TLC Characterization of Small Unilamellar Liposomes Containing D-myo-Inositol Derivatives

• Published in: Biomedical chromatography Vol. 10; no. 5; pp. 233 - 236
• Main Authors: Brailoiu, Eugen, Beschea, Corina, Brailoiu, Cristina, Costuleanu, Angela, Filipeanu, Catalin M., Costuleanu, Marcel, Fallgrens, Bo, Branisteanu, Dimitrie D.
• Format: Journal Article
• Language: English
• Published: Chichester, UK John Wiley & Sons, Ltd 01.09.1996
• Subjects: Animals; Aorta, Thoracic - drug effects; Aorta, Thoracic - physiology; Chromatography, Thin Layer; Endothelium, Vascular - drug effects; Endothelium, Vascular - physiology; Inositol 1,4,5-Trisphosphate - chemistry; Inositol Phosphates - chemistry; Liposomes - chemistry; Male; Phytic Acid - chemistry; Rats; Rats, Wistar
• ISSN: 0269-3879; 1099-0801
• DOI: 10.1002/(SICI)1099-0801(199609)10:5<233::AID-BMC594>3.0.CO;2-5

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 (α‐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 α‐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