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Nanofluid extraction of Ochratoxin A in food
Institution:1. The George Institute for Global Health, Sydney, NSW, 2042, Australia;2. Charles Perkins Centre and School of Life and Environmental Sciences, The University of Sydney, Sydney, NSW, 2006, Australia;3. Department of Epidemiology and Biostatistics, School of Public Health, Faculty of Medicine, Imperial College London, United Kingdom;1. CONICET- Universidad De Buenos Aires, Instituto de Investigaciones en Producción Animal, (INPA), CP C1427CWO, Buenos Aires, Argentina;2. Universidad Nacional del Litoral, Facultad de Ingeniería Química Programa De Investigación y Análisis de Residuos y Contaminantes Químicos (PRINARC), Santiago del Estero 2654 Piso 5-6, CP 3000 Santa Fe, Argentina;3. Universidade Federal do Paraná (UFPR), Pós-Graduação em Engenharia Ambiental, Departamento de Engenharia, CP 19020, Bairro Jardim Das Américas, Curitiba, Paraná, Brazil;1. Department of Biochemistry, Faculty of Biology and Biotechnology, University of Warmia and Mazury, Olsztyn, Poland;2. Department of Plant Breeding and Seed Production, University of Warmia and Mazury, Olsztyn, Poland;3. Division of Food Science, Institute of Animal Reproduction and Food Research of the Polish Academy of Sciences, Olsztyn, Poland;4. Department of Entomology, Phytopathology and Molecular Diagnostics, University of Warmia and Mazury, Olsztyn, Poland;1. Department of Chemistry, Wuhan University, Wuhan 430072, PR China;2. Hubei Provincial Institute for Food Supervision and Test, Wuhan 430075, PR China;3. HEJ Research Institute of Chemistry, International Center for Chemical and Biological Sciences, University of Karachi, Karachi, Pakistan;4. Frontier Science Center for Immunology and Metabolism, Wuhan University, Wuhan 430072, PR China;1. U.S. Department of Agriculture, Agricultural Research Service, Beltsville Human Nutrition Research Center, Methods and Application of Food Composition Laboratory, Beltsville, MD, US 20705, United States;2. Center for Intelligent Chemical Instrumentation, Department of Chemistry & Biochemistry, Ohio University, Athens, OH, 45701, United States;1. Livestock and Wildlife Laboratory, Arid Lands Institute, Medenine, Tunisia;2. Faculty of Sciences of Gabès, University of Gabès, Tunisia;3. Department of Bioactivity and Food Analysis, Food Lipid Biomarkers and Health Group, Institute of Food Science Research (CIAL), CSIC-UAM, Autónoma University of Madrid, Spain
Abstract:Monitoring of Ochratoxin A (OTA), a toxic and carcinogenic metabolite of fungi, requires accurate and precise analytical methods. Quantitative determination of OTA at trace level in raisin samples was evaluated by nanofluid extraction coupled with HPLC–FLD. The experimental parameters affecting the extraction efficiency of OTA were investigated and optimized. The validated method has low detection and quantification limit (0.2 and 0.5 ng g−1). Moreover, under optimum conditions, the repeatability of the method expressed as the relative standard deviation for intra-day and inter-day precision (RSD %) was below 15 % (n = 3). This method has also been successfully applied to the analysis of trace amounts of OTA in real samples with satisfactory relative recoveries in the range of 70.3–84.7 %.
Keywords:Food analysis  Food composition  Ochratoxin A  Raisin  Nanofluids extraction  HPLC
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