Methods for separation and content determination of chlorogenic acid type components in gynura procumbens
A technology of Pingwoju notoginseng and chlorogenic acid, applied in the quantitative determination of neochlorogenic acid and three kinds of isochlorogenic acids, chlorogenic acid in Pingwoju notoginseng extract, determination of Pingwoju notoginseng extract Quality inspection field
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0014] Example 1 Isolation and Identification of Chlorogenic Acids in Pingwo Jusanqi
[0015] 1. Preparation of Pingwoju Sanqi extract sample
[0016] 1.1 Extraction sample preparation Pingbu notoginseng is produced in Guangdong and identified by Mr. Zhang Bingkun of Wuhan Botanical Garden, Chinese Academy of Sciences. Take the dried stem (0.5kg) and crush it, add 5L of 80v / v% ethanol each time, reflux extraction at 85°C for 1h, extract 3 times in total, combine the extracts and concentrate and dry, the extract (density 1.40g / L) yield was 18.5%. Dissolve the extract in 50v / v% methanol (the ratio of extract to 50v / v% methanol is 0.1g: 1mL), and filter it with a 0.45μm microporous membrane for preparation.
[0017] The above experiment was repeated three times, and four batches of extracts were obtained in total, with batch numbers of 2012 / 6 / 14, 2012 / 6 / 20, 2012 / 6 / 21, and 2012 / 9 / 6 for subsequent experiments.
[0018] 1.2 Preparative chromatography and mass spectrometry conditi...
Embodiment 2
[0026] Example 2 The method for determining the content of chlorogenic acid, neochlorogenic acid and three kinds of isochlorogenic acids by external standard method
[0027] 2.1 Analytical chromatographic conditions
[0028] DIONEX UltiMate 3000 high performance liquid chromatograph; DIONEX C18 chromatographic column (250nm×4.6mm, 5μm), mobile phase is acetonitrile (A)-0.1w / v% phosphoric acid aqueous solution (B) (w / v unit is g / mL ), gradient elution: 0-65min, 9%-27%A (v / v%); 65-70min, 27%-9% (v / v%)A; time is 70min, volume flow 1.0mL / min , the injection volume was 10 μL, the detection wavelength was 326 nm, and the column temperature was 30°C.
[0029] 2.2 Solution preparation
[0030] 2.2.1 Sample preparation
[0031] Accurately weigh 100-250mg of the extract in Example 1, add 9mL of 50v / v% methanol to a 10mL volumetric flask, ultrasonicate at 20-40KHz for 15-30min in an ultrasonic instrument, let cool, add 50v / v% methanol to the mark Shake well and pass through a 0.45 μm m...
Embodiment 3 1
[0053] Embodiment 3 One test multiple evaluation method methodological investigation
[0054] 1 Calculation of relative correction factor On the basis of embodiment 2, calculate relative correction factor (f k / s ), calculation formula: f k / s =(C s ×A k ) / (C k ×A s ), the formula for calculating the mass concentration of the component to be tested: C k′ =(C s ×A k′ ) / (f k / s ×A s ), where C s is the concentration of the reference substance, A s is the chromatographic peak area of the reference substance, C k is the mass concentration of other control groups, A k is the peak area of other control chromatographic peaks, C k′ is the mass concentration of the component to be measured, A k′ is the area of the chromatographic peak of the component to be tested, and the results are shown in Table 3.
[0055] Table 3 f with chlorogenic acid as reference k / s (multi-point calibration method)
[0056]
[0057] 2 Inspection of the reproducibility of the correction ...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com