Department of Pharmaceutical Technology, School of Clinical Pharmacy, College of Pharmaceutical Sciences, Matsuyama University.
Chem Pharm Bull (Tokyo). 2023;71(9):687-694. doi: 10.1248/cpb.c23-00262.
Lactose is an excipient used extensively for bulking, diluting, and molding active pharmaceutical ingredients in tablet manufacturing. Particularly, granulated lactose (GL) intended for direct powder compression has distinct properties due to differences in manufacturing methods. It contributes to handling blended powders for tableting and tablet quality. In this study, we aimed to compare the functions of different forms of GL added as excipients during direct powder compression on the tablet properties and the effect of magnesium stearate (Mg-S) used as a lubricant on each type of GL. Different GL types obtained using different manufacturing methods (agitated granulation, GL-AG; spray-dried granulation, GL-SD; fluidized bed granulation, GL-FB) were blended with maize starch, low-substituted hydroxypropyl cellulose, and paracetamol in a V-type blender for 10 min. Mg-S was added at varying amounts (0.1, 1.0, and 2.0%) and blending times (5, 10, and 30 min) for the nine types of blended powders for tableting formulation. The powders were tableted, and the tablets were evaluated for weight and drug loading variations, tensile strength, friability, and disintegration time. When tablets with the same blending conditions were compared, the tensile strength and disintegration time were in the order of GL-FB > GL-SD > GL-AG. For each GL, we analyzed the effects of changes in the added amount of Mg-S and blending time using contour plots, evaluated the effects of blending conditions on tablet properties, and determined the target tablet properties. We investigated the optimization of the lubricant blending conditions to obtain suitable tablets.
乳糖是一种广泛用于制药行业的辅料,可用于增加、稀释和成型药物活性成分。特别是用于直接粉末压缩的颗粒状乳糖(GL),由于制造方法的不同,具有独特的性质。它有助于处理用于压片的混合粉末和片剂的质量。在这项研究中,我们旨在比较不同形式的 GL 作为辅料在直接粉末压缩中对片剂性质的影响,以及不同类型的 GL 中使用的硬脂酸镁(Mg-S)作为润滑剂的效果。使用不同的制造方法(搅拌制粒、GL-AG;喷雾干燥制粒、GL-SD;流化床制粒、GL-FB)获得的不同 GL 类型与玉米淀粉、低取代羟丙基纤维素和扑热息痛混合在 V 型混合器中混合 10 分钟。将不同量(0.1、1.0 和 2.0%)和不同混合时间(5、10 和 30 分钟)的 Mg-S 添加到九种用于压片制剂的混合粉末中。将粉末压制成片剂,并评估片剂的重量和药物负载变化、拉伸强度、脆性和崩解时间。当比较具有相同混合条件的片剂时,拉伸强度和崩解时间的顺序为 GL-FB>GL-SD>GL-AG。对于每种 GL,我们使用等高线图分析了添加的 Mg-S 量和混合时间变化的影响,评估了混合条件对片剂性质的影响,并确定了目标片剂性质。我们研究了优化润滑剂混合条件以获得合适片剂的方法。