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玻璃化形成能力对过饱和无定形固体分散体物理稳定性的影响。

Influence of Glass Forming Ability on the Physical Stability of Supersaturated Amorphous Solid Dispersions.

机构信息

Department of Pharmacy, University of Copenhagen, Universitetsparken 2, 2100 Copenhagen, Denmark.

Idorsia Pharmaceuticals Ltd, Hegenheimermattweg 91, CH-4123 Allschwil, Switzerland.

出版信息

J Pharm Sci. 2019 Aug;108(8):2561-2569. doi: 10.1016/j.xphs.2019.02.028. Epub 2019 Mar 13.

Abstract

In this study, the influence of the glass-forming ability (GFA) of a drug on its physical stability in a supersaturated solid dispersion was investigated. Nine drugs were classified according to their GFA using their respective critical cooling rate. Their respective solubility in poly(vinylpyrrolidone-co-vinyl acetate) 6:4 (PVPVA64) was predicted using the melting point depression method based on the Flory-Huggins lattice theory. Supersaturated amorphous solid dispersions at a level of 25% w/w drug above saturation solubility in the polymer were prepared by film-casting, and their respective physical stability at temperatures of 10°C or 20°C above or below their respective T (dry conditions) was monitored by the use of polarized light microscopy. This study showed that drugs with good GFA (class 3) on average have higher physical stability in supersaturated amorphous solid dispersion compared to drug with modest GFA (class 2), which in turn have higher physical stability in supersaturated amorphous solid dispersion than drugs with poor GFA (class 1). These results indicate that the GFA of a drug and its physical stability in a supersaturated amorphous solid dispersion stored at a temperature above or below its T are correlated.

摘要

在这项研究中,考察了药物的成玻璃能力(GFA)对其在过饱和固体分散体中物理稳定性的影响。根据各自的临界冷却速率,将 9 种药物按照 GFA 进行分类。根据 Flory-Huggins 晶格理论的熔点降低法,预测了它们在聚(乙烯基吡咯烷酮-co-醋酸乙烯酯)6:4(PVPVA64)中的溶解度。通过薄膜铸造法制备了 25%w/w 药物超过聚合物溶解度的过饱和无定形固体分散体,并在高于或低于各自 T(干燥条件)10°C 或 20°C 的温度下,通过偏光显微镜监测它们各自的物理稳定性。这项研究表明,具有良好 GFA(3 类)的药物在过饱和无定形固体分散体中的物理稳定性平均高于具有适度 GFA(2 类)的药物,而具有适度 GFA(2 类)的药物在过饱和无定形固体分散体中的物理稳定性又高于具有较差 GFA(1 类)的药物。这些结果表明,药物的 GFA 与其在高于或低于其 T 温度下储存的过饱和无定形固体分散体中的物理稳定性相关。

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