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首页> 外文期刊>European journal of pharmaceutics and biopharmaceutics: official journal of Arbeitsgemeinschaft fuer Pharmazeutische Verfahrenstechnik e.V >Fluorescent carbon dot-gated multifunctional mesoporous silica nanocarriers for redox/enzyme dual-responsive targeted and controlled drug delivery and real-time bioimaging
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Fluorescent carbon dot-gated multifunctional mesoporous silica nanocarriers for redox/enzyme dual-responsive targeted and controlled drug delivery and real-time bioimaging

机译:用于氧化还原的荧光碳点门络型多功能介孔二氧化硅纳米载体用于氧化还原的双响应靶向和受控药物递送和实时生物分析

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摘要

A distinctive and personalized nanocarrier is described here for controlled and targeted antitumor drug delivery and real-time bioimaging by combining a redox/enzyme dual-responsive disulfide-conjugated carbon dot with mesoporous silica nanoparticles (MSN-SS-CDHA). The carbon dot with controlling and targeting abilities was prepared through a polymerizing reaction by applying citric acid and HA as starting materials (named CDHA). The as-prepared MSN-SS-CDHA exhibited not only superior photostability and excellent biocompatibility, but also the ability to target A549 cells with overexpression of CD44 receptors. Upon loading the antitumor drug, doxorubicin (DOX), into the mesoporous channels of MSN nanoparticles, CDHA with a diameter size of 3 nm completely blocked the pore entrance of DOX-encapsulated MSN nanoparticles with a pore size of about 3 nm, thus preventing the premature leakage of DOX and increasing the antitumor activity until being triggered by specific stimuli in the tumor environment. The results of the cell imaging and cytotoxicity studies demonstrated that the redox/enzyme dual-responsive DOX-encapsulated MSN-SS-CDHA nanoparticles can selectively deliver and control the release of DOX into tumor cells. Ex vivo fluorescence images showed a much stronger fluorescence of MSN-SS-CDHA-DOX in the tumor site than in normal tissues, greatly facilitating the accumulation of DOX in the target tissue. However, its counterpart, MSN-SH-DOX exhibited no or much lower tumor cytotoxicity and drug accumulation in tumor tissue. In addition, MSN-SS-CD was also used as a control to investigate the ability of MSN-SS-CDHA to target A549 cells. The results obtained indicated that MSN-SS-CDHA possessed a higher cellular uptake through the CD44 receptor-mediated endocytosis compared with MSN-SS-CD in the A549 cells. Such specific redox/enzyme dual-responsive targeted nanocarriers are a useful strategy achieving selective controlled and targeted delivery of therapeutic reagents with realtime bioimaging, and may also facilitate the development of drug delivery systems for a number of clinical applications. (C) 2017 Elsevier B.V. All rights reserved.
机译:这里描述了一种独特的和个性化的纳米载波,用于通过将氧化还原/酶双响应二硫键 - 共轭碳点与中孔二氧化硅纳米颗粒(MSN-SS-CDHA)组合来进行控制和靶向抗肿瘤药物递送和实时生物载体。通过将柠檬酸和HA作为原料(命名为CDHA),通过聚合反应制备具有控制和靶向能力的碳点。制备的MSN-SS-CDHA不仅具有卓越的光稳定性和优异的生物相容性,而且还具有靶向A549细胞的能力,其具有过表达的CD44受体。在将抗肿瘤药物(DOX)加载到MSN纳米颗粒的中孔通道中时,直径尺寸为3nm的CDHA完全阻断了孔径为约3nm的DOX封装MSN纳米颗粒的孔入口,从而防止了DOX过早渗漏并增加抗肿瘤活性,直至通过肿瘤环境中的特异性刺激引发。细胞成像和细胞毒性研究的结果证明了氧化还原/酶双响应DOX封装的MSN-SS-CDHA纳米颗粒可以选择性地递送和控制DOX释放到肿瘤细胞中。在肿瘤部位显示出比正常组织中的MSN-SS-CDHA-DOX的荧光更强大,大大促进了DOX在靶组织中的积累。然而,其对应物,MSN-SH-DOX在肿瘤组织中表现出没有或更低的肿瘤细胞毒性和药物积累。此外,MSN-SS-CD也用作对照,以研究MSN-SS-CDHA靶向A549细胞的能力。得到的结果表明,与A549细胞中的MSN-SS-CD相比,MSN-SS-CDHA通过CD44受体介导的内吞作用具有更高的细胞吸收。这种特定的氧化还原/酶双响应靶向纳米载体是实现具有实时生物模拟的选择性控制和靶向递送治疗试剂的有用策略,并且还可以促进用于许多临床应用的药物递送系统。 (c)2017 Elsevier B.v.保留所有权利。

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