School of Pharmacy, Faculty of Health Sciences, University of Eastern Finland, Kuopio, Finland.
Early Product Development and Manufacturing, Pharmaceutical Sciences, BioPharmaceuticals R&D, AstraZeneca Gothenburg, 431 83 Mölndal, Sweden.
Eur J Pharm Sci. 2022 May 1;172:106151. doi: 10.1016/j.ejps.2022.106151. Epub 2022 Feb 23.
In early development, when active pharmaceutical ingredient (API) is in short supply, it would be beneficial to reduce the number of experiments by predicting a suitable L/S ratio before starting the product development. The aim of the study was to decrease development time and the amount of API needed for the process development of high drug load formulations for continuous twin-screw wet granulation (TSWG). Mixer torque rheometry was used as a pre-formulation tool to predict the suitable L/S ratios for granulation experiments. Three different values that were based on the MTR curves, were determined and assessed for their ability to predict the suitable L/S ratio for TSWG. Three APIs (allopurinol, paracetamol and metformin HCl) were used as model substances in high drug load formulations containing 60% drug substance. The MCC-mannitol ratio was varied to assess the optimal composition for the high-dose formulations. The API solubility affected the mixer torque rheometer (MTR) curves and the optimum L/S ratio for TSWG. The highly soluble metformin needed a much lower L/S ratio compared with allopurinol and paracetamol. A design space was determined for each API based on granule flowability and tablet tensile strength. The flowability of the granules and tensile strength of the tablets improved with an increasing L/S ratio. The MCC-mannitol filler ratio had a significant effect on tabletability for paracetamol and metformin, and these APIs having poor compaction properties needed higher MCC ratios to achieve the 2 MPa limit. The MCC-mannitol ratio had no effect on the granule flow properties. Instead, API properties had the largest influence on both granule flow properties and tensile strength. Based on this study, both the L/S ratio and MCC-mannitol ratio are crucial in controlling the critical quality attributes in high drug load formulations processed by TSWG. The optimum flow and tablet mechanical properties were achieved when using 75:25 MCC-mannitol ratio. Both start of the slope and 2/3 of the L/S ratio at the maximum torque in MTR provided a solid guideline to aim for in a TSWG experiment.
在早期开发阶段,当活性药物成分 (API) 供应不足时,如果在开始产品开发之前预测合适的固液比 (L/S),可以减少实验次数。本研究旨在减少高载药量制剂连续双螺杆湿法造粒 (TSWG) 工艺开发所需的开发时间和 API 用量。混合器转矩流变仪被用作预配方工具,以预测造粒实验的合适 L/S 比。基于 MTR 曲线确定了三个不同的值,并评估了它们预测 TSWG 合适 L/S 比的能力。三种 API(别嘌醇、对乙酰氨基酚和盐酸二甲双胍)被用作含有 60%药物的高载药量制剂的模型物质。MCC-甘露醇的比例变化,以评估高剂量制剂的最佳组成。API 溶解度影响混合器转矩流变仪 (MTR) 曲线和 TSWG 的最佳 L/S 比。高溶解度的二甲双胍与别嘌醇和对乙酰氨基酚相比,需要低得多的 L/S 比。基于颗粒流变性和片剂拉伸强度,为每个 API 确定了设计空间。随着 L/S 比的增加,颗粒的流变性和片剂的拉伸强度提高。MCC-甘露醇填充剂比例对对乙酰氨基酚和盐酸二甲双胍的可压性有显著影响,这些 API 压缩性能差,需要更高的 MCC 比例才能达到 2 MPa 的限制。MCC-甘露醇比例对颗粒流变性没有影响。相反,API 性质对颗粒流变性和拉伸强度都有最大的影响。基于这项研究,L/S 比和 MCC-甘露醇比在控制 TSWG 处理的高载药量制剂的关键质量属性方面都至关重要。当使用 75:25 的 MCC-甘露醇比例时,实现了最佳的流动和片剂力学性能。MTR 中最大扭矩处的斜率开始和 L/S 比的 2/3 都为 TSWG 实验提供了一个明确的目标。