SN/T 4744-2017 in English
VALIDDetermination of sexhormone residues of live animal for import and export一HPLC-MS/MS
- Issued on:2017-05-12
- Implemented on:2017-12-01
- File Format:PDF
- Delivery:Via email within 1~3 business days
$243.00
Introduction
Overview of detection method
This standard adopts high performance liquid chromatography-tandem mass spectrometry and solid phase extraction pretreatment technology to conduct qualitative and quantitative analysis of sex hormone residues in animal tissues. The main steps include:
Key instrument parameters
| Chromatographic column type | Mobile phase composition | Mass spectrometry mode | Detection limit (μg/kg) |
|---|---|---|---|
| C18 column (1.7μm) | Methanol-acetonitrile gradient | MRM | 0.5 |
| NH2 column | Ammonium acetate buffer | ESI+/- | 1.0 |
Technology evolution analysis
Compared to the traditional GC-MS method, the HPLC-MS/MS technology in this standard:
- Increases detection sensitivity by 10 times
- Shortens pre-treatment time by 40%
- Can simultaneously detect steroidal and estrogen compounds
Actual application case
A beef exporting company used this standard for testing and found that the residues of methyltestosterone in two batches of samples were 1.2μg/kg and 0.8μg/kg, respectively. After optimizing the feed formula, the detection values in subsequent batches dropped to below 0.3μg/kg.
Implementation Recommendations
- Laboratories should regularly verify the stability of the method using isotope internal standards such as testosterone-D3.
- For high-fat samples, it is recommended to add a frozen centrifugation step.
- Mass spectrometry parameters need to be fine-tuned according to the instrument model.

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