Complexation of α-Mangostin with γ-Cyclodextrin and Its Application in Alginate/Chitosan Hydrogel Mucoadhesive Film for Treatment of Recurrent Aphthous Stomatitis.

IF 4.1 2区 医学 Q2 IMMUNOLOGY Journal of Inflammation Research Pub Date : 2025-02-15 eCollection Date: 2025-01-01 DOI:10.2147/JIR.S482582
Ine Suharyani, Ahmed Fouad Abdelwahab Mohammed, Muchtaridi Muchtaridi, Ali El-Rayyes, Marline Abdassah, Cecep Suhandi, Nasrul Wathoni
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Abstract

Introduction: α-Mangostin (α-M), one of the xanthon compound isolated from Garcinia mangostana rind, demonstrates the efficacy in the treatment of recurrent aphthous stomatitis (RAS). The lack of solubility of α-mangostin in water limited its pharmacological application.

Purpose: The lack of solubility of α-mangostin in water limited its formulation and pharmacological application. This study was done to enhance the solubility of α-M by complexation with γ-cyclodextrin (γ-CD) and its application in Alginate/Chitosan Hydrogel Mucoadhesive Film (HMF) for RAS treatment.

Methods: This complex was made by dissolved α-M and γ-CD in separated solution. α-M solution gradualy added into γ-CD to formed α-M/γ-CD complex (α-M/γ-CD CX). This complex then evaporated to yield the dry complex powder. The complex was successfully formulated into hydrogel mucoadhesive film (HMF) preparations based on characterization using Scanning Electron Microscope (SEM), Fourier Transform Infra-Red (FTIR), and X-Ray Diffractometry (XRD). The complex was formulated in hydrogel mucoadhesive film, followed by in-vitro drug release and the study of recurrent aphthous stomatitis (RAS) activity in rats.

Results: The α-M/γ-CD CX HMF film has a higher mucoadhesive force and mucoadhesive time than other HMFs resulting in a prolonged retention time in the oral mucosa. The drug release of α-M/γ-CD CX HMF followed the Korsmeyer-Peppas Model with a total amount of drug released 80.34+0.32%. The inclusion complex of α-M/γ-CD CX HMF exhibited increased anti-RAS activity compared to HMF base, α-M HMF, and α-M/γ-CD PM HMF. This was evidenced by a significant decrease in wound area of approximately 79.05±3.30%, an increase in epithelial thickness of about 1.24±0.09 μm, and a decrease in neutrophil score 1.10±0.26. These findings highlight the potential use of α-M/γ-CD CX as an effective RAS agent in HMF.

Conclusion: The complex of α-M/γ-CD CX has improved solubility of α-M, resulting in the transparent and homogenous film. The film containing this complex has the better physical characteristic, increasing the release and RAS activity.

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α-山竹苷与γ-环糊精的络合及其在海藻酸盐/壳聚糖水凝胶黏合剂膜中治疗复发性口腔炎的应用。
α-山竹苷(α-M)是从山竹果皮中分离得到的一种黄原化合物,具有治疗复发性口疮性口炎(RAS)的疗效。α-山竹苷在水中缺乏溶解度,限制了其药理应用。目的:α-山竹苷在水中缺乏溶解度,限制了其制剂和药理应用。通过与γ-环糊精(γ-CD)络合提高α-M的溶解度,并将其应用于海藻酸盐/壳聚糖水凝胶粘接膜(HMF)中进行RAS处理。方法:将α-M和γ-CD溶解在分离液中制备该配合物。α-M溶液逐渐加入到γ-CD中,形成α-M/γ-CD配合物(α-M/γ-CD CX)。然后,这种复合物蒸发得到干燥的复合物粉末。通过扫描电镜(SEM)、傅里叶变换红外(FTIR)和x射线衍射(XRD)对该配合物进行表征,成功制备了水凝胶黏附膜(HMF)。采用水凝胶黏附膜制备该配合物,体外释放并研究其对大鼠复发性口疮性口炎(RAS)的活性。结果:α-M/γ-CD CX HMF膜比其他HMF具有更高的黏附力和黏附时间,使其在口腔黏膜的滞留时间延长。α-M/γ-CD CX HMF的释药符合Korsmeyer-Peppas模型,释药总量为80.34+0.32%。与HMF碱、α-M HMF和α-M/γ-CD PM HMF相比,α-M/γ-CD CX HMF包合物的抗ras活性增强。创面面积减少约79.05±3.30%,上皮细胞厚度增加约1.24±0.09 μm,中性粒细胞评分降低1.10±0.26。这些发现突出了α-M/γ-CD CX作为一种有效的RAS剂在HMF中的潜在应用。结论:α-M/γ-CD CX配合物提高了α-M的溶解度,形成透明均匀的膜。含有该配合物的膜具有较好的物理特性,提高了RAS的释放度和活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Inflammation Research
Journal of Inflammation Research Immunology and Microbiology-Immunology
CiteScore
6.10
自引率
2.20%
发文量
658
审稿时长
16 weeks
期刊介绍: An international, peer-reviewed, open access, online journal that welcomes laboratory and clinical findings on the molecular basis, cell biology and pharmacology of inflammation.
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