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Spectroscopic study of interactions between dye molecules in micelle and liposome nanovolumes

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Journal of Applied Spectroscopy Aims and scope

The efficiency of Förster resonance energy transfer (FRET) between pairs of different dyes in the nanovolumes of surfactant micelles and liposomes was studied using optical spectroscopy methods. More efficient FRET with the same solution concentrations of the dyes was observed in liposomes despite the greater diameter of liposomes compared with micelles (100 and 5 nm). Calculations showed that the observed effect was explained by the smaller amount of liposomes in the solution and, consequently, the larger local concentration of the dyes in the liposome lipid bilayer. It was shown that not only the spectral overlap integral and the Förster distance but also specific interactions between molecules in the nanovolume (electrostatic, vander-Waals, and steric) that were governed by structural features of the molecules affected the FRET efficiency.

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References

  1. M. E. Diaz Garcia and A. Sanz-Medel, Talanta, 33, 255–264 (1986).

    Article  Google Scholar 

  2. C.-C. Chang, Y.-T. Yang, J.-C. Yang, H.-D. Wu, and T. Tsai, Dyes Pigm., 79, 170–175 (2008).

    Article  Google Scholar 

  3. B. B. Bhowmik, S. Basu, and D. Ray, Chem. Phys. Lipids, 109, 175–183 (2001).

    Article  Google Scholar 

  4. S. Bracko and J. Span, Dyes Pigm., 50, 77–84 (2001).

    Article  Google Scholar 

  5. R. Blumenthal, S. A. Gallo, M. Viard, Y. Raviv, and A. Puri, Chem. Phys. Lipids, 116, 39–55 (2002).

    Article  Google Scholar 

  6. R. Sabate, M. Gallardo, A. de la Maza, and J. Estelrich, Langmuir, 17, 6433–6437 (2001).

    Article  Google Scholar 

  7. B. Simoncic and M. Kert, Dyes Pigm., 54, 221–237 (2002).

    Article  Google Scholar 

  8. J. Yang, J. Colloid Interface Sci., 274, 237–243 (2004).

    Article  Google Scholar 

  9. P. Forte-Taver, Dyes Pigm., 63, 181–189 (2004).

    Article  Google Scholar 

  10. B. Jain and K. Das, Chem. Phys. Lett., 433, 170–174 (2006).

    Article  ADS  Google Scholar 

  11. B. M. Aydin, M. Acar, M. Arik, and Y. Onganer, Dyes Pigm., 81, 156–160 (2009).

    Article  Google Scholar 

  12. A. S. Lebed, S. L. Yefimova, G. Ya. Guralchuk, A. V. Sorokin, I. A. Borovoy, and Yu. V. Malyukin, Zh. Prikl. Spektrosk., 77, No. 2, 198–203 (2010).

    Google Scholar 

  13. S. Yefimova, A. Lebed, A. Sorokin, G. Guralchuk, I. Borovoy, and Yu. Malyukin, J. Mol. Liq., 165, 113–118 (2012).

    Article  Google Scholar 

  14. C. C. You, A. Chompoosor, and V. M. Rotello, Nano Today, 2, No. 3, 34–43 (2007).

    Article  Google Scholar 

  15. A. Kozubek, J. Gubernator, E. Przeworska, and M. Stasiuk, Acta Biochim. Pol., 47, No. 3, 639–649 (2000).

    Google Scholar 

  16. P. Goyal, K. Goyal, S. G. V. Kumar, A. Singh, O. P. Katare, and D. N. Mishra, Acta Pharm., 55, 1–25 (2005).

    Google Scholar 

  17. R. A. Petros and J. M. DeSimone, Nat. Rev. Drug Discovery, 9, 615–627 (2010).

    Article  Google Scholar 

  18. N. Nishiyama and K. Kataoka, Pharmacol. Ther., 112, 630–648 (2006).

    Article  Google Scholar 

  19. S. L. Yefimova, A. S. Lebed, G. Ya. Guralchuk, A. V. Sorokin, I. Yu. Kurilchenko, N. S. Kavok, and Yu. V. Malyukin, Biopolym. Cell, 27, No. 1, 47–52 (2011).

    Article  Google Scholar 

  20. H. Chen, S. Kim, L. Li, S. Wang, K. Park, and J.-X. Cheng, Proc. Natl. Acad. Sci. USA, 105, No. 18, 6596–6601 (2008).

    Article  ADS  Google Scholar 

  21. H. Chen, S. Kim, W. He, H. Wang, P. S. Low, K. Park, and J.-X. Cheng, Langmuir, 24, 5213–5217 (2008).

    Article  Google Scholar 

  22. K. Shinoda, T. Nakagawa, H. Tamamushi, and T. I. Semura, Colloidal Surfactants, Some Physicochemical Properties, Academic Press, New York-London (1963).

    Google Scholar 

  23. B. Mui, L. Chow, and M. J. Hope, Methods Enzymol., 367, 3–14 (2003).

    Article  Google Scholar 

  24. S. Sreejith, P. Carol, P. Chithra, and A. Ajayaghosh, J. Mater. Chem., 18, 264–274 (2008).

    Article  Google Scholar 

  25. A. Ajayaghosh, Acc. Chem. Res., 38, 449–459 (2005).

    Article  Google Scholar 

  26. R. W. Bigelow and H. J. Freund, Chem. Phys., 107, 159–169 (1986).

    Article  ADS  Google Scholar 

  27. A. A. Ishchenko, Structure and Spectral-Luminescent Properties of Polymethine Dyes [in Russian], Naukova Dumka, Kiev (1994).

    Google Scholar 

  28. S. L. Yefimova, Yu. V. Malyukin, and K. Kemnitz, Zh. Prikl. Spekstrosk., 68, No. 5, 569–572 (2001).

    Google Scholar 

  29. Yu. V. Malyukin, S. L. Efimova, and K. Kemnitz, J. Lumin., 94–95, 239–242 (2001).

    Article  Google Scholar 

  30. S. L. Yefimova, A. V. Sorokin, A. N. Lebedenko, Yu. V. Malyukin, and E. N. Obukhova, Zh. Prikl. Spektrosk., 73, No. 2, 152–157 (2006).

    Google Scholar 

  31. S. L. Yefimova, A. S. Lebed, G. Ya. Guralchuk, A. V. Sorokin, and Yu. V. Malyukin, Mol. Cryst. Liq. Cryst., 535, 204–211 (2011).

    Google Scholar 

  32. A. S. Lebed, S. L. Yefimova, A. V. Sorokin, I. A. Borovoy, and Yu. V. Malyukin, Funct. Mater., 18, 5–11 (2011).

    Google Scholar 

  33. B. M. Aydin, M. Acar, M. Arik, and Y. Onganer, Dyes Pigm., 81, 156–160 (2009).

    Article  Google Scholar 

  34. S. H. Lee, A. H. Gore, T. Ferdous, S. M. Alam, and G. B. Kolecar, J. Mol. Liq., 168, 12–16 (2012).

    Article  Google Scholar 

  35. J. Nanda, P. K. Behera, H. L. Tavernier, and M. D. Fayer, J. Lumin., 115, 138–146 (2005).

    Article  Google Scholar 

  36. S. Pihlasalo, M. Hara, P. Hanninen, J. P. Slotte, J. Peltonen, and H. Harma, Anal. Biochem., 384, 231–237 (2009).

    Article  Google Scholar 

  37. A. Manna and S. Chakravorti, J. Mol. Liq., 168, 94–101 (2012).

    Article  Google Scholar 

  38. J. R. Lakowicz, Principles of Fluorescence Spectroscopy, Plenum Press, New York (1983).

    Book  Google Scholar 

  39. M. Z. Maksimov and I. M. Rozman, Opt. Spektrosk., 12, 606–609 (1962).

    Google Scholar 

  40. S. L. Yefimova, G. Ya. Guralchuk, A. V. Sorokin, Yu. V. Malyukin, I. A. Borovoy, and A. S. Lubyanaya, Zh. Prikl. Spektrosk., 75, No. 5, 646–652 (2008).

    Google Scholar 

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Authors and Affiliations

  1. Institute for Scintillation Materials, National Academy of Sciences of Ukraine, 60 Lenin Ave., Kharkov, 61001, Ukraine

    S. L. Yefimova, T. N. Tkacheva, A. V. Sorokin & Yu. V. Malyukin

  2. Slavyansk State Pedagogical University, Slavyansk, Ukraine

    I. Yu. Kurilchenko

Authors
  1. S. L. Yefimova
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  2. T. N. Tkacheva
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  3. I. Yu. Kurilchenko
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  4. A. V. Sorokin
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  5. Yu. V. Malyukin
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Correspondence to S. L. Yefimova.

Additional information

Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 79, No. 6, pp. 919–926, November–December, 2012.

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Yefimova, S.L., Tkacheva, T.N., Kurilchenko, I.Y. et al. Spectroscopic study of interactions between dye molecules in micelle and liposome nanovolumes. J Appl Spectrosc 79, 914–921 (2013). https://doi.org/10.1007/s10812-013-9694-7

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  • DOI: https://doi.org/10.1007/s10812-013-9694-7

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