PVA/Stevia/MIL-88A@AuNPs composite nanofibers as a novel sorbent for simultaneous extraction of eight agricultural pesticides in food and vegetable samples followed by HPLC-UV analysis.

Herein, an electrospun composite from poly(vinyl alcohol) (PVA) and Stevia extract as a cross-linked nanofibrous was prepared with incorporating Fe-metal organic framework@Au nanoparticles (MIL-88A@AuNPs). The final composite was characterized, and then used as an efficient sorbent in pipette-tip micro solid-phase extraction (PT-µSPE) of eight selected pesticides in food samples followed by HPLC-UV analysis. Under the opted conditions, the linearity was in the range of 1.0-1000.0 ng mL-1 for atrazine and ametryn, 3.0-1500.0 ng mL-1 for tribenuron-methyl, metribuzin, profenofos and chlorpyrifos, 5.0 to 1500.0 ng mL-1 for phosalone, and 5.0-2000.0 ng mL-1 for malation with coefficient of determination (r2) ≥ 0.9943. The LODs (based on S/N = 3) ranged from 0.3 to 1.5 ng m L-1. The relative standard deviations (RSDs) were between 5.2% and 6.6% (intra-day, n = 5) and 5.9%-7.4% (inter-day, n = 3) for three consecutive days. Ultimately, the capability of the method in various food samples was appraised with good recoveries (79.3 to 97.6%).

Simultaneous trace-level monitoring of seven opioid analgesic drugs in biological samples by pipette-tip micro solid phase extraction based on PVA-PAA/CNT-CNC composite nanofibers followed by HPLC-UV analysis.

Electrospun poly(vinyl alcohol)-(PVA)-poly(acrylic acid) (PAA)/carbon nanotubes(CNTs)-cellulose nanocrystal (CNC) (PVA-PAA/CNT-CNC) composite nanofibers were prepared and characterized using Fourier transform-infrared spectroscopy and field emission scanning electron microscopy. The resultant composite was used as an effective and novel sorbent for pipette-tip micro-solid phase extraction (PT-µSPE) of seven opioid analgesics (OAs) in biological samples followed by HPLC-UV analysis. Addition of CNT-CNC with the high specific surface area and plenty of OH-functional groups endows the nanofibers with considerable extraction efficiency. Under the optimum conditions, the linearity was obtained in the range 1.5 to 700.0 ng mL-1 for morphine, codeine, oxycodone, and tramadol, and 0.5 to 1000.0 ng mL-1 for nalbuphine, thebaine, and noscapine with coefficient of determination (r2) ≥ 0.9990. Detection limits (LODs) based on S/N = 3 were in the range of 0.15-0.50 ng mL-1. The relative standard deviations (RSDs) of 4.1-5.4% (intra-day, n = 5) and 5.2-6.4% (inter-day, n = 3) for three consecutive days were achieved. Finally, the efficiency of the PT-µSPE-HPLC-UV method was evaluated for the determination of OAs in human plasma and urine samples with good recoveries (87.3 to 97.8%). A: Schematic illustration for the preparation of PVA-PAA/CNT-CNC composite nanofibers. B: Schematic presentation of applying PVA-PAA/CNT-CNC composite nanofibers as the sorbent in pipette-tip micro solid-phase extraction (PT-µSPE) for the preconcentration of seven opioid analgesic drugs in biological samples before HPLC-UV analysis.