Suñé-Negre Josep M, Pérez-Lozano Pilar, Miñarro Montserrat, Roig Manel, Fuster Roser, Hernández Carmen, Ruhí Ramon, García-Montoya Encarna, Ticó Josep R
Pharmacy and Pharmaceutical Technology Department, University of Barcelona, Barcelona, Spain.
Eur J Pharm Biopharm. 2008 Aug;69(3):1029-39. doi: 10.1016/j.ejpb.2008.01.020. Epub 2008 Jan 31.
Application of the new SeDeM Method is proposed for the study of the galenic properties of excipients in terms of the applicability of direct-compression technology. Through experimental studies of the parameters of the SeDeM Method and their subsequent mathematical treatment and graphical expression (SeDeM Diagram), six different DC diluents were analysed to determine whether they were suitable for direct compression (DC). Based on the properties of these diluents, a mathematical equation was established to identify the best DC diluent and the optimum amount to be used when defining a suitable formula for direct compression, depending on the SeDeM properties of the active pharmaceutical ingredient (API) to be used. The results obtained confirm that the SeDeM Method is an appropriate system, effective tool for determining a viable formulation for tablets prepared by direct compression, and can thus be used as the basis for the relevant pharmaceutical development.
就直接压片技术的适用性而言,建议将新的SeDeM方法应用于辅料的盖仑性质研究。通过对SeDeM方法参数的实验研究及其后续的数学处理和图形表达(SeDeM图),分析了六种不同的直接压片稀释剂,以确定它们是否适合直接压片(DC)。基于这些稀释剂的性质,建立了一个数学方程,根据待使用的活性药物成分(API)的SeDeM性质,确定最佳的直接压片稀释剂以及在定义合适的直接压片配方时要使用的最佳用量。所得结果证实,SeDeM方法是一种合适的系统,是确定直接压片制备片剂可行配方的有效工具,因此可作为相关药物开发的基础。