Sugihara Shinji, Sudo Masahiro, Maeda Yasushi
Department of Applied Chemistry and Biotechnology, Graduate School of Engineering , University of Fukui , 3-9-1 Bunkyo , Fukui 910-8507 , Japan.
Langmuir. 2019 Feb 5;35(5):1346-1356. doi: 10.1021/acs.langmuir.8b01558. Epub 2018 Aug 27.
Biomimetic ABC triblock copolymers of poly[2-(methacryloyloxy)ethyl phosphorylcholine]- b-poly[2-(dimethylamino)ethyl methacrylate]- b-poly(2-hydroxypropyl methacrylate) (PMPC- b-PDMA- b-PHPMA) were synthesized by RAFT aqueous dispersion polymerization of 2-hydroxypropyl methacrylate (HPMA) in the presence of a PMPC- b-PDMA macromolecular chain transfer agent (macro-CTA). This ABC triblock copolymer deploys well-known biocompatible PMPC and PDMA for the coordination of Ag ions to form silver nanoparticles in situ on reduction, and PHPMA for assembling (core) in water. The synthesis of PMPC- b-PDMA- b-PHPMA starts when both the reactive steric stabilizer of PMPC- b-PDMA macro-CTA and HPMA monomer are dissolved in water. The growing PHPMA is not soluble in water and begins to assemble based on three-layer onion micelles, in which the outer and inner shells are PMPC and PDMA, respectively. In the synthesis of PMPC- b-PDMA- b-PHPMA at a constant 25% (w/w) solids concentration, the resultant assemblies change from spheres to worms to jellyfishes to vesicles when the targeted PHPMA chain length increases from 100mer to 400mer at full monomer conversion. Furthermore, in the synthesis of identical PMPC- b-PDMA- b-PHPMA copolymers, the assembly morphology can be controlled from vesicles to spheres through worms by varying the solids concentration in the polymerization mixture, decreasing from 25% (w/w) to 15% (w/w) at full monomer conversion. Thus, the final morphology can be tuned by the degree of polymerization of HPMA and the solids concentration in the polymerization mixture. Using the resultant three PMPC- b-PDMA- b-PHPMA assemblies as scaffolds, Ag(0) nanoparticles (Ag-NPs) are obtained through in situ reduction of AgNO facilitated by electrostatic interactions between the Ag ions and PDMA moieties. The resultant Ag-NPs loaded in the assemblies exhibit excellent stability, dispersibility, and activity of catalyst for the reduction of p-nitrophenol. The order of rate constants for the reduction using Ag-NPs loaded in the assemblies is worms > vesicles > spheres, which corresponds to the order of the surface areas of the assemblies of PMPC- b-PDMA- b-PHPMA. These results can be achieved thanks to the kinetically frozen PMPC- b-PDMA- b-PHPMA assemblies with identical compositions.
聚[2-(甲基丙烯酰氧基)乙基磷酰胆碱]-b-聚[2-(二甲氨基)乙基甲基丙烯酸酯]-b-聚(甲基丙烯酸2-羟丙酯)(PMPC-b-PDMA-b-PHPMA)的仿生ABC三嵌段共聚物是在PMPC-b-PDMA大分子链转移剂(macro-CTA)存在下,通过甲基丙烯酸2-羟丙酯(HPMA)的可逆加成-断裂链转移(RAFT)水分散聚合反应合成的。这种ABC三嵌段共聚物采用众所周知的生物相容性PMPC和PDMA来配位Ag离子,在还原时原位形成银纳米颗粒,并用PHPMA在水中进行组装(形成核)。当PMPC-b-PDMA macro-CTA的反应性空间稳定剂和HPMA单体都溶解在水中时,PMPC-b-PDMA-b-PHPMA的合成开始。生长的PHPMA不溶于水,并开始基于三层洋葱状胶束进行组装,其中外层和内层壳分别是PMPC和PDMA。在固体浓度恒定为25%(w/w)的情况下合成PMPC-b-PDMA-b-PHPMA时,当目标PHPMA链长在单体完全转化时从100聚体增加到400聚体时,所得组装体从球形变为蠕虫状再变为水母状最后变为囊泡状。此外,在合成相同的PMPC-b-PDMA-b-PHPMA共聚物时,通过改变聚合混合物中的固体浓度,在单体完全转化时从25%(w/w)降至15%(w/w),组装形态可以通过蠕虫状从囊泡状控制为球形。因此,最终形态可以通过HPMA的聚合度和聚合混合物中的固体浓度来调节。使用所得的三种PMPC-b-PDMA-b-PHPMA组装体作为支架,通过Ag离子与PDMA部分之间的静电相互作用促进AgNO的原位还原,获得Ag(0)纳米颗粒(Ag-NPs)。负载在组装体中的所得Ag-NPs表现出优异的稳定性、分散性和用于对硝基苯酚还原的催化剂活性。使用负载在组装体中的Ag-NPs进行还原的速率常数顺序为蠕虫状>囊泡状>球形,这与PMPC-b-PDMA-b-PHPMA组装体的表面积顺序相对应。由于具有相同组成的动力学冻结的PMPC-b-PDMA-b-PHPMA组装体,这些结果得以实现。