Designing of new cationic surfactant based micellar systems as drug carriers: an investigation into the drug cell membrane interactions

Abstract

This study highlights the utility of new pyridinium based cationic surfactants, N-(n-heptyl)-3-methylpyridinium bromide (Py7) and N-(n-nonyl)-3-methylpyridinium bromide (Py9), formed via a single step substitution reaction, for their application towards drugs delivery. Fourier-transform infrared (FT-IR) and nuclear magnetic resonance (NMR) spectroscopic methods have been employed for the characterization of these amphiphiles. Aggregation behavior of the surfactants in solution i.e. the critical micelle concentration (CMC), has been investigated by conductometric and spectrophotometric analyses. The results reveal that the amphiphiles can act as excellent surface active agents due to their low critical micelle concentration (CMC). Furthermore, the interaction of these surfactants with two anionic drugs i.e., Ketoprofen (KP, 2-(3-Benzoylphenyl)propanoic acid) and Diclofenac sodium (DF, Sodium 2-(2,6-dichloranilino) phenylacetate), has been explored below and above the CMC value using UV-visible spectroscopy. The enhanced absorption intensities of both the drugs in the presence of synthesized surfactants indicated stronger interactions between surfactants and drugs molecules.