Quercetin nanoparticles decorated on Arabic gum and polyvinyl alcohol composite as a film sensor for fluorescence detection of meropenem

Abstract

Moving towards green chemistry to minimize the diverse effect of chemicals on human health and environment has become a great issue in chemistry. On the other hand, determination of pharmaceuticals is an important issue for both human health and environment. In this regard two natural and benign compounds such as quercetin a polyphenolic flavonoid and Arabic Gum (AG) a polysaccharide were used to construct a sensor for meropenem. Herein, a new method was established for the synthesis of AG and polyvinyl alcohol (PVA) composite decorated by quercetin nanoparticles (QUENPs) as a fluorimetric film sensor to measure meropenem. In order to embed QUENPs in the polymer composite substrate, first QUENPs were synthesized and then added to the prepared composite solution under optimal conditions. The characteristics of AG and PVA composite (AG-PVA) and AG-PVA composite decorated by QUENPs films (QUENPs-AG-PVA), before and after the addition of meropenem was studied by TEM, FT-IR and EDX-Mapping. The developed film sensor was placed in a holder made with 3D printer. The difference in the fluorescence intensity of the fabricated film before and after the addition of meropenem was taken as the signal for measuring meropenem. The effect of different parameters on the fabrication of film fluorimetric sensor such as the concentration of polymer solutions, the volume of QUENPs and the volume of glycerol were investigated. Factors affecting the measurement of meropenem such as pH, type of buffer, volume of meropenem solution added on the sensor and time were also investigated. Under the obtained optimum conditions, the calibration graph was linear in the concentration range of 50–800 ng mL−1 with a correlation coefficient (r) of 0.9976 and the detection limit was 42.6 ng mL−1. The relative standard deviation was 3.5% and 1.4%, for eight replicate determinations of 100 ng mL−1 and 400 ng mL−1 of meropenem, respectively. The proposed method was successfully utilized for determination of meropenem in blood serum, human urine and pharmaceutical samples.