SN/T 5362-2021 in English
VALIDDetermination of the Sulfoxaflor residues in foods for export
- Issued on:2021-11-22
- Implemented on:2022-06-01
- File Format:PDF
- Delivery:Via email within 1~3 business days
$272.00
Introduction
Analysis of the core content of the standard
This standard specifies two detection technologies: liquid chromatography-mass spectrometry/mass spectrometer and high performance liquid chromatography. It is applicable to the analysis of sulfoxaflor residues in 13 types of food matrices. The lower limit of determination of the method is 0.005 mg/kg.
Comparative Analysis of Methods
| Dimensions | LC-MS/MS Method | HPLC Method |
|---|---|---|
| Detection Principle | Multiple Reaction Monitoring (MRM) Mode | UV Detection (264nm) |
| Sensitivity | 0.1μg/L(S/N Ratio≥10) | 0.5μg/L |
| Anti-interference Ability | Triple Quadrupole Mass Spectrometry Confirmation | Depends on Purification Effect |
| Operating Cost | Higher | Economical |
Key Technical Points
Sample Pretreatment Optimization
Differentiated cleanup schemes are used for different matrices:
1. High pigment samples (pepper/cucumber): Increase the amount of graphitized carbon black to 50mg
2. High protein samples (meat/liver): Use C18+PSA combination cleanup
Mass spectrometry parameter settings
It is recommended to use m/z 278.1→174.1 as the quantitative ion pair, collision energy 11eV, source temperature 550℃. Note that formic acid additives will enhance the positive ion mode response.
Implementation recommendations
- For complex matrices (such as honey), it is recommended to use a matrix matching standard curve to eliminate matrix effects
- Regularly verify the performance of the chromatographic column, and the column temperature of the C18 column should be controlled at 30±2℃
- The method validation should cover the MRL value specified in GB 2763-2019 (0.02-3mg/kg)

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