首页> 外文期刊>ACS Omega >Cancer Cell Membrane-Decorated Zeolitic-Imidazolate Frameworks Codelivering Cisplatin and Oleanolic Acid Induce Apoptosis and Reversed Multidrug Resistance on Bladder Carcinoma Cells
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Cancer Cell Membrane-Decorated Zeolitic-Imidazolate Frameworks Codelivering Cisplatin and Oleanolic Acid Induce Apoptosis and Reversed Multidrug Resistance on Bladder Carcinoma Cells

机译:癌细胞膜修饰的沸石-咪唑酸盐骨架编码顺铂和齐墩果酸诱导膀胱癌细胞凋亡和逆转的多药耐药性。

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Combination therapy is emerging as a preferable approach in cancer therapy with minimized side effects and elevated performance. Nevertheless, the poor targeting and drug loading of currently available drug delivery systems (DDSs) are the main difficulties to realize preferable combination therapy of cancer. As a result, a cancer cell membrane-decorated zeolitic-imidazolate framework hybrid nanoparticle (HP) was successfully constructed in our study to codeliver cisplatin (DDP) and oleanolic acid (OLA). Our results showed positive results of the platform (HP/DDP/OLA) for the treatment of bladder cancer (SW780). In detail, HP/DDP/OLA could enhance apoptosis while reverse multidrug resistance in SW780 cells than free drugs alone or monodelivery systems, which might be a suitable DDS for codelivery of different drugs with great promise.
机译:组合疗法作为具有最小化副作用和提高的性能的癌症疗法中的优选方法正在出现。然而,当前可用的药物递送系统(DDS)的较差的靶向性和药物负荷是实现优选的癌症联合治疗的主要困难。结果,在我们的研究中成功构建了癌细胞膜装饰的沸石-咪唑框架骨架杂化纳米粒子(HP),以编码顺铂(DDP)和齐墩果酸(OLA)。我们的结果显示该平台(HP / DDP / OLA)用于治疗膀胱癌(SW780)的积极结果。详细地讲,HP / DDP / OLA与单独的游离药物或单一递送系统相比,可以增强SW780细胞中的细胞凋亡,同时逆转多药耐药性,这可能是一种适用于不同药物共递送的DDS,前景广阔。

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