Gong Jianyu, Guo Rong, Xue Pengcheng, Zheng Yao, Qian Guangfu, Chen Changzhou, Min Douyong, Tong Yan, Lu Minsheng
Guangxi Key Laboratory of Clean Pulp & Papermaking and Pollution Control, School of Light Industry and Food Engineering, Guangxi University, Nanning 530004, China.
Guangxi Key Laboratory of Clean Pulp & Papermaking and Pollution Control, School of Light Industry and Food Engineering, Guangxi University, Nanning 530004, China.
Int J Biol Macromol. 2025 Apr;303:140712. doi: 10.1016/j.ijbiomac.2025.140712. Epub 2025 Feb 4.
The application of inorganic salt-regulated Hofmeister effects in cellulose nanocrystals (CNC)-based hydrogels is hindered by limitations, including poor biocompatibility and difficulties in achieving precise drug release. In this study, we show that the anionic polyelectrolyte regulated Hofmeister effect promotes the aggregation and crystallization of CNC and polyvinyl alcohol (PVA) chains. This structural transformation significantly enhances the controllability of drug release in CNC-based hydrogels. The incorporation of anionic polyelectrolytes into CNC-based hydrogels creates a semi-interpenetrating polymer network (semi-IPN), significantly enhancing their mechanical properties and improving in vitro drug release controllability. Our hydrogel exhibits significant flexibility in controlling both drug release duration and capacity, with adjustable release times ranging from 16 to 52 h and tunable drug release capacities between 10.13 mg/g and 19.21 mg/g. Furthermore, antibacterial and cytotoxicity assays confirm its favorable biocompatibility and moderate antibacterial properties. Overall, our research findings emphasize that the preparation of cellulose-based hydrogels using polyelectrolytes has certain flexible regulatory functions in drug release.
无机盐调控的霍夫迈斯特效应在基于纤维素纳米晶体(CNC)的水凝胶中的应用受到了限制,包括生物相容性差以及实现精确药物释放存在困难。在本研究中,我们表明阴离子聚电解质调控的霍夫迈斯特效应促进了CNC和聚乙烯醇(PVA)链的聚集和结晶。这种结构转变显著增强了基于CNC的水凝胶中药物释放的可控性。将阴离子聚电解质掺入基于CNC的水凝胶中形成了半互穿聚合物网络(半IPN),显著增强了它们的机械性能并改善了体外药物释放的可控性。我们的水凝胶在控制药物释放持续时间和容量方面表现出显著的灵活性,释放时间可在16至52小时之间调节,药物释放容量可在10.13毫克/克至19.21毫克/克之间调节。此外,抗菌和细胞毒性试验证实了其良好的生物相容性和适度的抗菌性能。总体而言,我们的研究结果强调,使用聚电解质制备纤维素基水凝胶在药物释放方面具有一定的灵活调控功能。