Novel gastroprotective activity of basella alba mucilage-based hydrogel beads on diclofenac sodium induced gastric ulcer

Moumita Chowdhury, Pintu Kumar De
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Abstract

Natural polysaccharides are emerging gastro-protective agents that need extensive characterization and subsequent commercialization. Diclofenac sodium, a non-steroidal anti-inflammatory drug, is generally used as a model drug to induce gastric ulcers experimentally. Therefore, in the present study, Basella alba mucilage is modified to form hydrogel beads, and its gastro-protective potential is judged by incorporating Diclofenac sodium in it and administered orally to Swiss albino rats at an equivalent weight of 50mg Diclofenac sodium/ kg bw for ten days. The results were compared with the rats administered Diclofenac sodium (50 mg/kg bw) and with the group of rats administered Diclofenac sodium (50mg/kg bw) and Pantoprazole (10mg/kg bw). Another group of rats were administered blank hydrogel beads, and another group served as control. The gastro-protective property was evaluated from the gastric secretory parameters, ulcer index, biochemical tests, and histopathology studies. The administration of Basella alba mucilage-based hydrogel beads in rats decreased the ulcer index, total and free acidity, lipid peroxidation, hydrogen peroxide level, and myeloperoxidase activity. It elevated the level of enzymic antioxidants and increased gastric juice's pH significantly compared to the Diclofenac-treated rats. All the evaluated parameters showed similar results for the rats treated with Diclofenac sodium-loaded Basella alba mucilage beads and those treated with Diclofenac sodium and Pantoprazole, with no significant differences. The histopathology analysis also supports the gastro-protective property of the beads. Thus, Basella alba mucilage-based hydrogel beads can be a promising gastro-protective agent against Diclofenac sodium-induced gastric ulcers.
基于白底藻粘液的水凝胶珠对双氯芬酸钠诱发的胃溃疡的新型胃保护作用
天然多糖是新兴的胃保护剂,需要广泛的表征和随后的商业化。双氯芬酸钠是一种非甾体抗炎药,在实验中一般作为模型药物诱导胃溃疡。因此,本研究将白底藻粘液修饰成水凝胶珠状,加入双氯芬酸钠,并以50mg双氯芬酸钠/ kg bw等量给药给瑞士白化大鼠10天,以此来判断其胃保护作用。将结果与双氯芬酸钠(50mg/kg bw)组和双氯芬酸钠(50mg/kg bw) +泮托拉唑(10mg/kg bw)组进行比较。另一组大鼠给予空白水凝胶珠,另一组作为对照组。从胃分泌参数、溃疡指数、生化试验和组织病理学研究评价其胃保护作用。大鼠给予白底菌黏液基水凝胶珠可降低溃疡指数、总酸度和游离酸度、脂质过氧化、过氧化氢水平和髓过氧化物酶活性。与双氯芬酸治疗的大鼠相比,它提高了酶抗氧化剂的水平,显著增加了胃液的pH值。所有评价参数显示,双氯芬酸钠负载的白底藻黏液珠与双氯芬酸钠和泮托拉唑处理的大鼠结果相似,无显著差异。组织病理学分析也支持这些小珠子的胃保护特性。因此,基于白底藻粘液的水凝胶珠可能是一种有前途的胃保护剂,可用于治疗双氯芬酸钠引起的胃溃疡。
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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