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6-丙基-2-硫脲嘧啶药物共晶体开发中的合理共形成物选择

Rational Coformer Selection in the Development of 6-Propyl-2-thiouracil Pharmaceutical Cocrystals.

作者信息

Acebedo-Martínez Francisco Javier, Alarcón-Payer Carolina, Verdugo-Escamilla Cristóbal, Martín Jesús, Frontera Antonio, Domínguez-Martín Alicia, Gómez-Morales Jaime, Choquesillo-Lazarte Duane

机构信息

Laboratorio de Estudios Cristalográficos, IACT, CSIC-Universidad de Granada, Avda. de las Palmeras 4, 18100 Armilla, Spain.

Servicio de Farmacia, Hospital Universitario Virgen de las Nieves, 18014 Granada, Spain.

出版信息

Pharmaceuticals (Basel). 2023 Feb 28;16(3):370. doi: 10.3390/ph16030370.

Abstract

Pharmaceutical multicomponent solids have proved to efficiently modulate the physicochemical properties of active pharmaceutical ingredients. In this context, polyphenols are interesting coformers for designing pharmaceutical cocrystals due to their wide safety profile and interesting antioxidant properties. The novel 6-propyl-2-thiouracil multicomponent solids have been obtained by mechanochemical synthesis and fully characterized by powder and single-crystal X-ray diffraction methods. The analysis of supramolecular synthons has been further performed with computational methods, with both results revealing a robust supramolecular organization influenced by the different positions of the hydroxyl groups within the polyphenolic coformers. All novel 6-propyl-2-thiouracil cocrystals show an enhanced solubility profile, but unfortunately, their thermodynamic stability in aqueous media is limited to 24 h.

摘要

药物多组分固体已被证明能有效调节活性药物成分的物理化学性质。在这种情况下,由于多酚具有广泛的安全性和有趣的抗氧化特性,它们是设计药物共晶体的有趣共形成物。通过机械化学合成获得了新型6-丙基-2-硫脲嘧啶多组分固体,并通过粉末和单晶X射线衍射方法进行了全面表征。利用计算方法进一步对超分子合成子进行了分析,结果均表明,多酚共形成物中羟基的不同位置影响了强大的超分子结构。所有新型6-丙基-2-硫脲嘧啶共晶体均显示出增强的溶解度,但遗憾的是,它们在水性介质中的热力学稳定性仅限于24小时。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5c0/10055029/e72e2bef74eb/pharmaceuticals-16-00370-sch001.jpg

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