We describe a comprehensive approach to the separation, quantitation, and characterization of phospholipids and lysophospholipids present in complex biological samples. The central feature is a normal-phase HPLC separation of individual phospholipid and lysophospholipid classes. In this single chrom
High-performance liquid chromatography of phospholipids: Quantitation by phosphate analysis
β Scribed by John R. Yandrasitz; Gerard Berry; Stanton Segal
- Publisher
- Elsevier Science
- Year
- 1983
- Tongue
- English
- Weight
- 381 KB
- Volume
- 135
- Category
- Article
- ISSN
- 0003-2697
No coin nor oath required. For personal study only.
β¦ Synopsis
Quantitation of individual phospholipids sepamted by HPLC from tissue extracts by calorimetric analysis of phosphate was investigated. Elution of inorganic phosphate and breakthrough of lecithin were determined using radioisotopes. A substance which interfered with sample phosphate determinations was found in the column eluant, and a method to minimize its effect was developed. This method allows accurate quantitation of individual phospholipids present at a minimum of 20 nmol phosphate.
π SIMILAR VOLUMES
The common mobile phase hexane/isopropanol/water used for separation of phospholipids on highperformance liquid chromatography silica columns poses several problems, such as incomplete separation and rapid column deterioration. By inclusion of 5 mM ammonium sulfate in the aqueous phase, we were able
## High Performance Liquid Chromatographic Analysis of Soybean Phospholipids \* ## B y N . S o t i r h o s , C h i -T a n g H o andStephenS. C h a n g * An HPLC method was optimized to analyze soybean phospholipids. It uses a silica column with W detection at 210 nm, and amobile phase consistin