Basit A W, Newton J M, Lacey L F
Department of Pharmaceutics, School of Pharmacy, University of London, U.K.
Pharm Dev Technol. 1999;4(4):499-505. doi: 10.1081/pdt-100101387.
The present study was concerned with the feasibility of formulating ranitidine into pellets with a range of alternative excipients in place of microcrystalline cellulose (MCC). Eight ranitidine formulations employing two or more of the excipients lactose, barium sulfate, glyceryl monostearate, and MCC were processed by extrusion-spheronization, and characterized according to a series of physico-mechanical and dissolution criteria. Formulations containing lactose produced unsatisfactory pellets of wide size distribution and irregular shape, whereas formulations incorporating barium sulfate and glyceryl monostearate with or without MCC resulted in relatively spherical pellets of narrow size distribution and good mechanical properties. Ranitidine release was found to be rapid and virtually complete within 15 min, regardless of the pellet formulation. A direct relationship was observed between the concentration of MCC in the formulation and the properties of the pellets. In general, the higher the concentration of MCC, the rounder, stronger, and less friable the pellets. However, even pellets without MCC were also successfully prepared with a superior size distribution and shape over those with MCC. Overall, these results confirm that ranitidine can be formulated into pellet dosage forms with little or no MCC by the extrusion-spheronization process.
本研究关注用一系列替代辅料取代微晶纤维素(MCC)将雷尼替丁制成微丸的可行性。采用挤出滚圆法制备了八种含有乳糖、硫酸钡、单硬脂酸甘油酯和MCC中的两种或更多种辅料的雷尼替丁制剂,并根据一系列物理机械和溶出标准对其进行了表征。含有乳糖的制剂制备出的微丸尺寸分布宽且形状不规则,质量不佳,而含有硫酸钡和单硬脂酸甘油酯(含或不含MCC)的制剂则得到尺寸分布窄且具有良好机械性能的相对球形的微丸。无论微丸制剂如何,雷尼替丁的释放都很快,且在15分钟内几乎完全释放。观察到制剂中MCC的浓度与微丸的性质之间存在直接关系。一般来说,MCC的浓度越高,微丸越圆、越强且越不易脆碎。然而,即使不含MCC的微丸也能成功制备,其尺寸分布和形状优于含MCC的微丸。总体而言,这些结果证实雷尼替丁可以通过挤出滚圆法制成几乎不含或不含MCC的微丸剂型。