Chen Xiaojie, Zou Jiafeng, Zhang Ke, Zhu Jingjing, Zhang Yue, Zhu Zhihong, Zheng Hongyue, Li Fanzhu, Piao Ji-Gang
College of Pharmaceutical Sciences, Zhejiang Chinese Medical University, Hangzhou 310053, China.
Libraries of Zhejiang Chinese Medical University, Zhejiang Chinese Medical University, Hangzhou 310053, China.
Acta Pharm Sin B. 2021 Jan;11(1):271-282. doi: 10.1016/j.apsb.2020.08.009. Epub 2020 Aug 26.
The chemotherapy combined with photothermal therapy has been a favorable approach for the treatment of breast cancer. In present study, nanoparticles with the characteristics of photothermal/matrix metalloproteinase-2 (MMP-2) dual-responsive, tumor targeting, and size-variability were designed for enhancing the antitumor efficacy and achieving "on-demand" drug release markedly. Based on the thermal sensitivity of gelatin, we designed a size-variable gelatin nanoparticle (GNP) to encapsulate indocyanine green (ICG) and doxorubicin (DOX). Under an 808 nm laser irradiation, GNP-DOX/ICG responded photothermally and swelled in size from 71.58 ± 4.28 to 160.80 ± 9.51 nm, which was beneficial for particle retention in the tumor sites and release of the loaded therapeutics. Additionally, GNP-DOX/ICG showed a size reduction of the particles to 33.24 ± 4.11 nm and further improved drug release with the degradation of overexpressed MMP-2 in tumor. In the subsequently performed experiments, it was confirmed that GNP-DOX/ICG could provide a therapeutic effect that was enhanced and synergistic. Consequently, GNP-DOX/ICG could efficiently suppress the growth of 4T1 tumor . In conclusion, this study may provide a promising strategy in the rational design of drug delivery nanosystems based on gelatin for chemo-photothermal therapy to achieve synergistically enhanced therapeutic efficacy against breast cancer.
化疗联合光热疗法一直是治疗乳腺癌的一种有效方法。在本研究中,设计了具有光热/基质金属蛋白酶-2(MMP-2)双响应、肿瘤靶向和尺寸可变特性的纳米颗粒,以显著提高抗肿瘤疗效并实现“按需”药物释放。基于明胶的热敏性,我们设计了一种尺寸可变的明胶纳米颗粒(GNP)来包裹吲哚菁绿(ICG)和阿霉素(DOX)。在808nm激光照射下,GNP-DOX/ICG发生光热响应,尺寸从71.58±4.28nm膨胀至160.80±9.51nm,这有利于颗粒在肿瘤部位的滞留和所载治疗药物的释放。此外,随着肿瘤中过表达的MMP-2的降解,GNP-DOX/ICG的颗粒尺寸减小至33.24±4.11nm,并进一步改善了药物释放。在随后进行的实验中,证实GNP-DOX/ICG可提供增强的协同治疗效果。因此,GNP-DOX/ICG可有效抑制4T1肿瘤的生长。总之,本研究可能为基于明胶的化疗-光热疗法药物递送纳米系统的合理设计提供一种有前景的策略,以实现对乳腺癌协同增强的治疗效果。