壳聚糖
生物相容性
生物高聚物
阿莫西林
石墨烯
化学
药物输送
凝聚
活力测定
抗菌活性
核化学
色谱法
材料科学
纳米技术
细菌
抗生素
体外
聚合物
有机化学
生物化学
生物
遗传学
标识
DOI:10.1016/j.ijbiomac.2023.127837
摘要
Biopolymers are crucial in pharmaceuticals, particularly for controlled drug release. In this study, we loaded the broad-spectrum antibacterial drug amoxicillin into sodium alginate, a well-known biopolymer. Graphene oxide was incorporated into the composite, and the hydrogel beads were coated with chitosan for its mucoadhesive properties. Various composites were formulated by adjusting the weight percentage of graphene oxide (GO). The fabricated beads demonstrated controlled and sustained drug release, with 98 % of the loaded drug molecules released over 24 h at gastric pH. The antibacterial test using the disc diffusion technique confirmed the drug release, exhibiting greater effectiveness against the gram-positive bacterium S. aureus than the gram-negative bacterium E. coli. The drug release data were optimized using zero order, first order, Higuchi, and Korsmeyer-Peppas models. The experimental data were best fit to the Korsmeyer-Peppas model with a relatively higher correlation coefficient value. Biocompatibility was evaluated through a cell viability test using mouse fibroblast cell lines (L929). The MTT viability assay confirmed high levels of cytocompatibility, even at higher concentrations (100 μg/mL), with 98.15 % viable cells. These results highlight the potential of the fabricated beads as an effective amoxicillin drug delivery system with biomedical applications.
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