光动力疗法
光敏剂
体内
癌症研究
肿瘤缺氧
缺氧(环境)
单线态氧
转移
活性氧
癌细胞
癌症
药理学
材料科学
医学
氧气
放射治疗
化学
生物
内科学
生物化学
光化学
生物技术
有机化学
作者
Yanan Wang,Jian Huo,Shuang Li,Ran Huang,Daopeng Fan,Hanghang Cheng,Bo Wan,Yongkun Du,Hua He,Gaiping Zhang
标识
DOI:10.1021/acsami.1c23121
摘要
Photodynamic therapy (PDT) can eradicate cancer cells under light irradiation, mainly because of reactive singlet oxygen (1O2) being transformed from intratumoral oxygen. Nonetheless, the consumption of oxygen during PDT results in serious hypoxic conditions and an elevated hypoxia-inducing factor-1α (HIF-1α) level that hamper further photodynamic efficacy and induce tumor metastasis. To address this problem, we developed hypoxia-assisted NP-co-encapsulating Ce6 (photosensitizer) and YC-1 (HIF-1α inhibitor) as a self-rectifiable nanoinhibitor for synergistic antitumor treatment. PDT-aggravated intracellular hypoxic stress facilitated NP dissociation to release the drug (YC-1), which achieved tumor killing and HIF-1α inhibition to further enhance the therapeutic effect of PDT and prevent tumor metastasis. Besides, in vivo studies revealed that the HC/PI@YC-1 NPs afforded synergistic anticancer efficacy with minimal toxicity. Therefore, this study provides a prospective approach against PDT drawbacks and combination cancer therapy.
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