You Ye-Zi, Zhou Qing-Hui, Manickam Devika Soundara, Wan Lei, Mao Guang-Zhao, Oupický David
Department of Pharmaceutical Sciences, Wayne State University, Detroit, MI 48202, USA.
Macromolecules. 2007;40(24):8617-8624. doi: 10.1021/ma071176p.
We report synthesis of temperature- and redox-responsive multiblock copolymers by reversible addition-fragmentation chain transfer (RAFT) polymerization. Well-defined α,ω-bis(dithioester)-functionalized poly(N-isopropylacrylamide) (PNIPAM) and poly(2-(dimethylamino) ethyl methacrylate) (PDMAEMA) were prepared using 1,4-bis(thiobenzoylthiomethyl)benzene and 1,4-bis(2-(thiobenzoylthio)prop-2-yl)benzene as RAFT agents, respectively. Dually responsive multiblock copolymers were synthesized in a single aminolysis/oxidation step from the α,ω-bis(dithioester)-terminated PNIPAM and PDMAEMA. The copolymers and their stimulus-responsive behavior were characterized by size exclusion chromatography, NMR, light scattering and atomic force microscopy. Due to the presence of redox-sensitive disulfide bonds between the blocks, the copolymers were readily reduced to the starting polymer blocks. The presence of temperature-responsive PNIPAM blocks provided the copolymers with the ability to assemble into core-shell nanostructures with hydrophobic PNIPAM as a core and cationic PDMAEMA as stabilizing shell when above the phase transition temperatures of PNIPAM. The temperature-induced assembly of the copolymers also showed substantial pH sensitivity. The phase transition temperature increased with decreasing pH, while molecular weight of the assemblies decreased.
我们报道了通过可逆加成-断裂链转移(RAFT)聚合反应合成温度和氧化还原响应性多嵌段共聚物。分别使用1,4-双(硫代苯甲酰硫甲基)苯和1,4-双(2-(硫代苯甲酰硫)丙-2-基)苯作为RAFT试剂,制备了结构明确的α,ω-双(二硫酯)官能化聚(N-异丙基丙烯酰胺)(PNIPAM)和聚(甲基丙烯酸2-(二甲氨基)乙酯)(PDMAEMA)。在一个氨解/氧化步骤中,由α,ω-双(二硫酯)封端的PNIPAM和PDMAEMA合成了双响应性多嵌段共聚物。通过尺寸排阻色谱、核磁共振、光散射和原子力显微镜对共聚物及其刺激响应行为进行了表征。由于嵌段之间存在氧化还原敏感的二硫键,共聚物很容易还原为起始聚合物嵌段。温度响应性PNIPAM嵌段的存在使共聚物能够在高于PNIPAM的相转变温度时组装成核壳纳米结构,其中疏水性PNIPAM为核,阳离子PDMAEMA为稳定壳。共聚物的温度诱导组装也表现出显著的pH敏感性。相转变温度随pH值降低而升高,而组装体的分子量降低。