Bhiri Nour, Labour Marie-Noëlle, Li Suming, Nasri Rim, Nasri Moncef, Hajji Mohamed
Laboratory of Enzyme Engineering and Microbiology, National School of Engineering of Sfax (ENIS), University of Sfax, P.O. Box 1173, Sfax 3038, Tunisia; Institut Européen des Membranes, IEM, UMR 5635, Univ Montpellier, CNRS, ENSCM, 34095 Montpellier, France.
ICGM, Univ Montpellier, CNRS, ENSCM, 34293 Montpellier, France; Ecole Pratique des Hautes Etudes, Paris, France.
Int J Biol Macromol. 2025 Jul;318(Pt 1):144880. doi: 10.1016/j.ijbiomac.2025.144880. Epub 2025 Jun 2.
Composite hydrogels were synthesized using carboxymethyl chitosan (CMCh) and polysaccharides (PS) extracted from Ononis natrix through chemical cross-linking with genipin, a naturally derived cross-linker. Hydrogels with different PS/CMCh ratios were characterized in terms of their structural, morphological, thermal, rheological, and biological properties. The results showed that an increase in PS concentration enhanced both the swelling capacity and viscoelastic properties of the hydrogels. In vitro drug release was carried out using ascorbic acid (Aas) and curcumin (Cur) as model of hydrophilic and hydrophobic bioactive molecules, respectively. Drug loading was achieved by immersion of lyophilized hydrogel in a drug solution. The release profiles showed a higher release rate at physiological pH (7.4) compared to acidic pH (5.5) due to enhanced hydrogel swelling under neutral conditions. Modeling with Korsmeyer-Peppas equation revealed Fickian diffusion-controlled release for Aas and non-Fickian diffusion-controlled release for Cur. Moreover, the composite hydrogels displayed notable antioxidant activity, and Aas-loaded hydrogel exhibited antibacterial effects against Staphylococcus aureus, highlighting their promise in counteracting oxidative damage and microbial infection, two crucial factors in the wound healing process. Therefore, it is concluded that the PS/CMCh composite hydrogel presents great potential for the development of biomaterials from renewable resources for controlled drug delivery systems and wound care applications.
采用羧甲基壳聚糖(CMCh)和从直立黄芪中提取的多糖(PS),通过与天然衍生的交联剂京尼平进行化学交联,合成了复合水凝胶。对不同PS/CMCh比例的水凝胶的结构、形态、热学、流变学和生物学特性进行了表征。结果表明,PS浓度的增加提高了水凝胶的溶胀能力和粘弹性。分别以抗坏血酸(Aas)和姜黄素(Cur)作为亲水性和疏水性生物活性分子的模型,进行了体外药物释放实验。通过将冻干的水凝胶浸入药物溶液中来实现药物负载。释放曲线显示,由于中性条件下水凝胶溶胀增强,在生理pH(7.4)下的释放速率高于酸性pH(5.5)。用Korsmeyer-Peppas方程建模表明,Aas的释放为菲克扩散控制释放,Cur的释放为非菲克扩散控制释放。此外,复合水凝胶表现出显著的抗氧化活性,负载Aas的水凝胶对金黄色葡萄球菌具有抗菌作用,突出了它们在对抗氧化损伤和微生物感染方面的前景,这是伤口愈合过程中的两个关键因素。因此,可以得出结论,PS/CMCh复合水凝胶在开发用于可控药物递送系统和伤口护理应用的可再生资源生物材料方面具有巨大潜力。