pH-induced vesicle-to-micelle transition in amphiphilic diblock copolymer : investigation by energy transfer between in situ formed polymer embedded gold nanoparticles and fluorescent dye

The ability to regulate the formation of nanostructures through self-assembly of amphiphilic block copolymers is of immense significance in the field of biology and medicine. In this work, a new block copolymer synthesized by using reversible addition-fragmentation chain transfer (RAFT) polymerizati...

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Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1999. - 31(2015), 1 vom: 08., Seite 32-41
1. Verfasser: Maiti, Chiranjit (VerfasserIn)
Weitere Verfasser: Banerjee, Rakesh, Maiti, Saikat, Dhara, Dibakar
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2015
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Fluorescent Dyes Methacrylates Micelles Rhodamines polyethylene glycol methacrylate Polyethylene Glycols 3WJQ0SDW1A Gold 7440-57-5
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520 |a The ability to regulate the formation of nanostructures through self-assembly of amphiphilic block copolymers is of immense significance in the field of biology and medicine. In this work, a new block copolymer synthesized by using reversible addition-fragmentation chain transfer (RAFT) polymerization technique from poly(ethylene glycol) monomethyl ether acrylate (PEGMA) and Boc-l-tryptophan acryloyloxyethyl ester (Boc-l-trp-HEA) was found to spontaneously form pH-responsive water-soluble nanostructures after removal of the Boc group. While polymer vesicles or polymerosomes were formed at physiological pH, the micelles were formed at acidic pH (< 5.2), and this facilitated a pH-induced reversible vesicle-to-micelle transition. Formation of these nanostructures was confirmed by different characterization techniques, viz. transmission electron microscopy, dynamic light scattering, and steady-state fluorescence measurements. Further, these vesicles were successfully utilized to reduce HAuCl4 and stabilize the resulting gold nanoparticles (AuNPs). These AuNPs, confined within the hydrophobic shell of the vesicles, could participate in energy transfer process with fluorescent dye molecules encapsulated in the core of the vesicles, thus forming a nanometal surface energy transfer (NSET) pair. Subsequently, following the efficiency of energy transfer between this pair, it was possible to monitor the process of transition from vesicles to micelles. Thus, in this work, we have successfully demonstrated that NSET can be used to follow the transition between nanostructures formed by amphiphilic block copolymers 
650 4 |a Journal Article 
650 4 |a Research Support, Non-U.S. Gov't 
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650 7 |a Methacrylates  |2 NLM 
650 7 |a Micelles  |2 NLM 
650 7 |a Rhodamines  |2 NLM 
650 7 |a polyethylene glycol methacrylate  |2 NLM 
650 7 |a Polyethylene Glycols  |2 NLM 
650 7 |a 3WJQ0SDW1A  |2 NLM 
650 7 |a Gold  |2 NLM 
650 7 |a 7440-57-5  |2 NLM 
700 1 |a Banerjee, Rakesh  |e verfasserin  |4 aut 
700 1 |a Maiti, Saikat  |e verfasserin  |4 aut 
700 1 |a Dhara, Dibakar  |e verfasserin  |4 aut 
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773 1 8 |g volume:31  |g year:2015  |g number:1  |g day:08  |g pages:32-41 
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