Phan Chau My, Luu Cuong Hung, Murugesan Mohanapriya, Nguyen Thi-Nhu-Quynh, Ha Nhu-Y Ngoc, Ngo Huong Lan, Nguyen Ngoc-Dan Ho, Pan Zhouyi, Phan V H Giang, Li Yi, Thambi Thavasyappan
College of Materials and Textile Engineering & Nanotechnology Research Institute, Jiaxing University, Jiaxing 314001, Zhejiang Province, PR China; Biomaterials and Nanotechnology Research Group, Faculty of Applied Sciences, Ton Duc Thang University, Ho Chi Minh City, Vietnam.
School of Environment and Science, Griffith University, Nathan, QLD 4111, Australia; Queensland Micro- and Nanotechnology Centre, Griffith University, Nathan, QLD 4111, Australia.
Int J Biol Macromol. 2025 Jan;284(Pt 1):137939. doi: 10.1016/j.ijbiomac.2024.137939. Epub 2024 Nov 26.
Pulpitis is inflammation of the dental pulp, often caused by bacterial infection from untreated cavities, leading to pain. The main challenge in treatment is eliminating infection while preserving tooth vitality. This study aims to address this challenge by developing a hydrogel for convenient insertion into the root canal system, securely attaching to dentin walls. An injectable hydrogel system is developed by chemically cross-linking natural polysaccharide pectin with gelatin (GPG) through reversible Schiff base reaction. The GPG system was then used to encapsulate and release drugs, such as ciprofloxacin (CIP) for infection prevention and deferoxamine (DFO) for promoting blood vessel proliferation and reducing inflammatory reactions. The GPGs absorbed significant amounts of CIP and DFO, enabling sustained release over a nearly ten-day period. When subcutaneously implanted, the GPGs formed stable gel depots, with only 50 % of the gels degrading after 3 weeks, indicating a sustained biodegradation pattern. Additionally, the GPG system demonstrated excellent antibacterial activity against both gram-negative and gram-positive bacteria. Results from in vitro scratch healing tests and in ovo chorioallantoic membrane chick model tests showed promising biocompatibility and promotion of vascular proliferation by the GPG. This study heralds a novel frontier in endodontic therapeutics, poised to potentially enable dental pulp regeneration.
牙髓炎是牙髓的炎症,通常由未经治疗的龋齿引发的细菌感染所致,会导致疼痛。治疗的主要挑战在于消除感染的同时保留牙齿活力。本研究旨在通过开发一种便于插入根管系统并牢固附着于牙本质壁的水凝胶来应对这一挑战。通过可逆席夫碱反应将天然多糖果胶与明胶(GPG)化学交联,开发出一种可注射水凝胶系统。然后使用GPG系统包封和释放药物,如用于预防感染的环丙沙星(CIP)以及用于促进血管增殖和减轻炎症反应的去铁胺(DFO)。GPG吸收了大量的CIP和DFO,能够在近十天的时间内持续释放。皮下植入时,GPG形成稳定的凝胶贮库,3周后仅有50%的凝胶降解,表明其具有持续的生物降解模式。此外,GPG系统对革兰氏阴性菌和革兰氏阳性菌均表现出优异的抗菌活性。体外划痕愈合试验和鸡胚尿囊膜模型试验的结果显示,GPG具有良好的生物相容性并能促进血管增殖。本研究开创了牙髓病治疗的新领域,有望实现牙髓再生。