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Cytotoxic Activity of Salicylic Acid-Containing Drug Models with Ionic and Covalent Binding

机译:具有离子和共价结合的水杨酸药物模型的细胞毒活性

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Three different types of drug delivery platforms based on imidazolium ionic liquids (ILs) were synthesized in high preparative yields, namely, the models involving (i) ionic binding of drug and IL; (ii) covalent binding of drug and IL; and (iii) dual binding using both ionic and covalent approaches. Seven ionic liquids containing salicylic acid (SAILs) in the cation or/and in the anion were prepared, and their cytotoxicity toward the human cell lines CaCo-2 (colorectal adenocarcinoma) and 3215 LS (normal fibroblasts) was evaluated. Cytotoxicity of SA-ILs was significantly higher than that of conventional imidazolium-based ILs and was comparable to the pure salicylic acid. It is important to note that the obtained SA-ILs dissolved in water more readily than salicylic acid, suggesting benefits of possible usage of traditional nonsoluble active pharmaceutical ingredients in an ionic liquid form.
机译:以高制备产率合成了基于咪唑鎓离子液体(IL)的三种不同类型的药物递送平台,即涉及以下模型:(i)药物与IL的离子结合; (ii)药物与IL的共价结合; (iii)使用离子和共价方法的双重结合。制备了七种在阳离子或阴离子中含有水杨酸(SAIL)的离子液体,并评估了它们对人细胞系CaCo-2(结肠直肠腺癌)和3215 LS(正常成纤维细胞)的细胞毒性。 SA-ILs的细胞毒性明显高于传统的咪唑类ILs,并且与纯水杨酸相当。重要的是要注意,所获得的SA-ILs比水杨酸更易溶于水,这暗示了可能以离子液体形式使用传统的不溶性活性药物成分的好处。

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