[1] M. Malmsten, Surfactants and Polymers in Drug Delivery, Taylor & Francis, New York, 2002.[2] K. Holmberg, D.O. Shah, M.J. Schwuger, Handbook of Applied Surface and Colloid Chemistry, Wiley, New York, 2002.[3] T.F. Tadros, Phase behaviour of surfactant systems, Applied Surfactants, Principles and Applications, Wiley-VCH Verlag GmbH & Co., KGA, 2005.[4] Y. Liu, X. Dong, Y. Sun, New development of reverse micelles and applications in protein separation and refolding, Chin. J. Chem. Eng. 16(2008) 949-955.[5] A.Z. Naqvi, M.A. Rub, Kabir-ud-Din, Study of phospholipid induced phase separation in amphiphilic drugs, Colloid J. 77(2015) 525-531.[6] Y. Konodo, H. Uchiyama, N. Yoshino, K. Nishiyama, M. Abe, Spontaneous vesicle formation from aqueous solutions of didodecyldimethylammonium bromide and sodium dodecyl sulfate mixtures, Langmuir 11(1995) 2380-2384.[7] A. Khan, E.F. Marques, Synergism and polymorphism in mixed surfactant systems, Curr. Opin. Colloid Interf. Sci. 4(1999) 402-410.[8] C. Tondre, C. Caillet, Properties of the amphiphilic films in mixed cationic/anionic vesicles:a comprehensive view from a literature analysis, Adv. Colloid Interf. Sci. 93(2001) 115-134.[9] N. Azum, M.A. Rub, A.M. Asiri, Analysis of surface and bulk properties of amphiphilic drug ibuprofenand surfactant mixture in the absence and presence of electrolyte, Colloids Surf. B 121(2014) 158-164.[10] N. Azum, M.A. Rub, A.M. Asiri, Experimental and theoretical approach to mixed surfactant system of cationic gemini surfactant with nonionic surfactant in aqueous medium, J. Mol. Liq. 196(2014) 14-20.[11] I.A. Khan, R. Mohammad, M.S. Alam, Surface properties and mixed micellization of cationic gemini surfactants with ethyleneamines, J. Chem. Eng. Data 55(2009) 370-380.[12] N. Azum, M.A. Rub, A.M. Asiri, Micellization and interfacial behavior of binary and ternary mixtures in aqueous medium, J. Mol. Liq. 216(2016) 94-98.[13] M.A. Rub, N. Azum, A.M. Asiri, Interaction of cationic amphiphilic drug nortriptyline hydrochloride with TX-100 in aqueous and urea solutions and the studies of physicochemical parameters of the mixed micelles, J. Mol. Liq. 218(2016) 595-603.[14] M.A. Rub, N. Azum, F. Khan, A.M. Asiri, Surface, micellar, and thermodynamic properties of antidepressant drug nortriptyline hydrochloride with TX-114 in aqueous/urea solutions, J. Phys. Org. Chem. 30(2017), e3676.[15] I.A. Khan, R. Mohammad, M.S. Alam, Kabir-ud-Din, Mixed micellization of cationic gemini surfactants with primary linear alkylamines, J. Surfactant Deterg. 13(2010) 179-188.[16] N. Azum, M.A. Rub, A.M. Asiri, W.A. Bawazeer, Micellar and interfacial properties of amphiphilic drug-non-ionic surfactants mixed systems:surface tension, fluorescence and UV-visible studies, Colloids Surf. A 522(2017) 183-192.[17] N. Azum, M.A. Rub, A.M. Asiri, Interaction of triblock copolymer with cationic gemini and conventional surfactants:a physicochemical study, J. Dispers. Sci. Technol. (2017)https://doi.org/10.1080/01932691.2017.1283510.[18] F.M. Menger, C.A. Littau, Gemini surfactants:a new class of self-assembling molecules, J. Am. Chem. Soc. 115(1993) 10083-10090.[19] D. Danino, Y. Talmon, R. Zana, Alkanediyl-a,x-bis(dimethylalkylammonium bromide) surfactants (dimeric surfactants). 5. Aggregation and microstructure in aqueous solutions, Langmuir 11(1995) 1448-1456.[20] J. Zhao, D.C. Sherril, B.M. Fung, Mixtures of monomeric and dimeric cationic surfactants, J. Phys. Chem. B 102(1998) 7613-7618.[21] N. Azum, A.Z. Naqvi, M.A. Rub, A.M. Asiri, Multi-technique approach towards amphiphilic drug-surfactant interaction:A physicochemical study, J. Mol. Liq. 240(2017) 189-195.[22] H. Siddiqui, M. Kamil, M. Panda, Kabir-ud-Din, Solubilization of phenanthrene and fluorine in equimolar binary mixtures of gemini/conventional surfactants, Chin. J. Chem. Eng. 22(2014) 1009-1015.[23] M.A. Rub, D. Kumar, N. Azum, F. Khan, A.M. Asiri, Study of the interaction between promazine hydrochloride and surfactant (conventional/gemini) mixtures at different temperatures, J. Solut. Chem. 43(2014) 930-949.[24] N. Azum, A.M. Asiri, M.A. Rub, A.O. Al-Youbi, Thermodynamic aspects of polymersurfactant interactions:gemini (16-5-16)-PVP-water system, Arab. J. Chem. 9(2016) S1660-S1664.[25] A.R. Tehrani-Bagha, K. Holmberg, Cationic ester-containing gemini surfactants:physical-chemical properties, Langmuir 26(2010) 9276-9282.[26] X. Wang, H. Yang, F. Wang, A cationic gemini-surfactant as effective inhibitor for mild steel in HCl solutions, Corros. Sci. 52(2010) 1268-1276.[27] M. Mobin, S. Masroor, Cationic gemini surfactants as novel corrosion inhibitor for mild steel in 1.0 M HCl, Int. J. Electrochem. Sci. 7(2012) 6920-6940.[28] M.A. Hegazy, Novel cationic surfactant based on triazole as a corrosion inhibitor for carbon steel in phosphoric acid produced by dihydrate wet process, J. Mol. Liq. 208(2015) 227-236.[29] W.C. Bowman, M.J. Rand, Textbook of pharmacology, Blackwell, Cambridge, UK, 1990.[30] L.R.S. Barbosa, I. Rosangela, W. Caetano, D.S. Neto, M. Tabak, Self-aggregation of phenothiazine compounds investigated by small angle scattering and electron paramagnetic resonance spectroscopy, J. Phys. Chem. B 112(2008) 4261-4269.[31] E.M. Glaser, S.B. Newling, Side effects of chlorpromazine hydrochloride, Br. J. Pharmacol. 10(1955) 429-433.[32] W.H. Halliwell, Cationic amphiphilic drug-induced phospholipidosis, Toxicol. Pathol. 25(1997) 53-60.[33] M.A. Rub, N. Azum, A.M. Asiri, M.E.M. Zayed, A.O. Al-Youbi, Solution properties of phenothiazine drug promazine hydrochloride with cationic hydrotropes in aqueous/electrolyte solution at different temperature, J. Phys. Org. Chem. 29(2016) 476-489.[34] N. Azum, M.A. Rub, A.M. Asiri, Energetics of clouding phenomenon in amphiphilic drug imipramine hydrochloride with pharmaceuticals excipients, Pharm. Chem. J. 48(2014) 201-208.[35] F. Khan, M.A. Rub, N. Azum, D. Kumar, A.M. Asiri, Interaction of an amphiphilic drug and sodium bis(2-ethylhexyl)sulfosuccinate at low concentrations in the absence and presence of sodium chloride, J. Solut. Chem. 44(2015) 1937-1961.[36] M.A. Rub, N. Azum, A.M. Asiri, Self-association behavior of an amphiphilic drug nortriptyline hydrochloride under the influence of inorganic salts, Russ. J. Phys. Chem. B 10(2016) 1007-1013.[37] M.S. Alam, A.Z. Naqvi, Kabir-ud-Din, Surface and micellar properties of some amphiphilic drugs in the presence of additives, J. Chem. Eng. Data 52(2007) 1326-1331.[38] N. Azum, M.A. Rub, A.M. Asiri, Micellization and interfacial behavior of the sodium salt of ibuprofen-BRIJ-58 in aqueous/brine solutions, J. Solut. Chem. 45(2016) 791-803.[39] M.A. Rub, N. Azum, A.M. Asiri, Binary mixtures of sodium salt of ibuprofen and selected bile salts:interface, micellar, thermodynamic, and spectroscopic study, J. Chem. Eng. Data (2017). https://doi.org/10.1021/acs.jced.7b00298.[40] N. Azum, M.A. Rub, A.M. Asiri, Self-assocaition and microenvironmental properties of sodium salt of ibuprofen with brij-56 under the influence of aqueous/urea solution, J. Dispers. Sci. Technol. 38(2017) 96-104.[41] N. Azum, A.M. Asiri, M.A. Rub, A.O. Al-Youbi, Thermodynamic properties of ibuprofen sodium salt in aqueous/urea micellar solutions at 298.15 K, Russ. J. Phys. Chem. A 91(2017) 685-691.[42] M.A. Rub, F. Khan, M.S. Sheikh, N. Azum, A.M. Asiri, Tensiometric, fluorescence and 1H NMR study of mixed micellization of non-steroidal anti-inflammatory drug sodium salt of ibuprofen in the presence of non-ionic surfactant in aqueous/urea solutions, J. Chem. Thermodyn. 96(2016) 196-207.[43] M.K. Al-Muhanna, M.A. Rub, N. Azum, S.B. Khan, A.M. Asiri, Effect of gelatin on micellization and microstructural behavior of amphiphilic amitriptyline hydrochloride drug solution:a detailed study, J. Chem. Thermodyn. 89(2015) 112-122.[44] S. De, V.K. Aswal, P.S. Goyal, S. Bhattacharya, Role of spacer length in dimeric micellar organization. Small angle neutron scattering and fluorescence studies, J. Phys. Chem. 100(1996) 11664-11671.[45] I.A. Khan, R. Mohammad, M.S. Alam, Kabir-ud-Din, The interaction of cationic gemini surfactant 1, 4-butanediyl-α,ω-bis (dimethylcetylammonium bromide) with primary linear alkanols, J. Dispers. Sci. Technol. 31(2009) 129-137.[46] S. Schreier, S.V.P. Malheiros, E. de Paula, Surface active drugs:self association and interaction with membranes and surfactants. Physico-chemical and biological aspects, Biochim. Biophys. Acta 1508(2000) 210-234.[47] N. Azum, A.Z. Naqvi, M. Akram, Kabir-ud-Din, Properties of mixed aqueous micellar solutions formed by cationic alkanediyl-α,ω-bis(tetradecyldimethylammonium bromide) and alkyltrimethylammonium bromides:Fluorescence and conductivity studies, J. Chem. Eng. Data 54(2009) 1518-1523.[48] N. Azum, A.M. Asiri, M.A. Rub, A.A.P. Khan, A. Khan, M.M. Rahman, D. Kumar, A.O. AlYoubi, Mixed micellization of gemini surfactant with nonionic surfactant in aqueous media:a fluorometric study, Colloid J. 75(2013) 263-268.[49] J.H. Clint, Surfactant Aggregation, Chapman and Hall, New York, 1992.[50] D.N. Rubingh, Solution Chemistry of Surfactants, Plenum, New York, 1979.[51] A.K. Sood, H. Kaur, T.S. Banipal, Interactions in the mixed micelles of monomeric and gemini surfactants:influence of some co-solvents as a function of temperature, Arab. J. Chem. (2016)https://doi.org/10.1016/j.arabjc.2015.12.009.[52] M.J. Rosen, X.Y. Hua, Surface concentrations and molecular interactions in binary mixtures of surfactants, J. Colloid Interface Sci. 86(1982) 164-172.[53] D.K. Chattoraj, K.S. Birdi, Adsorption and Gibbs surface excess, Plenum, New York, 1984.[54] K. Tsubone, Y. Arakawa, M.J. Rosen, Structural effects on surface and micellar properties of alkanediyl-α,ω-bis(sodium N-acyl-β-alaninate) gemini surfactants, J Colloid Interface Sci. 262(2003) 516-524.[55] R. Miller, V. Dutschk, V.B. Fainerman, Influence of molecular processes at liquid interfaces on dynamic surface tensions and wetting kinetics, J. Adhes. 80(2004) 549-561.[56] G. Sugihara, A.M. Miyazono, S. Nagadome, T. Oida, Y. Hayashi, J.S. Ko, Adsorption and micelle formation of mixed surfactant systems in water ii:a combination of cationic gemini-type surfactant with mega-10, J. Oleo Sci. 52(2003) 449-461.[57] M.A. Rub, N. Azum, A.M. Asiri, S.Y.M. Alfaifi, S.S. Alharthi, Interaction between antidepressant drug and anionic surfactant in low concentration range in aqueous/salt/urea solution:a conductometric and fluorometric study, J. Mol. Liq. 227(2017) 1-14.[58] C. Parkanyi, C. Boniface, J.J. Aaron, M. Maafi, A quantitative study of the effect of solvent on the electronic absorption and fluorescence spectra of substituted phenothiazines:evaluation of their ground and excited singlet-state dipole moments, Spectrochim. Acta 49(1993) 1715-1725. |