An insight to optical studies of acridine orange cationic dye within nanometer-sized microemulsions at fixed water content

Authors

  • Abbas Rahdar Department of Physics, University of Zabol, Zabol, P. O. Box. 98613-35856, Islamic Republic of Iran
  • Bijan Paul Department of Chemistry, Jadavpur University, Kolkata 700032, India
  • Havva Esmailzaee ghale kohne Department of Physics, University of Sistan and Baluchestan, Zahedan, Islamic Republic of Iran
  • Mousa Aliahmad Department of Physics, University of Sistan and Baluchestan, Zahedan, Islamic Republic of Iran
Abstract:

Cationic dye Acridine orange (AO) has wide applications especially in biologicalfields such as analysis of lysosomal and mitochondria content by flow cytometryand so on. In the current work, spectroscopy of acridine orange (AO) dye at bothlow concentrations (mdye/mwater=6.25×10-5, 3.12×10-5) and high concentrations(mdye/mwater=0.002, 0.001) was studied in confined water nanodroplets withinwater/AOT/n-hexane microemulsions (MEs) at a constant water content (W=[Water]/[AOT]=10) and as a function of mass fraction of droplet (MFD) usingabsorption and fluorescence spectroscopic techniques. The absorption spectraof the dye at high concentrations of Acridine orange (AO) dye molecules showedthat the absorption spectra of the samples deviated from Beer’s law, and arebroadened at larger MFD due to the interactions of AO dye molecules. Thefluorescence spectrum investigated at two higher concentrations (0.002, 0.001)and low concentrations (6.25×10-5, 3.12×10-5). At high concentration of the dye,quenching of fluorescence intensity observed due to the accumulation of the dyemolecules, coupled with a red shift with increasing MFD. However, in the lowerconcentration regime, enhancement of fluorescence intensity was observed withincreasing MFD. The Stokes’ shift of the dye for both high and low concentrationsincreased with MFD, but largely at high concentrations compared to that at lowconcentrations.

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Journal title

volume 7  issue 1

pages  31- 42

publication date 2020-03-01

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