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pubmed-article:8930747pubmed:abstractTextThe recent increased use of cell cultures to model physiological events, in particular signal transduction and traumatic injury, has produced a need for a quantitative, high-performance liquid chromatographic separation of neutral lipid classes with a high degree of resolution and reproducibility. We report an isocratic separation using a Phenomenex Selectosil silica column (5 microns). Two solvents were used, 1.2% 2-propanol in n-hexane containing 0.1% acetic acid (90%) and n-hexane (10%) at a flow-rate of 0.6 ml/min. Column temperature was maintained at 55 degrees C and this temperature was critical for baseline resolution of 1,3-diacylglycerol and cholesterol. The use of 10% n-hexane permitted the resolution of low polarity compounds such as butylated hydroxytoluene, triacylglycerols and cholesteryl esters. All of the detectors used produced standard curves with linearity over a wide concentration range.lld:pubmed
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pubmed-article:8930747pubmed:authorpubmed-author:HorrocksL ALAlld:pubmed
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pubmed-article:8930747pubmed:dateRevised2007-11-14lld:pubmed
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pubmed-article:8930747pubmed:articleTitleSeparation of neutral lipids by high-performance liquid chromatography: quantification by ultraviolet, light scattering and fluorescence detection.lld:pubmed
pubmed-article:8930747pubmed:affiliationDepartment of Medical Biochemistry, Ohio State University, Columbus 43210, USA.lld:pubmed
pubmed-article:8930747pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:8930747pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
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