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    双刺激响应型纳米载药系统的构建及性能

    Development and Properties of Dual Stimuli Responsive Nanocarrier for Drug Delivery

    • 摘要: 采用聚乙二醇单甲醚(mPEG)为亲水段,聚赖氨酸(PzLL)为疏水段,通过二硫键和碳氮双键串联桥连合成了两嵌段共聚物(mPEG-CN-SS-PzLL),其中的二硫键具有还原敏感性,碳氮双键具有pH酸敏感性。通过红外光谱和核磁共振谱等手段测试分析了产物的化学结构。将聚合物通过透析法自组装制备得到双刺激响应型纳米载药粒子。结果表明:该纳米载药粒子的药物包封率较高,达到52%。该载药系统在还原环境或酸性环境下具有良好的体外释药性能。

       

      Abstract: A block copolymer mPEG-CN-SS-PzLL was synthesized using methoxypolyethylene glycols (mPEG) as hydrophilic segment and poly (ε-benzyloxycarbonyl-L-lysine) (PzLL) as hydrophobic segment. The redox sensitive disulfide bond S=S and pH sensitive bond C=N were simultaneously incorporated in the copolymer structure. The resultant copolymers were comprehensively characterized by Fourier Transform Infrared Spectra (FT-IR) and 1H Nuclear Magnetic Resonance(1H-NMR). The copolymer could self assemble into dual stimuli responsive drug loaded nanoparticles by dialysis method. Results showed that these nanoparticles had prominent drug loading capability with high drug loaded efficiency up to 52%. The drug carrier system had a good in vitro release performance in reducing or acidic environment.

       

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