State Key Laboratory of Chemical Engineering, School of Chemical Engineering and Technology, Tianjin University , Tianjin , P. R. China.
Key Laboratory Modern Drug Delivery, High Efficiency in Tianjin University , Tianjin , P. R. China.
Pharm Dev Technol. 2019 Nov;24(9):1175-1180. doi: 10.1080/10837450.2019.1641517. Epub 2019 Jul 22.
Lenalidomide (LDM) is a blockbuster drug for multiple myeloma and non-Hodgkin's lymphoma, and contributed $ 6.974 billion in sales for Celgene in 2016. The aim of this research is to expand the crystal form landscape, characterize the physicochemical properties and thoroughly investigate the potential solid forms transformation for this famous drug. In this study, a comprehensive solid-state screening was carried out. The physicochemical properties, stability and phase transformation were fully investigated using powder X-ray diffraction (PXRD), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), solid state nuclear magnetic resonance (solid state NMR) and Infrared Spectroscopic Analysis (IR). Finally the differences of dissolution behavior were compared through powder dissolution test. Two new anhydrous forms (α and β) and one new dihydrate form (DH) of LDM were discovered through a comprehensive solid-state screening experiment. The new discovered DH showed better stability under accelerated storage condition (40 °C/75% RH) and in most organic solvents than other forms. The new discovered form α exhibited faster dissolution rate in the early phase and larger apparent solubility than the currently marketed form. These new forms exhibit a new chance for drug development in view of their pharmaceutical properties and intellectual property.
来那度胺(LDM)是多发性骨髓瘤和非霍奇金淋巴瘤的重磅药物,2016 年为 Celgene 带来了 69.74 亿美元的销售收入。本研究旨在拓展其晶型景观,对其物理化学性质进行全面表征,并深入研究该知名药物潜在的固体形式转变。 在本研究中,进行了全面的固态筛选。采用粉末 X 射线衍射(PXRD)、热重分析(TGA)、差示扫描量热法(DSC)、固态核磁共振(固体 NMR)和红外光谱分析(IR)全面研究了其物理化学性质、稳定性和相转变。最后通过粉末溶解试验比较了溶解行为的差异。 通过全面的固态筛选实验,发现了来那度胺的两种新无水形式(α和β)和一种新的二水合物形式(DH)。新发现的 DH 在加速储存条件(40°C/75%RH)和大多数有机溶剂中比其他形式具有更好的稳定性。新发现的形式α在早期阶段表现出更快的溶解速率和更大的表观溶解度,优于目前市售的形式。 鉴于其药物特性和知识产权,这些新形式为药物开发提供了新的机会。