Filipa Carreiró
Research Subjects
Research Interests
Filipa Carreiró has a total of 5 co-authors. Here are the top co-authors by number of shared publications:
- Ana Rita Soares Mateus
National Institute for Agricultural and Veterinary Research (INIAV), I.P., Rua dos Lagidos, Lugar da Madalena, Vairão, 4485-655 Vila do Conde, Portugal
1 shared publication - Ana Sanches Silva
Centre for Study in Animal Science (CECA), Instituto de Ciências, Tecnologias e Agroambiente (ICETA), University of Porto, 4050-053 Porto, Portugal
1 shared publication - Angelina Pena
University of Coimbra, Faculty of Pharmacy, Polo III, Azinhaga de Stª Comba, 3000-548 Coimbra, Portugal
1 shared publication - Carla Brites
National Institute for Agricultural and Veterinary Research (INIAV), I.P., Av. da República, Quinta do Marquês, 2780-157 Oeiras, Portugal
1 shared publication - Sílvia Cruz Barros
National Institute for Agricultural and Veterinary Research (INIAV), I.P., Av. da República, Quinta do Marquês, 2780-157 Oeiras, Portugal
1 shared publication
Latest Publications
- 16 July 2026
- Published by Oxford University Press (OUP) in Journal of AOAC INTERNATIONAL
QuEChERS–UHPLC–TOF-MS method for regulated and emerging mycotoxins including ergot alkaloids in rice
Background: Rice is susceptible to contamination by mycotoxins and ergot alkaloids, posing significant risks to food safety. Despite growing evidence of their co-occurrence, few methods allow simultaneous determination of regulated, emerging mycotoxins and ergot alkaloids in rice. Objective: A screening method based on the of Quick, Easy, Cheap, Effective, Rugged and Safe (QuEChERS) method coupled with ultra-high performance liquid chromatography combined with time-of-flight mass spectrometry (UHPLC–TOF-MS) was develop and validated for the simultaneous determination of 11 mycotoxins and 12 ergot alkaloids in rice. Methods: Chromatographic parameters, including column selection, gradient program, flow rate, and injection volume, were optimized to ensure adequate separation and sensitivity. Two extraction approaches, solid–liquid extraction (SLE) and QuEChERS, were systematically compared, and key parameters such as extraction solvent, extraction time, and salt composition were optimized to maximize recoveries across chemically diverse analytes. The validated method was applied to 41 commercially available rice samples from the Portuguese market. Results: The validated method showed recoveries between 71% and 119%, repeatability (RSDr ≤20%), inter-day precision (RSDR ≤25%), and LOQs compliant with European Union (EU) performance criteria. Aflatoxin G2 and sterigmatocystin were the most frequently detected mycotoxins, with three samples exceeding the legal limit for total aflatoxins (4 µg/kg). Mycophenolic acid was also detected in two samples. Conclusion: The developed method demonstrated adequate sensitivity, selectivity, and precision for multi-mycotoxin surveillance, highlighting the relevance of monitoring emerging mycotoxins in rice. Highlights: QuEChERS combined with UHPLC–TOF-MS enables simultaneous screening of 23 analytes, including ergot alkaloids and regulated and emerging myxotoxins. The method was validated according to Regulation (EU) 2023/2782. Aflatoxin G2 and sterigmatocystin were detected in Portuguese market rice. Mycophenolic acid was detected as an emerging contaminant.
- 16 July 2026
- Published by Oxford University Press (OUP) in Journal of AOAC INTERNATIONAL
QuEChERS–UHPLC–TOF-MS method for regulated and emerging mycotoxins including ergot alkaloids in rice
Background: Rice is susceptible to contamination by mycotoxins and ergot alkaloids, posing significant risks to food safety. Despite growing evidence of their co-occurrence, few methods allow simultaneous determination of regulated, emerging mycotoxins and ergot alkaloids in rice. Objective: A screening method based on the of Quick, Easy, Cheap, Effective, Rugged and Safe (QuEChERS) method coupled with ultra-high performance liquid chromatography combined with time-of-flight mass spectrometry (UHPLC–TOF-MS) was develop and validated for the simultaneous determination of 11 mycotoxins and 12 ergot alkaloids in rice. Methods: Chromatographic parameters, including column selection, gradient program, flow rate, and injection volume, were optimized to ensure adequate separation and sensitivity. Two extraction approaches, solid–liquid extraction (SLE) and QuEChERS, were systematically compared, and key parameters such as extraction solvent, extraction time, and salt composition were optimized to maximize recoveries across chemically diverse analytes. The validated method was applied to 41 commercially available rice samples from the Portuguese market. Results: The validated method showed recoveries between 71% and 119%, repeatability (RSDr ≤20%), inter-day precision (RSDR ≤25%), and LOQs compliant with European Union (EU) performance criteria. Aflatoxin G2 and sterigmatocystin were the most frequently detected mycotoxins, with three samples exceeding the legal limit for total aflatoxins (4 µg/kg). Mycophenolic acid was also detected in two samples. Conclusion: The developed method demonstrated adequate sensitivity, selectivity, and precision for multi-mycotoxin surveillance, highlighting the relevance of monitoring emerging mycotoxins in rice. Highlights: QuEChERS combined with UHPLC–TOF-MS enables simultaneous screening of 23 analytes, including ergot alkaloids and regulated and emerging myxotoxins. The method was validated according to Regulation (EU) 2023/2782. Aflatoxin G2 and sterigmatocystin were detected in Portuguese market rice. Mycophenolic acid was detected as an emerging contaminant.