光敏剂
脂质体
光动力疗法
蓖麻毒素
适体
化学
药理学
生物物理学
纳米技术
医学
生物化学
分子生物学
材料科学
生物
光化学
毒素
有机化学
作者
Chun Hong Li,Jia Xie,Chen Men,Lin Liu,Cheng Zhi Huang,Chun Mei Li,Shu Jun Zhen
出处
期刊:ACS materials letters
[American Chemical Society]
日期:2024-04-18
卷期号:6 (5): 2050-2058
标识
DOI:10.1021/acsmaterialslett.4c00350
摘要
Ricin, a potent protein synthesis inhibitor, shows significant potential as an anticancer agent. However, the limited delivery efficiency to tumor cells hampers its therapeutic efficacy. Here, we propose a novel approach for precise delivery of ricin A-chain (RTA) to tumors using aptamer-functionalized liposomes. RTA initially binds to Golgi-targeting carbon dots (CDs), followed by the encapsulation of CDs–RTA conjugates in aptamer-functionalized liposomes. Leveraging the precise recognition between nucleolin and aptamers and CDs' Golgi targeting, we achieve efficient transportation of RTA to tumor cells, thereby facilitating its potent chemotherapeutic effect. Furthermore, we enhanced the therapeutic efficacy by incorporating the photosensitizer pheophorbide a (PPa) into liposomes. Combined with near-infrared laser-mediated photodynamic therapy and chemotherapy, the liposomal system exhibits superior antitumor activity compared to monotherapy. This synergistic bimodal approach holds great promise for various biomedical applications, particularly in the field of cancer therapy.
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