Detection method for detecting agilawood quality by using high-performance liquid chromatography
A technology of high-performance liquid chromatography and a detection method, which is applied in the detection field of high-performance liquid chromatography to determine the quality of agarwood, can solve the problems of low accuracy of detection results, one-sided quality evaluation of agarwood medicinal materials, etc., and achieve prolonged storage time and good accuracy , High detection efficiency
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
preparation example Construction
[0085] ②. Preparation of the mother liquor of the reference substance. Accurately weigh 0.30 mg of agarotetrol, 0.30 mg of 6-hydroxy-2-[2-(4′-methoxy)phenethyl]chromone, and 0.30 mg of 6- Hydroxy-2-(2-phenylethyl)chromone, 0.30mg of 6,7-dimethoxy-2-[2-(4'-methoxy)phenethyl]chromone and 0.30mg of 6 , 7-dimethoxy-2-(2-phenylethyl) chromone, the five chromones, were dissolved in methanol after filtering through a 0.22 μm microporous membrane and degassed, and the volume was adjusted to 5ml, and sealed and stored Store in a refrigerator at 4°C for later use, then take 1ml and mix them to form 1ml of a mixed solution containing 60μg of chromone, and filter through a 0.22μm microporous membrane to obtain the mother solution of the reference substance;
[0086] ③. Sample analysis
[0087] ③-1. Sample pretreatment: Grind agarwood, take an appropriate amount of agarwood powder passed through a 40-mesh sieve, accurately weigh 1.00mg, add 50ml of methanol that has been filtered through ...
Embodiment 2
[0104] The difference from Example 1 is that in step ① of this example, the column temperature is 30°C; the mobile phase flow rate is 0.5ml / min; the linear gradient is:
[0105] 0-15min: 80% of phase A + 20% of phase B;
[0106] 16-30min: 65% of phase A + 35% of phase B;
[0107] 31-80min: 60% phase A + 40% phase B;
[0108] 81-90min: 10% phase A + 90% phase B;
[0109] In step ③ of this embodiment, the amount of methanol added is 30ml, and the extraction time of the agarwood powder by methanol is 0.8h.
Embodiment 3
[0111] The difference from Example 1 is that in this example, in the chromatographic conditions of step ①, the column temperature is 38°C; the mobile phase flow rate is 1.0ml / min; the linear gradient is:
[0112] 0-15min: 82% of phase A + 18% of phase B;
[0113] 16-30min: 70% of phase A + 30% of phase B;
[0114] 31-80min: 65% of phase A + 35% of phase B;
[0115] 81-90min: 10% phase A + 90% phase B;
[0116] In step ③ of this embodiment, the amount of methanol added is 60ml, and the extraction time of the agarwood powder by methanol is 1.2h.
[0117] 2.4, Embodiment 4
[0118] The difference from Example 1 is that in this example, in the chromatographic conditions of step ①, the column temperature is 35°C; the mobile phase flow rate is 0.8ml / min; the linear gradient is:
[0119] 0-15min: 85% of phase A + 15% of phase B;
[0120] 16-30min: 65% of phase A + 35% of phase B;
[0121] 31-80min: 65% of phase A + 35% of phase B;
[0122] 81-90min: 10% phase A + 90% phase B; ...
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