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ORIGINAL RESEARCH article

Front. Bioeng. Biotechnol.

Sec. Tissue Engineering and Regenerative Medicine

Volume 13 - 2025 | doi: 10.3389/fbioe.2025.1655809

This article is part of the Research TopicApplication of Tissue Engineering in Bone, Joints, Ligaments Injuries and Cartilage RegenerationView all 13 articles

PRP-Loaded Hydrogel for Rotator Cuff Repair by Promoting Osteogenic Differentiation and Tendon Regeneration

Provisionally accepted
Rusen  ZhangRusen Zhang1Zhi-Yang  ZhengZhi-Yang Zheng2Guo-Qing  ZhuGuo-Qing Zhu1Chao-Rong  LuoChao-Rong Luo1Jing-Min  YuanJing-Min Yuan1Yi-Lin  YeYi-Lin Ye1Ze-Qin  ZhuangZe-Qin Zhuang1Ze-Zheng  LiuZe-Zheng Liu2*Qingchu  LiQingchu Li2*Xi-Zhao  HuangXi-Zhao Huang1*
  • 1Guangdong Province Women and Children Hospital, Guangzhou, China
  • 2The Third Affiliated Hospital of Southern Medical University, Guangzhou, China

The final, formatted version of the article will be published soon.

Objective: Rotator cuff injuries are a common and challenging shoulder joint pathology that significantly impacts shoulder function and quality of life. Current treatments, particularly arthroscopic repair, face high failure rates due to the difficulty of regenerating the native tendon-bone interface. This study aimed to develop and evaluate a platelet-rich plasma–carboxymethyl chitosan–tannic acid composite hydrogel (PRP-CMCS-TA), designed to address these limitations and enhance the repair and regeneration of the tendon-bone interface. Methods: The composite hydrogel was synthesized by creating a CMCS-TA hydrogel via chemical cross-linking, which was then integrated with PRP. Its functionality was assessed through a series of in vitro biocompatibility, bioactivity, and sustained-release assays, and its efficacy in promoting tendon-bone interface regeneration was evaluated in a rat rotator cuff injury model using micro-CT, biomechanical testing, and histological analysis. Results: In vitro experiments demonstrated the biocompatibility and bioactivity of PRP-CMCS-TA. The hydrogel supported cell viability and proliferation, and sustained the release of PRP components, which are critical for promoting tenogenic and osteogenic differentiation. The in vitro results indicated that PRP-CMCS-TA could provide a suitable environment for cell growth and tissue repair. In vivo studies were conducted using a rat rotator cuff injury model. The model was divided into three groups: Control, CMCS-TA, and PRP-CMCS-TA. Micro-CT scans and histological analyses were performed at predetermined time points to evaluate the repair capability of the composite hydrogel. The results showed that PRP-CMCS-TA significantly promoted bone regeneration and achieved superior tendon-bone interface repair compared to the other groups. Conclusion: The PRP-CMCS-TA composite hydrogel exhibits good biocompatibility and effectively repairs the tendon-bone interface by promoting osteogenic differentiation and tendon regeneration. This study provides new insights into the application of bioactive materials for rotator cuff injuries and offers a promising strategy for improving the outcomes of rotator cuff repair. Further research and clinical trials are needed to translate these findings into practical applications and to establish the hydrogel as a standard treatment option for rotator cuff injuries.

Keywords: Rotator cuff injury, Platelet-Rich Plasma, Biomaterials, Hydrogel, Tendon-bone interface

Received: 28 Jun 2025; Accepted: 13 Oct 2025.

Copyright: © 2025 Zhang, Zheng, Zhu, Luo, Yuan, Ye, Zhuang, Liu, Li and Huang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence:
Ze-Zheng Liu, 296572577@qq.com
Qingchu Li, liqingchu12@qq.com
Xi-Zhao Huang, heywong@qq.com

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