Alexander B. Cook, Raoul Peltier, Tammie R. Barlow, Joji Tanaka, James A. Burns, Sébastien Perrier
{"title":"RAFT支链聚(丙烯酸乙酯三甲基鏻-共-PEGA):用于核酸络合的阳离子聚铵的替代品","authors":"Alexander B. Cook, Raoul Peltier, Tammie R. Barlow, Joji Tanaka, James A. Burns, Sébastien Perrier","doi":"10.1002/jin2.50","DOIUrl":null,"url":null,"abstract":"<p>Cationic and highly branched poly (trimethylphosphonium ethylacrylate-<i>co</i>-poly (ethylene glycol) acrylate) (p (TMPEA-<i>co</i>-PEGA)), and its ammonium equivalent, have been synthesised from post-polymerisation modification of a poly (bromo ethylacrylate-<i>co</i>-poly (ethylene glycol) acrylate) (p (BEA-<i>co</i>-PEGA)) precursor polymer produced using reversible addition fragmentation chain transfer (RAFT) polymerisation. The cationic polymers were evaluated for their ability to complex nucleic acids, their i<i>n vitro</i> cytotoxicity and their GFP pDNA transfection efficiency. The results show RAFT copolymerisation of BEA and PEGA is a simple route to polyphosphoniums showing reduced cytotoxicities and higher transfection efficiencies than their polyammonium alternatives.</p>","PeriodicalId":91547,"journal":{"name":"Journal of interdisciplinary nanomedicine","volume":"3 4","pages":"164-174"},"PeriodicalIF":0.0000,"publicationDate":"2018-12-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/jin2.50","citationCount":"8","resultStr":"{\"title\":\"Branched poly (trimethylphosphonium ethylacrylate-co-PEGA) by RAFT: alternative to cationic polyammoniums for nucleic acid complexation\",\"authors\":\"Alexander B. Cook, Raoul Peltier, Tammie R. Barlow, Joji Tanaka, James A. Burns, Sébastien Perrier\",\"doi\":\"10.1002/jin2.50\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Cationic and highly branched poly (trimethylphosphonium ethylacrylate-<i>co</i>-poly (ethylene glycol) acrylate) (p (TMPEA-<i>co</i>-PEGA)), and its ammonium equivalent, have been synthesised from post-polymerisation modification of a poly (bromo ethylacrylate-<i>co</i>-poly (ethylene glycol) acrylate) (p (BEA-<i>co</i>-PEGA)) precursor polymer produced using reversible addition fragmentation chain transfer (RAFT) polymerisation. The cationic polymers were evaluated for their ability to complex nucleic acids, their i<i>n vitro</i> cytotoxicity and their GFP pDNA transfection efficiency. The results show RAFT copolymerisation of BEA and PEGA is a simple route to polyphosphoniums showing reduced cytotoxicities and higher transfection efficiencies than their polyammonium alternatives.</p>\",\"PeriodicalId\":91547,\"journal\":{\"name\":\"Journal of interdisciplinary nanomedicine\",\"volume\":\"3 4\",\"pages\":\"164-174\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2018-12-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1002/jin2.50\",\"citationCount\":\"8\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of interdisciplinary nanomedicine\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/jin2.50\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of interdisciplinary nanomedicine","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/jin2.50","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Branched poly (trimethylphosphonium ethylacrylate-co-PEGA) by RAFT: alternative to cationic polyammoniums for nucleic acid complexation
Cationic and highly branched poly (trimethylphosphonium ethylacrylate-co-poly (ethylene glycol) acrylate) (p (TMPEA-co-PEGA)), and its ammonium equivalent, have been synthesised from post-polymerisation modification of a poly (bromo ethylacrylate-co-poly (ethylene glycol) acrylate) (p (BEA-co-PEGA)) precursor polymer produced using reversible addition fragmentation chain transfer (RAFT) polymerisation. The cationic polymers were evaluated for their ability to complex nucleic acids, their in vitro cytotoxicity and their GFP pDNA transfection efficiency. The results show RAFT copolymerisation of BEA and PEGA is a simple route to polyphosphoniums showing reduced cytotoxicities and higher transfection efficiencies than their polyammonium alternatives.