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Title: Purification of plasma vitamin D metabolites for radioimmunoassay. Author: Taylor GA, Peacock M, Pelc B, Brown W, Holmes A. Journal: Clin Chim Acta; 1980 Dec 08; 108(2):239-46. PubMed ID: 6969637. Abstract: The ability of four solvent systems to extract tritiated 25-hydroxy vitamin D3, 24,25-dihydroxy vitamin D3, 25,26-dihydroxy vitamin D3 and 1 alpha, 25-dihydroxy vitamin D3 from plasma was compared. Diethyl ether gave the highest yield of metabolites and lowest yield of "lipid" materials, the dihydroxylated metabolites were more readily extracted than 25-hydroxy vitamin D3. Following extraction with ether the vitamin D metabolites could be separated, without prior purification, on a 6.2 mm X 250 mm Zorbax-Sil high pressure liquid chromatography (HPLC) column, a simplification of previous methods. Plasma 1 alpha, 25-dihydroxy vitamin D levels measured after purification by this method were not significantly different from those obtained by an established, more complex method.[Abstract] [Full Text] [Related] [New Search]