- About Us
- Products
- Services
- Pharma Applications
-
Support Hub
- FAQs
- References
- Liposome Preparation
- Lipid-DNA Preparation (Transfection)
- Storage and handling of lipids
-
Analytical Procedures
- Determination of Phospholipid Oxidation by UV/VIS Spectroscopy
- Thin Layer Chromatography (TLC) Analysis of Phospholipids
- Procedure for TLC of synthetic PIPs
- TLC Solvent Systems – Lipid Migration
- Detection Methods for Thin Layer Chromatography
- Fatty Acid Analysis of Phospholipids by GC/FID
- Determination of Total Phosphorus
- Fatty Acid Composition
- Physical Properties
- Contract Manufacturing & Packaging
- Lipid Extraction
- Ordering Information
- Limited Warranty
- Blog
- Contact Us
What Is The Enantiomeric Purity Of Avanti’s Phospholipids?
Avanti’s phospholipids are prepared using a precursor (GPC) derived from soybean lecithin, therefore the stereochemistry of the chiral carbon is dictated by the biological system from which it was derived. Since biological systems only manufacture the L-isomer, Avanti’s phospholipids are 100% L-isomer form. We have confirmed this by optical rotation and enzymatic digestion using phospholipase A2 (PLA2). PLA2 cleaves the sn-2 ester bond generating LPC and free fatty acid. The enzyme is specific for the L-isomer form, in fact the D-isomer acts as a competitive inhibitor. Treatment of Avanti’s synthetic PC’s results in complete digestion of the diacyl compound indicating absolute stereochemical purity. Spiking Avanti’s PC with 1% D-isomer PC as a control produces incomplete digestion (>1% residual diacyl PC remaining).