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GB 31656.13-2021: (National Food Safety Standard Determination of Multi-residue Nitrofuran Metabolites in Aquatic Products Liquid Chromatography-Tandem Mass Spectrometry)
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(National Food Safety Standard Determination of Multi-residue Nitrofuran Metabolites in Aquatic Products Liquid Chromatography-Tandem Mass Spectrometry)
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GB 31656.13-2021
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Basic data | Standard ID | GB 31656.13-2021 (GB31656.13-2021) | | Description (Translated English) | (National Food Safety Standard Determination of Multi-residue Nitrofuran Metabolites in Aquatic Products Liquid Chromatography-Tandem Mass Spectrometry) | | Sector / Industry | National Standard | | Classification of Chinese Standard | X04 | | Word Count Estimation | 8,836 | | Issuing agency(ies) | National Health Commission of the People's Republic of China, State Administration for Market Regulation | GB 31656.13-2021: (National Food Safety Standard Determination of Multi-residue Nitrofuran Metabolites in Aquatic Products Liquid Chromatography-Tandem Mass Spectrometry)
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National food safety standards
Determination of multiple residues of nitrofuran metabolites in aquatic products
Liquid chromatography-tandem mass spectrometry
National Standards of People's Republic of China
Released by the National Health Commission of the People's Republic of China
State Administration for Market Regulation
Ministry of Agriculture and Rural Affairs of the People's Republic of China
Foreword
This document complies with the provisions of GB/T 1:1-2020 "Standardization Work Guidelines Part 1: Structure and Drafting Rules of Standardization Documents"
Drafting:
This document is published for the first time:
National food safety standards
Determination of multiple residues of nitrofuran metabolites in aquatic products
Liquid chromatography-tandem mass spectrometry
1 Scope
This document specifies the nitrofuran metabolites 3-amino-2-oxazolidinone (AOZ) and 5G in aquatic products:
Morpholinomethyl-3-amino-2-oxazolidinone (5-morpholinomethyl-3-amino-2-oxazolidinone, AMOZ), 1-amino-2G hydantoin
Methods for sample preparation and liquid chromatography-tandem mass spectrometry determination of (1-aminohydantoin, AHD) and semicarbazide (SEM) residues:
This document applies to AOZ, AMOZ, AHD and SEM residues of nitrofuran metabolites in edible tissues of fish, sea cucumbers, turtles and other aquatic products:
Determination of retention amount, as well as determination of AOZ, AMOZ and AHD in edible tissues of crustaceans such as shrimps and crabs:
2 Normative reference documents
The contents of the following documents constitute essential provisions of this document through normative citations in the text: Among them, referenced documents with dates are only
The version corresponding to the date applies to this document; for undated referenced documents, the latest version (including all amendments) applies to this document:
GB/T 6682 Specifications and test methods for water used in analytical laboratories
GB/T 30891-2014 Sampling specifications for aquatic products
3 Terms and definitions
There are no terms or definitions that need to be defined in this document:
4 Principles
The remaining nitrofuran protein-bound metabolites in the sample were hydrolyzed under acidic conditions, derivatized with 2-nitrobenzaldehyde, and treated with ethyl acetate:
Ester liquid-liquid extraction, high-speed centrifugal purification, liquid chromatography-tandem mass spectrometry, and internal standard method for quantitation:
5 Reagents and materials
Unless otherwise specified, all reagents are of analytical grade and the water is first-grade water that complies with GB/T 6682:
5:1 Reagents
5:1:1 Methanol (CH₃OH): chromatographically pure:
5:1:2 Ammonium acetate (CH₃COONH₄) is chromatographically pure:
5:1:3 Ethyl acetate (C₄H₈O₂): chromatographically pure:
5:1:4 Dimethyl sulfoxide [(CH₃)₂SO]: chromatographically pure:
5:1:5 2-nitrobenzaldehyde (C₇H₅NO₃): chromatographically pure:
5:1:6 Anhydrous dipotassium hydrogen phosphate (K₂HPO):
5:1:7 Hydrochloric acid (HCD:
5:2 Solution preparation
5:2:1 0:5 mol/L hydrochloric acid solution: Take 42mL of hydrochloric acid, dilute it with water to 1000mL, and mix well:
5:2:20:002 mol/L ammonium acetate solution: Take 0:15g of ammonium acetate, dissolve it in water and dilute it to 1000mL, and mix well:
5:2:30:05 mol/L 2-nitrobenzaldehyde solution: Take 0:076 g of 2-nitrobenzaldehyde, dissolve it in dimethyl sulfoxide and dilute it to 10 mL, mix well, and prepare it now:
5:2:41:0 mol/L dipotassium hydrogen phosphate solution: Take 87:1 g of anhydrous dipotassium hydrogen phosphate, dissolve and dilute to 500mL with water, and mix well:
5:2:55% methanol solution: Take 5mL of methanol, dilute to 100mL with water, and mix well:
5:3 Standard products
5:3:1 Nitrofuran metabolites: AOZ, AMOZ, AHD·HCl and SEM·HCl, the content is ≥99:0%, see Appendix A for details:
5:3:2 Internal standards: AOZ-D₄, AMOZ-D, AHD-³C₃ and SEM·HCl-³C, 15N2, the contents are all ≥99:0%, see the attachment for details
Record A:
5:4 Preparation of standard solution
5:4:1 Standard stock solution: Take an appropriate amount of each of the AOZ, AMOZ, AHD·HCl, and SEM·HC1 standards (equivalent to 10 mg of active ingredient), weigh it accurately, add an appropriate amount of methanol to dissolve it, and dilute it to a 10mL brown volumetric flask: Prepare a standard stock solution with a concentration of 1:0 mg/mL: Store at -18℃ away from light, valid for 6 months:
5:4:2 Mixed standard intermediate solution: Accurately measure an appropriate amount of the standard stock solution, dilute it step by step with methanol, and prepare a mixed standard intermediate solution with a concentration of 1:0 μg/mL: Store at 2℃~8℃ away from light, valid for 1 month:
5:4:3 Mixed standard working solution: Accurately measure 1 mL of the mixed standard intermediate solution into 10 mL and 100 mL brown volumetric flasks, dilute to the mark with methanol, and prepare mixed standard working solutions with concentrations of 100 μg/L and 10 μg/L: Ready for use:
5:4:4 Isotope internal standard standard stock solution: Take appropriate amounts of each of AOZ-D₄, AMOZ-D₅, AHD-³C₃ and SEM·HCI-³C, ⁵N₂ standards (equivalent to 10 mg of active ingredient), weigh them accurately, and add an appropriate amount of methanol: Dissolve and dilute to a 10mL brown volumetric flask, and prepare to a concentration of
1:0 mg/mL internal standard standard stock solution: Store at -18℃ away from light, valid for 6 months:
5:4:5 Mixed internal standard standard working solution: Accurately measure an appropriate amount of the isotope internal standard standard stock solution, dilute it step by step with methanol, and prepare a mixed internal standard standard working solution with a concentration of 100 μg/L: Store at -18℃ away from light, valid for 3 months:
6Instruments and equipment
6:1 Liquid chromatography-tandem mass spectrometer: equipped with electrospray ionization source:
6:2 Analytical balance: sensitive to 0:01g and 0:00001g:
6:3 Centrifuge: 6000 r/min:
6:4 High-speed centrifuge: 14000 r/min:
6:5 Vortex mixer:
6:6 Constant temperature oscillator:
6:7 Nitrogen blower:
7 Preparation and preservation of samples
7:1 Preparation of samples
Prepare samples according to the requirements of Appendix B of GB/T 30891-2014:
a) Take the homogeneous test material as the test material;
b) Take a homogeneous blank sample as a blank sample;
c) Take a homogeneous blank sample, add a standard solution of appropriate concentration, and add the sample as a blank:
7:2 Storage of samples
Store below -18℃:
8 Measurement steps
8:1 Hydrolysis and derivatization
Take 2g of the sample (accurate to ±0:01g), put it into a 50mL polypropylene centrifuge tube, add exactly 50μL of the mixed internal standard standard working solution, vortex and mix for 1 minute, add 5mL of hydrochloric acid solution and 0:15mL of 2-nitrobenzaldehyde solution: , vortex and mix for 1 min, place in a constant temperature oscillator, and oscillate at 37°C in the dark for 16 h:
8:2 Extraction and purification
Take out the centrifuge tube and cool it to room temperature, adjust the pH to 7:0~7:5 with dipotassium hydrogen phosphate solution, add 8 mL of ethyl acetate, vortex for 30 s, centrifuge at 6000 r/min for 5 min, transfer the supernatant to a 10 mL glass centrifuge tube, 40 ℃ nitrogen blow dry: Add 1:0 mL of 5% methanol solution to dissolve the residue, then transfer the solution to a 1:5 mL centrifuge tube, centrifuge at 14000 r/min for 10 min, and pass the clear liquid through a 0:22 μm filter membrane for liquid chromatography-tandem mass spectrometry analysis:
8:3 Preparation of standard curve
Accurately transfer 0:05 mL, 0:1 mL, and 0:2 mL of the 10 μg/L and 100 μg/L mixed standard working solutions into six 50 mL centrifuge tubes: Follow steps 7:1 and 7:2 except that no sample is added to obtain the final concentration: 0:5μg/L, 1:0μg/L, 2:0μg/L respectively
5:0μg/L, 10μg/L, 20μg/L, measured according to 7:4: Taking the measured characteristic ion mass chromatographic peak external standard and internal standard peak area ratio as the ordinate and the corresponding standard solution concentration as the abscissa, draw a standard curve and find the regression equation and correlation coefficient:
8:4 Determination
8:4:1 Liquid Chromatography Reference Conditions
a) Chromatographic column: Cis chromatographic column (100mm×2:1 mm, 3:5μm), or equivalent:
b) Column temperature: 35℃;
c) Injection volume: 10 μL;
d) Flow rate: 0:35 mL/min;
e) Mobile phase: A is 0:002 mol/L ammonium acetate solution, B is methanol: Gradient elution conditions are shown in Table 1: 8:4:2 Mass spectrometry reference conditions
a) Ion source: electrospray ion source;
b) Scanning method: positive ion scanning;
c) Detection method: multiple reaction ion monitoring (MRM);
d) The desolvation gas, cone gas, and collision gas are all high-purity nitrogen or other suitable gases;
e) Spray voltage, collision energy and other parameters should be optimized to optimal sensitivity;
D) See Table 2 for the monitored ion parameters:
8:5 Determination method
8:5:1 Qualitative determination
Under the same test conditions, the ratio of the retention time of nitrofuran metabolites in the sample solution to the retention time of nitrofuran metabolites in the standard solution is within ±2:5%, and the relative ion abundance detected , should be consistent with the relative abundance of the calibration standard solution of equivalent concentration: The allowable deviation should comply with the requirements of Table 3:
8:5:2 Quantitative determination
Take the sample solution and the corresponding standard solution, conduct single-point or multi-point calibration, quantify it based on the chromatographic peak area, and calculate it according to the internal standard method: The response values of the nitrofuran metabolites in the standard solution and the sample solution should be on the instrument: within the linear range of detection: Under the above liquid chromatography-mass spectrometry conditions, the liquid chromatography-mass spectrum of the standard solution of nitrofuran metabolites is shown in Appendix B:
8:6 Blank test
Take a blank sample and perform parallel operations using the same measurement steps except that no standard solution is added:
9Result calculation and presentation
The residual amount of nitrofuran metabolites in the sample is calculated according to the standard curve method or formula (1):
10 Sensitivity, accuracy and precision of detection methods
10:1 Sensitivity
The detection limits of AOZ, SEM, AMOZ and AHD of this method are all 0:5 μg/kg, and the quantification limits are all 1:0 pg/kg:
10:2 Accuracy
The recovery rate of this method at the added concentration level of 1:0 μg/kg to 10 μg/kg is 70% to 120%:
10:3 Precision
The intra-batch relative standard deviation of this method is ≤15%, and the inter-batch relative standard deviation is ≤15%:
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