Abstract
5-hydroxymethyl furfural (HMF) exhibits mutagenic and DNA strand-breaking activity. It is a useful tool to evaluate the effect of heat and time on foodstuffs processing. The fluorescence interaction of HMF with HSA has not been explored to date. Therefore, this work reports the interaction mechanism of HMF with HSA via fluorescence spectroscopy analysis in a simulated physiological environment. The experimental tries showed that HMF intensely quenched the native fluorescence of HSA via the dynamic quenching. According to fluorescence quenching calculations, the binding constants Kb are 1.26x10-4, 2.71x10-4 and 3.19x10-4 M-1 at 298, 303 and 308 K respectively, and the number of binding sites n is almost 1. Thermodynamic parameters values expose that both electrostatic and hydrophobic interactions are accountable for the interaction of HSA and HMF. The presented quenching method for the assay of HMF exhibited a good linearity in the range of 0.1 to 6.66 µg/mL with a detecting limit of 0.0184 µg/mL. These values made the developed method appropriate to be used in the estimation of HMF in samples of bee honey after its extraction using SupelcleanTM ENVI™ -18 SPE Tube. Five bee honey samples show a positive response of HMF after exposing these samples for inappropriate storage or extreme heating.
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