Jingcun Wu | Authors

This method has greater sensitivity and a shorter LC analysis time than the AOAC method. It also requires less instrument maintenance, enhances column lifetime by requiring a smaller sample volume, and reduces cost by replacing acetonitrile with methanol in the mobile phase.

Mycotoxins are toxic metabolites produced by fungal species often found in agricultural products. An accurate method for analyzing 12 regulated mycotoxins is described using UHPLC–MS/MS. The method demonstrated limits of quantitation (LOQs) for all analytes below stringent regulatory limits, making the method suitable for routine mycotoxin analysis.

Tobacco-specific nitrosamines are important carcinogens in tobacco products. This article describes a fast, sensitive, selective, and robust method for analysis of these compounds in various tobacco samples by liquid chromatography–tandem mass spectrometry (LC–MS/MS). The separation of analytes from matrix interfering components was performed using a C18 column with simple LC–MS mobile phases. To minimize sample matrix effects on each analyte, a separate internal standard was used for each analyte. Two MS/MS ion pairs were used for each analyte for analyte confirmation and quantification, further enhancing the method’s selectivity and accuracy. The method was validated using different tobacco matrices.