Tao Jing, Pandey Preetanshu, Bindra Dilbir S, Gao Julia Z, Narang Ajit S
Drug Product Science and Technology, Bristol-Myers Squibb, New Brunswick, New Jersey, 08901.
J Pharm Sci. 2015 Jul;104(7):2323-33. doi: 10.1002/jps.24504. Epub 2015 May 25.
This work aimed to evaluate the commonly used scale-up rules for high-shear wet granulation process using a microcrystalline cellulose-lactose-based low drug loading formulation. Granule properties such as particle size, porosity, flow, and tabletability, and tablet dissolution were compared across scales using scale-up rules based on different impeller speed calculations or extended wet massing time. Constant tip speed rule was observed to produce slightly less granulated material at the larger scales. Longer wet massing time can be used to compensate for the lower shear experienced by the granules at the larger scales. Constant Froude number and constant empirical stress rules yielded granules that were more comparable across different scales in terms of compaction performance and tablet dissolution. Granule porosity was shown to correlate well with blend tabletability and tablet dissolution, indicating the importance of monitoring granule densification (porosity) during scale-up. It was shown that different routes can be chosen during scale-up to achieve comparable granule growth and densification by altering one of the three parameters: water amount, impeller speed, and wet massing time.
本研究旨在使用基于微晶纤维素 - 乳糖的低药物负载制剂,评估高剪切湿法制粒过程中常用的放大规则。使用基于不同叶轮速度计算或延长湿混时间的放大规则,在不同规模下比较了颗粒特性,如粒径、孔隙率、流动性和可压性,以及片剂溶出度。观察到恒定叶尖速度规则在较大规模下产生的制粒物料略少。较长的湿混时间可用于补偿较大规模下颗粒所经历的较低剪切力。恒定弗劳德数和恒定经验应力规则产生的颗粒在压实性能和片剂溶出度方面在不同规模之间更具可比性。颗粒孔隙率与混合物料可压性和片剂溶出度显示出良好的相关性,表明在放大过程中监测颗粒致密化(孔隙率)的重要性。结果表明,在放大过程中可以选择不同的途径,通过改变水量、叶轮速度和湿混时间这三个参数之一,来实现可比的颗粒生长和致密化。