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    张蕾蕾, 唐安琪, 王章慧, 张梦晓, 徐丽, 朱利平. 以ZIF-8为模板制备聚多巴胺/聚乙二醇复合纳米胶囊[J]. 功能高分子学报, 2018, 31(6): 546-552. doi: 10.14133/j.cnki.1008-9357.20180714001
    引用本文: 张蕾蕾, 唐安琪, 王章慧, 张梦晓, 徐丽, 朱利平. 以ZIF-8为模板制备聚多巴胺/聚乙二醇复合纳米胶囊[J]. 功能高分子学报, 2018, 31(6): 546-552. doi: 10.14133/j.cnki.1008-9357.20180714001
    ZHANG Lei-lei, TANG An-qi, WANG Zhang-hui, ZHANG Meng-xiao, XU Li, ZHU Li-ping. Preparation of Polydopamine/Poly(ethylene glycol) Composite Nanocapsules with ZIF-8 Nanoparticles as Templates[J]. Journal of Functional Polymers, 2018, 31(6): 546-552. doi: 10.14133/j.cnki.1008-9357.20180714001
    Citation: ZHANG Lei-lei, TANG An-qi, WANG Zhang-hui, ZHANG Meng-xiao, XU Li, ZHU Li-ping. Preparation of Polydopamine/Poly(ethylene glycol) Composite Nanocapsules with ZIF-8 Nanoparticles as Templates[J]. Journal of Functional Polymers, 2018, 31(6): 546-552. doi: 10.14133/j.cnki.1008-9357.20180714001

    以ZIF-8为模板制备聚多巴胺/聚乙二醇复合纳米胶囊

    Preparation of Polydopamine/Poly(ethylene glycol) Composite Nanocapsules with ZIF-8 Nanoparticles as Templates

    • 摘要: 在水相条件下,多巴胺(DA)在沸石咪唑酯骨架材料(ZIF-8)模板上自聚-复合,并进一步接枝聚乙二醇(PEG),制备了以ZIF-8纳米颗粒为核,聚多巴胺/聚乙二醇(PDA/PEG)为壳的PDA/PEG@ZIF-8复合纳米粒子。进一步将ZIF-8模板蚀刻去除,得到PDA/PEG复合纳米胶囊。利用红外光谱、X射线衍射、扫描电镜、透射电镜、纳米粒度和Zeta电位分析仪等手段对复合纳米粒子和纳米胶囊的化学结构、晶相结构和形貌进行了表征。结果表明:通过该方法可制备粒径为80 nm左右的PDA/PEG@ZIF-8复合纳米粒子,将ZIF-8蚀刻后得到的PDA/PEG复合纳米胶囊平均粒径缩小到34 nm,PEG的引入有利于提高纳米粒子和纳米胶囊在水中的分散性和稳定性。

       

      Abstract: Nanocapsules have been widely applied in drug delivery and controlled release. In this work, a class of polydopamine/poly(ethylene glycol) (PDA/PEG) composite nanocapules were developed with a zeolite imidazole frameworks (ZIF-8) as the template. PDA was first coated onto the as-synthesized ZIF-8 nanoparticles by mussel-inspired oxidation and self-polymerization of dopamine in alkaline aqueous condition. PEG chains were then grafted onto the PDA-coated ZIF-8 particles by the Michael addition or Shiff-base reaction between amine-terminated PEG and PDA coatings. Further, the ZIF-8 templates were etched and removed by the decrease of pH value of the suspension, and the PDA/PEG composite nanocapsules were obtained. The chemical compositions, crystal structures, physical morphologies, particle size distribution and charged characteristics of the intermediates PDA@ZIF-8 and PDA/PEG@ZIF-8 nanoparticles were characterized in detail. The experimental results showed that the PDA/PEG@ZIF-8 composite nanoparticles were prepared successfully and the average particle size was about 80 nm. The average size of the PDA/PEG composite nanocapsules reduced to about 34 nm due to the etching and removal of ZIF-8 templates. The introduction of PEG brushes was advantageous to improve the dispersion and stability of nanoparticles and nanocapsules in water. This work develops a new approach for the preparation of polymer nanocapsules used in drug delivery and controlled release.

       

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