The preparation of sugar polymer-coated nanocapsules by the layer-by-layer deposition on the liposome

We intended to combine the liposomal preparation and the layer-by-layer deposition to prepare a nanosized capsule. Chitosan (CHI) was deposited to form the cationic polymeric layer onto a negatively charged liposomal surface and further deposition was carried out using anionic polymers dextran sulfa...

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Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1991. - 25(2009), 17 vom: 01. Sept., Seite 10020-5
1. Verfasser: Fukui, Yuuka (VerfasserIn)
Weitere Verfasser: Fujimoto, Keiji
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2009
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Carbohydrates Cations Detergents Liposomes Nanocapsules Polymers Surface-Active Agents Octoxynol mehr... 9002-93-1 Glucose IY9XDZ35W2 Alendronate X1J18R4W8P
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245 1 4 |a The preparation of sugar polymer-coated nanocapsules by the layer-by-layer deposition on the liposome 
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520 |a We intended to combine the liposomal preparation and the layer-by-layer deposition to prepare a nanosized capsule. Chitosan (CHI) was deposited to form the cationic polymeric layer onto a negatively charged liposomal surface and further deposition was carried out using anionic polymers dextran sulfate (DXS) or deoxyribonucleic acid (DNA). zeta-Potentials of nanocapsules changed between positive and negative charges at each deposition. FE-TEM revealed that the liposome remained a spherical shape even after the layer-by-layer (LbL) deposition. The capsule wall showed a dramatic increase in stability against the surfactant Triton X-100 compared to a bare liposome, and the stability was controllable by the adsorption amount of the polymer. These suggest that the polymer multilayer was generated on the liposome surface by the layer-by-layer depositions of polysaccharides. The three kinds of chemical substances with different charges, 1-hydroxy pyrene-3,6,8-trisulfonic acid (HPTS), alendronate, and glucose, were encapsulated into nanocapsules and the release was suppressed by the polymeric capsule wall irrespective of charges. The release from DNA-deposited nanocapsules (liponano-CHI-DNA) was clearly increased by raising temperature from 25 to 60 degrees C. This indicates that the temperature-dependent release was achieved by applying DNA denaturation as a temperature-dependent "switch", which influenced the permeability of the capsule wall 
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650 4 |a Research Support, Non-U.S. Gov't 
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650 7 |a Cations  |2 NLM 
650 7 |a Detergents  |2 NLM 
650 7 |a Liposomes  |2 NLM 
650 7 |a Nanocapsules  |2 NLM 
650 7 |a Polymers  |2 NLM 
650 7 |a Surface-Active Agents  |2 NLM 
650 7 |a Octoxynol  |2 NLM 
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650 7 |a Glucose  |2 NLM 
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650 7 |a Alendronate  |2 NLM 
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700 1 |a Fujimoto, Keiji  |e verfasserin  |4 aut 
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