We focused on the critical role of crystallization of active pharmaceutical ingredients (APIs) in drug development, with particular emphasis on stability, solubility, and the feasibility of drug formulation and manufacturing. We explored polymorphism in APIs and the formation of multicomponent crystals, including salt and cocrystal screening, underscoring the significance of regulatory and intellectual property considerations in recognizing salts and cocrystals of solid forms. Our study led to the design of seven new multicomponent crystalline forms of imatinib, an oncology API. Using X-ray crystallography and solid-state NMR, we elucidated hydrogen bonding interactions and proton transfer, unveiling multicomponent interactions in the crystalline solid forms along the salt-cocrystal continuum. Most of the new solid forms demonstrated improved aqueous solubility compared to that of the free base form. This research provides valuable insights into the structural details of solid forms of pharmaceutical compounds and emphasizes the importance of understanding solid-state interactions for the rational design of crystalline APIs, thereby enhancing the drug development process.
机构:
USM, Inst Univ Sains Malaysia, Xray Crystallog Unit, Sch Phys, George Town 11800, MalaysiaIndian Sch Mines, Dept Appl Chem, Dhanbad 826004, Jharkhand, India
Fun, Hoong-Kun
Isik, Samil
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机构:
Ondokuz Mayis Univ, Fac Art & Sci, Dept Phys, TR-55139 Kurupelit, TurkeyIndian Sch Mines, Dept Appl Chem, Dhanbad 826004, Jharkhand, India