微波辅助黄胶接枝银纳米复合水凝胶用于双氯芬酸钠缓释制剂和抗菌检测

Nano Select Pub Date : 2024-07-09 DOI:10.1002/nano.202300200
Sharnappa Chapi, G. Babaladimath, M. V. Murugendrappa, A. Raghu
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引用次数: 0

摘要

本研究利用过二硫酸铵和N,N-亚甲基双丙烯酰胺在微波辐射下对TG、2-丙烯酰胺基-2-甲基丙磺酸和N,N-亚甲基双丙烯酰胺进行自由基共聚,合成了交联的接枝共聚物网络,从而合成了新型黄原胶-接枝-聚(2-丙烯酰胺基-2-甲基丙磺酸)(TG-g-PAMPS)水凝胶。利用柠檬酸三钠还原硝酸银,形成并稳定了银纳米粒子(SN)。利用傅立叶变换红外光谱(FTIR)、热重分析(TGA)、X 射线衍射(XRD)、扫描电子显微镜(SEM)、电致发光(EDS)和电子显微镜(TEM)技术对 TG-g-PAMPS 凝胶及其纳米复合材料进行了表征和确认。结果表明,SNs 的存在大大提高了 TG-g-PAMPS 凝胶的溶胀能力。采用土壤掩埋法对两种水凝胶进行了降解研究,并测定了各自的重量损失。研究发现,SNs 的存在使凝胶对铜绿假单胞菌和大肠杆菌具有明显的抗菌特性。此外,还将 TG-g-PAMPS 凝胶和 TG-g-PAMPS-SN 作为释放药物(双氯芬酸钠)的基质材料进行了评估,并考察了 SN 对药物释放的影响。使用经验方程分析了体外释放数据,以了解释放机理。在各种模型中,释放数据与 Korsmeyer-Peppas 方程拟合良好,释放动力学遵循非菲克扩散。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Microwave‐Assisted Tragacanth Gum–Based Grafted Silver Nanocomposite Hydrogel for Sustained Release Formulations of Diclofenac Sodium and Antibacterial Assay
In this work, novel tragacanth gum‐graft‐poly(2‐acrylamido‐2‐methylpropanesulfonic acid) (TG‐g‐PAMPS) hydrogel was synthesized via free radical copolymerization of TG, 2‐acrylamido‐2‐methylpropanesulfonic acid by using ammonium peroxodisulfate and N,N‐methylene‐bis‐acrylamide under microwave radiation, resulting in the cross‐linked graft copolymer network. Silver nanoparticles (SNs) were formed and stabilized by the reduction of silver nitrate using tri‐sodium citrate. The TG‐g‐PAMPS gel and its nanocomposite were characterized and confirmed using FTIR, TGA, XRD, SEM, EDS, and TEM techniques. It is observed that the presence of SNs significantly improves the swelling ability of the TG‐g‐PAMPS gel. Degradation studies of both hydrogels were studied using the soil burial method and determining the respective weight loss. The presence of SNs is found to impart significant antibacterial properties to the gel against Pseudomonas aeruginosa and Escherichia coli bacteria. Further, the TG‐g‐PAMPS gel and TG‐g‐PAMPS‐SN were evaluated as matrix materials for the release of the drug (diclofenac sodium) and the effect of SNs on the release was examined. The in‐vitro released data were analyzed using empirical equations to understand the mechanism of release. Among the various models, the released data were well fitted into the Korsmeyer–Peppas equation and the released kinetics followed non‐Fickian diffusion.
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