Simple turn-off fluorescence sensor for determination of raloxifene using gold nanoparticles stabilized by chitosan hydrogel.

It is essential to develop a simple, applicable, and reliable assay to anticancer drug raloxifene (RAF) because of its significant usage and side effect due to entering residue in the environment. Fluorescence sensors developed and widely used because of them high selectivity, fast-response, and highly-sensitivity. The gold nanoparticles using chitosan hydrogel was synthesized and applied as a fluorescence sensor to determine the trace amount of RAF. The characterization methods including DLS, FE-SEM, EDX, XRD, and FT-IR were performed to confirm the synthesized structure. This sensor turned off the fluorescent signals proportional to RAF concentrations at 400 nm. The RAF can be detected in the linear range from 5 × 10-7 to 5 × 10-5 M. Limits of detection and quantification were obtained as 34 × 10-8 and 11 × 10-7 M as well as the relative standard deviation calculated as 1.63% in RAF measuring. The effective parameters on quenching efficiency were studied by central composite design (CCD) with response surface methodology (RSM). The effective parameters in RAF determination, include analyte concentration, temperature, contact time, and pH, were obtained as 35 µM, 30 °C, 8 min, and pH = 8.5. The sensor was applied to determine the RAF concentrations in biological and environmental samples with satisfactory recoveries between 97.5% and 109%.

Magnetic nanoparticles based on cerium MOF supported on the MWCNT as a fluorescence quenching sensor for determination of 6-mercaptopurine.

In this study, a new magnetic nanocomposite was developed as an efficient and fast-response fluorescence quenching sensor for determination of anticancer drug 6-mercaptopurine (6-MP). For this purpose, the needle-shape fluorescence metal-organic framework of cerium (Ce-MOF) were successfully synthesized on the surface of multiwalled carbon nanotubes using 1,3,5-benzenetricarboxylic acid ligand via a facile solvothermal assisted route and magnetized. The accuracy of the proposed synthesis was confirmed using the FT-IR, FE-SEM, XRD, and VSM methods. The obtained product as presented the fluorescence emission in 331 nm by excitation of 293 nm in excitation/emission slit widths of 10.0 nm. The operation of suggested method is based on quenching the fluorescence signal in accordance with increasing the 6-MP concentration. The proposed assay effectively detected the trace amount of 6-MP in the linear range of 1.0 × 10-6 to 7 × 10-5 M. The limit of detection and limit of quantification were obtained as 8.6 × 10-7 and 2.86 × 10-6 M, respectively. The analyte molecule was determined in real samples with satisfactory recoveries between 98.75 and 105.33.

Application of dispersive liquid-liquid-solidified floating organic drop microextraction and ETAAS for the preconcentration and determination of indium.

A new, simple and efficient method, including dispersive liquid-liquid-solidified floating organic drop microextraction and then electrothermal atomic absorption spectrometry, has been developed for the preconcentration and determination of ultratrace amounts of indium. The method was applied to preconcentrate the indium-1-(2-pyridylazo)-2-naphthol complex in 25 µL 1-undecanol. The various factors affecting the extraction efficiency, such as pH, type and volume of extraction solvent, type and volume of disperser solvent, sample volume, ionic strength, and ligand concentration, were investigated and optimized. Under the optimum conditions, an enrichment factor of 62.5, precision of ±4.75%, a detection limit of 55.6 ng L-1, and for the calibration graph a linear range of 96.0-3360 ng L-1 were obtained. The method was used for the extraction and determination of indium in water and standard samples with satisfactory results. Graphical Abstract Preconcentration of indium ions via liquid-liquid-solidified floating organic drop microextraction method and determination by ETAAS.