LAQV, Requimte, Departamento de Química, Faculdade de Ciências e Tecnologia, Universidade Nova de Lisboa, Caparica 2829-516, Portugal.
UCIBIO, Life Sciences Department, Faculdade Ciências e Tecnologia, Universidade Nova de Lisboa, Caparica 2829-516, Portugal.
Eur J Pharm Biopharm. 2019 Apr;137:227-232. doi: 10.1016/j.ejpb.2019.03.004. Epub 2019 Mar 2.
The major challenge of the pharmaceutical industry is to find potential solvents for poorly water-soluble drug molecules. Ionic liquids (ILs) have attracted this industry as (co-) solvents due to their unique physicochemical and biological properties. Herein, a straightforward approach for the enhancement of the water solubility of paracetamol and sodium diclofenac is presented, using new biocompatible N-acetyl amino acid N-alkyl cholinium-based ionic liquids as co-solvents (0.2-1 mol%). These new ionic liquids were able to increase the water solubility of these drugs up to four times that in pure water or in an inorganic salt solution. In the presence of these ILs, the drugs lipophilicity (log P was not significantly changed for paracetamol, but for sodium diclofenac it was possible to decrease significantly its lipophilicity. Concerning cytotoxicity in human dermal fibroblasts it was observed that ILs did not show a significant toxicity, and were able to improve cell viability compared with the respective precursors.
制药行业的主要挑战是寻找潜在的溶剂来溶解水溶性差的药物分子。离子液体(ILs)由于其独特的物理化学和生物特性而引起了该行业的关注,被用作(共)溶剂。本文提出了一种简单的方法,使用新的生物相容性 N-乙酰氨基酸 N-烷基胆碱基离子液体作为共溶剂(0.2-1 mol%)来提高对乙酰氨基酚和双氯芬酸钠的水溶性。这些新的离子液体能够将这些药物的水溶性提高至纯水中或无机盐溶液中的四倍。在这些 ILs 的存在下,药物的亲脂性(log P 对乙酰氨基酚的变化不明显,但对于双氯芬酸钠,其亲脂性可以显著降低。关于人皮肤成纤维细胞的细胞毒性,观察到 ILs 没有表现出明显的毒性,并且与各自的前体相比,能够提高细胞活力。