Medicinal and Pharmaceutical Chemistry Department, Pharmaceutical and Drug Industries Research Institute, National Research Centre, 33 EL Bohouth st. (former EL Tahrir st.), P.O.12622, Affiliation ID: 10014618, Dokki, Giza, Egypt.
Medicinal and Pharmaceutical Chemistry Department, Pharmaceutical and Drug Industries Research Institute, National Research Centre, 33 EL Bohouth st. (former EL Tahrir st.), P.O.12622, Affiliation ID: 10014618, Dokki, Giza, Egypt.
J Pharm Sci. 2024 Aug;113(8):2274-2285. doi: 10.1016/j.xphs.2024.03.012. Epub 2024 Mar 19.
The appropriate design of experiments (DoE) could support post-approval lean-stability approaches. A three-factor three-level face-centered design was constructed to evaluate the long-term stability of gliclazide (GLZ) alginate-gelatin beads. The formulation variables were GLZ%(X), alginate:gelatin ratio(X), and glutaraldehyde%(X). The studied responses included GLZ release at predefined intervals in 0.1 N HCl (2 h) followed by phosphate buffer (pH 7.4). Model-dependent and independent approaches were utilized for comparison. DoE-model validation and reduction were implemented. All the studied formulations showed non-significant changes in the particle size (p > 0.05) and most of them showed similar release profiles before and after storage. The directions of the relationships between the factors' main effects and the responses (Y:Q, Y:Q and Y:Q) remained unchanged after storage. The optimal factor settings based on the proposed optimization criteria were defined. The optimized formulations (OP-1 and OP-2) showed non-significant changes in the particle size after storage. The release profiles and kinetics of OP-1 and OP-2 remained unchanged after storage. No chemical change was indicated (FT-IR). DSC-thermograms of OP-1 indicated GLZ conversion to a more stable polymorph after storage. While OP-2 showed a change in GLZ crystallinity. The stored and fresh beads' surfaces after GLZ release were almost similar. DoE could be utilized to evaluate, optimize, and predict the effects of different formulation variables on the long-term stability of GLZ alginate-gelatin beads.
适当的实验设计(DoE)可以支持批准后精益稳定性方法。构建了一个三因素三水平的中心复合设计,以评估格列齐特(GLZ)海藻酸钠-明胶珠的长期稳定性。制剂变量为 GLZ%(X)、海藻酸钠:明胶比例(X)和戊二醛%(X)。研究的响应包括在 0.1 N HCl(2 h)后按预定间隔释放 GLZ,然后是磷酸盐缓冲液(pH 7.4)。采用模型依赖和独立的方法进行比较。实施了 DoE 模型验证和简化。所有研究的制剂在粒径(p > 0.05)方面均未发生显著变化,并且大多数在储存前后均显示出相似的释放曲线。在储存后,因素主效应和响应之间的关系(Y:Q、Y:Q 和 Y:Q)的方向保持不变。根据提出的优化标准定义了最佳因素设置。基于优化标准的优化配方(OP-1 和 OP-2)在储存后粒径没有明显变化。OP-1 和 OP-2 的释放曲线和动力学在储存后保持不变。没有表明发生化学变化(FT-IR)。OP-1 的 DSC 图谱表明 GLZ 在储存后转化为更稳定的多晶型物。而 OP-2 显示 GLZ 结晶度发生变化。GLZ 释放后储存和新鲜珠粒的表面几乎相似。DoE 可用于评估、优化和预测不同制剂变量对 GLZ 海藻酸钠-明胶珠长期稳定性的影响。