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Interaction of the antibiotic norfloxacin with ionic micelles: pH-dependent binding

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Abstract

The interaction of the antimicrobial drug norfloxacin (NFX) with anionic sodium dodecyl sulfate (SDS) and cationic cetyltrimethylammonium bromide (CTAB) micelles was studied using the intrinsic spectroscopic properties of NFX to obtain association constants and molecular modifications. Nonionic Tween® 20 micelles were also investigated, but the spectroscopic properties of NFX did not detect interactions with these micelles, and quenching by iodide suggested a weak association constant around 47 M−1. For SDS and CTAB, UV–Vis absorption spectroscopy, steady-state and time-resolved fluorometry were monitored as a function of surfactant concentration ranging from the premicellar to micellar region. It was found that cationic (pH 4.0) and zwitterionic NFX (pH 7.4) associate with SDS micelles, with binding constants equal to 5.4 × 103 and 1.7 × 103 M−1, respectively. Premicellar interaction slightly decreases the critical micelle concentration of SDS. Association of anionic NFX (pH 10.6) is very weak. The fluorescence spectrum and lifetime showed that SDS-associated NFX is cationic and that the heterocycle penetrates the interfacial environment of decreased polarity. Cationic CTAB micelles do not bind cationic NFX, and the association constant with zwitterionic NFX is two orders of magnitude lower than that of SDS micelles. From a pharmacological point of view, it is important that at neutral pH, NFX presented a two orders of magnitude higher affinity for anionic than for cationic sites, and did not interact significantly with nonionic or zwitterionic micelle interfaces.

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References

  • Albini A, Monti S (2003) Photophysics and photochemistry of fluoroquinolones. Chem Soc Rev 32:238–250

    Article  PubMed  CAS  Google Scholar 

  • Andriole VT (Ed.) (2000) The Quinolones, Academic Press, San Diego, California, USA

  • Appelbaum PC, Hunter PA (2000) The fluoroquinolone antibacterials: past, present and future perspectives. Int J Antimicrob Agents 16:5–15

    Article  PubMed  CAS  Google Scholar 

  • Benesi HA, Hildebrand JH (1949) A spectrophotometric investigation of the interaction of iodine with aromatic hydrocarbons. J Am Chem Soc 71:2703–2707

    Article  CAS  Google Scholar 

  • Bensikaddour H, Snoussi K, Lins L, Van Bambeke F, Tulkens PM, Brasseur R, Goormaghtigh E, Mingeot-Leclercq M-P (2008a) Interactions of ciprofloxacin with DPPC and DPPG: fluorescence anisotropy, ATR-FTIR and 31P NMR spectroscopies and conformational analysis. Biochim Biophys Acta 1778:2535–2543

    Article  PubMed  CAS  Google Scholar 

  • Bensikaddour H, Fa N, Burton I, Deleu M, Lins L, Schanck A, Brasseur R, Dufrêne YF, Goormaghtigh E, Mingeot-Leclercq M-P (2008b) characterization of the interactions between fluoroquinolone antibiotics and lipids: a multitechnique approach. Biophys J 94:3035–3046

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  • Bilski P, Martinez LJ, Koker EB, Chignell CF (1996) photosensitization by norfloxacin is a function of pH. Photochem Photobiol 64:496–500

    Article  PubMed  CAS  Google Scholar 

  • Drakopoulos AI, Ioannou PC (1997) Spectrofluorimetric study of the acid–base equilibria and complexation behavior of the fluoroquinolone antibiotics ofloxacin, norfloxacin, ciprofloxacin and pefloxacin in aqueous solution. Anal Chim Acta 354:197–204

    Article  CAS  Google Scholar 

  • Drlica K, Hiasa H, Kerns R, Malik M, Mustaev A, Zhao X (2009) Quinolones: action and resistance updated. Curr Top Med Chem 9:981–998

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  • Emami S, Shafiee A, Foroumadi A (2005) Quinolones: recent structural and clinical developments. Iran J Pharm Res 4:123–136

    CAS  Google Scholar 

  • Guo LN, Arnaud I, Petit-Ramel M, Gauthier R, Monnet C, Le Perchec P, Chevalier Y (1994) Solution behavior of dye-surfactant associations. J Colloid Interface Sci 163:334–346

    Article  CAS  Google Scholar 

  • Hernández-Borrell J, Montero MT (2003) Does ciprofloxacin interact with neutral bilayers? An aspect related to its antimicrobial activity. Int J Pharm 252:149–157

    Article  PubMed  Google Scholar 

  • King DE, Malone R, Lilley SH (2000) New classification and update on the quinolone antibiotics. Am Fam Physician 61:2741–2748

    PubMed  CAS  Google Scholar 

  • Louro SRW, Nascimento OR, Tabak M (1994) Charge- and pH-dependent binding sites for dibucaine in ionic micelles: a fluorescence study. Biochim Biophys Acta 1190:319–328

    Article  PubMed  CAS  Google Scholar 

  • Luiz FCL, Garcia LS, Goes Filho LS, Teixeira LR, Louro SRW (2011) Fluorescence studies of gold(iii)-norfloxacin complexes in aqueous solutions. J Fluoresc 21:1933–1940

    Article  PubMed  CAS  Google Scholar 

  • Park H-R, Kim TH, Bark K-M (2002) Physicochemical properties of quinolone antibiotics in various environments. Eur J Med Chem 37:443–460

    Article  PubMed  CAS  Google Scholar 

  • Popović G, Milovanović LJ, Kapetanović V (1998) Study of acid–base equilibria of fleroxacin. J Pharm Biomed Anal 18:859–863

    Article  PubMed  Google Scholar 

  • Sortino S (2006) Selective entrapment of the cationic form of norfloxacin within anionic sodium dodecyl sulfate micelles at physiological pH and its effect on the drug photodecomposition. Photochem Photobiol 82:64–70

    Article  PubMed  CAS  Google Scholar 

  • Sortino S, De Guidi G, Giuffrida S (2001) Drastic photochemical stabilization of lomefloxacin through selective and efficient self-incorporation of its cationic form in anionic sodium dodecyl sulfate (SDS) micelles. New J Chem 25:197–199

    Article  CAS  Google Scholar 

  • Tocanne JF, Teissié J (1990) Ionization of phospholipids and phospholipid-supported interfacial lateral diffusion of protons in membrane model systems. Biochim Biophys Acta 1031:111–142

    Article  PubMed  CAS  Google Scholar 

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Acknowledgments

This work was partly supported by the Brazilian Agencies Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq), Fundação de Amparo à Pesquisa do Estado do Rio de Janeiro (FAPERJ), Fundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG), and the project inct-INAMI (CNPq).

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Correspondence to Sonia Renaux Wanderley Louro.

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Muniz, G.S.V., Teixeira, L.R. & Louro, S.R.W. Interaction of the antibiotic norfloxacin with ionic micelles: pH-dependent binding. Eur Biophys J 43, 477–483 (2014). https://doi.org/10.1007/s00249-014-0978-5

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  • DOI: https://doi.org/10.1007/s00249-014-0978-5

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