An Adhesive Immune‐Stimulating Multifunctional Hydrogel for Potent Tumor Chemoimmunotherapy and Postoperative Wound Healing Promotion

Tianran Wang(University of Science and Technology of China), Junfeng Ding(University of Science and Technology of China), Shuang Liang(University of Science and Technology of China), Zhiqiang Lin(University of Science and Technology of China), Jiaxuan Yang(University of Science and Technology of China), Zhen Zhang(University of Science and Technology of China), Zheng Zou(University of Science and Technology of China), Gao Li(University of Science and Technology of China), Xuesi Chen(University of Science and Technology of China), Chaoliang He(University of Science and Technology of China)
Advanced Functional Materials
December 27, 2023
Cited by 35

Abstract

Abstract Surgical excision is the first choice for clinical cancer therapy. However, major challenges, such as postoperative tumor recurrence and unsatisfactory wound healing after surgery, remain. In this study, an adhesive hydrogel is developed as a multifunctional platform for antitumor chemoimmunotherapy and postoperative wound treatment. The hydrogel adheres firmly to diverse tissues and degrades within 4 weeks in vivo with good histocompatibility. The immune‐stimulating hydrogel ((DOX+R837@HN)@Gel) is fabricated by encapsulating doxorubicin (DOX) and imiquimod‐loaded HSA nanoparticles (R837@HNs) into the hydrogel. When combined with immune checkpoint blockade (ICB) therapy, intratumorally administering (DOX+R837@HN)@Gel exhibits markedly enhanced systemic antitumor efficacy and strengthened antitumor immunity. For tumor surgical resection, (DOX+R837@HN)@Gel can adhere to the wounds and effectively prevents tumor recurrence and achieves long‐term immune memory with ICB therapy. Moreover, the hydrogel achieves rapid hemostasis and promotes wound healing after treating surgical wound models. Therefore, this multifunctional hydrogel has great significance for clinical postsurgical cancer treatment.


Related Papers

No related papers found

Powered by citation graph analysis