GB/T 40643-2021 in English
VALIDDetermination of hyperoside in extract of crataegus pinnatifida leaf—HPLC
- Issued on:2021-10-11
- Implemented on:2022-05-01
- File Format:PDF
- Delivery:Via email within 1~3 business days
$97.00
《GB/T 40643-2021山楂叶提取物中金丝桃苷的检测 高效液相色谱法》由TC558(全国林化产品标准化技术委员会)归口,主管部门为国家林业和草原局。
Introduction
Technical background and scope of application of the standard
This standard was proposed by the State Forestry and Grassland Administration and is under the jurisdiction of the National Forest Products Standardization Technical Committee. It specifies the method for determining the content of hyperoside in hawthorn leaf extract using high performance liquid chromatography. As a flavonoid active ingredient, the content of hyperoside directly affects the quality evaluation of Chinese medicinal materials.
Core Detection Principle
| Technical Elements | Parameter Requirements | Scientific Basis |
|---|---|---|
| Separation Principle | Reversed Phase C18 Column Gradient Elution | Based on the Polarity Characteristics of Hyperoside |
| Detection Wavelength | 360nm | Maximum Ultraviolet Absorption Peak |
| Quantitative Method | External Standard Method | Standard Product ≥98% Purity |
Key Instrument and Reagent Specifications
High performance liquid chromatograph must be equipped with UV detector and gradient elution function, and the chromatographic column specification clearly requires a 250mm×4.6mm C18 column. Reagents emphasize:
- Methanol must be chromatographically pure
- Experimental water meets GB/T6682 first-level standard
- Standard purity≥98%
Operation process quality control points
Sample processing should pay attention to: Ultrasonic extraction time is 10-30 minutes, and room temperature must be restored before constant volume. The mobile phase in the chromatographic conditions is a gradient mixture of 0.5% glacial acetic acid aqueous solution and methanol. The specific elution procedure is shown in Standard Table 1.
Method validation requirements: Linear range 0.02-1.0mg/mL, RSD<5%, spike recovery rate 90-110%.
Implementation suggestions and common problems
1. The standard solution should be prepared before use and stored away from light
2. The filter membrane should be 0.45μm organic phase filter
3. When the sample concentration exceeds the linear range, the extraction quality should be adjusted or diluted

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