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首页> 外文期刊>Colloids and Surfaces, B. Biointerfaces >Temperature and H2O2-operated nano-valves on mesoporous silica nanoparticles for controlled drug release and kinetics
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Temperature and H2O2-operated nano-valves on mesoporous silica nanoparticles for controlled drug release and kinetics

机译:介孔二氧化硅纳米粒子的温度和H2O2操作纳米阀用于受控药物释放和动力学

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摘要

Temperature and H2O2 dual-responsive nanoparticles were fabricated from ferrocene modified mesoporous silica (MSN-Fc) and beta-cyclodextrin-poly(N-isopropylacrylamide) (beta-CD-PNIPAM) star-shaped polymer due to the host-guest interactions for controlled drug release. The formation and structure of beta-CD-PNIPAM@MSN-Fc composite nanoparticles was confirmed by FTIR, TGA, TEM and N-2 adsorption-desorption isotherms. The size of nanoparticles was about 100-150 nm with well-ordered mesoporous structure and PNIPAM chains coating on the surface as outer shell. The channels of MSNs and hydrophobic cavities of beta-CD were all contributed to the high drug loading capacity for nanoparticles. The release of DOX from nanoparticles was enhanced with the increase of temperature above LCST or adding H2O2 in ambient O-2. The release kinetics were studied using different models to explain drug release mechanism. Furthermore, the drug loaded composite nanoparticles exhibited excellent anti-cancer activity.
机译:由于对受控的主机相互作用,由二茂铁改性的介孔二氧化硅(MSN-Fc)和β-环糊精)(β-Cd-PNIPAM)(β-Cd-丙烯酰胺)星形聚合物制成温度和H 2 O 2双响应纳米颗粒。药物释放。通过FTIR,TGA,TEM和N-2吸附 - 解吸等温线确认β-CD-PNIPAM @ MSN-Fc复合纳米颗粒的形成和结构。纳米颗粒的尺寸约为100-150nm,具有良好有序的介孔结构和表面上的泊米链涂层作为外壳。 β-CD的MSN和疏水性腔的通道都有助于纳米颗粒的高药物负载能力。随着LCST的温度的增加或在环境O-2中加入H2O2,增强了从纳米颗粒的DOX释放。使用不同的模型研究了释放动力学来解释药物释放机制。此外,药物负载复合纳米粒子表现出优异的抗癌活性。

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