Preparation and Properties of Crosslinked Quaternized Chitosan-Based Hydrogel Films Ionically Bonded with Acetylsalicylic Acid for Biomedical Materials.

IF 4.9 2区 医学 Q1 CHEMISTRY, MEDICINAL
Marine Drugs Pub Date : 2024-09-30 DOI:10.3390/md22100450
Jingjing Zhang, Linqing Wang, Yingqi Mi, Fang Dong, Zhanyong Guo
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Abstract

The aim of the current study is to develop chitosan-based biomaterials which can sustainably release acetylsalicylic acid while presenting significant biological activity. Herein, an innovative ionic bonding strategy between hydroxypropyl trimethyl ammonium chloride chitosan (HACC) and acetylsalicylic acid (AA) was proposed, skillfully utilizing the electrostatic attraction of the ionic bond to achieve the controlled release of drugs. Based on this point, six crosslinked N-[(2-hydroxy-3-trimethylammonium)propyl]chitosan acetylsalicylic acid salt (CHACAA) hydrogel films with varying acetylsalicylic acid contents were prepared by a crosslinking reaction. The results of 1H nuclear magnetic resonance spectroscopy (1H NMR) and scanning electron morphology (SEM) confirmed the crosslinked structure, while the obtained hydrogel films possessed favorable thermal stability, mechanical properties, and swelling ability. In addition, the drug release behavior of the hydrogel films was also investigated. As expected, the prepared hydrogel films demonstrated the capability for the sustainable release of acetylsalicylic acid due to ion pair attraction dynamics. Furthermore, the bioactivities of CHACAA-3 and CHACAA-4 hydrogel films with acetylsalicylic acid molar equivalents of 1.25 and 1.5 times those of HACC were particularly pronounced, which not only exhibited an excellent drug sustained-release ability and antibacterial effect, but also had a higher potential for binding and scavenging inflammatory factors, including NO and TNF-α. These findings suggest that CHACAA-3 and CHACAA-4 hydrogel films hold great potential for applications in wound dressing, tissue engineering scaffolds, and drug carriers.

用于生物医学材料的与乙酰水杨酸离子键合的交联季铵化壳聚糖基水凝胶膜的制备及其性能
本研究的目的是开发壳聚糖基生物材料,这种材料既能持续释放乙酰水杨酸,又具有显著的生物活性。本研究提出了羟丙基三甲基氯化铵壳聚糖(HACC)与乙酰水杨酸(AA)之间的创新离子键策略,巧妙地利用了离子键的静电吸引力来实现药物的控制释放。在此基础上,通过交联反应制备了六种不同乙酰水杨酸含量的交联 N-[(2-羟基-3-三甲基铵)丙基]壳聚糖乙酰水杨酸盐(CHACAA)水凝胶薄膜。1H 核磁共振波谱(1H NMR)和扫描电子显微镜(SEM)结果证实了交联结构,所制备的水凝胶薄膜具有良好的热稳定性、机械性能和溶胀能力。此外,还研究了水凝胶薄膜的药物释放行为。不出所料,制备的水凝胶薄膜在离子对吸引动力学的作用下表现出了持续释放乙酰水杨酸的能力。此外,乙酰水杨酸摩尔当量分别为 HACC 1.25 倍和 1.5 倍的 CHACAA-3 和 CHACAA-4 水凝胶薄膜的生物活性尤为明显,不仅表现出优异的药物持续释放能力和抗菌效果,而且具有更高的结合和清除 NO 和 TNF-α 等炎症因子的潜力。这些研究结果表明,CHACAA-3 和 CHACAA-4 水凝胶薄膜在伤口敷料、组织工程支架和药物载体方面具有巨大的应用潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Marine Drugs
Marine Drugs 医学-医药化学
CiteScore
9.60
自引率
14.80%
发文量
671
审稿时长
1 months
期刊介绍: Marine Drugs (ISSN 1660-3397) publishes reviews, regular research papers and short notes on the research, development and production of drugs from the sea. Our aim is to encourage scientists to publish their experimental and theoretical research in as much detail as possible, particularly synthetic procedures and characterization information for bioactive compounds. There is no restriction on the length of the experimental section.
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