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pH- and redox-triggered synergistic controlled release of a ZnO-gated hollow mesoporous silica drug delivery system

机译:pH和氧化还原触发的ZnO门控中空介孔二氧化硅药物传递系统的协同控制释放

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摘要

Hollow mesoporous silica spheres (HMSS) have a hierarchical mesoporous structure composed of a hollow cavity and mesoporous shell available for high capacity drug storage. The covalent attachment of ZnO quantum dots (QDs) to the HMSS outer surface as gatekeepers via disulfide-conjugated two amide linkages encapsulated the anticancer drugs doxorubicin (DOX) within the HMSS cavities and pores, and minimized premature release of the drug. The controlled release of the drug from the ZnO-gated HMSS delivery system was realized by the dissolution of ZnO QDs upon a decrease in pH and cleavage of the disulfide bonds, which indicates that the pH-and redox-responsive controlled release of the drugs could be synergically stimulated by tumor cells with weakly acidic environments and high-expressed glutathione. The constructed ZnO-gated HMSS delivery system has promising applications in site-specific drug release for tumor chemotherapy.
机译:空心介孔二氧化硅球(HMSS)具有由中空空腔和介孔壳组成的分层介孔结构,可用于高容量药物存储。 ZnO量子点(QDs)通过二硫键结合的两个酰胺键作为守门员共价附着于HMSS外表面,将抗癌药阿霉素(DOX)封装在HMSS腔和孔内,并最大程度地减少了药物的过早释放。药物从ZnO门控HMSS递送系统中的控释是通过在pH值降低和二硫键断裂时ZnO QD的溶解来实现的,这表明pH和氧化还原响应性控释药物可以在弱酸性环境和高表达的谷胱甘肽中被肿瘤细胞协同刺激。构建的ZnO门控HMSS输送系统在肿瘤化疗的特定部位药物释放中具有广阔的应用前景。

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