Školáková Tereza, Patera Jan, Zámostný Petr
University of Chemistry and Technology, Prague, Department of Organic Technology, Technická 5, 166 28 Prague 6, Czech Republic.
University of Chemistry and Technology, Prague, Department of Organic Technology, Technická 5, 166 28 Prague 6, Czech Republic.
Int J Pharm. 2017 Sep 15;530(1-2):107-112. doi: 10.1016/j.ijpharm.2017.07.029. Epub 2017 Jul 15.
Many newly developed active pharmaceutical ingredients (APIs) have very low solubility in aqueous media. The preparation of solid dispersions (SDs) is one way of avoiding this problem. However, compound wettability and thus solubility are influenced by surface energy. In this study, we used inverse gas chromatography (IGC) to evaluate the surface energies of prepared SDs, and compared them with those obtained for physical mixtures (PMs). SDs containing different weight ratios of crystalline acetaminophen and one of three polymers (Kollidon 12 PF, Kollidon VA 64 or Soluplus) were prepared by the melt-quenching of corresponding PMs. In all cases, as the polymer content increased, the surface energy decreased significantly. For the SDs and PMs containing Soluplus, this decrease in surface energy showed the same non-linear trend. In the cases of Kollidon 12 PF and Kollidon VA 64, the trend was linear, with the SDs showing a steeper decrease in surface energy than the corresponding PMs. Typically, such decreases are ascribed to the dissolution of the crystalline structure of an API. Our results suggest that in the case of the Kollidons, the steeper decrease is caused by another mechanism, namely, strong API-Kollidon interaction leading to the less wettable surface of SDs.
许多新开发的活性药物成分(API)在水性介质中的溶解度非常低。制备固体分散体(SD)是避免这一问题的一种方法。然而,化合物的润湿性以及溶解度会受到表面能的影响。在本研究中,我们使用反相气相色谱法(IGC)来评估所制备SD的表面能,并将其与物理混合物(PM)的表面能进行比较。通过相应PM的熔融淬冷制备了含有不同重量比的结晶对乙酰氨基酚和三种聚合物之一(聚乙烯吡咯烷酮12 PF、聚乙烯吡咯烷酮VA 64或固体分散体增强剂)的SD。在所有情况下,随着聚合物含量的增加,表面能显著降低。对于含有固体分散体增强剂的SD和PM,表面能的这种降低呈现相同的非线性趋势。在聚乙烯吡咯烷酮12 PF和聚乙烯吡咯烷酮VA 64的情况下,趋势是线性的,SD的表面能下降比相应的PM更陡峭。通常,这种下降归因于API晶体结构的溶解。我们的结果表明,在聚乙烯吡咯烷酮的情况下,更陡峭的下降是由另一种机制引起的,即API与聚乙烯吡咯烷酮的强相互作用导致SD的表面润湿性降低。