首页> 美国卫生研究院文献>ACS Omega >Ultrasonic De-cross-linking of the pH- and Magneto-ResponsivePHEMA/PMMA Microgel to Janus Nanoparticles: A New Synthesis Basedon Grafting from/Grafting to Polymerization
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Ultrasonic De-cross-linking of the pH- and Magneto-ResponsivePHEMA/PMMA Microgel to Janus Nanoparticles: A New Synthesis Basedon Grafting from/Grafting to Polymerization

机译:超声波与磁响应的解联PhEMA / PMMA微凝胶到Janus纳米粒子:基于新的合成从/移植到嫁接至聚合

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摘要

Stimuli-responsiveJanus nanoparticles (NPs) with a two-facialstructure have been used widely in biomedical applications. Amongseveral methods to prepare these NPs, surface-initiated atom transferradical polymerization (SI-ATRP) has received much attention due tothe precise deposition of polymers on the surface of the substrate.In this study, Janus nanoparticles with asymmetric surface chemistrywere prepared through a masking method in three steps involving thecovalent deposition of super paramagnetic iron oxide nanoparticles(SPIONs) on the cross-linked substrate based on methotrexate (MTX)-graftedpoly(2-hydroxyethyl methacrylate) (CPM), surface functionalizationof unreacted sites of immobilized SPIONs with 2-bromoisobutyryl bromide(BIBB) in order to prepare the macro-initiator (Br-Fe3O4-CPM), growing poly(methyl methacrylate) (PMMA) on the surfaceof the macro-initiator through the SI-ATRP method. Optical microscopywas utilized to monitor the successful modification of SPIONs. Poly(methylmethacrylate)-iron oxide-poly(2-hydroxyethyl methacrylate) (PMMA-Fe3O4-PHEMA) microgel was exposed to optimum ultrasound(US) waves to prepare the PMMA-Fe3O4-PHEMA nanoparticle.Transmission electron microscopy (TEM) was used to confirm the precisedeposition of polymers and the Janus structure. The MTX release ofUS-synthesized Janus NPs was studied in PBS at pH values of 7.4 and5.8. The release data were analyzed using the Excel add-in DDSolverprogram to evaluate the kinetics of the drug release process fromthe nanocarrier under different pH values.
机译:刺激反应Janus纳米粒子(NPS)用双面部结构已广泛用于生物医学应用中。之中几种准备这些NPS的方法,表面发起的原子转移自由基聚合(SI-ATRP)由于基材表面上的聚合物精确沉积。在本研究中,Janus纳米粒子具有不对称的表面化学通过掩蔽方法在涉及的三个步骤中制备超顺磁性氧化铁纳米粒子的共价沉积基于甲氨蝶呤(MTX) - 移植的交联基材上的(酱)聚(2-羟乙基甲基丙烯酸甲酯)(CPM),表面官能化用2-溴异丁酰基溴离防盐的未反应位点(BIBB)为了制备宏引发剂(BR-FE3O4-CPM),在表面上生长聚(甲基丙烯酸甲酯)(PMMA)通过SI-ATRP方法的宏引发剂。光学显微镜用于监测酱的成功修改。聚(甲基甲基丙烯酸酯) - 铁氧化物 - 聚(2-羟乙基甲基丙烯酸酯)(PMMA-FE3O4-PHEMA)微凝胶暴露于最佳超声波(美国)波以制备PMMA-FE3O4-PHEMA纳米粒子。透射电子显微镜(TEM)用于确认精确聚合物和Janus结构的沉积。 MTX释放在PB值的PBS中,在7.4和pH值中研究了美国合成的Janus NPS5.8。使用Excel加载程序进行分析释放数据DDSolver评估药物释放过程的动力学的计划在不同pH值下的纳米载体。

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