GB/T 38086-2019 in English
VALIDDetermination of metallothionein (MT) in biological samples
- Issued on:2019-10-18
- Implemented on:2019-10-18
- File Format:PDF
- Delivery:Via email within 1~3 business days
$175.00
《GB/T 38086-2019生物样品中金属硫蛋白含量的测定》由TC387(全国生化检测标准化技术委员会)归口,主管部门为国家标准化管理委员会。
Introduction
1. Standard Overview
GB/T 38086-2019 specifies the method for determining the content of rabbit metallothionein (MT-I and MT-Ⅱ) in biological samples using liquid chromatography-tandem mass spectrometry. This method is suitable for the detection of metallothionein in biological preparations or extracts, with a detection limit of 6.2~mg/kg.
2. Technical Interpretation and Implementation Guide
| Project | MT-I | MT-Ⅱ | Detection Method |
|---|---|---|---|
| Scope of Application | MT-I from Rabbit in Biological Samples | MT-Ⅱ from Rabbit in Biological Samples | Liquid Chromatography-Tandem Mass Spectrometry |
| Detection Limit | 6.2~mg/kg | 6.2~mg/kg | LC-MS/MS |
| Standard curve | The peak area of the characteristic peptide is proportional to the concentration | The peak area of the characteristic peptide is proportional to the concentration | Linear regression analysis |
2.1 Selection and synthesis of characteristic peptides
The characteristic peptide CAQGCICK (labeled as LCAM) was used to detect MT-I and MT-II. The relative molecular mass of the peptide is 995, the purity is over 95%, and the appearance is white powder.
2.2 Quantitative and qualitative analysis
The parent ion m/z 498.7 and the daughter ion m/z 637.3 were selected for quantification by liquid chromatography and tandem mass spectrometry. The qualitative judgment was based on the maximum allowable deviation of retention time and relative ion abundance (Table 1).
| Relative ion abundance | >50% | >20%~50% | >10%~20% | ≤10% |
|---|---|---|---|---|
| Maximum allowable deviation | ±20% | ±25% | ±30% | ±50% |
3. Implementation Suggestions
To ensure the effective implementation of the standard, it is recommended that:
- Use reagents and instruments that meet the requirements.
- Strictly follow the enzymatic hydrolysis and sample preparation steps.
- Regularly calibrate the instrument and perform blank tests to verify the accuracy of the method.
- Ensure the recovery rate is within the range of 80%~120% in the spike recovery test.

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