GB/T 23504-2009 PDF in English
GB/T 23504-2009 (GB/T23504-2009, GBT 23504-2009, GBT23504-2009)
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| GB/T 23504-2009 | English | 90 |
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Determination of zearalenone in food -- High performance liquid chromatographic method with immunoaffinity column clean-up
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Standards related to (historical): GB/T 23504-2009
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GB/T 23504-2009: PDF in English (GBT 23504-2009) GB/T 23504-2009
GB
NATIONAL STANDARD
OF THE PEOPLE’S REPUBLIC OF CHINA
ICS 67.050
X 04
Determination of zearalenone in food - High
performance liquid chromatographic method with
immunoaffinity column clean-up
ISSUED ON. APRIL 08, 2009
IMPLEMENTED ON. MAY 01, 2009
Issued by. General Administration of Quality Supervision, Inspection and
Quarantine of the People's Republic of China;
Standardization Administration of the PRC.
Table of contents
Foreword ... 3
1 Scope ... 4
2 Normative references ... 4
3 Method summary ... 4
4 Reagents and materials ... 5
5 Instruments and equipment ... 5
6 Analysis procedures ... 6
7 Result calculation ... 8
8 Recovery ... 8
9 Repeatability ... 8
Appendix A (Informative) Liquid chromatogram of zearalenone standard ... 9
Foreword
Appendix A of this standard is an informative appendix.
This standard was proposed by the National Food Industry Standardization
Technical Committee (SAC/TC 64).
This standard shall be under the jurisdiction of the National Food Industry
Standardization Technical Committee Food General Detection Technology
Technical Committee Branch (SAC/TC 64 /SC 8)
The drafting organizations of this standard. Qingdao Product Quality
Supervision and Inspection Institute, the People's Republic of China Shandong
Entry-Exit Inspection and Quarantine Bureau, Clover Technology Group Inc.,
Tsingtao Brewery Co., Ltd.
The main drafters of this standard. Zhang Huizhen, Dong Jianjun, Lv Ning, Li
Hongwei, Li Huiying, Zhai Shixing, Wang Xiong.
Determination of zearalenone in food - High
performance liquid chromatographic method with
immunoaffinity column clean-up
1 Scope
This standard specifies the method for the determination of zearalenone in
foods by high performance liquid chromatographic method with immunoaffinity
column clean-up.
This standard is applicable to the determination of zearalenone in food and
grain products, alcohol, soy sauce, vinegar, sauce and sauces.
The limit of detection of this method is 20 μg/kg for food and grain products; 20
μg/kg for alcohol; AND 50 μg/kg for soy sauce, vinegar, sauce and sauces.
2 Normative references
The provisions in following documents become the provisions of this Standard
through reference in this Standard. For the dated references, the subsequent
amendments (excluding corrections) or revisions do not apply to this Standard;
however, parties who reach an agreement based on this Standard are
encouraged to study if the latest versions of these documents are applicable.
For undated references, the latest edition of the referenced document applies.
GB/T 6682 Water for analytical laboratory use - Specification and test methods
(GB/T 6682-2008, ISO 3696.1987, MOD)
3 Method summary
USE the extraction solution to extract the zearalenone from the test specimen;
after making it be purified by immunoaffinity column, USE the high performance
chromatography fluorescence detector to determine it and the external
standard method to quantify it.
5.5 Glass syringe. 10 mL.
5.6 Test screen. 1 mm aperture.
5.7 Air pressure pump.
6 Analysis procedures
6.1 Sample preparation and extraction
6.1.1 Food and grain products. GRIND samples; USE high-speed universal mill
to grind the hard grain and MAKE it pass the test sieve (5.6); DO not grind it
into powder. WEIGH 50 g of ground test specimen (accurate to 0.01 g) and
PLACE it into a 100 mL volumetric flask; ADD 5 g of sodium chloride; USE the
extraction solution (4.3) to make its volume reach to the mark; MIX it uniformly;
TRANSFER it into a homogeneous cup; MAKE it subjected to high-speed
stirring and extraction for 2 min. USE the quantitative filter paper to filter it;
TRANSFER 10.0 mL of filtrate into a 50 mL volumetric flask; ADD water to make
its volume reach to the mark; MIX it uniformly; USE glass fiber filter paper to
the filter it until the filtrate is clean; COLLECT the filtrate A into a clean container.
6.1.2 Alcohols. TAKE 20 g of alcohol samples (the alcohol containing carbon
dioxide is refrigerated at 4 °C for 30 min, filtered or degassed ultrasonically prior
to use) or other alcohol samples containing no carbon dioxide (accurate to 0.01
g) into a 50 mL volumetric flask; USE acetonitrile to make its volume reach to
the mark; SHAKE it uniformly; TRANSFER 10.0 mL of filtrate into a 50 mL
volumetric flask; ADD water to make the volume reach to the mark; MIX it
uniformly; USE glass fiber filter to filter it until the filtrate is clean; COLLECT the
filtrate B into a clean container.
6.1.3 Soy sauce, vinegar, sauce and sauce products. WEIGH 25 g (accurate to
0.01 g) of uniformly mixed test specimen; USE acetonitrile to make the volume
reach to 100.0 mL; MAKE it subjected to ultrasonic extraction for 2 min; USE
the quantitative filter paper to filter it; TRANSFER 10.0 mL of filtrate into a 50
mL volumetric flask; ADD water to make the volume reach to the mark; MIX it
uniformly; USE glass fiber filter to filter it until the filtrate is clean; COLLECT the
filtrate C into a clean container.
6.2 Purification
CONNECT the immunoaffinity column to under the glass syringe (5.5);
accurately PIPETTE 10.0 mL of the filtrate A or B or C as mentioned in 6.1 into
the glass syringe. CONNECT the air pressure pump to the glass syringe;
ADJUST the pressure so that the solution can pass through the immunoaffinity
......
Source: Above contents are excerpted from the PDF -- translated/reviewed by: www.chinesestandard.net / Wayne Zheng et al.
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