Camouflaged Virus‐Like‐Nanocarrier with a Transformable Rough Surface for Boosting Drug Delivery

• Published in: Angewandte Chemie International Edition Vol. 62; no. 14; pp. e202216188 - n/a
• Main Authors: Yu, Hongyue, Yu, Yan, Lin, Runfeng, Liu, Minchao, Zhou, Qiaoyu, Liu, Mengli, Chen, Liang, Wang, Wenxing, Elzatahry, Ahmed A., Zhao, Dongyuan, Li, Xiaomin
• Format: Journal Article
• Language: English
• Published: Germany Wiley Subscription Services, Inc 27.03.2023
• Edition: International ed. in English
• Subjects: Antitumor Agents; Blood circulation; Cell Line, Tumor; Doxorubicin - pharmacology; Drug Carriers; Drug Delivery; Drug Delivery Systems; Endocytosis; Nanomedicines; Nanoparticles; pH-Response; Polymers; Silicon Dioxide; Tumor microenvironment; Tumors; Viruses; pH-Response; Drug Delivery; Antitumor Agents; Nanomedicines
• ISSN: 1433-7851; 1521-3773
• DOI: 10.1002/anie.202216188

Due to non‐specific strong nano–bio interactions, it is difficult for nanocarriers with permanent rough surface to cross multiple biological barriers to realize efficient drug delivery. Herein, a camouflaged virus‐like‐nanocarrier with a transformable rough surface is reported, which is composed by an interior virus‐like mesoporous SiO2 nanoparticle with a rough surface (vSiO2) and an exterior acid‐responsive polymer. Under normal physiological pH condition, the spikes on vSiO2 are hidden by the polymer shell, and the non‐specific strong nano–bio interactions are effectively inhibited. While in the acidic tumor microenvironment, the nanocarrier sheds the polymer camouflage to re‐expose its rough surface. So, the retention ability and endocytosis efficiency of the nanocarrier are great improved. Owing to it's the dynamically variable rough surface, the rationally designed nanocarrier exhibits extended blood‐circulation‐time and enhanced tumor accumulation. A nanocarrier with variable surface roughness was designed. At physiological pH, the virus‐like spikes are hidden by a polymer shell, which effectively inhibits the non‐specific strong nano–bio interaction between the nanocarrier and protein/normal tissue induced by the rough surface. In the acidic tumor microenvironment, the nanocarrier sheds the polymer camouflage to re‐expose its rough surface, thus promoting endocytosis of the nanocarrier by tumor cells.