基于壳聚糖/羟丙基甲基纤维素的含有姜黄素的黏附性胃黏膜微颗粒,用于预防胃溃疡

IF 5.2 2区 医学 Q1 PHARMACOLOGY & PHARMACY International Journal of Pharmaceutics Pub Date : 2025-04-15 Epub Date: 2025-03-09 DOI:10.1016/j.ijpharm.2025.125454
Maurício Palmeira Chaves de Souza , Suzana Gonçalves Carvalho , Larissa Spósito, Bruna Almeida Furquim de Camargo, Tais Maria Bauab, Andréia Bagliotti Meneguin, Marlus Chorilli
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摘要

胃溃疡(GU)是一种以胃粘膜表面溃疡病变为特征的疾病,主要由健康相关疾病、非甾体抗炎药(NSAIDs)的使用和幽门螺杆菌感染引起。这种疾病的治疗要求药物与作用部位保持接触,然而,由于胃排空,常规剂型在该器官的停留时间有限。姜黄素(Curcumin, CUR)是从姜黄植物的根茎中提取的一种化合物,在传统的印度药物中使用了许多世纪。然而,它的使用受到限制,因为它在水介质中溶解度低。此外,胃疾病的治疗需要药物与该部位保持接触,但常规剂型在该器官的停留时间有限。克服这些限制的一个策略是使用胃保留剂和黏液输送系统。因此,本研究旨在开发聚合物壳聚糖和羟丙基甲基纤维素基微颗粒来释放CUR,并评估它们在体内的胃保护作用。微颗粒呈球形,粒径在620 ~ 820µm之间,包封效率超过50%,24 h后CUR完全释放。热分析表明聚合物和CUR结构发生变化,表明新的超分子相互作用的建立。微颗粒对粘蛋白盘表现出较高的生物粘附力。这组结果表明,这些系统是预防与使用非甾体抗炎药相关的胃病变的有希望的工具,其胃保护指数与奥美拉唑相似。
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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Chitosan/hydroxypropylmethylcellulose based-mucoadhesive gastroretentive microparticles containing curcumin intended for the prevention of gastric ulcers
Gastric ulcer (GU) is a disease characterized by ulcerative lesions on the surface of the stomach mucosa caused mainly by health-related conditions, non-steroidal anti-inflammatory drugs (NSAIDs) use, and Helicobacter pylori infections. The treatment for this disease requires that the drug remains in contact with the site of action, however, the residence time of conventional dosage forms in this organ is limited due to gastric emptying. Curcumin (CUR) is a compound obtained from the rhizomes of the Curcuma longa plant and has been used in traditional Indian medicine for many centuries. However, its use is limited because it has low solubility in aqueous media. In addition, the treatment of gastric diseases requires the drug to remain in contact with the area, but the residence time of conventional dosage forms in this organ is limited. One strategy to overcome these limitations is the use of a gastroretentive and mucoadhesive delivery system. Therefore, this study aimed to develop polymeric chitosan and hydroxypropylmethylcellulose-based microparticles for the release of CUR and to evaluate their in vivo gastroprotective action. The microparticles had a spherical shape and size between 620 and 820 µm, and the encapsulation efficiency was over 50 %, with complete release of CUR after 24 h. Thermal analysis showed changes in the structure of the polymers and CUR, suggesting the establishment of new supramolecular interactions. Microparticles showed high bioadhesive forces to the mucin disc. This set of results, suggest that these systems are promising tools for the prevention of gastric lesions associated with the use of NSAIDs, with a gastroprotective index similar to that conferred by omeprazole.
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来源期刊
CiteScore
10.70
自引率
8.60%
发文量
951
审稿时长
72 days
期刊介绍: The International Journal of Pharmaceutics is the third most cited journal in the "Pharmacy & Pharmacology" category out of 366 journals, being the true home for pharmaceutical scientists concerned with the physical, chemical and biological properties of devices and delivery systems for drugs, vaccines and biologicals, including their design, manufacture and evaluation. This includes evaluation of the properties of drugs, excipients such as surfactants and polymers and novel materials. The journal has special sections on pharmaceutical nanotechnology and personalized medicines, and publishes research papers, reviews, commentaries and letters to the editor as well as special issues.
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