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Thermodynamics and preliminary pharmaceutical characterization of a melatonin-pimelic acid cocrystal prepared by a melt crystallization method

机译:熔融结晶法制备的褪黑素-庚二酸共晶体的热力学和初步药物表征

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摘要

Pharmaceutical cocrystals have been extensively investigated as a promising approach to improve drugs' physicochemical properties. Cocrystals are usually prepared using solution-mediated methods and grinding methods. In this study, a cocrystal of pimelic acid with poorly soluble melatonin was produced using a melt crystallization method by controlling the crystallization within a specific temperature range. The cocrystal was characterized by infrared spectroscopy, powder and single crystal X-ray diffraction. The binary phase diagram and the formation enthalpy established by differential scanning calorimetry provided the rationale for this spontaneous cocrystallization system. The cocrystal exhibited higher apparent solubility, a faster dissolution rate and acceptable stability as compared to the original melatonin. The study has shown that the melt crystallization method can be considered as a competitive route for producing pharmaceutical cocrystals with improved properties and the thermodynamic investigation can provide in depth understanding and guidance on the melt crystallization of cocrystals.
机译:药用共晶体已被广泛研究作为改善药物理化性质的一种有前途的方法。通常使用溶液介导的方法和研磨方法制备共晶体。在这项研究中,通过将结晶控制在特定的温度范围内,采用熔融结晶法生产了庚二酸与褪黑素难溶性的共晶体。通过红外光谱,粉末和单晶X射线衍射对共晶体进行表征。通过差示扫描量热法建立的二元相图和形成焓提供了这种自发共结晶体系的原理。与原始褪黑激素相比,该共晶体表现出更高的表观溶解度,更快的溶解速率和可接受的稳定性。研究表明,熔融结晶法可被认为是生产具有改进性能的药物共结晶的竞争途径,而热力学研究可提供对共结晶熔融结晶的深入理解和指导。

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