Faculty of Pharmacy, Bahauddin Zakriya University, Multan, Pakistan.
Lahore Pharmacy College, Lahore Medical and Dental College, Lahore, Pakistan.
Drug Des Devel Ther. 2020 Jun 22;14:2435-2448. doi: 10.2147/DDDT.S244016. eCollection 2020.
Severe bleeding and perforation of the colon and rectum are complications of ulcerative colitis which can be treated by a targeted drug delivery system.
Development of colon-targeted delivery usually involves a complex formulation process and coating steps of pH-sensitive methacrylic acid based Eudragit. The current work was purposefully designed to develop dicalcium phosphate (DCP) facilitated with Eudragit-S100-based pH-dependent, uncoated mesalamine matrix tablets.
Mesalamine formulations were compressed using wet granulation technique with varying compositions of dicalcium phosphate (DCP) and Eudragit-S100. The developed formulations were characterized for physicochemical and drug release profiles. Infrared studies were carried out to ensure that there was no interaction between active ingredients and excipients. Artificial neural network (ANN) was used for the optimization of final DCP-Eudragit-S100 complex and the experimental data were employed to train a multi-layer perception (MLP) using quick propagation (QP) training algorithm until a satisfactory root mean square error (RMSE) was reached. The ANN-aided optimized formulation was compared with commercially available Masacol.
Compressed tablets met the desirability criteria in terms of thickness, hardness, weight variation, friability, and content uniformity, ie, 5.34 mm, 7.7 kg/cm 585±5 mg (%), 0.44%, and 103%, respectively. In-vitro dissolution study of commercially available mesalamine and optimized formulation was carried out and the former showed 100% release at 6 h while the latter released only 12.09% after 2 h and 72.96% after 12 h which was fitted to Weibull release model with b value of 1.3, indicating a complex release mechanism.
DCP-Eudragit-S100 blend was found explicative for mesalamine release without coating in gastric and colonic regions. This combination may provide a better control of ulcerative colitis.
结肠和直肠的严重出血和穿孔是溃疡性结肠炎的并发症,可以通过靶向药物输送系统进行治疗。
开发结肠靶向递送系统通常涉及复杂的制剂工艺和 pH 敏感的甲基丙烯酸共聚物 Eudragit 的包衣步骤。目前的工作旨在开发基于磷酸氢钙(DCP)的 pH 依赖性、无涂层美沙拉嗪基质片剂,该片剂由 Eudragit-S100 辅助。
使用湿法制粒技术,用不同比例的磷酸氢钙(DCP)和 Eudragit-S100 压缩美沙拉嗪制剂。对所开发的制剂进行物理化学和药物释放特性的表征。进行了红外研究以确保活性成分和赋形剂之间没有相互作用。人工神经网络(ANN)用于优化最终的 DCP-Eudragit-S100 复合物,并用快速传播(QP)训练算法对实验数据进行训练,直到达到满意的均方根误差(RMSE)。将 ANN 辅助优化的配方与市售的 Masacol 进行比较。
片剂在厚度、硬度、重量差异、脆碎度和含量均匀度方面均符合理想标准,分别为 5.34mm、7.7kg/cm 585±5mg(%)、0.44%和 103%。对市售美沙拉嗪和优化配方进行了体外溶出度研究,前者在 6 小时时达到 100%释放,而后者在 2 小时时仅释放 12.09%,在 12 小时时释放 72.96%,符合 Weibull 释放模型,b 值为 1.3,表明释放机制复杂。
在胃和结肠区域不进行包衣的情况下,DCP-Eudragit-S100 混合物对美沙拉嗪的释放具有解释性。这种组合可能为溃疡性结肠炎的治疗提供更好的控制。