Moraes John, Peltier Raoul, Gody Guillaume, Blum Muriel, Recalcati Sebastien, Klok Harm-Anton, Perrier Sébastien
Department of Chemistry, University of Warwick, Coventry CV4 7AL, United Kingdom.
Faculty of Pharmacy and Pharmaceutical Sciences, Monash University, 381 Royal Parade, Parkville, VIC 3052, Australia.
ACS Macro Lett. 2016 Dec 20;5(12):1416-1420. doi: 10.1021/acsmacrolett.6b00652. Epub 2016 Dec 9.
The use of polymers has revolutionized the field of drug delivery in the past two decades. Properties such as polymer size, charge, hydrophilicity, or branching have all been shown to play an important role in the cellular internalization of polymeric systems. In contrast, the fundamental impact of monomer distribution on the resulting biological properties of copolymers remains poorly studied and is always only investigated for biologically active self-assembling polymeric systems. Here, we explore the fundamental influence of monomer distribution on the cellular uptake of nonaggregating and biologically passive copolymers. Reversible addition-fragmentation chain-transfer (RAFT) polymerization was used to prepare precisely defined copolymers of three hydrophilic acrylamide monomers. The cellular internalization of block copolymers was compared with the uptake of a random copolymer where monomers are statistically distributed along the chain. The results demonstrate that monomer distribution in itself has a negligible impact on copolymer uptake.
在过去二十年中,聚合物的使用彻底改变了药物递送领域。聚合物的大小、电荷、亲水性或支化等性质均已表明在聚合物体系的细胞内化过程中发挥重要作用。相比之下,单体分布对共聚物最终生物学性质的根本影响仍研究不足,且一直仅针对具有生物活性的自组装聚合物体系进行研究。在此,我们探究单体分布对非聚集性且无生物活性的共聚物细胞摄取的根本影响。采用可逆加成-断裂链转移(RAFT)聚合反应制备了三种亲水性丙烯酰胺单体的精确限定共聚物。将嵌段共聚物的细胞内化与单体沿链呈统计分布的无规共聚物的摄取情况进行了比较。结果表明,单体分布本身对共聚物摄取的影响可忽略不计。