Gellan gum-based microbeads for Colon-targeted drug delivery: A promising polysaccharide for controlled and site-specific release

IF 8.5 1区 化学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY International Journal of Biological Macromolecules Pub Date : 2025-04-19 DOI:10.1016/j.ijbiomac.2025.143276
Soumyadip Ghosh, Ankita Basak
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Abstract

Targeting drug delivery to the colon presents significant challenges due to unfavorable pH conditions and enzymatic activity in the upper gastrointestinal tract. This obstacle can be overcome with colon-targeted microbeads, which have led to significant advancements in treating colonic diseases such as inflammatory bowel disease and colorectal cancer, as well as in achieving sustained delivery of macromolecules like peptides and proteins. Polysaccharide-based microbeads (MBs) formulated with gellan gum (GLG) offer a robust platform for controlled and site-specific drug release. GLG, a natural anionic polysaccharide, is renowned for its gelation properties in the presence of divalent cations, biocompatibility, and enzymatic degradability, making it ideal for colon-specific applications. In this review, we explored the potential of GLG-MBs for colon-targeted drug delivery and their physicochemical properties, drug release mechanisms, formulation strategies, therapeutic applications, methods for analytical characterizations, highlighting their advantages over conventional drug delivery, and target specificity towards the colonic disease. Furthermore, we discussed the significant limitations of GLG-MBs, such as burst release, processing, scaling up production, regulatory challenges, and clinical uniformity towards colonic environments. We explored the strategies to overcome key limitations in clinical translation, such as uniformity and regulatory hurdles. The review concludes by outlining the direction of advancing GLG-MBs, emphasizing their potential in achieving efficient and targeted drug delivery towards the colon.

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结冷胶微珠用于结肠靶向给药:一种有前景的多糖,可用于控制和特定部位的释放
由于上消化道的 pH 值条件和酶活性不佳,向结肠靶向给药面临巨大挑战。结肠靶向微珠可以克服这一障碍,在治疗结肠疾病(如炎症性肠病和结肠直肠癌)以及实现肽和蛋白质等大分子的持续给药方面取得了重大进展。用结冷胶(GLG)配制的基于多糖的微珠(MBs)为控制和特定部位的药物释放提供了一个强大的平台。GLG 是一种天然阴离子多糖,因其在二价阳离子存在下的凝胶特性、生物相容性和酶降解性而闻名,是结肠特异性应用的理想选择。在这篇综述中,我们探讨了 GLG-MB 在结肠靶向给药方面的潜力,以及它们的理化性质、药物释放机制、配制策略、治疗应用、分析表征方法,突出了它们与传统给药相比的优势,以及对结肠疾病的靶向特异性。此外,我们还讨论了 GLG-MB 的重大局限性,如猝发释放、加工、扩大生产规模、监管挑战以及结肠环境的临床一致性。我们探讨了克服临床转化中关键限制的策略,如统一性和监管障碍。综述最后概述了 GLG-MB 的发展方向,强调了它们在实现结肠高效靶向给药方面的潜力。
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来源期刊
International Journal of Biological Macromolecules
International Journal of Biological Macromolecules 生物-生化与分子生物学
CiteScore
13.70
自引率
9.80%
发文量
2728
审稿时长
64 days
期刊介绍: The International Journal of Biological Macromolecules is a well-established international journal dedicated to research on the chemical and biological aspects of natural macromolecules. Focusing on proteins, macromolecular carbohydrates, glycoproteins, proteoglycans, lignins, biological poly-acids, and nucleic acids, the journal presents the latest findings in molecular structure, properties, biological activities, interactions, modifications, and functional properties. Papers must offer new and novel insights, encompassing related model systems, structural conformational studies, theoretical developments, and analytical techniques. Each paper is required to primarily focus on at least one named biological macromolecule, reflected in the title, abstract, and text.
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