Zhang Yeye, Lu Guangzhao, Yu Yuan, Zhang He, Gao Jie, Sun Zhiguo, Lu Ying, Zou Hao
Department of Pharmaceutical Sciences, School of Pharmacy, Second Military Medical University, Shanghai 200433, China.
Department of Pharmacy, Zhongshan Hospital, Fudan University, Shanghai 201203, China.
ACS Appl Bio Mater. 2019 Jan 22;2(1):495-503. doi: 10.1021/acsabm.8b00681. Epub 2019 Jan 11.
Light has several advantages as the stimulus for a triggered drug release. Currently, the applications of phototriggered drug-release devices (PDDs) are largely limited by two factors: the limited tissue penetration and detrimental effects caused by excitation light (ultraviolet or visible light). To address this disadvantage, this study developed nanocomposites based on upconversion nanoparticles (UC), which could convert near-infrared light to ultraviolet-visible light and trigger drug release. By loading UC and doxorubicin (DOX) into photoresponsive copolymer PEG-NMAB-PLA (PNP), near-infrared responsive copolymer upconversion nanocomposites (PNP-DOX-UC) were constructed. We proved that PNP-DOX-UC showed the fast release and strong cytotoxicity under near-infrared irradiation in vitro. The therapeutic efficacy study indicated that PNP-DOX-UC+ had the enhanced antitumor efficiency. In the study, UC becoming an internal ultraviolet-visible light source for near-infrared excitation develops an applicable and efficient approach to meet the requirements for UV/vis excitation, which is a major disadvantage in photosensitive materials developed for pharmaceutical and biomedical applications.
作为触发药物释放的刺激因素,光具有若干优势。目前,光触发药物释放装置(PDDs)的应用在很大程度上受到两个因素的限制:组织穿透性有限以及激发光(紫外线或可见光)造成的有害影响。为解决这一缺点,本研究开发了基于上转换纳米颗粒(UC)的纳米复合材料,其可将近红外光转换为紫外-可见光并触发药物释放。通过将UC和阿霉素(DOX)负载到光响应共聚物PEG-NMAB-PLA(PNP)中,构建了近红外响应共聚物上转换纳米复合材料(PNP-DOX-UC)。我们证明,PNP-DOX-UC在体外近红外照射下表现出快速释放和强细胞毒性。治疗效果研究表明,PNP-DOX-UC+具有增强的抗肿瘤效率。在该研究中,UC成为用于近红外激发的内部紫外-可见光光源,开发了一种适用且有效的方法来满足对紫外/可见光激发的要求,而这是为药物和生物医学应用开发的光敏材料中的一个主要缺点。