2012
DOI: 10.1016/j.jphotochem.2012.07.004
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Binding and stabilization of curcumin by mixed chitosan–surfactant systems: A spectroscopic study

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Cited by 52 publications
(39 citation statements)
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“…The changes in fluorescence behavior of curcumin have been attributed to the solute-solvent interactions, intramolecular charge transfer character, intermolecular hydrogen bonding with polar solvents, and p-p interaction with molecules possessing aromatic entity [57]. The plots of fluorescence intensity (FI) vs. concentration of the surfactants are shown in Fig.…”
Section: Fluorescence Spectral Behaviormentioning
confidence: 99%
“…The changes in fluorescence behavior of curcumin have been attributed to the solute-solvent interactions, intramolecular charge transfer character, intermolecular hydrogen bonding with polar solvents, and p-p interaction with molecules possessing aromatic entity [57]. The plots of fluorescence intensity (FI) vs. concentration of the surfactants are shown in Fig.…”
Section: Fluorescence Spectral Behaviormentioning
confidence: 99%
“…The absorption maxima around 425 nm region is due to the enol group and that at 360 nm is due to the keto group. Since polar solvents facilitated the existence of enol form [73][74][75], the wavelength is selected at 425 nm.…”
Section: Resultsmentioning
confidence: 99%
“…Assuming 1:1 complex formation between chitosan and curcumin, linear plot has been made by following the absorbance changes at a suitable wavelength, as a function of reciprocal concentration of chitosan or curcumin according to the equation, the modified Benesi-Hildebrand equation (3) is given below [24][25][26] :…”
Section: Resultsmentioning
confidence: 99%
“…[18] The useful features of chitosan, e.g., its abundance, flexibility, nontoxicity, hydrophilicity, biocompatibility, biodegradability, antibacterial property, and high resistance to heat makes chitosan suitable for biomedical application such as drug delivery, tissue engineering, wound dressing, etc. [18][19][20][21][22][23][24][25][26][27][28] Because of the high content of amine functional groups, as well as the hydroxyl groups on the glucosamine unit (Scheme 1), the protonated amine groups can attract metal anions, viz., molybdate, vanadate, palladate, chromate, cadmium, etc., and can absorb a number of dyes such as reactive, basic, acidic, disperse dyes in acidic (pH < 5) solutions. [29][30][31][32][33] Chitosan also binds the herbal pigment curcumin with high affinity at considerably high pH (7.0-10.5) through its glucosamine unit.…”
Section: Introductionmentioning
confidence: 99%
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