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压缩涂层脉冲式时间治疗系统:基于 QbD 的优化。

Compression-coated pulsatile chronomodulated therapeutic system: QbD assisted optimization.

机构信息

Department of Pharmaceutics, Faculty of Pharmacy, King Abdulaziz University, Jeddah, Saudi Arabia.

Center of Excellence for Drug Research and Pharmaceutical Industries, King Abdulaziz University, Jeddah, Saudi Arabia.

出版信息

Drug Deliv. 2022 Dec;29(1):2258-2268. doi: 10.1080/10717544.2022.2094500.

Abstract

Pulsatile drug delivery systems have drawn attention in contemporary research for designing chronotherapeutic systems. The current work aims to design pulsatile ketorolac tromethamine tablets using compression coating for delayed delivery with a lag time suitable for the treatment of morning stiffness in arthritis. Rapidly disintegrating core tablets of ketorolac tromethamine were formulated using super-disintegrants, and the optimized formulation was compression using PEO WSR coagulant and Eudragit RLPO for delaying the release. The central composite design and response surface methodology were employed to optimize the formulation and process parameters namely PEO WSR Coagulant (X), Eudragit RLPO (X), and Hardness (X). The dependent variables optimized were lag time and time required for 95% drug release. Analysis using response surface graphs and mathematical modeling of the results allowed identifying and quantifying the formulation variables active on the selected responses. A polynomial equation fitted to the data was used to predict the composition with optimum responses. Compression-coated pulsatile tablets' optimized composition exhibited a lag time of 9 h and released 95% of the ketorolac tromethamine in 17.42 h. Validation of the mathematical model assured the reliability of QBD in formulation design. X-ray imaging and pharmacokinetic studies established a strong relationship between the coated polymers maintaining the desired lag time for delayed delivery of the active to coincide with the chronobiology for enhanced bioavailability at the right time when needed.

摘要

脉冲药物递送系统在当代研究中引起了关注,旨在设计时间治疗系统。本工作旨在设计脉冲酮咯酸氨丁三醇片,采用压缩包衣延迟释放,时滞适合关节炎晨僵的治疗。采用超崩解剂制备酮咯酸氨丁三醇速崩核心片,并采用 PEO WSR 凝结剂和 Eudragit RLPO 进行优化,以延迟释放。采用中心组合设计和响应面法优化处方和工艺参数,即 PEO WSR 凝结剂 (X)、Eudragit RLPO (X)和硬度 (X)。优化的变量是时滞和 95%药物释放所需的时间。通过响应面图和结果的数学模型分析,可以确定和量化对所选响应有影响的配方变量。拟合数据的多项式方程用于预测具有最佳响应的组合物。压缩包衣脉冲片的优化组成显示时滞为 9 小时,17.42 小时内释放 95%的酮咯酸氨丁三醇。对数学模型的验证确保了 QBD 在配方设计中的可靠性。X 射线成像和药代动力学研究表明,涂层聚合物之间存在很强的关系,可以维持所需的时滞,以延迟活性成分的释放,使其与生物节律相吻合,从而在需要时提高生物利用度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff19/9477481/920ccdd24d32/IDRD_A_2094500_F0001_C.jpg

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