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Frontal polymerization synthesis and drug delivery behavior of thermo-responsive poly(N-isopropylacrylamide) hydrogel

机译:热敏性聚(N-异丙基丙烯酰胺)水凝胶的前沿聚合反应及药物传递行为

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摘要

Thermo-responsive hydrogels of poly(N-isopropylacrylamide) (PNIPAm) were prepared by fontal polymerization and investigated as a temperature-triggered delivery device for the model drug aspirin. The influence of relative amount of reactant components on the feature of the polymerization front was studied. Furthermore, aspirin was loaded into hydrogels prepared by fontal polymerization method and classical polymerization, respectively, and its release characteristics were determined under different temperature conditions (25 °C and 37 °C). The drug storages and kinetic parameters for two hydrogels indicated that drug-loading capacity and drug release of frontal polymerization (FP) hydrogel were improved as compared with the classical polymerization (CP) one. Scanning electronic microscope and differential scanning calorimetry (DSC) results could account for these improvements in drug delivery for FP hydrogel. The above results indicate that FP can be an alternative method for the preparation of PNIPAm hydrogels used as drug delivery devices with less time consuming and easier protocols.
机译:聚(N-异丙基丙烯酰胺)(PNIPAm)的热响应水凝胶是通过字体聚合制备的,并作为模型药物阿司匹林的温度触发传递装置进行了研究。研究了反应物组分的相对量对聚合前沿特征的影响。此外,将阿司匹林分别装入通过常规聚合法和经典聚合法制备的水凝胶中,并在不同温度条件下(25℃和37℃)测定其释放特性。两种水凝胶的药物储存和动力学参数表明,与经典的聚合(CP)相比,额叶聚合(FP)水凝胶的载药量和药物释放得到改善。扫描电子显微镜和差示扫描量热法(DSC)的结果可以解释FP水凝胶在药物递送方面的这些改进。以上结果表明,FP可以作为制备PNIPAm水凝胶的替代方法,该PNIPAm水凝胶用作药物输送装置,耗时少,操作简便。

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