Study on polycyclic macromolecular drug solid stability: A case exploration of methylcobalamin

甲钴胺 化学 药品 高分子 药理学 医学 生物化学 维生素B12
作者
Zhaoxia Ao,Shijian Feng,Chenyang Zhao,Shilin Guo,Kangli Li,Dandan Han,Junbo Gong
出处
期刊:International Journal of Pharmaceutics [Elsevier]
卷期号:644: 123326-123326
标识
DOI:10.1016/j.ijpharm.2023.123326
摘要

As one of derivatives of Vitamin B12, methylcobalamin (MeCbl) is an indispensable “Life Element” and plays an essential role in maintaining human normal physiology function and clinical medicine application. Because of the intricate molecular structure, strong hygroscopicity and optical instability, maintaining its solid stability is a great challenge in pharmaceutical preparation. Based on the structure features of MeCbl hydrates, this study explored the drug solid stability by designing solid-solid phase transformation (SSPT) experiments. Three hydrate powders of MeCbl that had special structure with isolated site and channel water molecules were discovered. It was found that drying condition and surrounding humidity were controlling factors influencing the final solid form. The inter-conversion relations relevant to heating-induced and humidity-induced structure changes were established among the three hydrate powders. Powder X-ray diffraction, thermogravimetric analysis, differential scanning calorimetry, high performance liquid chromatography and dynamic vapor sorption were used to characterize the differences and related properties of stably prepared MeCbl hydrate powders. The particle size of product could be regulated and controlled by optimizing operating conditions of crystallization process, where ultrasound-assisted and seeding-introduced were applied as promising strategies to enhance solution crystallization process. This study opens up the possibility for the stable preparation and large-scale production of polycyclic macromolecular bulk drugs like methylcobalamin.
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