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Core-Shell Structure Design of Hollow Mesoporous Silica Nanospheres Based on Thermo-Sensitive PNIPAM and pH-Responsive Catechol-Fe3+ Complex

机译:基于热敏PNIPAM和pH响应型邻苯二酚-Fe3 +配合物的中孔二氧化硅纳米球核-壳结构设计

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摘要

A kind of core-shell hybrid nanoparticle comprised of a hollow mesoporous silica nanoparticles (HMS) core and a copolymer shell bearing N-(3,4-dihydroxyphenethyl) methacrylamide (DMA) and N-isopropylacrylamide (NIPAM) as responsive moieties was prepared. Moreover, the factors that could impact the surface morphology and hierarchical porous structure were discussed. In the presence of Fe , catechol-Fe complexes were formed to achieve pH-responsive polymer shell, combining with thermal-sensitiveness of poly(N-isopropylacrylamide). Doxorubicin (DOX) was applied as a model drug and the behaviors of its loading/release behaviors were investigated to prove the idea. The results exhibited a significant drug loading capacity of 8.6% and embed efficiency of 94.6% under 1 mg ml DOX/PBS solution. In fact, the loading capacity of drug can be easily improved to as high as 28.0% by increasing the DOX concentration. The vitro cytotoxicity assay also indicated that the as-prepared nanoparticles have no significant cytotoxicity on RAW 264.7 cells. The in vitro experiment showed that the cumulative release of DOX was obviously dependent on the temperature and pH values. This pH/temperature-sensitive hollow mesoporous silica nanosphere is expected to have potential applications in controlled drug release.
机译:制备了一种核-壳杂化纳米颗粒,其由中空介孔二氧化硅纳米颗粒(HMS)核和带有N-(3,4-二羟基苯乙基)甲基丙烯酰胺(DMA)和N-异丙基丙烯酰胺(NIPAM)作为响应部分的共聚物壳组成。此外,讨论了影响表面形态和分层多孔结构的因素。在Fe的存在下,形成邻苯二酚-Fe配合物以实现pH响应的聚合物壳,并结合了聚(N-异丙基丙烯酰胺)的热敏性。阿霉素(DOX)被用作模型药物,并对其负载/释放行为进行了研究以证明这一想法。结果显示,在1 mg ml DOX / PBS溶液中,显着的载药量为8.6%,包埋率为94.6%。实际上,通过增加DOX浓度可以很容易地将药物的载量提高到28.0%。体外细胞毒性试验还表明,所制备的纳米颗粒对RAW 264.7细胞没有明显的细胞毒性。体外实验表明,DOX的累积释放明显取决于温度和pH值。预期这种对pH /温度敏感的空心中孔二氧化硅纳米球在控制药物释放方面具有潜在的应用。

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