A Stereoselective Synthesis of the C(13)-C(23) Fragment of Iriomoteolide-1b

Yang, Zhen; Peng, Jing; She, Xuegong

doi:10.6023/cjoc1104192

Cited by 1 publication

(1 citation statement)

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“…21 This method was improved using an IAC cleanup method with reversed-phase HPLC-FLD determination (AOAC-IUPAC Official Method 2001.4), obtaining recoveries of 97-110%, repeatability values of 8-22%, and reproducibility values of 26-35% at contamination levels ranging from 130 to 920 mg kg À1 FB1. 18 Specic immunochemical methods for fumonisin detection are robust alternatives to HPLC analysis, 22,23 the more common methods include both ELISA (enzyme-linked immunosorbent analysis), [24][25][26][27] and lateral ow devices (dipsticks) usually for screening purposes. 28,29 A variety of antibody-based ELISAs for fumonisins have been introduced in the past decade, 25-27 some of them available as commercial quantitative kits, with detection limits ranging from about 1-10 ng mL À1 of FB1.…”

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confidence: 99%

A validated multi-channel electrochemical immunoassay for rapid fumonisin B1 determination in cereal samples

Ezquerra

Vidal

Bonel³

et al. 2015

Anal. Methods

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Fumonisin mycotoxins are natural contaminants of cereals mostly found in maize samples. Owing to their acute and chronic toxicity, very strict regulations have been imposed on the levels of fumonisin mycotoxins in cereal and cereal-based foods worldwide. We report a rapid direct competitive multi-channel electrochemical immunoassay for fumonisin B1 (FB1) determination in cereal and cereal-based foods. Monoclonal antibodies against FB1 were immobilized on the surface of modified magnetic beads (2.8 mm diameter), and the transduction was performed on an 8Â screen-printed array allowing the multichannel electrochemical detection of eight samples in parallel (amperometric detection, E ¼ À0.35 V).The FB1 electrochemical immunoassay has a limit of detection of 0.58 AE 0.05 mg L À1 and EC 50 ¼ 4.34 AE 0.15 mg L À1 , for FB1 concentration in the range of up to 54 mg L À1 . The precision (within-day, betweendays) was in the range of about 7-13% RSD. The optimized method (extraction and the electrochemical immunoassay determination) was successfully validated with maize certified reference materials at various levels of concentrations, and with an official AOAC liquid chromatography with fluorescence detection (HPLC-FLD) method (2001.04). We also compared our results with a commercial enzymelinked immunosorbent analysis (ELISA) kit. Cross-reactivities with other mycotoxins (ochratoxins and deoxynivalenol) were less than 10%. The lifetime of immobilized antibodies was about 28 days. The reported FB1 multi-channel electrochemical immunoassay is a rapid and reliable alternative to HPLC methods.

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