Heikal Eman J, Kaoud Rashad M, Gad Shadeed, Mokhtar Hatem I, Alattar Abdullah, Alshaman Reem, Zaitone Sawsan A, Moustafa Yasser M, Hammady Taha M
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.
Gels. 2023 Mar 23;9(4):264. doi: 10.3390/gels9040264.
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.
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。