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用于结肠特异性药物递送的含姜黄素-美沙拉嗪组合的新型pH敏感型丙烯酸树脂包衣微丸的研制。

Development of Novel pH-Sensitive Eudragit Coated Beads Containing Curcumin-Mesalamine Combination for Colon-Specific Drug Delivery.

作者信息

Heikal Eman J, Kaoud Rashad M, Gad Shadeed, Mokhtar Hatem I, Alattar Abdullah, Alshaman Reem, Zaitone Sawsan A, Moustafa Yasser M, Hammady Taha M

机构信息

Department of Pharmaceutics and Industrial Pharmacy, Faculty of Pharmacy, Suez Canal University, Ismailia 41522, Egypt.

Faculty of Pharmacy, The University of Mashreq, Baghdad 11001, Iraq.

出版信息

Gels. 2023 Mar 23;9(4):264. doi: 10.3390/gels9040264.

DOI:10.3390/gels9040264
PMID:37102876
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10137603/
Abstract

This research aims to develop a drug delivery system that effectively treats colitis while administering curcumin/mesalamine by coating alginate/chitosan beads with Eudragit® S-100 to target the colon. Beads were tested to determine their physicochemical characteristics. Coating with Eudragit® S-100 prevents drug release at a pH of less than 7; this was demonstrated by in-vitro release conducted in a medium with gradually varying pH to mimic circumstances in various regions of the gastrointestinal tract. This study examined the efficacy of the coated beads in treating acetic acid-induced colitis in rats. Results showed that spherical beads were formed with an average diameter of 1.6-2.8 mm, and the obtained swelling ranged from 409.80% to 890.19%. The calculated entrapment efficiency ranged from 87.49% to 97.89%. The optimized formula F13 (which was composed of mesalamine-curcumin active ingredients, Sodium alginate as a gelling agent, chitosan as a controlled release agent, CaCl2 as a crosslinking agent, and Eudragit S-100 as a pH-sensitive coating agent) demonstrated the best entrapment efficiency (97.89% ± 1.66), swelling (890.19% ± 60.1), and bead size (2.7 ± 0.62 mm). In formulation #13, which was coated with Eudragit S 100, curcumin (6.01 ± 0.04%) and mesalamine (8.64 ± 0.7%), were released after 2 h at pH 1.2; 6.36 ± 0.11% and 10.45 ± 1.52% of curcumin and mesalamine, respectively, were then released after 4 h and at pH 6.8. Meanwhile, at pH 7.4, after 24 h, approximately 85.34 ± 2.3% (curcumin) and 91.5 ± 1.2% (mesalamine) were released. Formula #13 significantly reduced the colitis, and this suggests that the developed hydrogel beads can be used for delivering curcumin-mesalamine combinations to treat ulcerative colitis after adequate research.

摘要

本研究旨在开发一种药物递送系统,通过用尤特奇®S - 100包衣海藻酸钠/壳聚糖珠来靶向结肠,从而在施用姜黄素/美沙拉嗪时有效治疗结肠炎。对珠子进行测试以确定其物理化学特性。用尤特奇®S - 100包衣可防止药物在pH值小于7时释放;在模拟胃肠道不同区域环境的pH值逐渐变化的介质中进行的体外释放实验证明了这一点。本研究考察了包衣珠治疗大鼠乙酸诱导的结肠炎的疗效。结果表明,形成了平均直径为1.6 - 2.8毫米的球形珠子,获得的溶胀率在409.80%至890.19%之间。计算得到的包封率在87.49%至97.89%之间。优化配方F13(由美沙拉嗪 - 姜黄素活性成分、海藻酸钠作为凝胶剂、壳聚糖作为控释剂、氯化钙作为交联剂以及尤特奇S - 100作为pH敏感包衣剂组成)表现出最佳的包封率(97.89%±1.66)、溶胀率(890.19%±60.1)和珠子尺寸(2.7±0.62毫米)。在涂有尤特奇S 100的配方#13中,姜黄素(6.01±0.04%)和美沙拉嗪(8.64±0.7%)在pH 1.2时2小时后释放;在pH 6.8时4小时后,姜黄素和美沙拉嗪分别又释放了6.36±0.11%和10.45±1.52%。同时,在pH 7.4时,24小时后,大约85.34±2.3%(姜黄素)和91.5±1.2%(美沙拉嗪)被释放。配方#13显著减轻了结肠炎,这表明经过充分研究后,所开发的水凝胶珠可用于递送姜黄素 - 美沙拉嗪组合来治疗溃疡性结肠炎。

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