ABSTRACT Citrate as a naturally occurring ion with important biological roles, especially in metabolic cycles, and as an important biomarker in the early diagnosis of many diseases, including prostate cancer, has received special attention. In the present study, a novel, sensitive, fast and simple colorimetric bisazo-based chemosensor was developed for sequential determination and naked-eye detection of Cu2+ and citrate. UV-Vis spectroscopic studies showed that Reactive Red 141 (RR141) exhibits high selectivity and sensitivity towards Cu2+ in the presence of many other cations in deionised water (10 mmol L−1 MES(2-(N-morpholino)ethanesulfonic acid)/NaOH buffer solution, pH 6.0) and complex real samples as well. The obvious colorimetric response while interaction with copper and citrate is due to complexation between RR141 and Cu2+, and then the citrate detection occurred through metal transfer from the RR141-Cu2+ towards the citrate anion releasing RR141 via an indicator displacement route. The mechanism of detection has been carefully investigated using the semi-empirical calculation method of MM2 molecular mechanics. The proposed detection method for citrate ion has a detection limit of 0.15 µmol L−1 and a satisfactory linear range of 1.92–45.96 µmol L−1, which is consistent with the desired average diagnostic concentration in prostate cancer (less than 2 mmol L−1). Our studies’ results indicate the high capability of the developed chemical sensor for quantitative and qualitative citrate detection in various complex media, including biological and clinical real samples.
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