Voinovich D, Campisi B, Moneghini M, Vincenzi C, Phan-Tan-Luu R
Department of Pharmaceutical Sciences, University of Trieste, Piazzale Europa 1, I-34127, Trieste, Italy.
Int J Pharm. 1999 Nov 10;190(1):73-81. doi: 10.1016/s0378-5173(99)00278-1.
The effects of process conditions on the granulometric characteristics of a placebo formulation prepared in a 10 l high shear mixer by single-step melt granulation were studied. The factors under investigation were: binder grade, mixer load, presence of the deflector (all of analysed at two levels), binder concentration, impeller speed, massing time, type of impeller blades (these four at three levels) and jacket temperature (considered at four levels). Two granule characteristics were analysed: the geometric mean diameter and the percentage of particles finer than 315 microm. In order to screen simultaneously the above-mentioned factor levels, an asymmetrical factorial design was adopted, which allowed the reduction in the number of runs from 2592 to 25. Additionally, this technique permitted the selection of the factor levels which have the major 'weight' on the two granule characteristics under study. Two additional trials were performed to attest the screening validity.
研究了工艺条件对在10升高剪切混合器中通过一步熔融制粒制备的安慰剂制剂粒度特性的影响。研究的因素有:粘合剂等级、混合器负载、导流板的存在(所有这些因素均在两个水平上进行分析)、粘合剂浓度、叶轮速度、造粒时间、叶轮叶片类型(这四个因素在三个水平上进行分析)和夹套温度(在四个水平上进行考虑)。分析了两种颗粒特性:几何平均直径和小于315微米的颗粒百分比。为了同时筛选上述因素水平,采用了非对称析因设计,这使得实验次数从2592次减少到25次。此外,该技术允许选择对所研究的两种颗粒特性具有主要“权重”的因素水平。进行了另外两项试验以证明筛选的有效性。