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Visible-light-sensitive titanium dioxide nanoplatform for tumor-responsive Fe2+ liberating and artemisinin delivery

机译:可见光敏感的二氧化钛纳米平台可释放肿瘤并释放Fe2 +和青蒿素

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摘要

Artemisinin is a kind of Fe2+-dependent drugs. Artemisinin and Fe2+ co-transport systems can improve its anti-tumor effect. In this study, a visible light-sensitive nanoplatform (HA-TiO2-IONPs/ART) was developed. Detailed investigation demonstrated that HA-TiO2-IONPs/ART could realize Fe2+ and artemisinin synchronous co-delivery and tumor-responsive release. This feature enhanced the anti-tumor efficiency of artemisinin significantly. In vitro results proved that hyaluronic acid modification could improve the biocompatibility, dispersion stability and cytophagy ability of nanocarriers. Furthermore, this drug delivery system could generate reactive oxygen species under visual light irradiation. In vitro and in vivo experiments demonstrated that HA-TiO2-IONPs/ART combining with laser irradiation displayed the best anti-tumor efficacy. This study affords a promising idea to improve the curative efficiency of artemisinin analogs for cancer therapy.
机译:青蒿素是一种Fe 2 + 依赖性药物。青蒿素和Fe 2 + 共转运系统可提高其抗肿瘤作用。在这项研究中,开发了可见光敏感的纳米平台(HA-TiO2-IONPs / ART)。详细研究表明,HA-TiO2-IONPs / ART可以实现Fe 2 + 和青蒿素的同步共释放和肿瘤反应释放。该特征显着增强了青蒿素的抗肿瘤效率。体外实验结果表明,透明质酸修饰可以提高纳米载体的生物相容性,分散稳定性和细胞吞噬能力。此外,该药物递送系统可以在可见光照射下产生活性氧。体外和体内实验表明,HA-TiO2-IONPs / ART与激光照射相结合显示出最佳的抗肿瘤功效。这项研究提供了一个有前途的想法,以提高青蒿素类似物治疗癌症的疗效。

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