Alaee Reyhaneh, Mohammadi Toraj, Mahinroosta Mostafa
Center of Excellence for Membrane Science and Technology, Department of Chemical, Petroleum and Gas Engineering, Iran University of Science and Technology (IUST), Narmak, Tehran, Iran.
Center of Excellence for Membrane Science and Technology, Department of Chemical, Petroleum and Gas Engineering, Iran University of Science and Technology (IUST), Narmak, Tehran, Iran.
Int J Biol Macromol. 2025 Jul;318(Pt 2):145112. doi: 10.1016/j.ijbiomac.2025.145112. Epub 2025 Jun 9.
In this study, pH-sensitive xanthan-glycerol hydrogels were developed for the controlled delivery of amoxicillin. The detailed characterization of the hydrogel matrix involved evaluating various parameters, including Fourier-transform infrared spectroscopy (FTIR), Scanning electron microscopy (SEM), drug loading percentage, swelling and degradation behavior, drug release kinetics, antibacterial activity, and cytotoxicity were performed. FTIR analysis confirmed successful synthesis of the hydrogel, while SEM revealed its smooth surface and porous structure. By optimizing the formulation parameters, 75.43 % of the total drug was successfully loaded in the hydrogel samples. The pH-responsive nature of the hydrogels was demonstrated by variations in swelling and degradation at different pH levels, with significantly higher swelling and degradation observed in basic environments due to the larger pore size. At pH of 7.5, the swelling ratio after 8 h and degradation after 48 h were 722.5 % and 19.99 %, respectively. Drug release studies indicated that cumulative release was pH-dependent, increasing from 18.4 % at pH of 2 to 88 % at pH of 8.5 after 8 h in in vitro conditions (PBS buffer at temperature of 37 °C). Additionally, the hydrogel demonstrated significant antibacterial activity, exhibiting 26 mm inhibition zone against Staphylococcus aureus, while cytotoxicity assays confirmed its biocompatibility. These findings underscored the potential of xanthan-glycerol hydrogels as effective and responsive wound dressings for controlled antibiotic delivery.
在本研究中,开发了用于阿莫西林控释的pH敏感型黄原胶-甘油水凝胶。对水凝胶基质的详细表征涉及评估各种参数,包括进行傅里叶变换红外光谱(FTIR)、扫描电子显微镜(SEM)、载药百分比、溶胀和降解行为、药物释放动力学、抗菌活性和细胞毒性。FTIR分析证实了水凝胶的成功合成,而SEM显示其表面光滑且具有多孔结构。通过优化配方参数,75.43%的总药物成功负载在水凝胶样品中。水凝胶的pH响应特性通过不同pH水平下溶胀和降解的变化得以证明,由于孔径较大,在碱性环境中观察到显著更高的溶胀和降解。在pH为7.�时,8小时后的溶胀率和48小时后的降解率分别为722.5%和19.99%。药物释放研究表明,体外条件下(37°C的PBS缓冲液)8小时后,累积释放量与pH相关,从pH为2时的18.4%增加到pH为8.5时的88%。此外,水凝胶表现出显著的抗菌活性,对金黄色葡萄球菌的抑菌圈为26毫米,而细胞毒性试验证实了其生物相容性。这些发现强调了黄原胶-甘油水凝胶作为用于控释抗生素的有效且响应性伤口敷料的潜力。