Institute of Nanochemistry and Nanobiology, School of Environmental and Chemical Engineering, Shanghai University, Shanghai 200444, China; Key Laboratory of Smart Drug Delivery, Ministry of Education, Department of Pharmaceutics, School of Pharmacy, Fudan University, Shanghai 201203, China.
Institute of Nanochemistry and Nanobiology, School of Environmental and Chemical Engineering, Shanghai University, Shanghai 200444, China.
J Colloid Interface Sci. 2025 Jan;677(Pt B):79-90. doi: 10.1016/j.jcis.2024.08.037. Epub 2024 Aug 8.
Photothermal therapy combined with chemotherapy has shown great promise in the treatment of cancer. In this synergistic system, a safe, stable, and efficient photothermal agent is desired. Herein, an effective photothermal agent, carbon quantum dots (CQDs), was initially synthesized and then rationally constructed a folic acid (FA)-targeted photothermal multifunctional nanoplatform by encapsulating CQDs and the anticancer drug doxorubicin (DOX) in the liposomes. Indocyanine green (ICG), a near infrared (NIR) photothermal agent, approved by the U.S. Food and Drug Administration, was embedded in the bilayer membrane to further enhance the photothermal effects and facilitate the rapid cleavage of liposomes for drug release. Triggered by the NIR laser, this engineered photothermal multifunctional nanoplatform, not only exhibited an excellent performance with the photothermal conversion efficiency of up to 47.14%, but also achieved controlled release of the payloads. In vitro, and in vivo experiments demonstrated that the photothermal multifunctional nanoplatform had excellent biocompatibility, enhanced tumor-specific targeting, stimuli-responsive drug release, effective cancer cell killing and tumor suppression through multi-modal synergistic therapy. The successful construction of this NIR light-triggered targeted photothermal multifunctional nanoplatform will provide a promising strategy for the design and development of synergistic chemo-photothermal combination therapy and improve the therapeutic efficacy of cancer treatment.
光热疗法联合化学疗法在癌症治疗中显示出巨大的应用前景。在这种协同系统中,需要一种安全、稳定且高效的光热试剂。本文中,我们首先合成了一种有效的光热试剂——碳量子点(CQDs),然后通过将 CQDs 和抗癌药物阿霉素(DOX)封装在脂质体中,合理构建了叶酸(FA)靶向的光热多功能纳米平台。美国食品和药物管理局批准的近红外(NIR)光热试剂吲哚菁绿(ICG)被嵌入双层膜中,以进一步增强光热效应,并促进脂质体的快速裂解以释放药物。在近红外激光的触发下,这种工程化的光热多功能纳米平台不仅表现出高达 47.14%的光热转换效率,还实现了载药的可控释放。体外和体内实验表明,该光热多功能纳米平台具有优异的生物相容性、增强的肿瘤特异性靶向、刺激响应性药物释放、有效杀伤癌细胞和通过多模式协同治疗抑制肿瘤。这种 NIR 光触发的靶向光热多功能纳米平台的成功构建将为协同化疗-光热联合治疗的设计和开发提供一种有前景的策略,并提高癌症治疗的疗效。