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animal origin lc-ms/ms method applicable matrix livestock lc-ms/ms method animal fat export introduction technical evolution hydrodynamic sliding bearings gear reducer scopethis standard ammonium salts
SN/T 5140-2019 in English

SN/T 5140-2019 in English

VALID

Determination of sulfonamides residues in foodstuffs of animal origin for export

  • Issued on:2019-10-25
  • Implemented on:2020-05-01
  • File Format:PDF
  • Delivery:Via email within 5 business days
Price(USD): $540.00
$524.00
Standard No: SN/T 5140-2019
Document status: VALID
Title in English: Determination of sulfonamides residues in foodstuffs of animal origin for export
Title in Chinese: 出口动物源食品中磺胺类药物残留量的测定
Language: English
File Format: Electronic (PDF)
Delivery: Via email within 5 business days
Issued on: 2019-10-25
Implemented on: 2020-05-01
Superseding: SN 0498-1995 Method for the determination of sulfadimethoxine residues in meat for export
SN/T 1965-2007 Determination of sulfonamides residues in eels and eel products - High performance liquid chromatographic method
SN/T 2580-2010 Determination of Sixteen Sulfonamides Residues in Royal Jelly for Import and Export - HPLC-MS/MS
Professional Classification: SN-Import&Export Inspection
Related Keywords: animal origin
lc-ms/ms method applicable matrix livestock
lc-ms/ms method
animal fat
export introduction technical evolution
Related Topics: animal source
drug residue
drug in english
export medicine
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Introduction

Technical evolution and background of standards

This standard integrates and replaces the three old standards SN 0498-1995, SN/T 1965-2007 and SN/T 2580-2010. The main technical improvements include:

  • Detection range expansion: HPLC method adds livestock and poultry muscle matrix and 9 sulfonamide drugs (sulfathiazole, sulfapyridine, etc.)
  • Method upgrade: LC-MS/MS method adds honey/fat matrix and 2 drugs sulfacetamide and sulfachloropyridine
  • Technology integration: unified pretreatment methods for different matrices, optimized chromatographic separation conditions

Comparison of core detection methods

Dimensions HPLC method LC-MS/MS method
Applicable matrix Livestock and poultry muscle, aquatic products Muscle/liver/fat/egg/milk/honey/royal jelly
Detection drugs 17 kinds 19 kinds (sulfacetamide and sulfachloropyridine were newly added)
Detection limit (μg/kg) 10 2.0 (bee products 5.0)
Quantification method External standard method Isotope internal standard method

Key operating points

Pretreatment process optimization

HPLC method adopts ethyl acetate extraction → n-hexane defatting → MCX column purification; LC-MS/MS method adds a trichloroacetic acid solution extraction step to the fat matrix, and the royal jelly needs to be purified twice by C18 column.

Instrument parameter setting

  • HPLC conditions: C18 column (4.6×250mm, 5μm), gradient elution (methanol/0.3% acetic acid-2mM ammonium acetate), detection wavelength 268nm
  • LC-MS/MS conditions: ESI positive ion mode, multiple reaction monitoring (MRM), see Appendix D for specific collision energy

Implementation suggestions

  1. For high-fat samples (such as animal fat), it is recommended to use the LC-MS/MS method to ensure the recovery rate (85-115%)
  2. When detecting bee products, special attention should be paid to the matrix effect, and the use of isotope internal standard compensation is recommended
  3. Regularly verify the performance of the solid phase extraction column, and the methanol activation volume should be no less than 5mL

Technical indicator verification

Typical recovery data (pork matrix):

  • Sulfadiazine: 75.4-90.0% (10μg/kg spike level)
  • Sulfadimethoxine: 91.2-116.3% (20μg/kg)
  • Sulfaquinoxaline: 89.5-114.3% (200μg/kg)

Sample only — not a preview of SN/T 5140-2019
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