ANALYSIS OF MYCOTOXINS IN FOOD MATRICES

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ANALYSIS OF MYCOTOXINS IN FOOD MATRICES Agilent Ultivo Triple Quadrupole LC/MS System Introduction Mycotoxins are compounds produced by fungi that grow on crops ranging from grains to fruits, vegetables, nuts, and spices. Mycotoxins can be harmful to humans and livestock through consumption of contaminated crops; therefore, mycotoxin levels are monitored in foods to minimize the risk of ingestion1. Regulatory agencies around the globe set Maximum Residue Limits (MRLs), which range from <1 to >5 ppb to ensure harmful levels of mycotoxins do not enter the food supply. It is important to detect and accurately quantify mycotoxin contents at low levels across various food matrices, as each matrix composition poses different detection challenges. This study demonstrates the accurate and sensitive quantification of up to 1 regulated mycotoxin compounds in three commonly regulated foods using the Agilent Ultivo Triple Quadrupole LC/MS. (Figure 1). Figure 1. Agilent Ultivo Triple Quadrupole LC/MS integrated into the Agilent 16 Infinity II Prime LC. For more information, visit: www.agilent.com/chem/ultivo

Agilent Ultivo Triple Quadrupole LC/MS Ultivo is designed to address many of the challenges faced by labs performing environmental and food safety analyses. The innovative technologies housed within Ultivo allowed us to achieve a reduced overall footprint, while conserving the performance found in many larger MS systems. Innovations such as VacShield, Cyclone Ion Guide, Vortex Collision Cell, and Hyperbolic Quads maximize quantitative performance in a small package, enhancing instrument reliability and robustness, resulting in greater uptime. Ultivo reduces user intervention for system maintenance, making it easy for the nonexpert MS user to operate and maintain. Agilent MassHunter software simplifies data acquisition, method setup, data analysis, and reporting. This results in the fastest acquisition-to-reporting time possible, increasing lab productivity and confidence in results. Experimental Sample preparation Corn, peanut, and black pepper were chosen as commonly regulated food crops of diverse matrix components for mycotoxins. Twelve mycotoxins in corn and peanut matrices, and five mycotoxins in black pepper matrix were quantified using dynamic MRM (dmrm) in a 9-minute LC/Triple Quad method. Mycotoxin standards were spiked into matrix extracts for analysis. A 5 g sample of corn flour, 5 g of peanuts, or g of black pepper were extracted with 1 ml of ACN, 1 ml H O, and EN Extraction Salts (598-565). Dispersive SPE for fruits and vegetables (598-558) was used on corn, and a universal dispersive SPE kit (598-9) was used for black pepper. A novel modified lipid removal sorbent inflow through a cartridge format was used on each matrix as a final cleanup step. Spiked black pepper extracts were diluted 3:7 extract/water prior to analysis.

Instrument parameters Table 1. LC and MS parameters. Agilent 19 Infinity II LC Column Agilent Eclipse Plus C18, 3. 15 mm, 1.8 µm Column temperature 45 C Injection volume Corn: µl, Peanut: 1 µl, Black pepper: 1 µl Mobile phase Flow rate A) Water,.5 mm NH 4 F + 5 mm NH 4 formate +.1 % formic acid B) MeOH,.5 mm NH 4 F + 5 mm NH 4 formate +.1 % formic acid.45 ml/min Gradient Time (min) %B 3.5 3 7.5 1 9. 1 9.1 3 Agilent Ultivo Drying gas temperature 5 C Drying gas flow 8 L/min Sheath gas temperature 35 C Sheath gas flow Nebulizer pressure Capillary voltage Nozzle voltage Cycle time 1 L/min 3 psi 3,3 V(+),,8 V( ) V(+), V( ) 5 ms Results and Discussion Mycotoxin signal response Excellent precision and sensitivity was attained for mycotoxins in various food matrices due to a combination of sample preparation techniques, LC separation, and the innovative technology designed into the Ultivo triple quadrupole mass spectrometer. 1 1..9.8.7.6.5.4.3..1.6.8 3. 3. 3.4 3.6 3.8 4. 4. 4.4 4.6 4.8 5. 5. 5.4 5.6 5.8 6. 6. 6.4 6.6 6.8 7. 7. 7.4 7.6 7.8 Figure. Detection of mycotoxins at 1/1th MRL in corn matrix.

Mycotoxin maximum residue limits and sensitivity Outstanding sensitivity was achieved, with the majority of the mycotoxin compounds in each matrix studied reaching a limit of quantitation (LOQ) at 1/th the assigned MRL. Table. Maximum residue limits for mycotoxins used in this study. EU reg No. 1881/6 and 15/1 used for reference. All assigned MRLs in this study are equal to or lower than SANTE MRLs. Mycotoxin EU MRL for mycotoxins,3 Assigned MRL level used Corn Peanut Black pepper Corn and peanut Black pepper Aflatoxin B1 ppb ppb 5 ppb a ppb 5 ppb Aflatoxin B Aflatoxins: 4 ppb Aflatoxins: 4 ppb Aflatoxins: 1 ppb ppb 5 ppb Aflatoxin G1 ppb 5 ppb Aflatoxin G ppb 5 ppb Ochratoxin A 3 ppb N/A 15 ppb b 3 ppb 15 ppb Fumonisin B1 5 ppb N/A N/A 5 ppb Not included Fumonisin B Fumonisins: 1, ppb N/A N/A 5 ppb Not included Fumonisin B3 N/A N/A 5 ppb Not included Deoxynivalenol 75 ppb N/A N/A 75 ppb Not included Zearalenone 1 ppb N/A N/A 1 ppb Not included T- Toxin N/A N/A N/A 1 ppb Not included HT- Toxin N/A N/A N/A 5 ppb Not included No. of mycotoxins 14 1 1 8 6 4 1 1 1 1 1/5 MRL 1/1 MRL 1/ MRL Corn Peanut Black pepper Matrix Figure 3. Quantitation limit for all mycotoxins studied in each matrix, defined as a fraction of the assigned MRL. 3

Precision and linearity of mycotoxins Excellent linearities were obtained for all compounds in this study, with R values >.999 over the calibration ranges used. Precision values obtained for mycotoxins in the matrices investigated rendered %RSD values of <1 % at the LOQs. No. of mycotoxins 14 1 1 8 6 4 3 3 9 9 RSD 5 1 % RSD 5 % Corn Peanut Black pepper Matrix Figure 4. Calibration curves for PFOS, PFOA, N-EtFOSAA, and PFBS. 3 1 1..6.8.7.6.5.4.3..1 Corn Aflatoxin B1 1 ppt 1. RSD% = 1.75 Avg. S/N = 36.6.8.7.6.5.4.3..1 Peanut Aflatoxin B1 1 ppt 1. RSD% =.34 Avg. S/N = 169.6.8.7.6.5.4.3..1 Black pepper Aflatoxin B1 ppt RSD% = 5.65 Avg. S/N = 53.6 5.5 5.55 5.6 5.65 5.5 5.55 5.6 5.65 5.5 5.55 5.6 5.65 Figure 5. Excellent precision demonstrated for Aflatoxin B1 at 1/1th MRL ( ppt or 5 ppt) in all matrices.

1 3 4.4 4. 3.6 3..8..8.4 1 4 1.4 1..8.6.4. Ochratoxin A.5 3 ppb R =.999 3 6 9 1 15 18 1 4 7 3 1 4 6. HT- Toxin 5.4 5 5, ppb 4.8 R =.999 4. 3.6 3. 1.8.6 8 1,6,4 3, 4, 4,8 Aflatoxin B1.1 ppb R =.999 4 6 8 1 1 14 16 18 1 3 3.3 3..7.1 1.8 1.5.9.6.3 1 4 6.4 5.6 4.8 4. 3..8 1 4 1.4 1..8.6.4. Deoxynivalenol.375 75 ppb R =.999 75 15 5 3 375 45 55 6 675 75 Zearalenone 5 1, ppb R =.999 75 15 5 3 375 45 55 6 675 75 Aflatoxin G.1 ppb R =.999 4 6 8 1 1 14 16 18 Figure 6. Exceptional linearity was demonstrated for all compounds, with r values.99 for all compounds, in all matrices. Pictured above, examples of linearity for 6 mycotoxins in corn matrix. References 1. Bennett, J. W.; Klich, M. Mycotoxins. Clinical Microbiology Reviews 3, 16(3), 497-516.. Commission Regulation (EC) No 1881/6. Setting maximum levels for certain contaminants in foodstuffs. Official Journal of the European Union. L 364/5-4. 19 December 6. 3. Commission Regulation (EU) No 15/1. Amending Regulation (EC) No 1881/6 setting maximum levels for certain contaminants in foodstuffs as regards ochratoxin A. L 35/7-8. Official Journal of the European Union. 5 February 1. Conclusions The Agilent Ultivo Triple Quadrupole LC/MS is an exceptionally innovative new mass spectrometer that can minimize laboratory workspace needs, as well as reduce maintenance challenges, creating a productive work environment for high throughput laboratories. Ultivo is a small, yet powerful tool enabling the accurate and sensitive detection of commonly regulated mycotoxins in various food matrices well below established MRL levels. Agilent MassHunter software provides an easy-to-use, all-inclusive tool for managing and reporting LC/MS data. www.agilent.com Information, descriptions and specifications in this publication are subject to change without notice. Agilent Technologies, Inc. 17 Published in USA, May 3, 17 5991-816EN