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Journal of Lipid Research, Vol 37, 1823-1829, Copyright © 1996 by Lipid Research, Inc.
R Wagener, B Kobbe and W Stoffel
A highly sensitive analytical method was developed that allows the
separation of ganglioside mixtures and quantification of individual non-
derivatized gangliosides in the concentration range between 2 pmol and 1
nmol. Gangliosides were separated with a gradient of acetonitrile/phosphate
buffer on a 1 mm diameter microbore HPLC column packed with Spherisorb-NH2.
They eluted according to their number of sialic acid residues with
increasing phosphate and decreasing acetonitrile concentrations. The
separation of different gangliosides with equal sialic acid content is also
described. The column effluent was monitored at the maximum of absorption
at 197 nm. The sensitivity is higher than resorcinol staining of
fractionated gangliosides by thin layer chromatography, previously the
standard method for ganglioside analysis. The separated gangliosides can be
analyzed by further methods. The HPLC method described here has been
applied to the analysis of serum and oligodendroglioma specimens.
ARTICLES
Quantification of gangliosides by microbore high performance liquid chromatography
Institute of Biochemistry, Medical Faculty, University of Cologne, Germany.
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