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Effect of drug substance particle size on the characteristics of granulation manufactured in a high-shear mixer

机译:原料药粒径对高剪切混合机制粒特性的影响

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摘要

DPC 963 is a non-nucleoside reverse transcriptase inhibitor with low aqueous solubility. The effect of DPC 963 drug substance particle size on the characteristics of granules manufactured by high-shear wet granulation was evaluated. The wet granulation process was used to manufacture a DPC 963 formulation with high drug loading. The formulation was manufactured using drug substance lots with different particle size distributions. Granulation particle size distribution, porosity, and compressibility were determined. A uniaxial compression test was also performed on moist compacts of the formulation prepared with different particle size distributions. Particle agglomeration behavior was affected by drug substance particle size. Granulation geometric mean diameter and fraction with particle size greater than 250 μm was inversely proportional to the drug substance particle size. Mercury intrusion porosimetry revealed higher pore volumes for the granules manufactured using the drug substance with the smaller particle size, suggesting lower tendency for granule densification than for that manufactured with the larger drug substance particle size. Granulation compressibility was also sensitive to changes in drug substance particle size. A decreased drug substance particle size led to increased granulation compressibility. Results from the uniaxial compression experiments suggested that the effect of particle size on granulation growth is the results of increased densification propensity, which in turn results from increased drug substance particle size.
机译:DPC 963是水溶性低的非核苷类逆转录酶抑制剂。评估了DPC 963原料药粒径对通过高剪切湿法制粒生产的颗粒特性的影响。湿法制粒工艺用于制造具有高载药量的DPC 963配方。使用具有不同粒度分布的原料药生产制剂。测定了颗粒大小分布,孔隙率和可压缩性。还对以不同粒度分布制备的制剂的湿压块进行了单轴压缩试验。颗粒附聚行为受原料药粒径影响。造粒几何平均直径和粒径大于250μm的级分与原料药粒径成反比。汞侵入孔隙率法显示,使用较小粒径的药物生产的颗粒具有较高的孔体积,这表明与使用较大粒径的药物生产的颗粒相比,颗粒致密化的趋势较低。颗粒可压缩性也对原料药粒径的变化敏感。减小的药物粒径导致增加的颗粒可压缩性。单轴压缩实验的结果表明,颗粒大小对造粒生长的影响是致密化倾向增加的结果,而致密化倾向又是由增加的药物颗粒大小引起的。

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