SAXS Study of Influence of Gemini Surfactant, 1,1'-(1,4-butanediyl)bis 3-cyclododecyloxymethylimidazolium di-chloride, on the Fully Hydrated DMPC

• Authors: Z. Pietralik , M. Taube , A. Skrzypczak , M. Kozak
• Languages of publication: EN

Abstracts

EN

The study has been performed on model systems of biological membranes obtained on the basis of 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC) and cationic gemini surfactant - derivative of 1,1'-(1,4-butane)bis 3-alkylo-xyme-thyli-mida-zolium chlorides with cyclic chains. The small angle X-ray scattering SAXS results implied a gradual disappearance (as a function of surfactant concentration) of the lamellar phase typical of DMPC and formation of unilamellar phase - probably a bicellar phase.

Keywords

EN

61.05.cf; 87.16.dt; 87.14.Cc; 82.70.Uv

Discipline

• 87.14.Cc: Lipids
• 87.16.dt: Structure, static correlations, domains, and rafts
• 82.70.Uv: Surfactants, micellar solutions, vesicles, lamellae, amphiphilic systems, (hydrophilic and hydrophobic interactions)(see also 82.30.Rs Hydrogen bonding, hydrophilic effects in specific chemical reactions)
• 61.05.cf: X-ray scattering (including small-angle scattering)

• Publisher: Institute of Physics, Polish Academy of Sciences
• Journal: Acta Physica Polonica A
• Year: 2010
• Volume: 117
• Issue: 2
• Pages: 311-314

Dates

published

2010-02

Contributors

author

Z. Pietralik

• Department of Macromolecular Physics, Faculty of Physics, A. Mickiewicz University, Umultowska 85, 61-614 Poznań, Poland

author

M. Taube

• Department of Macromolecular Physics, Faculty of Physics, A. Mickiewicz University, Umultowska 85, 61-614 Poznań, Poland

author

A. Skrzypczak

• Institute of Chemical Technology and Engineering, Poznań University of Technology, Marii Skłodowskiej-Curie 2, 61-542 Poznań, Poland

author

M. Kozak

• Department of Macromolecular Physics, Faculty of Physics, A. Mickiewicz University, Umultowska 85, 61-614 Poznań, Poland

References

• 1. R. Koynova, M. Caffrey, BBA-Rev. Biomembranesg 1376, 91 (1998)
• 2. J. Swenson, F. Kargl, P. Berntsen, C. Svanberg. J. Chem. Phys. 129, 045101 (2008)
• 3. J. Katsaras, T.A. Harroun, J. Pencer, M.P. Nieh, Naturwissenschafteng 92, 355 (2005)
• 4. M. Kozak, M. Kempka, M. Szpotkowski, S. Jurga. J. Non-Cryst. Solidsg 353, 4246 (2007)
• 5. R.D. Harvey, R.K. Heenan, D.J. Barlow, M.J. Lawrence, Langmuirg 20, 9282 (2004)
• 6. M. Kozak, K. Szpotkowski, A. Kozak, R. Zieliński, D. Wieczorek, M.J. Gajda, L. Domka, Radiat. Phys. Chem. 78, S129 (2009)
• 7. K. Kato, P. Walde, N. Koine, S. Ichikawa, T. Ishikawa, R. Nagaharna, T. Ishihara, T. Tsujii, M. Shudou, Y. Omokawa, T.T. Kuroiwa, Langmuirg 24, 10762 (2008)
• 8. O. Lopez, M. Cocera, E. Wehrli, J.L. Parra, A. de la Maza, Archiv. Biochem. Biophys. 367, 153 (1999)
• 9. J. Singh, Z. Unlu, R. Ranganathan, P. Griffiths, J. Phys. Chem. B 112, 3997 (2008)
• 10. G. Klose, B. Madler, H. Schafer, K.P. Schneider, J. Phys. Chem. B 103, 3022 (1999)
• 11. M. Kozak, A. Wypych, K. Szpotkowski, S. Jurga, A. Skrzypczak, J. Non-Cryst. Solids 356, 747 (2010)
• 12. B. Madler, H. Binder, G. Klose, J. Coll. Interface Sci. 202, 124 (1998)
• 13. K. Szpotkowski, M. Kozak, A. Kozak, R. Zieliński, D. Wieczorek, S. Jurga, Acta Phys. Pol. A 115, 561 (2009)
• 14. B. Rozycka-Roszak, A. Przyczyna, Chem. Phys. Lipidsg 123, 209 (2003)
• 15. S.Q. Wang, J.B. Huang, Q. Song, H.L. Fu, J. Coll. Interface Sci. 311, 296 (2007)
• 16. H.H. Chang, R.K. Bhagat, R. Tran, P. Dea, J. Phys. Chem. B 103, 3022 (1999)
• 17. R. Zana, Adv. Colloid Interface Sci. 97, 205 (2002)
• 18. S.D. Wettig, R.E. Verrall, M. Foldvari, Curr. Gene Therapyg 8, 9 (2008)
• 19. I. Badea, R. Verrall, M. Baca-Estrada, S. Tikoo, A. Rosenberg, P. Kumar, M. Foldvari, J. Gene Med. 7, 1200 (2005)
• 20. P. Luciani, C. Bombelli, M. Colone, L. Giansanti, S. Ryhaenen, V.M.J. Saily, G. Mancini, P.K.J, Kinnunen, Biomacromoleculesg 8, 1999 (2007)
• 21. D. Uhríková, I. Zajac, M. Dubnicková, M. Pisarcik, S.S. Funari, G. Rapp, P. Balgavý, Coll. Surf. B 42, 59 (2005)
• 22. E. Urbanik, J. Zabielska-Matejuk, A. Skrzypczak, J. Pernak, Mater. Organismeng 31, 246 (1997)
• 23. N. Rabjohn, Organic Synthese. Coll. Vol. 4, Wiley, New York 1963, p. 748
• 24. M. Królikowska, J. Garbarczyk, Z. Kristallogr. NCSg 220, 103 (2005)
• 25. Á. Csiszár, E. Klumpp, A. Bota, K. Szegedi, Chem. Phys. Lipidsg 126, 155 (2003)
• 26. Y. Cerenius, K. Ståhl, L.A. Svensson, T. Ursby, Å. Oskarsson, J. Albertsson, A. Liljas, J. Synchrotron Rad. 7, 203 (2000)
• 27. M. Knaapila, C. Svensson, J. Barauskas, M. Zackrisson, S.S. Nielsen, N. Nørgaard Toft, B. Vestergaard, L. Arleth, Y. Cerenius, J. Synchrotron Rad. 16, 498 (2009)
• 28. T.C. Huang, H. Toraya, T.N. Blanton, Y. Wu, J. Appl. Crystallogr. 26, 180 (1993)
• 29. P.V. Konarev, V.V. Volkov, A.V. Sokolova, M.H.J. Koch, D.I. Svergun, J. Appl. Crystallogr. 36, 1277 (2003)
• 30. S. Lesieur, D. Charon, P. Lesieur, C. Ringard-Lefebvre, V. Muguet, D. Duchene, D. Wouessidjewe, Chem. Phys. Lipidsg 106, 127 (2000)
• 31. J. Eisenblätter, R. Winter. Biophys. J. 90, 956 (2006)
• 32. J. Bolze, T. Fujisawa, T. Nagao, K. Norisada, H. Saito, A. Naito, Chem. Phys. Lett. 329, 215 (2000)

Identifiers

DOI

10.12693/APhysPolA.117.311