Synthesis and applications of shell cross-linked thermoresponsive hybrid micelles based on poly(N-isopropylacrylamide-co-3-(trimethoxysilyl)propyl methacrylate)-b-poly(methyl methacrylate)

Shell cross-linked (SCL) thermoresponsive hybrid micelles consisting of a cross-linked thermoresponsive hybrid hydrophilic shell and a hydrophobic core domain were synthesized from poly(N-isopropylacrylamide-co-3- (trimethoxysilyl)propyl methacrylate)-b-polymethyl methacrylate (P(NIPAAm-co-MPMA)-b-P...

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Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1992. - 24(2008), 9 vom: 06. Mai, Seite 4564-70
1. Verfasser: Wei, Hua (VerfasserIn)
Weitere Verfasser: Cheng, Cheng, Chang, Cong, Chen, Wen-Qin, Cheng, Si-Xue, Zhang, Xian-Zheng, Zhuo, Ren-Xi
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2008
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Acetates Acrylamides Cross-Linking Reagents Methacrylates Micelles Organosilicon Compounds poly(N-isopropylacrylamide-b-methyl methacrylate) 3-(trimethoxysilyl)propyl methacrylate mehr... JV48X1M2EQ Prednisone VB0R961HZT
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245 1 0 |a Synthesis and applications of shell cross-linked thermoresponsive hybrid micelles based on poly(N-isopropylacrylamide-co-3-(trimethoxysilyl)propyl methacrylate)-b-poly(methyl methacrylate) 
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520 |a Shell cross-linked (SCL) thermoresponsive hybrid micelles consisting of a cross-linked thermoresponsive hybrid hydrophilic shell and a hydrophobic core domain were synthesized from poly(N-isopropylacrylamide-co-3- (trimethoxysilyl)propyl methacrylate)-b-polymethyl methacrylate (P(NIPAAm-co-MPMA)-b-PMMA) amphiphilic block copolymers. Transmission electron microscopy (TEM) images showed that the SCL micelles formed regularly globular nanoparticles. The SCL micelles showed reversible dispersion/aggregation in response to temperature cycles through an outer polymer shell lower critical solution temperature (LCST) for PNIPAAm at around 33 degrees C, observed by turbidity measurements and dynamic light scattering (DLS). The drug loading and in vitro drug release properties of the SCL micelles bearing a silica-reinforced PNIPAAm shell were further studied, which showed that the SCL micelles exhibited a much improved entrapment efficiency (EE) as well as a slower release rate which allowed the entrapped molecules to be slowly released over a much longer period of time as compared with pure PNIPAAm-b-PMMA micelles 
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650 4 |a Research Support, Non-U.S. Gov't 
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650 7 |a Acrylamides  |2 NLM 
650 7 |a Cross-Linking Reagents  |2 NLM 
650 7 |a Methacrylates  |2 NLM 
650 7 |a Micelles  |2 NLM 
650 7 |a Organosilicon Compounds  |2 NLM 
650 7 |a poly(N-isopropylacrylamide-b-methyl methacrylate)  |2 NLM 
650 7 |a 3-(trimethoxysilyl)propyl methacrylate  |2 NLM 
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700 1 |a Cheng, Cheng  |e verfasserin  |4 aut 
700 1 |a Chang, Cong  |e verfasserin  |4 aut 
700 1 |a Chen, Wen-Qin  |e verfasserin  |4 aut 
700 1 |a Cheng, Si-Xue  |e verfasserin  |4 aut 
700 1 |a Zhang, Xian-Zheng  |e verfasserin  |4 aut 
700 1 |a Zhuo, Ren-Xi  |e verfasserin  |4 aut 
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