GB 31656.11-2021 English PDF

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GB 31656.11-2021: (National Food Safety Standard Determination of Oxytetracycline, Tetracycline, Chlortetracycline and Doxycycline Residues in Aquatic Products)
Status: Valid

Standard ID	USD	BUY PDF	Lead-Days	Standard Title (Description)	Status
GB 31656.11-2021	239	Add to Cart	3 days	(National Food Safety Standard Determination of Oxytetracycline, Tetracycline, Chlortetracycline and Doxycycline Residues in Aquatic Products)	Valid

Similar standards

GB 31650.1   GB/T 37517   GB/T 30636   GB 31656.16   GB 31656.17   GB 31656.15   

Basic data

Standard ID: GB 31656.11-2021 (GB31656.11-2021)
Description (Translated English): (National Food Safety Standard Determination of Oxytetracycline, Tetracycline, Chlortetracycline and Doxycycline Residues in Aquatic Products)
Sector / Industry: National Standard
Classification of Chinese Standard: X04
Word Count Estimation: 12,176
Issuing agency(ies): National Health Commission of the People's Republic of China, State Administration for Market Regulation

GB 31656.11-2021: (National Food Safety Standard Determination of Oxytetracycline, Tetracycline, Chlortetracycline and Doxycycline Residues in Aquatic Products)

---This is a DRAFT version for illustration, not a final translation. Full copy of true-PDF in English version (including equations, symbols, images, flow-chart, tables, and figures etc.) will be manually/carefully translated upon your order.
National food safety standards Oxytetracycline, tetracycline, chlortetracycline, Determination of doxycycline residues 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 Replace GB/T 22961-2008

1 Scope

This document specifies a high-performance liquid chromatography method for the determination of oxytetracycline, tetracycline, chlortetracycline and doxycycline residues in aquatic products: This document is applicable to the determination of oxytetracycline, tetracycline, chlortetracycline and doxycycline residues in the edible tissues of aquatic products such as fish, shrimp, crab, turtle and sea cucumber: Determination:

2 Normative reference documents

The contents of the following documents constitute essential provisions of this document through normative citations in the text: Among them, the cited 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: 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

After the oxytetracycline, tetracycline, chlortetracycline and doxycycline in the sample were extracted with citric acid buffer solution, the solid phase extraction column was purified, and the liquid chromatography fluorescence Detection by detector and quantification by external standard method:

5 Reagents and materials

The reagents used below are of analytical grade unless otherwise noted; 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 Magnesium acetate (C₄H₆O₄Mg·4H₂O): 5:1:3 Imidazole (C₃H₄N₂): 5:1:4 Potassium dihydrogen phosphate (KH₂PO): 5:1:5 Citric acid (C₆H₈O₃·H₂O): excellent grade pure: 5:1:6 Disodium hydrogen phosphate (Na₂HPO₄): superior grade pure: 5:1:7 Disodium ethylenediaminetetraacetate (Na₂EDTA·2H₂O): superior grade pure: 5:1:8 Glacial acetic acid (CH₃COOH): 5:2 Solution preparation 5:2:1 Potassium dihydrogen phosphate solution: Take 13:6 g of potassium dihydrogen phosphate, add an appropriate amount of water to dissolve and dilute to 1000 mL: 5:2:2 Methanol solution: Take 5 mL of methanol and 95 mL of water, and mix well: 5:2:3 Citric acid buffer: Take 6:30 g of citric acid, 13:8 g of disodium hydrogen phosphate, and 1:86 g of disodium ethylenediaminetetraacetate, add 400 mL of water to dissolve, adjust the pH to 4:0 with glacial acetic acid, and then dilute to 500 mL with water: : 5:2:4 Imidazole buffer solution: Take 68:0g of imidazole, 0:40g of disodium ethylenediaminetetraacetate, and 10:0g of magnesium acetate, add 800mL of water to dissolve, and dissolve with Adjust the pH to 7:2 with glacial acetic acid, dilute it with water to 1000mL, filter it through a 0:45μm aqueous phase microporous membrane and set aside: 5:2:5 Methanol-imidazole buffer solution: Take 20 mL of methanol and 80 mL of imidazole buffer solution, and mix well: 5:3 Standard products The contents of tetracycline hydrochloride, chlortetracycline hydrochloride, oxytetracycline hydrochloride, and doxycycline hydrochloride are all ≥95%: See Appendix A for details: 5:4 Preparation of standard solution 5:4:1 Standard stock solution (100pg/mL): Accurately weigh appropriate amounts of standards, dissolve and dilute to constant volume with methanol to prepare standards with concentrations of 100 μg/mL for oxytetracycline, tetracycline, chlortetracycline and doxycycline: Stock solution: Store away from light below -18 ℃, valid for 1 month: 5:4:2 Mix standard intermediate solution: accurately pipette 1:0mL, 1:0mL, oxytetracycline, tetracycline, chlortetracycline and doxycycline standard stock solutions respectively: 2:0 mL and 2:0 mL in a 100 mL volumetric flask, dilute with methanol and adjust to volume, and prepare the concentrations of oxytetracycline, tetracycline, chlortetracycline and doxycycline Mixed standard intermediate solutions of 1:0μg/mL, 1:0μg/mL, 2:0μg/mL and 2:0μg/mL respectively: Store away from light below -18 ℃, validity period is 7 days: 5:5 Materials 5:5:1 Solid phase extraction column: 500 mg/6 mL, Oasis HLB or equivalent: 5:5:2 Water phase microporous filter membrane: 0:22μm: 6Instruments and equipment 6:1 High performance liquid chromatograph: equipped with fluorescence detector: 6:2 Analytical balance: sensitivity 0:01 g: 6:3 Analytical balance: sensitivity 0:00001 g: 6:4 Vortex Oscillator, 6:5 Centrifuge: speed 6000 r/min or above: 6:6 Solid phase extraction device (with negative pressure suction filter): 6:7 Nitrogen blower: 6:8 Tissue homogenizer:

7 Preparation and preservation of specimens

7:1 Preparation of specimens Prepare samples according to the requirements of Appendix B of GB/T 30891-2014: a) Take the homogenized test sample as the test sample; b) Take the homogenized blank sample as the blank sample; c) Take the homogenized blank sample, add standard working solution of appropriate concentration, and add the sample as a blank: 7:2 Storage of specimens Store below -18℃:

8 Measurement steps

8:1 Extraction Take 5g of sample (accurate to ±0:05g), add 20mL of citric acid buffer, vortex for 2 minutes, extract with ultrasonic for 10 minutes, centrifuge at 6000 r/min for 10 minutes, and take the supernatant in another 50mL centrifuge tube: : Add 10 mL of citric acid buffer to the residue, repeat the extraction twice, and combine the supernatants from three times for purification: 8:2 Purification Activate the Oasis HLB solid-phase extraction column with 10 mL of methanol, 10 mL of water, and 5 mL of citric acid buffer in sequence, transfer the solution to be purified, rinse with 10 mL of methanol solution, 10 mL of water, drain, add 10 mL of methanol for elution, and collect the eluate , blow dry with nitrogen at 40℃, add potassium dihydrogen phosphate to dissolve Dissolve the residue in 1:0 mL of solution, sonicate for 1 min, and pass through a 0:22 μm aqueous phase microporous membrane for high-performance liquid chromatography measurement: 8:3 Preparation of standard curve Accurately transfer an appropriate amount of the mixed standard intermediate solution of oxytetracycline, tetracycline, chlortetracycline and doxycycline, and dilute it with methanol-imidazole buffer solution to make the concentrations of oxytetracycline and tetracycline respectively 50 ng/mL, 100 ng/mL and:200 ng/mL, 500ng/mL, 1000ng/mL, mixed standard series working solutions with chlortetracycline and doxycycline concentrations of 100ng/mL,:200ng/mL, 400ng/mL, 1000ng/mL, and:2000ng/mL respectively: High performance liquid chromatography determination: Draw a standard curve with the peak area of the analyte as the ordinate and the corresponding standard solution concentration as the abscissa: Calculate the regression equation and correlation coefficient: 8:4 Determination 8:4:1 Liquid Chromatography Reference Conditions a) Chromatographic column: Cu chromatographic column (250mm×4:6mm, 5μm), or equivalent; b) Column temperature: 40℃; c) Injection volume: 30gL; d) Flow rate: 0:8mL/min; e) Excitation wavelength: 380 nm; f) Emission wavelength: 520 nm; g) Mobile phase: methanol-imidazole buffer solution: 8:4:2 Determination method Take the sample solution and the corresponding standard solution, perform single-point or multi-point calibration, quantify the chromatographic peak area, and calculate using the external standard method: The response values of oxytetracycline, tetracycline, chlortetracycline and doxycycline in the standard working solution and sample solution should be within the linear range of instrument detection: The HPLC chromatogram of the standard solution is shown in Figure B:1 in Appendix B: 8:5 Blank test Take the empty 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 the substance to be tested in the sample is calculated according to the standard curve or formula (1): 10 Sensitivity, accuracy and precision of detection methods 10:1 Sensitivity The detection limit of oxytetracycline and tetracycline in the edible tissues of aquatic products by this method is 10:0 μg/kg, and the detection limit of doxycycline and chlortetracycline is 10:0 μg/kg: Both are 20:0 μg/kg; the quantitation limits of oxytetracycline and tetracycline are both 20:0 μg/kg, and the quantification limits of doxycycline and chlortetracycline are both 40:0 μg/kg: 10:2 Accuracy The recovery rates of oxytetracycline and tetracycline at the added concentration of 20:0 μg/kg to:200 μg/kg were 60% to 110%; the recovery rates of doxycycline and chlortetracycline were The recovery rate at the added concentration of 40:0 μg/kg ~ 400 μg/kg is 60% ~ 110%: 10:3 Precision The intra-batch relative standard deviation of this method is ≤15%, and the inter-batch relative standard deviation is ≤15%: Method two liquid chromatography-tandem mass spectrometry 11 Scope This document specifies a liquid chromatography-tandem mass spectrometry method for the determination of oxytetracycline, tetracycline, chlortetracycline and doxycycline residues in aquatic products: This document is applicable to the determination of oxytetracycline, tetracycline, chlortetracycline and doxycycline residues in the edible tissues of aquatic products such as fish, shrimp, crab, turtle and sea cucumber: 12Normative reference documents The contents of the following documents constitute essential provisions of this document through normative references in the text: Among them, for dated reference documents, only the version corresponding to the date applies to this document; for undated reference documents, the latest version (including all amendments) applies to this document: GB/T 6682 Specifications and test methods for water use in analytical laboratories GB/T 30891-2014 Specifications for sampling of aquatic products 13 Terms and Definitions There are no terms or definitions to be defined in this document: 14 Principles The remaining oxytetracycline, tetracycline, chlortetracycline and doxycycline in the sample were extracted with Na₂EDTA-Mcllvaine buffer solution and precipitated with lead acetate: precipitation, n-hexane degreasing, solid phase extraction column purification, liquid chromatography-tandem mass spectrometry measurement, and matrix calibration standard curve for external standard method quantification: 15Reagents and materials The reagents used below are of analytical grade unless otherwise noted; the water is first-grade water that complies with GB/T 6682: 15:1 Reagents 15:1:1 Acetonitrile (CH₃CN): chromatographically pure: 15:1:2 Methanol (CH₃OH): chromatographically pure: 15:1:3 Ethyl acetate (CH₃COOC₂H₅): chromatographically pure: 15:1:4 n-hexane (C₅H₈): chromatographically pure: 15:1:5 Formic acid (HCOOH): chromatographically pure: 15:1:6 Hydrochloric acid (HCD: 15:1:7 Sodium hydroxide (NaOH): 15:1:8 Citric acid (C₆H₈O₇·H₂O): excellent grade pure: 15:1:9 Disodium hydrogen phosphate (Na₂HPO₄): superior grade pure: 15:1:10 Disodium ethylenediaminetetraacetate (Na₂EDTA·2H₂O): superior grade pure: 15:1:11 Lead acetate [Pb(CH₃COO)₂·3H₂O]: 15:2 Solution preparation 15:2:1 Na₂EDTA-Mellvaine buffer solution (0:1mol/L): Weigh 12:9 g of citric acid, 10:9 g of disodium hydrogen phosphate, and ethylenediamine tetrahydrofuran: Disodium acetate 37:2g, add appropriate amount of water to dissolve each, mix, dilute to 1000mL with water, adjust pH to 4:0 (±0:05) with 0:1 mol/L HCl or 0:1 mol/L NaOH: 15:2:2 Lead acetate solution (20:0g/L): Take 20:0g of lead acetate, add water to dissolve and dilute to 1000 mL: 15:2:3 Formic acid solution (0:1%): Take 0:1mL of formic acid, add water to dissolve and dilute to 100mL: 15:2:4 Methanol solution: Take 5 mL of methanol and 95 mL of water, and mix well: 15:2:5 Methanol-ethyl acetate: Take 10 mL of methanol and 90 mL of ethyl acetate, and mix well: 15:2:6 Formic acid solution (0:1%)-acetonitrile: Take 90 mL of 0:1% formic acid solution and 10 mL of acetonitrile, and mix well: 15:3 Standard products The contents of tetracycline hydrochloride, chlortetracycline hydrochloride, oxytetracycline hydrochloride, and doxycycline hydrochloride are all ≥95%: See Appendix A for details: 15:4 Preparation of standard solutions 15:4:1 Standard stock solution (100 μg/mL): Take 10 mg of the standard substance, weigh it accurately, add methanol to dissolve it and dilute it to 100 mL volumetric flask, and prepare oxytetracycline, tetracycline, chlortetracycline and doxycycline The standard stock solution with a concentration of 100 μg/mL was used: Store below -18 ℃ away from light, valid for 1 month: 15:4:2 Mixed standard intermediate solution (1:0 μg/mL): Accurately transfer 1 mL of the standard stock solutions of oxytetracycline, tetracycline, chlortetracycline and doxycycline into a 100 mL volumetric flask, dilute to the mark with methanol, and prepare the concentration All are 1:0μg/mL mixed standard intermediate solution: Store below -18 ℃ away from light, valid for 7 days: 15:5 Materials 15:5:1 Solid phase extraction column: 60 mg/3 mL: Oasis HLB or equivalent: 15:5:2 Polypropylene centrifuge tube: 50mL: 15:5:3 Microporous filter membrane: 0:22 μm: 16 Instruments and Equipment 16:1 Liquid chromatography-tandem quadrupole mass spectrometer: equipped with electrospray ion source (ESI): 16:2 Analytical balance: sensitivity 0:01 g: ......

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