Traylor T D, Koontz D A, Hogan E L
J Chromatogr. 1983 Jan 14;272(1):9-20. doi: 10.1016/s0378-4347(00)86098-3.
A new quantitative procedure for the high-performance liquid chromatographic (HPLC) resolution of human brain gangliosides employing reversed-phase chromatography is described. To provide a derivative which can be determined by UV absorption techniques, p-nitrobenzyloxyamine was coupled to the gangliosides. Derivatization involves ozonation and cleavage of the ceramide double bond followed by oxime formation to the nascent aldehyde. Individual gangliosides, as they were resolved by HPLC, were collected. These fractions were then identified by thin-layer chromatography (TLC) and by gas chromatography of their monosaccharides. Quantitative results were obtained along with a marked increase in sensitivity over conventional resorcinol-hydrochloric acid quantitation of TLC-resolved gangliosides.
本文描述了一种采用反相色谱法对人脑海藻糖脂进行高效液相色谱(HPLC)分离的新定量方法。为了提供一种可通过紫外吸收技术测定的衍生物,对硝基苄氧基胺与神经节苷脂偶联。衍生化包括神经酰胺双键的臭氧化和裂解,然后与新生醛形成肟。通过HPLC分离的各个神经节苷脂被收集起来。然后通过薄层色谱(TLC)及其单糖的气相色谱对这些馏分进行鉴定。获得了定量结果,并且与传统的用间苯二酚 - 盐酸对TLC分离的神经节苷脂进行定量相比,灵敏度有显著提高。