Synthesis, characterization, and liposome partition of a novel tetracycline derivative using the ionic liquids framework

被引:31
作者
Alves, Filipa [1 ]
Oliveira, Filipe S. [2 ]
Schroeder, Bernd [3 ]
Matos, Carla [1 ]
Marrucho, Isabel M. [1 ,2 ]
机构
[1] Univ Nova Lisboa, Inst Tecnol Quim & Biol, P-2780157 Oeiras, Portugal
[2] Univ Aveiro, Dept Quim, CICECO, P-3810193 Aveiro, Portugal
[3] UFP, Escola Super Saude, CIAGEB Fac Ciencias Saude, P-4200150 Oporto, Portugal
关键词
Tetracycline; Docusate; Ionic Liquids; Synthesis; Drug-like properties; Solubility; Partition Coefficient; Liposomes; UV-VIS spectroscopy; ACTIVE PHARMACEUTICAL INGREDIENTS; HYDROCHLORIDE FORMS; COEFFICIENTS; ANTIBIOTICS; SOLUBILITY; CIPROFLOXACIN; SOLVENTS; SALTS; WATER;
D O I
10.1002/jps.23487
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Recently, efforts have been put on the development of new drug formulations using ionic liquid framework. In this work, two different species of abroad-spectrum polyketide antibiotic, tetracycline, are studied in terms of some important properties for antibiotics such as solubility in water and hydrophilichydrophobic balance. Tetracycline was used as cation, whereas docusate, a biocompatible anion, which enables the tailoring of the hydrophilicity of salts, was chosen as the anion. The developed innovative ion pair, tetracycline docusate, was characterized in terms of its thermal stability, water solubility, octanolwater, and liposomewater partition coefficients, using UVvis spectrophotometry because of the absorbance of tetracycline around 270nm. Egg yolk phosphatidylcholine liposomes were used as cell membrane models, and the interactions of both tetracycline hydrochloride and tetracycline docusate with the liposomes were quantified by determination of the partition coefficient using derivative spectrophotometry. A theoretical model based on simple partition drugs between two different media was used to determine the partition coefficient in liposomes. (c) 2013 Wiley Periodicals, Inc. and the American Pharmacists Association J Pharm Sci 102:15041512, 2013
引用
收藏
页码:1504 / 1512
页数:9
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