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dc.contributor.authorToprak, M. and Meryem Aydn, B. and Ark, M. and Onganer, Y.
dc.date.accessioned2021-04-08T12:10:21Z
dc.date.available2021-04-08T12:10:21Z
dc.date.issued2011
dc.identifier10.1016/j.jlumin.2011.05.049
dc.identifier.issn00222313
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-79959190272&doi=10.1016%2fj.jlumin.2011.05.049&partnerID=40&md5=732858b9fa0f63276f45030303205261
dc.identifier.urihttp://acikerisim.bingol.edu.tr/handle/20.500.12898/5000
dc.description.abstractThe fluorescence quenching of fluorescein (FL) by merociyanine 540 (MC540) was examined in L-egg lecithin phosphatidycholine (PC) liposomes using spectroscopic methods. The type of quenching mechanism (dynamic or static) was evaluated using the SternVolmer plots. Findings were also supported by the temperature studies and florescence decay measurements. The SternVolmer equation was utilized to calculate bimolecular quenching constants (Kq). Furthermore, the bimolecular quenching constant of the quencher in the liposomes (KSV), partition coefficient (Kp), binding constant (K), and corresponding thermodynamic parameters ΔH, ΔS, and ΔG were calculated. The quenching property was also used in determining quantitatively (Kp) the partition coefficient of Merociyanini 540 in PC liposome.The obtained data indicated that static quenching occurred in the system and the KSV values decreased with increasing lipid concentration. In addition, thermodynamic analysis suggested that van der Waals interactions and hydrogen bonding were the main acting forces between fluorescein and merociyanine 540 molecules in the medium. © 2011 Elsevier B.V. All rights reserved.
dc.language.isoEnglish
dc.sourceJournal of Luminescence
dc.titleFluorescence quenching of fluorescein by Merocyanine 540 in liposomes


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