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praziquantel residue % purity praziquantel standard feed samples export- -lc-ms/ms method introduction technical background live animals analysis comparison conditions technical data package optical sending components
SN/T 5111-2019 in English

SN/T 5111-2019 in English

VALID

Determination of praziquantel residue in live animals and feed for import and export- -LC-MS/MS method

  • Issued on:2019-09-03
  • Implemented on:2020-03-01
  • File Format:PDF
  • Delivery:Via email within 1~3 business days
Price(USD): $150.00
$146.00
Standard No: SN/T 5111-2019
Document status: VALID
Title in English: Determination of praziquantel residue in live animals and feed for import and export- -LC-MS/MS method
Title in Chinese: 进出口食用动物、饲料吡喹酮药物残留测定 液相色谱-质谱/质谱法
Language: English
File Format: Electronic (PDF)
Delivery: Via email within 1~3 business days
Issued on: 2019-09-03
Implemented on: 2020-03-01
Professional Classification: SN-Import&Export Inspection
Related Keywords: praziquantel residue
% purity praziquantel standard
feed samples
export- -lc-ms/ms method introduction technical background
live animals
Related Topics: liquid chromatography mass spectrometry
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food animals
drug residue
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Introduction

Technical background of the standard

This standard is formulated to address the residual risk of Praziquantel in food animals and feed. As a broad-spectrum antiparasitic drug, its residues may threaten human health through the food chain. The General Administration of Customs issued this standard in 2019, filling the gap in my country's detection technology in this field.


Core parameters of the method

Technical elements Parameter requirements International comparison
Limit of detection (LOD) 0.25μg/kg EU standard 0.5μg/kg
Limit of quantification (LOQ) 1μg/kg Codex 1μg/kg
Recovery range 76%-99% Meet CAC/GL 71 requirements

Key Operation Flow

Sample Pretreatment

Use HLB solid phase extraction column (500mg/6mL) for purification, extract with 4:1 acetonitrile-water mixed solution, filter through 0.22μm filter membrane and inject. Typical cases show that muscle tissue samples need to be homogenized and accurately weighed 2.00±0.01g.

Chromatographic Conditions

Use C18 chromatographic column (150×2.0mm,5μm), gradient elution procedure see standard Appendix B, column temperature maintained at 30℃, flow rate 0.3mL/min.


Optimization of mass spectrometry parameters

The ESI+ ion source was used to monitor the parent ions m/z 313→203 (quantitative ion) and 313→83 (qualitative ion), with collision energies of 14V and 24V, respectively. In actual applications, it was found that the best response was obtained when the source temperature was 550℃.


Implementation suggestions

  1. The laboratory needs to regularly verify the sensitivity of the mass spectrometer to ensure that it meets the requirements for low-concentration detection
  2. It is recommended to verify the extraction efficiency of different matrix samples, and special attention should be paid to lipid interference in feed samples
  3. The standard solution should be prepared using a ≥98% purity praziquantel standard (CAS: 55268-74-1)

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