1. TLC characterization of small unilamellar liposomes containing D-myo-inositol derivatives.
- Author
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Brailoiu E, Beschea C, Brailoiu C, Costuleanu A, Filipeanu CM, Costuleanu M, Fallgren B, and Branisteanu DD
- Subjects
- Animals, Aorta, Thoracic drug effects, Aorta, Thoracic physiology, Endothelium, Vascular drug effects, Endothelium, Vascular physiology, Inositol 1,4,5-Trisphosphate chemistry, Male, Phytic Acid chemistry, Rats, Rats, Wistar, Chromatography, Thin Layer, Inositol Phosphates chemistry, Liposomes chemistry
- Abstract
The thin-layer chromatographic (TLC) behaviour of small unilamellar liposomes containing inositol phosphates (IPs) was studied. The vesicles contained different concentrations of D-myo-inositol 1,4,5-triphosphate (IP3), D-myo-inositol 1,2,6-triphosphate (alpha-trinositol, PP 56, a novel Perstorp Pharma derivative), D-myo-inositol 1,3,4,5-tetraphosphate (IP4), D-myo-inositol 1,3,4,5,6-pentakisphosphate (IP5) and D-myo-inositol 1,2,3,4,5,6-hexakisphosphate (IP6). Migration of all liposome batches was compared to that of control liposomes (multilamellar and small unilamellar, both containing only triple-distilled water), and to that of free phosphatidylcholine (PC). The same amount of lipid was used in all situations. Thin-layer chromatography was performed with silica gel as adsorbent. The developing solvent was an n-buthanol:ethanol:water mixture in a 4:3:3 volume ratio. At doses higher than 10(-2) M liposomes containing alpha-trinositol and IP6 had a different migration than PC, MLV or SUV as well as all batches of liposomes. Physiological studies (using as model endothelized rat aorta rings) proved that in this situation they had no effects.
- Published
- 1996
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