Li Siqi, Wang Qingshuang, Li Zhilin, Zhang Jiahe, Jiang Xue, Liu Shuai, Lu Changshun, Liu Tianhui, Feng Xiangru
College of Life Science and Technology, Changchun University of Science and Technology, Changchun 130022, Jilin, China.
College of Life Science and Technology, Changchun University of Science and Technology, Changchun 130022, Jilin, China.
Nanomedicine. 2025 Feb;64:102802. doi: 10.1016/j.nano.2025.102802. Epub 2025 Jan 7.
Exploiting the unique physiological and biochemical characteristics of the tumor microenvironment, the development of a polypeptide nanogel capable of responding to these specific properties holds great promise as an effective antitumor strategy. In this study, we synthesized a glutathione-responsive (GSH-responsive) methylated poly (ethylene glycol)-poly (phenylalanine)-poly (cystine) block copolymer (mPPC) through one-step ring-opening polymerization. Shikonin (SHK) was encapsulated within nanogel, designated as mPPC/SHK. The biocompatible and safe nature of mPPC facilitated its accumulation at the tumor site through enhanced permeability and retention effect, leading to efficient release of SHK upon stimulation by high concentrations of GSH. As anticipated, the group of mPPC/SHK displayed enhanced efficacy against tumors, resulting in a tumor inhibition rate of 69.97 % in the 4T1 breast cancer model. Overall, this GSH-responsive polypeptide nanogel encapsulating SHK has tremendous potential as a promising biomedical agent for effective tumor nanotherapy.
利用肿瘤微环境独特的生理和生化特性,开发一种能够响应这些特定特性的多肽纳米凝胶作为一种有效的抗肿瘤策略具有巨大的潜力。在本研究中,我们通过一步开环聚合合成了一种谷胱甘肽响应型(GSH响应型)甲基化聚(乙二醇)-聚(苯丙氨酸)-聚(胱氨酸)嵌段共聚物(mPPC)。将紫草素(SHK)包裹在纳米凝胶中,命名为mPPC/SHK。mPPC的生物相容性和安全性通过增强的渗透和滞留效应促进了其在肿瘤部位的积累,导致在高浓度GSH刺激下SHK的有效释放。正如预期的那样,mPPC/SHK组对肿瘤显示出增强的疗效,在4T1乳腺癌模型中的肿瘤抑制率为69.97%。总体而言,这种包裹SHK的GSH响应型多肽纳米凝胶作为一种有前途的生物医学剂用于有效的肿瘤纳米治疗具有巨大的潜力。