School of Pharmacy, University of Wisconsin-Madison, 777 Highland Avenue, Madison, Wisconsin 53707, United States.
Department of Pharmaceutical Sciences, University of Puerto Rico, San Juan, Puerto Rico 00936, United States.
Mol Pharm. 2024 Aug 5;21(8):4074-4081. doi: 10.1021/acs.molpharmaceut.4c00444. Epub 2024 Jul 15.
Amorphous solid dispersions (ASDs) can be used to enhance the solubility and bioavailability of poorly soluble drugs. An ASD is often a ternary system containing a drug, a surfactant, and a polymer. Recent work on binary ASDs has observed significant differences between surface and bulk compositions, with impacts on wettability and stability. Here we investigate a ternary ASD composed of the antifungal posaconazole, the surfactant Span 80, and a dispersion polymer (PVP or PVP/VA). The surfactant loading was fixed at the typical level of 5 wt %, and the drug/polymer ratio was varied. We observed strong surface enrichment of the surfactant and simultaneous depletion of the drug. This effect is already pronounced in the binary drug-surfactant system and is enhanced by the addition of the polymers. Between the two polymers, the more hydrophilic PVP causes a stronger enhancement of the surface enrichment effect. These results demonstrate the impact of component interactions on the surface composition of ASDs and the performance.
无定形固体分散体(ASD)可用于提高难溶性药物的溶解度和生物利用度。ASD 通常是一种包含药物、表面活性剂和聚合物的三元体系。最近关于二元 ASD 的研究观察到表面和体相组成之间存在显著差异,这对润湿性和稳定性有影响。在这里,我们研究了一种由抗真菌药物泊沙康唑、表面活性剂 Span 80 和分散聚合物(PVP 或 PVP/VA)组成的三元 ASD。表面活性剂的负载量固定在典型的 5wt%,药物/聚合物的比例变化。我们观察到表面活性剂的强烈富集和药物的同时耗尽。这种效应在二元药物-表面活性剂体系中已经很明显,并且通过添加聚合物得到增强。在两种聚合物中,亲水性更强的 PVP 导致表面富集效应的增强更为显著。这些结果表明了成分相互作用对 ASD 的表面组成和性能的影响。