对血浆中性糖鞘脂进行定量分析。

Quantitative analysis of plasma neutral glycosphingolipids by high performance liquid chromatography of their perbenzoyl derivatives.

作者信息

Ullman M D, McCluer R H

出版信息

J Lipid Res. 1977 May;18(3):371-8.

PMID:405444
Abstract

A quantitative high performance liquid chromatography method for the analysis of neutral glycosylceramides as their perbenzoyl derivatives has been devised. Samples containing more than 2.5 nmol each of mono-, di-, tri-, and tetraglycosylceramide are benzoylated with 10% benzoyl chloride in pyridine at 37degrees C for 16 hr. The products are separated from excess reagents by solvent distribution and injected onto a pellicllar silica gel (Zipax) column (2.1 mm X 50 cm). The derivatives are eluted with a 10 min linear gradient of 2-17% ethyl acetate in hexane at 2 ml/min and absorbance at 280 nm is recorded. The detector response was proportional to the weight of sample used (2-30 nmol) and the lower limit of detection was about 70 pmol. The procedure has been applied to the quantitative analysis of erythrocyte and plasma glycolipids. As little as 0.5 ml of plasma can be used for analysis. The relative standard deviation of repetitive analyses ranged between 2.0% for glucosylceramide to 5.4% for galactosyllactosylceramide.

摘要

已设计出一种定量高效液相色谱法,用于分析作为其过苯甲酰衍生物的中性糖基神经酰胺。含有每种单糖基、二糖基、三糖基和四糖基神经酰胺各超过2.5 nmol的样品,在37℃下用吡啶中的10%苯甲酰氯进行苯甲酰化反应16小时。通过溶剂分配将产物与过量试剂分离,并注入到 pellicllar 硅胶(Zipax)柱(2.1 mm×50 cm)上。衍生物用己烷中2 - 17%乙酸乙酯的10分钟线性梯度以2 ml/min的流速洗脱,并记录280 nm处的吸光度。检测器响应与所用样品重量(2 - 30 nmol)成正比,检测下限约为70 pmol。该方法已应用于红细胞和血浆糖脂的定量分析。分析时血浆用量低至0.5 ml即可。重复分析的相对标准偏差范围为,葡萄糖基神经酰胺为2.0%至半乳糖基乳糖基神经酰胺为5.4%。

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