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pH-responsive metallo-supramolecular nanogel for synergistic chemo-photodynamic therapy

机译:pH响应的金属超分子纳米凝胶用于协同化学光动力疗法

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摘要

Benefited from the high orientation of coordinated interaction, metallo-supramolecular materials have attracted enormous interest in many fields. Herein, a novel metallo-supramolecular nanogel (SNG)-based drug delivery system for synergistic chemo-photodynamic therapy is explored to enhance anticancer efficacy. It is fabricated by the metallo-supramolecular-coordinated interaction between tetraphenylporphyrin zinc (Zn-Por) and histidine. It can respond to tumor acid microenvironment to release the co-delivered anticancer drug and photosensitizer to kill the lesion cells. Zn-Por moieties in SNG keep the photosensitivity in the range of visible wavelength and possess the ability of generating active oxygen species for photodynamic therapy. The drug-loaded SNG provides a di-functional platform for chemotherapy and photodynamic therapy. Compared with the single chemotherapy of free doxorubicine (DOX) or photodynamic therapy of Zn-Por in SNG, DOX-loaded SNG with irradiation shows higher in vitro cytotoxicity and in vivo anticancer therapeutic activity, endowing the SNG with great potential in cancer treatments.
机译:得益于配位相互作用的高度取向,金属超分子材料在许多领域引起了极大的兴趣。在本文中,探索了用于协同化学光动力疗法的新型基于金属超分子纳米凝胶(SNG)的药物递送系统,以增强抗癌功​​效。它是由四苯基卟啉锌(Zn-Por)和组氨酸之间的金属-超分子配位相互作用制成的。它可以对肿瘤的酸性微环境作出反应,释放出共同提供的抗癌药物和光敏剂,以杀死病变细胞。 SNG中的Zn-Por部分可将光敏性保持在可见波长范围内,并具有为光动力疗法产生活性氧的能力。载有药物的SNG为化学疗法和光动力疗法提供了一个双功能平台。与游离阿霉素(DOX)的单一化学疗法或Zn-Por在SNG中的光动力疗法相比,带有DOX的SNG照射具有更高的体外细胞毒性和体内抗癌治疗活性,这使SNG在癌症治疗中具有巨大潜力。

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