Elasticity of vesicles assessed by electron spin resonance, electron microscopy and extrusion measurements

Citation
Bai. Van Den Bergh et al., Elasticity of vesicles assessed by electron spin resonance, electron microscopy and extrusion measurements, INT J PHARM, 217(1-2), 2001, pp. 13-24
Citations number
31
Categorie Soggetti
Pharmacology & Toxicology
Journal title
INTERNATIONAL JOURNAL OF PHARMACEUTICS
ISSN journal
03785173 → ACNP
Volume
217
Issue
1-2
Year of publication
2001
Pages
13 - 24
Database
ISI
SICI code
0378-5173(20010417)217:1-2<13:EOVABE>2.0.ZU;2-X
Abstract
The composition of Vesicles determines the physical state and elasticity of their bilayers. Fatty acid spin labels were incorporated into vesicles, co mposed of the single chain non-ionic surfactant octaoxyethylenelaurate-este r (PEG-8-L), the sucrose laurate-ester L-595 and cholesterol sulfate (CS) t o monitor local dynamic properties of lipid molecules in vesicle bilayers a nd to study the elasticity of vesicle bilayers. Studies with the spin label probes 5-, 12- and 16-doxyl stearic acid (DSA) indicated that both the ord er parameter and the rotational correlation times increased when the doxyl group was positioned closer to the headgroup region. These findings indicat e that the fluidity of membranes decreased near the headgroup region. Compa ring 16-DSA incorporated in vesicle formulations with either 30 or 70 mol% showed no difference in alkyl chain mobility as was reflected by the order parameter. The rotational correlation times, however, showed a slowdown fro m 0.38 to 0.71 and 1.13 ns when the PEG-8-L molar content was decreased fro m 100 to 70 and 30 mol% for PEG-X-L:L-595:CS vesicles, respectively. Extrus ion measurements indicated an increase in elasticity of vesicle bilayers as the molar content of PEG-8-L was increased from 10 to 90 mol%. Incorporati on of cholesterol sulfate stabilizes vesicles and thereby, decreases the el asticity. The increased elasticity correlated excellent with a reduction in the rotational correlation times observed. In conclusion, these results de monstrate that when the molar content of the single chain non-ionic surfact ant PEG-8-L in vesicles is increased the elasticity is enhanced and the rot ational correlation time is reduced. The enhanced elasticity might contribu te to an optimal design of Vesicles as drug carriers for transdermal applic ation. (C) 2001 Elsevier Science B.V. All rights reserved.