体外光动力治疗中基于卵清蛋白、磷酸a和Zn2+的多组分协同组装纳米药物

Xiaoyan Ma , Yamei Liu , Shukun Li , Kenji Ogino , Ruirui Xing , Xuehai Yan
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引用次数: 2

摘要

光动力疗法(PDT)是一种无创、副作用小的治疗方法。然而,光敏剂(PS)作为PDT的主要成分,在给药过程中会发生聚集,限制活性氧(ROS)的产生,导致PDT的治疗效果不理想。在此,我们展示了一种基于金属结合蛋白(卵清蛋白,OVA)、金属离子(Zn2+)和光敏药物(PheoA)结合的多组分配位共组装策略,用于构建抗肿瘤PDT的超分子光敏纳米药物。所得光敏剂纳米药物具有明确的纳米棒结构、良好的胶体分散性和高包封效率。最重要的是,多组分共组装纳米棒在肿瘤细胞中具有良好的生理环境稳定性和对酸性环境的按需释放PS的能力。这些特点导致肿瘤细胞中ROS生成水平较高,有利于体外PDT治疗效果的增强。
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Multicomponent coassembled nanodrugs based on ovalbumin, pheophorbide a and Zn2+ for in vitro photodynamic therapy

Photodynamic therapy (PDT) has been considered as a therapeutic method based on non-invasiveness and lower side effect. However, photosensitizers (PS), as a major component of PDT, suffer from aggregation and limit reactive oxygen species (ROS) generation in the delivery process, thus causing unsatisfactory therapeutic effect of PDT. Herein, we demonstrate a multicomponent coordination coassembly strategy based on the combination of metal-binding protein (ovalbumin, OVA), metal ions (Zn2+) and a photosensitive drug (pheophorbide a, PheoA) for constructing supramolecular photosensitive nanodrugs towards antitumor PDT. The resulting photosensitizer nanodrugs exhibit well-defined nanorod structures, good colloidal dispersity, and high encapsulation efficiency. Most importantly, multicomponent coassembled nanorods possess favorable stability of physiological environment and on-demand release of PS in response to an acidic ambient in tumor cells. These features result in the high level of ROS generation in tumor cells, benefiting for enhanced therapeutic effect of in vitro PDT.

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