Lansoprazole/β-Cyclodextrin-Based Metal-Organic Frameworks: Development, Characterization, and Anti-Ulcer Activity Evaluation on Rats.

IF 3
Bader B Alsulays
{"title":"Lansoprazole/β-Cyclodextrin-Based Metal-Organic Frameworks: Development, Characterization, and Anti-Ulcer Activity Evaluation on Rats.","authors":"Bader B Alsulays","doi":"10.2174/0115672018449532260409081159","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Gastric ulcers are among the most common diseases worldwide, affecting individuals of all ages and genders. Lansoprazole (LNS) is one of the first-choice treatments for ulcers. In this study, β-Cyclodextrin-based metal-organic frameworks (β-CD-MOFs), which have recently attracted attention for biomedical applications, were used as carriers for LNS to enhance its physicochemical properties.</p><p><strong>Methods: </strong>β-CD-MOF crystals were prepared, and LNS was successfully loaded into the crystals in the presence of MgO. Pure LNS and the formulation were characterized using Differential Scanning Calorimetry (DSC), Powder X-Ray Diffraction (PXRD), Fourier-Transform Infrared spectroscopy (FTIR), Scanning Electron Microscopy (SEM), and in vitro release studies. The anti-ulcer activity was evaluated in male Wistar albino rats.</p><p><strong>Results: </strong>Dissolution studies revealed that approximately 90% of LNS was released from the formulation within 60 minutes, and the formulation's color remained unchanged after exposure to light. The formulation demonstrated a significant reduction in mucosal erythema and mucosal surface lesions, as well as a higher percentage of ulcer index inhibition.</p><p><strong>Discussion: </strong>Loading of LNS into β-CD-MOF enhanced its release and photostability. In vivo studies suggest that the formulation has a potent anti-ulcerogenic capability comparable to that of LNS.</p><p><strong>Conclusion: </strong>β-CD-MOF, a promising carrier in drug delivery, improves the properties of LNS and further enhances its anti-ulcer activity.</p>","PeriodicalId":94287,"journal":{"name":"Current drug delivery","volume":" ","pages":""},"PeriodicalIF":3.0000,"publicationDate":"2026-04-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current drug delivery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/0115672018449532260409081159","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction: Gastric ulcers are among the most common diseases worldwide, affecting individuals of all ages and genders. Lansoprazole (LNS) is one of the first-choice treatments for ulcers. In this study, β-Cyclodextrin-based metal-organic frameworks (β-CD-MOFs), which have recently attracted attention for biomedical applications, were used as carriers for LNS to enhance its physicochemical properties.

Methods: β-CD-MOF crystals were prepared, and LNS was successfully loaded into the crystals in the presence of MgO. Pure LNS and the formulation were characterized using Differential Scanning Calorimetry (DSC), Powder X-Ray Diffraction (PXRD), Fourier-Transform Infrared spectroscopy (FTIR), Scanning Electron Microscopy (SEM), and in vitro release studies. The anti-ulcer activity was evaluated in male Wistar albino rats.

Results: Dissolution studies revealed that approximately 90% of LNS was released from the formulation within 60 minutes, and the formulation's color remained unchanged after exposure to light. The formulation demonstrated a significant reduction in mucosal erythema and mucosal surface lesions, as well as a higher percentage of ulcer index inhibition.

Discussion: Loading of LNS into β-CD-MOF enhanced its release and photostability. In vivo studies suggest that the formulation has a potent anti-ulcerogenic capability comparable to that of LNS.

Conclusion: β-CD-MOF, a promising carrier in drug delivery, improves the properties of LNS and further enhances its anti-ulcer activity.

兰索拉唑/β-环糊精为基础的金属有机骨架:开发、表征和大鼠抗溃疡活性评价。
胃溃疡是世界上最常见的疾病之一,影响所有年龄和性别的个体。兰索拉唑(Lansoprazole, LNS)是治疗溃疡的首选药物之一。本研究利用近年来在生物医学领域备受关注的β-环糊精基金属有机骨架(β-CD-MOFs)作为LNS的载体,增强其理化性能。方法:制备β-CD-MOF晶体,在MgO存在的情况下将LNS成功加载到晶体中。采用差示扫描量热法(DSC)、粉末x射线衍射(PXRD)、傅里叶变换红外光谱(FTIR)、扫描电镜(SEM)和体外释放研究对纯LNS及其制剂进行了表征。对雄性Wistar白化大鼠进行抗溃疡活性评价。结果:溶出度研究表明,约90%的LNS在60分钟内从配方中释放出来,并且在光照后配方的颜色保持不变。该配方证明了粘膜红斑和粘膜表面病变的显著减少,以及溃疡指数抑制的更高百分比。讨论:在β-CD-MOF中加入LNS增强了其释放性和光稳定性。体内研究表明,该制剂具有与LNS相当的抗溃疡能力。结论:β-CD-MOF是一种很有前景的药物递送载体,可以改善LNS的性能,进一步增强其抗溃疡活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书