The 2nd International Conference on Drug Discovery & Therapy: Dubai, February 1 - 4, 2010


Session Speaker

To Study the Effect of Furosemide on Micellar Behaviour of Ionic Surfactants - A Physicochemical Approach
S. Chauhan, V.K. Syal, M.S. Chauhan and D. Kaushal

Micellar solubilization is an effective way for the dissolution of hydrophobic drugs in aqueous environment. Pharmacologically active compounds, also known as drugs are amphiphilic in nature and can, therefore undergo different kinds of associations in a surfactant-like manner. Ionic surfactants are found to be better solubilizing agents than non-ionic surfactants and amongst ionic surfactants, solubility is found to be very high in anionic surfactant as compared to cationic one. Due to clinical importance of Furosemide - a cardiovascular drug, a large number of analytical methods to detect the presence of this drug in pharmaceutical and physiological samples using surfactants have been developed. Critical micellar concentration (CMC) values for Sodium dodecyl sulfate (SDS) are found to be lowered in the presence of drug indicating its greater solubility.

In the present work, therefore we provide a concept of micellar solubilization of drugs in surfactant systems in the concentration range 0.001M and 0.01M of Furosemide with surfactants SDS and Cetyltrimethylammonium bromide (CTAB) by measuring different transport properties viz : Conductance measurements of anionic surfactant SDS and cationic surfactant CTAB have been measured in solutions of aqueous Furosemide (0.001and 0.01M) in the temperature range 20 – 40ºC. From these measurements, CMC’s of SDS and CTAB have been determined in the above said aqueous Furosemide solutions. From CMC data, various thermodynamic parameters viz. ΔHºm, ΔSºm and ΔGºm have been evaluated. Sound velocity and density measurements are used to calculate the compressibility coefficient (β), apparent molar volume (φV) and apparent molar compressibility (φK). The viscosity studies of SDS and CTAB have also been included in order to calculate relative viscosity (ηr). All these parameters provide insight in terms of drug – surfactant interactions as a consequence of various electrostatic and hydrophobic interactions.



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