Materials Research Institute, Athlone Institute of Technology, Dublin Rd, Athlone, Westmeath, Ireland; Synthesis and Solid State Pharmaceutical Centre (SSPC), Athlone Institute of Technology, Dublin Rd, Athlone, Westmeath, Ireland.
Materials Research Institute, Athlone Institute of Technology, Dublin Rd, Athlone, Westmeath, Ireland.
Int J Pharm. 2018 Oct 5;549(1-2):50-57. doi: 10.1016/j.ijpharm.2018.07.039. Epub 2018 Jul 26.
The investigation of the miscibility between active pharmaceutical ingredients (API's) and polymeric excipients is of great interest for the formulation and development of amorphous solid dispersions, especially in the context of the prediction of the stability of these systems. Two different methods were applied to determine the miscibility between model compounds poly(vinylpyrrolidone-co-vinyl acetate) (PVPVA) and indomethacin (IND), viz. the measurement of the glass transition temperature (T) and the melting point depression method framed on the Flory-Huggins theory. Measurement of the glass transition temperatures of the binary blends showed the formation of an amorphous single phase system between the PVPVA and the IND regardless of the composition. Variation of T with the composition was well described by the Gordon-Taylor equation leading to the error of concluding lack of intermolecular interactions between the materials. Application of the Brostow-Chiu-Kalogeras-Vassilikou-Dova (BCKV) model shows a negative interaction parameter (a) suggesting the presence of drug-drug intermolecular interactions. Application of the melting point depression method within the framework of the Flory-Huggins theory proved the miscibility of the system at temperatures close to the melting point of IND.
研究活性药物成分(API)与高分子赋形剂之间的混溶性对于无定形固体分散体的配方和开发非常重要,特别是在预测这些系统的稳定性方面。本文应用了两种不同的方法来确定模型化合物聚乙烯吡咯烷酮-乙酸乙烯酯共聚物(PVPVA)和吲哚美辛(IND)之间的混溶性,即测量玻璃化转变温度(T)和基于 Flory-Huggins 理论的熔点降低法。二元混合物玻璃化转变温度的测量表明,无论组成如何,PVPVA 和 IND 之间形成了非晶单相体系。T 随组成的变化很好地用 Gordon-Taylor 方程描述,导致错误地得出材料之间不存在分子间相互作用的结论。Brostow-Chiu-Kalogeras-Vassilikou-Dova(BCKV)模型的应用表明存在药物-药物分子间相互作用,具有负相互作用参数(a)。在 Flory-Huggins 理论框架内应用熔点降低法证明了在接近 IND 熔点的温度下,该体系具有混溶性。