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Marques, J.G., Gaspar, V.M. and Costa, E. (2014) Synthesis and Characterization of Micelles as Carriers of Non-steroidal Anti-Inflammatory Drugs (NSAIDs) for Application in Breast Cancer Therapy. Colloids and Surfaces B: Biointerfaces, 113, 375-383.
https://doi.org/10.1016/j.colsurfb.2013.09.037

has been cited by the following article:

• TITLE: The Extent of Solubilization of Flurbiprofen and Ketoprofen by Cetyltrimethylammonium Micelles Using Semi-Equilibrium Dialysis

  AUTHORS: Jimmy D. Roach, Ibrahim Laswi, Malik Mushannen, Ali Chaari, Mandy Bondaruk

  KEYWORDS: Flurbiprofen, Ketoprofen, CTAB, Micelle, Solubilization

  JOURNAL NAME: Advances in Materials Physics and Chemistry, Vol.10 No.4, April 29, 2020

  ABSTRACT: The partitioning of two non-steroidal anti-inflammatory drugs (NSAIDs), flurbiprofen and ketoprofen, into cationic cetyltrimethylammonium micelles was investigated using semi-equilibrium dialysis at 37℃ in phosphate buffered saline. The micellar-water solubilization equilibrium constants for both NSAIDs, in their deprotonated forms, were observed to decrease linearly with increasing mole fraction of drug in micelles. For flurbiprofen, the solubilization constant in the limit as mole fraction of drug in micelles approaches zero was found to be 11,200 (co = 1 M), while for ketoprofen the value was 1950 (co = 1 M). Using 1H-NMR and UV spectroscopic techniques, the locus of solubilization for ketoprofen was found to be towards the charged exterior of the micelles, in the Stern layer, whereas flurbiprofen was found to solubilize more in the micellar interior.