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Anticrystal Engineering of Ketoprofen and Ester Local Anesthetics: Ionic Liquids or Deep Eutectic Mixtures?

机译:酮洛芬和酯类局部麻醉剂的反晶体工程:离子液体还是深共晶混合物?

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摘要

Ionic liquids (ILs) and deep eutectic mixtures (DEMs) are potential solutions to the problems of low solubility, polymorphism, and low bioavailability of drugs. The aim of this work was to develop and investigate ketoprofen (KET)-based ILs/DEMs containing an ester local anesthetic (LA): benzocaine (BEN), procaine (PRO) and tetracaine (TET) as the second component. ILs/DEMs were prepared via a mechanosynthetic process that involved the mixing of KET with an LA in a range of molar ratios and applying a thermal treatment. After heating above the melting point and quench cooling, the formation of supercooled liquids with Tgs that were dependent on the composition was observed for all KET-LA mixtures with exception of that containing 95 mol% of BEN. The KET-LA mixtures containing either ≥ 60 mol% BEN or 95 mol% of TET showed crystallization to BEN and TET, respectively, during either cooling or second heating. KET decreased the crystallization tendency of BEN and TET and increased their glass-forming ability. The KET-PRO systems showed good glass-forming ability and did not crystallize either during the cooling or during the second heating cycle irrespective of the composition. Infrared spectroscopy and molecular modeling indicated that KET and LAs formed DEMs, but in the KET-PRO systems small quantities of carboxylate anions were present.
机译:离子液体(IL)和深共晶混合物(DEM)是解决药物溶解度低,多态性和生物利用度低的问题的潜在解决方案。这项工作的目的是开发和研究基于酮洛芬(KET)的IL / DEM,其中含有酯类局部麻醉剂(LA):苯佐卡因(BEN),普鲁卡因(PRO)和丁卡因(TET)作为第二成分。 ILs / DEMs是通过机械合成过程制备的,该过程涉及将KET与LA以一定摩尔比范围混合并进行热处理。在加热到熔点以上并骤冷后,对于所有的KET-LA混合物,除了含95mol%的BEN外,均观察到了Tgs过冷液体的形成,该液体取决于组成。含有≥60 mol%BEN或95 mol%TET的KET-LA混合物在冷却或第二次加热过程中分别显示出结晶为BEN和TET。 KET降低了BEN和TET的结晶趋势,并提高了它们的玻璃形成能力。无论组成如何,KET-PRO系统均具有良好的玻璃形成能力,并且在冷却过程中或第二个加热周期中均不会结晶。红外光谱和分子建模表明,KET和LA形成了DEM,但是在KET-PRO系统中存在少量的羧酸根阴离子。

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