Literature DB >> 9635773

New sterically stabilized vesicles based on nonionic surfactant, cholesterol, and poly(ethylene glycol)-cholesterol conjugates.

S Beugin1, K Edwards, G Karlsson, M Ollivon, S Lesieur.   

Abstract

Monomethoxypoly(ethylene glycol) cholesteryl carbonates (M-PEG-Chol) with polymer chain molecular weights of 1000 (M-PEG1000-Chol) and 2000 (M-PEG2000-Chol) have been newly synthesized and characterized. Their aggregation behavior in mixture with diglycerol hexadecyl ether (C16G2) and cholesterol has been examined by cryotransmission electron microscopy, high-performance gel exclusion chromatography, and quasielastic light scattering. Nonaggregated, stable, unilamellar vesicles were obtained at low polymer levels with optimal shape and size homogeneity at cholesteryl conjugate/ lipids ratios of 10 mol% M-PEG1000-Chol or 5 mol% M-PEG2000-Chol, corresponding to the theoretically predicted brush conformational state of the PEG chains. At 20 mol% M-PEG1000-Chol or 10 mol% M-PEG2000-Chol, the saturation threshold of the C16G2/cholesterol membrane in polymer is exceeded, and open disk-shaped aggregates are seen in coexistence with closed vesicles. Higher levels up to 30 mol% lead to the complete solubilization of the vesicles into disk-like structures of decreasing size with increasing PEG content. This study underlines the bivalent role of M-PEG-Chol derivatives: while behaving as solubilizing surfactants, they provide an efficient steric barrier, preventing the vesicles from aggregation and fusion over a period of at least 2 weeks.

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Year:  1998        PMID: 9635773      PMCID: PMC1299660          DOI: 10.1016/S0006-3495(98)78026-9

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  37 in total

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Authors:  K Edwards; M Johnsson; G Karlsson; M Silvander
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4.  Controlled environment vitrification system: an improved sample preparation technique.

Authors:  J R Bellare; H T Davis; L E Scriven; Y Talmon
Journal:  J Electron Microsc Tech       Date:  1988-09

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Authors:  M N Azmin; A T Florence; R M Handjani-Vila; J F Stuart; G Vanlerberghe; J S Whittaker
Journal:  J Pharm Pharmacol       Date:  1985-04       Impact factor: 3.765

6.  Quasielastic light-scattering studies of aqueous biliary lipid systems. Mixed micelle formation in bile salt-lecithin solutions.

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Authors:  C A Hunter; T F Dolan; G H Coombs; A J Baillie
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8.  The therapeutic effect of sodium stibogluconate in BALB/c mice infected with Leishmania donovani is organ-dependent.

Authors:  K C Carter; A J Baillie; J Alexander; T F Dolan
Journal:  J Pharm Pharmacol       Date:  1988-05       Impact factor: 3.765

9.  The distribution of doxorubicin in mice following administration in niosomes.

Authors:  A Rogerson; J Cummings; N Willmott; A T Florence
Journal:  J Pharm Pharmacol       Date:  1988-05       Impact factor: 3.765

10.  Non-ionic surfactant vesicles, niosomes, as a delivery system for the anti-leishmanial drug, sodium stibogluconate.

Authors:  A J Baillie; G H Coombs; T F Dolan; J Laurie
Journal:  J Pharm Pharmacol       Date:  1986-07       Impact factor: 3.765

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