Pakawadee Sutthivaiyakit

New Reagent for Trace Determination of Protein-Bound Metabolites of Nitrofurans in Shrimp Using Liquid Chromatography with Diode Array Detector

The synthesis of derivatives of metabolites from furazolidone, furaltadone, nitrofurazone, and nitrofurantoin using a new derivatizing reagent, 2-naphthaldehyde (NTA), is described. The reaction product was used in liquid chromatography with diode array detector (LC-DAD) for determination of protein-bound metabolites of nitrofurans in shrimp followed by two steps of liquid-liquid extraction. Derivatives of nitrofuran metabolites are well separated from NTA remaining in the extract upon separation on a ChromSpher 5 Pesticide (250 x 4.6 mm, 5 microm) column at 40 degrees C with acetonitrile/5 mM ammonium acetate adjusted to pH 7.5 gradient as the mobile phase and DAD detection at 308 nm except for naphthyl derivative of 1-aminohydantoin at 310 nm. The high absorptivity of these derivatives makes simultaneous screening of these metabolites in shrimp at 1 microg/kg possible for the first time using LC-DAD. The method was validated using blank shrimp fortified with all four metabolites at 1, 1.5, and 2 microg/kg. Recoveries were >86% with relative standard deviations of <14% for all four metabolites. Comparison between LC-DAD and APCI-MS/MS shows very good agreement for shrimp samples.

Photocatalytic degradation of 3,4-dichlorophenylurea in aqueous gold nanoparticles-modified titanium dioxide suspension under simulated solar light.

The TiO(2) modified with nanosized gold particles was prepared by deposition-precipitation at pH 7 and calcination in air at various temperatures up to 973 K. The materials were characterized by transmission electron microscope, X-ray diffraction spectrometry, and atomic absorption spectroscopy. The highest photocatalytic efficiency was obtained at the calcination temperature of 873 K. The decrease in 3,4-dichlorophenylurea concentration follows first order kinetics with a half life of 36.6 ± 2.0 min in 100 mg L(-1) of 0.83 wt% Au/TiO(2). Fifteen degradation products were identified using LC/MS/MS and IC. Degradation pathway was proposed on the basis of the observed transformation products.

Determination of Nitrofurans in Chicken Feed by High-Performance Liquid Chromatography–Tandem Mass Spectrometry

Liquid chromatography with tandem mass spectrometry was used for the determination of nitrofurantoin, nitrofurazone, furazolidone, and furaltadone in chicken feed. The nitrofurans were extracted with phosphate buffer (pH 7) and sodium chloride. Proteins and lipids were removed with acetonitrile and hexane before purification with ethyl acetate, dilution in 1:1 acetonitrile-5 millimolar ammonium acetate at pH 7.3, and filtration prior to analysis. The limits of detection were 1.69, 1.74, 2.01, and 1.45 microgram per kilogram for nitrofurantoin, nitrofurazone, furazolidone, and furaltadone, respectively. The mean recoveries were between 84.6 and 110.6 percent. The method was employed to determine nitrofurans in chicken feed.

Degradation products of profenofos as identified by high-field FTICR mass spectrometry: Isotopic fine structure approach

ABSTRACT This study was performed to identify the degradation products of profenofos “a phenyl organothiophosphate insecticide” in raw water (RW) collected from the entry point of Metropolitan Water Works Authority “Bangkaen, Thailand” and ultrapure water (UPW) with and without TiO2 under simulated sunlight irradiation. Degradation of profenofos was followed with ultrahigh performance liquid chromatography (UHPLC) and follows pseudo first-order kinetic. Accordingly, high-field FTICR mass spectrometry coupled to an electrospray ionization source was used to reveal the degradation routes of profenofos and the isotopic fine structures (IFS) elucidations to approve the chemical structures of its degradation products. More degradation products were detected in UPW as compared to RW. Consequently, two main degradation pathways namely (i) interactive replacements of bromine and hydrogen by hydroxyl functional groups and (ii) rupture of PO, PS, CBr and CCl bonds were observed. None interactive replacement of chlorine by hydroxyl functional group was detected. Accordingly, mechanistical pathways of the main degradation products were established.

Microscale ecotoxicity testing of Moselle river watershed (Lorraine Province, France) sediments

The ecotoxic potential of seven Moselle river watershed sediments was assessed with a battery of bioassays comprised of rapid phototrophic [LuminoTox solid phase (L-SPA) and elutriate (L-ELU) assays] and bacterial [Microtox solid phase assay (M-SPA)] exposure tests, as well as with two micro-invertebrate solid phase tests conducted with Hydra attenuata (lethal and sublethal effects solid phase assay, HL-SPA and HSL-SPA) and Chironomus riparius. Measured effects of sediments and their elutriates were varied and reflected responses that were ecotoxicity test-, endpoint- and site-dependent, suggesting some degree of risk toward benthic and water column organisms, respectively, at specific sites. Correlation analysis demonstrated that L-SPA and M-SPA ecotoxicity responses were significantly linked with the Hydra HSL-SPA assay, indicating their ability to predict ecotoxicity towards an invertebrate taxonomic group representing secondary consumers. While the L-SPA and M-SPA assays hold promise as rapid screens for sediment ecotoxicity, correlation analysis with grain size (L-SPA: r=–0.795, P=0.033; M-SPA: r=–0.73, P=0.07) points out that their responses can be influenced by the presence of fines (i.e., sediment particles ≤0.063 mm in size) and that this information is essential to properly interpret ecotoxicity data generated with these assays. Finally, notable differences observed in trophic level sensitivities once again recall the importance of employing a test battery to adequately appraise the ecotoxicity of sediments.

Magnetic molecularly imprinted polymer prepared by microwave heating for confirmatory determination of chloramphenicol in chicken feed using high-performance liquid chromatography-tandem mass spectrometry

Abstract A magnetic molecularly imprinted polymer (MMIP) for chloramphenicol was prepared using a surface-imprinted and microwave-heating-induced polymerization method. The surfaces of the magnetic particles were first double-bond functionalized with 3-(trimethoxysilyl)propyl methacrylate (γ-MPS), followed by the copolymerization of 4-vinyl pyridine (4-VP) and trimethylolpropane trimethacrylate (TRIM) in the presence of chloramphenicol as a template and 1,1-azobis(cyclohexane-carbonitrile) (ABCN) as an initiator in a mixture of dimethyl sulfoxide and water with microwave heating at 80°C. The magnetic polymer possesses supraparamagnetic properties and was used to concentrate and cleanup chicken feed extract, followed by chromatographic separation using a Lichrospher®100 RP C8 column and detection with two multi-reaction monitoring transitions at m/z 321→ 152 and m/z 321→ 257. The mean recoveries obtained at two spiking levels were in the range of 94.6–100% The relative intra- and inter-day standard deviations were in the range of 1.4–2.6% and 5.1–5.7%, respectively. The detection limit of the method was 0.12 µg kg−1. This confirmatory method was successfully applied to determine chloramphenicol in chicken feed samples.