Tan Bernice Mei Jin, Tay Justin Yong Soon, Wong Poh Mun, Chan Lai Wah, Heng Paul Wan Sia
GEA-NUS Pharmaceutical Processing Research Laboratory, Department of Pharmacy, National University of Singapore, Singapore, Singapore.
GEA-NUS Pharmaceutical Processing Research Laboratory, Department of Pharmacy, National University of Singapore, Singapore, Singapore.
Eur J Pharm Biopharm. 2015 Jan;89:208-15. doi: 10.1016/j.ejpb.2014.12.007. Epub 2014 Dec 10.
Size reduction or milling of the active is often the first processing step in the design of a dosage form. The ability of a mill to convert coarse crystals into the target size and size distribution efficiently is highly desirable as the quality of the final pharmaceutical product after processing is often still dependent on the dimensional attributes of its component constituents. The F10 Fine Grind mill is a mechanical impact mill designed to produce unimodal mid-size particles by utilizing a single-pass two-stage size reduction process for fine grinding of raw materials needed in secondary processing. Box-Behnken designs were used to investigate the effects of various mill variables (impeller, blower and feeder speeds and screen aperture size) on the milling of coarse crystals. Response variables included the particle size parameters (D10, D50 and D90), span and milling rate. Milled particles in the size range of 5-200 μm, with D50 ranging from 15 to 60 μm, were produced. The impeller and feeder speeds were the most critical factors influencing the particle size and milling rate, respectively. Size distributions of milled particles were better described by their goodness-of-fit to a log-normal distribution (i.e. unimodality) rather than span. Milled particles with symmetrical unimodal distributions were obtained when the screen aperture size was close to the median diameter of coarse particles employed. The capacity for high throughput milling of particles to a mid-size range, which is intermediate between conventional mechanical impact mills and air jet mills, was demonstrated in the F10 mill. Prediction models from the Box-Behnken designs will aid in providing a better guide to the milling process and milled product characteristics.
原料药的粉碎或研磨通常是剂型设计中的首个加工步骤。由于最终药品加工后的质量往往仍取决于其成分的尺寸属性,因此,非常希望研磨机能高效地将粗晶体转化为目标尺寸和粒度分布。F10精细研磨机是一种机械冲击式研磨机,旨在通过采用单通道两级粉碎工艺对二次加工所需的原材料进行精细研磨,从而生产单峰中尺寸颗粒。采用Box-Behnken设计来研究各种研磨变量(叶轮、鼓风机和给料器速度以及筛孔尺寸)对粗晶体研磨的影响。响应变量包括粒度参数(D10、D50和D90)、跨度和研磨速率。生产出了粒径范围为5 - 200μm、D50范围为15 - 60μm的研磨颗粒。叶轮速度和给料器速度分别是影响粒径和研磨速率的最关键因素。与跨度相比,研磨颗粒的粒度分布通过其与对数正态分布的拟合优度(即单峰性)能得到更好的描述。当筛孔尺寸接近所用粗颗粒的中值直径时,可获得具有对称单峰分布的研磨颗粒。F10研磨机展示了将颗粒高通量研磨至中尺寸范围的能力,该范围介于传统机械冲击式研磨机和气流粉碎机之间。Box-Behnken设计的预测模型将有助于为研磨过程和研磨产品特性提供更好的指导。