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GB 5009.118-2016

Chinese Standard: 'GB 5009.118-2016'
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BASIC DATA
Standard ID GB 5009.118-2016 (GB5009.118-2016)
Description (Translated English) Determination of T-2 toxin in cereals
Sector / Industry National Standard
Classification of Chinese Standard X09
Word Count Estimation 14,131
Date of Issue 2016-12-23
Date of Implementation 2017-06-23
Older Standard (superseded by this standard) GB/T 23501-2009; GB/T 5009.118-2008; SN/T 1771-2006; SN/T 2676-2010
Regulation (derived from) National Health and Family Planning Commission Notice No.17 of 2016
Issuing agency(ies) National Health and Family Planning Commission of the People's Republic of China, State Food and Drug Administration

GB 5009.118-2016
NATIONAL STANDARD OF THE
PEOPLE’S REPUBLIC OF CHINA
National Food Safety Standard -
Determination of T-2 toxin in foods
食品安全国家标准
食品中 T-2毒素的测定
ISSUED ON: DECEMBER 23, 2016
IMPLEMENTED ON: JUNE 23, 2017
Issued by: National Health and Family Planning Commission of the PRC;
China Food and Drug Administration.
Table of Contents
Foreword ... 4
1 Scope ... 5
2 Principle ... 5
3 Reagents and materials ... 5
4 Instruments and apparatuses ... 6
5 Analysis steps ... 7
6 Precision ... 10
7 Precision ... 10
8 Principle ... 10
9 Reagents and materials ... 10
10 Instruments and apparatuses ... 12
11 Analysis steps ... 12
12 Description of the analysis result ... 13
13 Precision ... 14
14 Others ... 14
15 Principles and basis ... 14
16 Reagents and materials ... 15
17 Instruments and apparatuses ... 16
18 Analysis steps ... 17
19 Description of the analysis result ... 18
20 Precision ... 19
21 Others ... 20
Appendix A Liquid chromatogram of T-2 toxin standard substance ... 21
National Food Safety Standard -
Determination of T-2 Toxin in Foods
1 Scope
This Standard specifies methods for the determination of T-2 toxin in foods.
Method 1 of this Standard is applicable to the determination of T-2 toxin content in
food and food products, alcohol, soy sauce, vinegar, sauce and sauce products.
Method 2 and Method 3 are applicable to the determination of T-2 toxin in food and
food products.
Method 1 - Immunoaffinity chromatography purification
liquid chromatography
2 Principle
Use extract to extract T-2 toxin in the sample; after it is purified and derived by the
immunoaffinity column, use high-performance liquid chromatography fluorescence
detector to measure, and use external standard method to quantify.
3 Reagents and materials
Unless otherwise specified, all the reagents in this method are analytical reagents, the
water is grade-1 water that is specified by GB/T 6682.
3.1 Reagents
3.1.1 Methanol (CH3OH): chromatographic pure.
3.1.2 Acetonitrile (CH3CH): chromatographic pure.
3.1.3 Toluene (C6H5CH3): chromatographic pure.
3.1.4 4-dimethylaminopyridine.
3.1.5 1-anthroylnitrile,1-AN.
3.2 Preparation of reagents
4.7 Air pressure pump.
4.8 Test sieve: aperture of 1.0 mm.
4.9 Balance: sensitivity of 0.000 1 g and 0.01 g.
4.10 Ultrasonic generator: power > 180 W.
4.11 Glass syringe: 10 mL.
5 Analysis steps
5.1 Extraction
5.1.1 Food and food products
Grind the sample; for hard food or the like, use a high-speed pulverizer to grind well,
and use a test sieve to filter. Weigh 25.0 g (accurate to 0.1g) of sieved sample in a
volumetric flask; use extract to fix-volume to 100 mL; transfer it to a homogenizing cup;
use a homogenizer to stir and extract at high speed for 2 min; use a quantitative filter
paper to filter it. Pipette 10.0 mL of the filtrate into 40 mL of water; dilute and mix; use
a glass-fiber filter paper to filter it until the filtrate is clarified; reserve the filtrate for later
use.
5.1.2 Soy sauce, vinegar, sauce and sauce products
Weigh 25.0 g (accurate to 0.1 g) of the mixed sample; use methanol to fix-volume to
50.0 mL; ultrasonically extract it for 10 min; use quantitative filter paper to filter. Pipette
10.0 mL of the filtrate into 40 mL of water; dilute and mix; use a glass-fiber filter paper
to filter it until the filtrate is clarified; reserve the filtrate for later use.
5.1.3 Alcohol
Take 20.0 g (accurate to 0.1 g) of degassed alcohol samples (alcohols which contain
carbon dioxide, before using, shall be placed in a refrigerator at 4°C for 30 min, and
filtered or ultrasonically degassed) or other alcohol samples which do not contain
carbon dioxide in a 50 mL volumetric flask; use methanol to fix-volume to the scale;
shake well; use quantitative filter paper to filter. Pipette 10.0 mL of the filtrate into 40
mL of water; dilute; use a glass-fiber filter paper to filter it until the filtrate is clarified;
reserve the filtrate for later use.
5.2 Purification and elution
Connect the immunoaffinity column to a glass syringe; accurately transfer and inject
10 mL of filtrate which is extracted in 5.1 into the glass syringe. Connect the air
pressure pump to the glass syringe; adjust the pressure, so that the solution slowly
Where:
y -- the peak area ratio of the target substance;
a -- the slope of the regression curve;
x -- the concentration of the target substance;
b -- the intercept of the regression curve.
The response values of the test substance in both the standard working solution and
the sample solution shall be within the linear response range of the instrument; if the
sample content exceeds the standard curve range, it needs be diluted before
measurement.
5.5 Blank test
Do not weigh the sample; do a blank test according to the steps of 5.1, 5.2 and 5.3. It
shall be confirmed that it does not contain any substance that interferes with the to-
be-test component.
5.6 Result calculation
Calculate the content of T-2 toxin in the sample according to Formula (2):
Where:
X -- the content of T-2 toxin in the sample, in micrograms per kilogram (μg/kg);
ρ -- the concentration of T-2 toxin in the sample solution, in nanograms per milliliter
(ng/mL);
V -- the constant volume after derivatization, in milliliters (mL);
1 000 -- unit conversion coefficient;
m -- the weighing sample, in grams (g);
f -- dilution ratio.
Note: The calculation result needs to be deducted from the blank value, and retain two
significant figures.
9.1.5 Ethyl acetate (C4H8O2).
9.1.6 Dimethylformamide (C3H7NO).
9.1.7 Tetramethylbenzidine (TMB).
9.1.8 Tween-20 (C58H114O26).
9.1.9 30% hydrogen peroxide (30% H2O2).
9.1.10 Sodium carbonate (Na2CO3).
9.1.11 Sodium bicarbonate (NaHCO3).
9.1.12 Monopotassium phosphate (KH2PO4).
9.1.13 Disodium hydrogen phosphate (Na2HPO4·12H2O).
9.1.14 Sodium chloride (NaCl)
9.1.15 Potassium chloride (KCl).
9.1.16 Citric acid (C6H8O7·H2O).
9.1.17 Antibody: a specific monoclonal antibody against T-2 toxin that is produced by
hybridoma cell lines.
9.1.18 Antigen: conjugate of T-2 toxin and carrier protein-bovine serum albumin (BSA).
9.1.19 Conjugate of rabbit anti-mouse immunoglobulin and horseradish peroxidase
(enzyme-labeled secondary antibody).
9.2 Preparation of reagents
9.2.1 ELISA buffer system.
9.2.1.1 The coating buffer is carbonate buffer of pH 9.6. Weigh 1.59 g of sodium
carbonate, 2.93 g of sodium bicarbonate; add water to dilute to 1 000 mL.
9.2.1.2 The washing solution is a phosphate buffer (PBS-T for short) of pH 7.4, which
contains 0.05% of Tween-20. The preparation method is as follows: weigh 0.2 g of
monopotassium phosphate, 2.9 g of disodium hydrogen phosphate, 8.0 g of sodium
chloride, 0.2 g of potassium chloride, 0.5 mL of Tween-20; add water to 1 000 mL.
9.2.1.3 The substrate buffer is a phosphoric acid-citric acid buffer of pH 5.0. The
preparation method is: 0.1 mol/L of citric acid, that is, weigh 19.2 g of citric acid; add
water to 1 000 mL, which is liquid A; AND, 0.2 mol/L of disodium hydrogen phosphate,
that is, weigh 71.7 g of disodium hydrogen phosphate; add water to 1 000 mL, which
is liquid B. Take 24.3 mL of liquid A and 25.7 mL of liquid B; add water to 100 mL.
Weigh 20.0 g of sample which is pulverized and passed through a 20-mesh sieve;
place it in a 200 mL stoppered conical flask; add 8 mL of water and 100 mL of
trichloromethane-absolute ethanol (4:1, volume ratio); stuff up the stopper; shake for
1 h; filter it through a filter paper; take 25 mL of filtrate in an evaporating dish; place it
on a water bath at 90°C to volatilize it. Use 50 mL of petroleum ether, in several times,
to dissolve the residue in the evaporating dish; wash it into a 250 mL separatory funnel;
use 20 mL of methanol-water (4:1) to wash it for several times; transfer to the same
separatory funnel; shake for 1.5 min; let stand for 15 min; collect the lower methanol-
water extract; purify it through the chromatography column.
Pour the eluent which passes the column into the evaporating dish; concentrate it to
dryness in the water bath; add 3 mL of ethyl acetate while hot; heat to boiling; dry it;
repeat again; lastly, add 3 mL of ethyl acetate; after it becomes as cool as the room
temperature, transfer it to the flask. Use an appropriate amount of ethyl acetate to
wash the evaporating dish; incorporate it into a flask; place the flask in a 95°C water
bath; after it becomes dry and cool, use PBS of 20% methanol to fix-volume, which is
used for later ELISA test.
11.2 Test
11.2.1 Use T-2-BSA (4 μg/mL) to coat the enzyme-labeled plate, with 100 μL per well;
let it stand overnight at 4°C.
11.2.2 Use PBS-T to wash the enzyme-labeled plate 3 times; for each time, after 3
minutes, add standard working solution of different concentrations (to make the
standard curve) or mixture of sample extract (to test the toxin content in sample) and
antibody solution (1:1, volume ratio; 100 μL per well; the mixture shall be prepared the
day before use and placed overnight at 4°C); let stand at 37°C for 1 h.
11.2.3 Wash the enzyme-labeled plate 3 times; for each time, after 3 min, add enzyme-
labeled secondary antibody, 100 μL per well, at 37°C for 1.5 h.
11.2.4 After the same washing with the above, add the substrate solution, 100 μL per
well, at 37°C for 30 min.
11.2.5 Use 1 mol/L sulfuric acid solution to stop the reaction, 50 μL per well; measure
the absorbance at 450 nm.
12 Description of the analysis result
Calculate the content of T-2 toxin in the sample according to Formula (3):
add the reaction substrate; use the enzyme-labeled instrument to measure the
absorbance; obtain T-2 toxin content in the sample according to the absorbance value.
16 Reagents and materials 
Unless otherwise specified, all the reagents in this method are analytical reagents, the
water is grade-1 water that is specified by GB/T 6682.
16.1 Reagents
16.1.1 Methanol (CH3OH).
16.1.2 Petroleum ether (C7H7BrMg).
16.1.3 Trichloromethane (CHCl3).
16.1.4 Absolute ethanol (C2H5OH).
16.1.5 Ethyl acetate (C4H8O2).
16.1.6 Dimethylformamide (C3H7NO).
16.1.7 Tetramethylbenzidine (TMB).
16.1.8 Tween-20 (C58H114O26).
16.1.9 30% hydrogen peroxide (30% H2O2).
16.1.10 Conjugate of anti-T-2 toxin monoclonal antibody and horseradish peroxidase.
16.1.11 Antigen: conjugate of T-2 toxin and carrier protein-bovine serum albumin (T-
2-BSA).
16.2 Preparation of reagents
16.2.1 ELISA buffer system.
16.2.1.1 The coating buffer is carbonate buffer of pH 9.6. Weigh 1.59 g of sodium
carbonate (Na2CO3), 2.93 g of sodium bicarbonate (NaHCO3); add water to dilute to 1
000 mL.
16.2.1.2 The washing solution is a phosphate buffer (PBS-T for short) of pH 7.4, which
contains 0.05% of Tween-20. The preparation method is as follows: weigh 0.2 g of
monopotassium phosphate, 2.9 g of disodium hydrogen phosphate, 8.0 g of sodium
chloride, 0.2 g of potassium chloride, 0.5 mL of Tween-20; add water to 1 000 mL.
16.2.1.3 Sample diluent: phosphate buffer (PBS for short) of pH 7.2. The preparation
method is as follows: weigh 0.55 g of sodium dihydrogen phosphate (NaH2PO4·H2O),
17.5 Balance: sensitivity of 0.000 1 g, 0.01 g.
17.6 Homogenizer.
17.7 Pulverizer.
18 Analysis steps
18.1 Extraction
18.1.1 Direct ELISA 1
Weigh 20 g of sample which is pulverized and passed through a 20-mesh sieve; place
it in a 200 mL stoppered conical flask; add 8 mL of water and 100 mL of
trichloromethane-absolute ethanol (4:1, volume ratio); stuff up the stopper; shake for
1 h; filter it through a filter paper; take 25 mL of filtrate in an evaporating dish; place it
on a water bath at 90°C to volatilize it. Use 50 mL of petroleum ether, in several times,
to dissolve the residue in the evaporating dish; wash it into a 250 mL separatory funnel;
use 20 mL of methanol-water (4:1, volume ratio) to wash it for several times; transfer
to the same separatory funnel; shake for 1.5 min; let stand for 15 min; collect the lower
methanol-water extract; purify it through the chromatography column.
Pour the eluent which passes the column into the evaporating dish; concentrate it to
dryness in the water bath; add 3 mL of ethyl acetate while hot; heat to boiling; dry it;
repeat again; lastly, add 3 mL of ethyl acetate; after it becomes as cool as the room
temperature, transfer it to the flask. Use an appropriate amount of ethyl acetate to
wash the evaporating dish; incorporate it into a flask; place the flask in a 95°C water
bath; after it becomes dry and cool, use PBS of 20% methanol to fix-volume, which is
used for later ELISA test.
18.1.2 Direct ELISA 2
Use the method of quartering to reduce the sample to 1 kg; grind all of them into
particles of which the size can pass through the 20-mesh sieve; mix well; evenly divide
them into two portions as samples; respectively place them into clean containers and
seal. Weigh 25.0 g of the sample (accurate to 0.1 g); add 125 mL of methanol-water
(7:3, volume ratio); homogenize for 1 min ~ 2 min; centrifuge at 5 000 r/min for 10 min.
After centrifugation, add 50 μL of the filtrate to 300 μL of the sample dilution; mix. Take
50 μL for enzyme-linked immunoassay; the final dilution factor is 35. For high-
concentration samples, if the toxin content is beyo......
Related standard:   GB 5009.111-2016  GB 5009.138-2017
Related PDF sample:   GB 5009.121-2016  GB 5009.124-2016
   
 
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