Active pharmaceutical ingredients based on salicylate ionic liquids: insights into the evaluation of pharmaceutical profiles

被引:52
作者
Pinto, Paula C. A. G. [1 ]
Ribeiro, Diogo M. G. P. [1 ]
Azevedo, Ana M. O. [1 ]
Dela Justina, Vanessa [1 ]
Cunha, E. [1 ]
Bica, K. [2 ]
Vasiloiu, M. [2 ]
Reis, Salette [1 ]
Saraiva, M. Lucia M. F. S. [1 ]
机构
[1] Univ Porto, Dept Quim, Fac Farm, REQUIMTE, P-4050313 Oporto, Portugal
[2] Vienna Univ Technol, Inst Appl & Synthet Chem, A-1060 Vienna, Austria
关键词
CRITICAL MICELLE CONCENTRATION; PARTITION-COEFFICIENTS; BINDING; WATER; AGGREGATION; BEHAVIOR; ACID; TRANSPORT; SOLVENTS; TRENDS;
D O I
10.1039/c3nj00731f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This work is based on the evaluation of the protein binding affinity, partition coefficients (with a biomimetic membrane) and surfactant properties of three pharmaceutically active ionic liquids based on the salicylate anion. Fluorescence spectroscopy was used for the evaluation of the binding of ionic liquids to human serum albumin and for the determination of critical micelle concentrations. Partition coefficients were determined using micelles of hexadecylphosphocholine and UV-Vis derivative spectroscopy. The results indicate that all the compounds bind strongly and spontaneously to human serum albumin and exhibit the ability to form micelles. The determined partition coefficients were up to 6 times higher than those of the starting materials, evidencing that the ionic liquid form has greater affinity for the lipid phase than the inorganic salt form of salicylate. Generally, the studied salicylate ionic liquids exhibit an interesting pharmaceutical profile presenting favorable properties regarding the incorporation of the compounds in antimicrobial pharmaceutical formulations. It was evidenced that the tested ionic liquids can exert direct effects on cell membranes as indicated by their surfactant properties and high ability to partition to hydrophobic environments.
引用
收藏
页码:4095 / 4102
页数:8
相关论文
共 49 条
[11]  
Copeland R. A., 2000, ENZYMES
[12]   Exploring an Anti-Crystal Engineering Approach to the Preparation of Pharmaceutically Active Ionic Liquids [J].
Dean, Pamela M. ;
Turanjanin, Jelena ;
Yoshizawa-Fujita, Masahiro ;
MacFarlane, Douglas R. ;
Scott, Janet L. .
CRYSTAL GROWTH & DESIGN, 2009, 9 (02) :1137-1145
[13]   In vitro genotoxicity and cytotoxicity of benzalkonium chloride [J].
Deutschle, T. ;
Porkert, U. ;
Reiter, R. ;
Keck, T. ;
Riechelmann, H. .
TOXICOLOGY IN VITRO, 2006, 20 (08) :1472-1477
[14]   Development of novel ionic liquids based on ampicillin [J].
Ferraz, Ricardo ;
Branco, Luis C. ;
Marrucho, Isabel M. ;
Araujo, Joao M. M. ;
Rebelo, Luis Paulo N. ;
da Ponte, Manuel Nunes ;
Prudencio, Cristina ;
Noronha, Joao Paulo ;
Petrovski, Zeljko .
MEDCHEMCOMM, 2012, 3 (04) :494-497
[15]   Ionic Liquids as Active Pharmaceutical Ingredients [J].
Ferraz, Ricardo ;
Branco, Luis C. ;
Prudencio, Cristina ;
Noronha, Joao Paulo ;
Petrovski, Zeljko .
CHEMMEDCHEM, 2011, 6 (06) :975-985
[16]   Alternative measures of lipophilicity: From octanol-water partitioning to IAM retention [J].
Giaginis, Costas ;
Tsantili-Kakoulidou, Anna .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2008, 97 (08) :2984-3004
[17]   Ionic liquids then and now: From solvents to materials to active pharmaceutical ingredients [J].
Hough, Whitney L. ;
Rogers, Robin D. .
BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 2007, 80 (12) :2262-2269
[18]   The third evolution of ionic liquids:: active pharmaceutical ingredients [J].
Hough, Whitney L. ;
Smiglak, Marcin ;
Rodriguez, Hector ;
Swatloski, Richard P. ;
Spear, Scott K. ;
Daly, Daniel T. ;
Pernak, Juliusz ;
Grisel, Judith E. ;
Carliss, Richard D. ;
Soutullo, Morgan D. ;
Davis, James H., Jr. ;
Rogers, Robin D. .
NEW JOURNAL OF CHEMISTRY, 2007, 31 (08) :1429-1436
[19]  
Kadokawa JI, 2013, IONIC LIQUIDS - NEW ASPECTS FOR THE FUTURE, P1, DOI 10.5772/45605
[20]  
Khan AM, 2008, J CHEM SOC PAKISTAN, V30, P186