挤压
溶解
无定形固体
共晶
溶解度
化学
生物利用度
烟酰胺
溶剂
热稳定性
化学工程
材料科学
分子
结晶学
有机化学
复合材料
氢键
酶
工程类
生物
生物信息学
作者
Peiya Shen,Chun-Feng Zhang,Enshi Hu,Yuan Gao,Yuanfeng Wei,Jianjun Zhang,Shuai Qian,Weili Heng
标识
DOI:10.1021/acs.molpharmaceut.3c00059
摘要
Cocrystal (CC) and coamorphous (CM) techniques have become green technologies to improve the solubility and bioavailability of water-soluble drugs. In this study, hot-melt extrusion (HME) was employed to produce CC and CM formulations of indomethacin (IMC) and nicotinamide (NIC) due to its advantages like solvent-free and large-scale manufacturing. Interestingly, for the first time, IMC–NIC CC and CM were selectively prepared depending on the barrel temperatures of HME at a constant screw speed of 20 rpm and a feed rate of 1.0 g/min. IMC–NIC CC was obtained at 105–120 °C, IMC–NIC CM was produced at 125–150 °C, and the mixture of CC and CM was obtained between 120 and 125 °C (like a door switch of CC and CM). SS NMR combined with RDF and Ebind calculations revealed the formation mechanisms of CC and CM, where strong interactions between heteromeric molecules formed at lower temperatures favored periodic molecular organization of CC, whereas discrete and weak interactions formed at higher temperatures promoted disordered molecular arrangement of CM. Additionally, IMC–NIC CC and CM showed enhanced dissolution and stability over crystalline/amorphous IMC. This study provides an easy-to-operate and environmentally friendly strategy for the flexible regulation of CC and CM formulations with different properties through modulation of the barrel temperature of HME.
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