Method for determining content of triterpenoid saponin component in sapindus mukurossi
A technology for sapindus saponin and determination method, which is applied in the field of content determination of sapindus triterpenoid saponins, can solve problems such as surface activity, poor foaming property, uneven quality of raw materials, inability to effectively control quality, etc., and achieves short running time. , good resolution, high response value and high sensitivity
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0041] Determination method and results of Rarasaponin III, a triterpenoid saponin in Sapindus chinensis
[0042] 1.1. Drawing the standard curve: Accurately weigh an appropriate amount of Rarasaponin III reference substance, put it in a 10mL volumetric flask, dissolve it ultrasonically with 6mL methanol, constant volume, shake well, filter with a 0.45μm microporous membrane, take the subsequent filtrate, and dilute into a series of standards Working solutions: 69.80 μg / mL, 87.25 μg / mL, 174.5 μg / mL, 349.0 μg / mL, 698.0 μg / mL, 872.5 μg / mL. According to 1.3 chromatographic conditions sample injection analysis, obtain RarasaponinIII standard substance high performance liquid chromatogram (see figure 1 ); With the logarithm of peak area (A) as ordinate, the logarithm of concentration (C) as abscissa, carry out linear regression, regression equation is lnA=1.6937lnC-7.096(R 2=0.9984) (see Image 6 ).
[0043] 1.2. Preparation of the solution of the sample to be tested: Take the S...
Embodiment 2
[0049] Determination method and result of sapinmusaponion M content
[0050] 1.1. Drawing the standard curve: Accurately weigh about 10 mg of the Sapinmusaponion M reference substance, put it in a 10 mL volumetric flask, dissolve it with 6 mL of methanol sonication, constant volume, and shake well to make a solution containing 1000 μg per 1 mL, and use a 0.45 μm microporous filter membrane Filter, take the filtrate, and dilute into a series of standard working solutions: 50μg / mL, 62.5μg / mL, 125μg / mL, 250μg / mL, 500μg / mL, 625μg / mL. According to 1.3 chromatographic conditions sample injection analysis, obtain Sapinmusaponion M standard substance high performance liquid chromatogram (see figure 2 ); take the logarithm of peak area (A) as ordinate, and the logarithm of concentration (C) as abscissa, carry out linear regression, regression equation is lnA=1.6846lnC-6.3988(R 2 =0.9984) (see Figure 7 ).
[0051] 1.2. Preparation of the solution to be tested: same as step 1.2 of "...
Embodiment 3
[0055] Determination method and result of total saponin content of triterpenoid saponins in Sapindus chinensis
[0056] 1.1. Standard curve drawing: Accurately weigh an appropriate amount of triterpenoid total saponins reference substance, put it in a 10mL volumetric flask, dissolve it with 6mL of methanol sonication, constant volume, shake well, filter with a 0.45μm microporous membrane, take the subsequent filtrate, and dilute A series of standard working solutions: 1.023mg / mL, 2.047mg / mL, 4.094mg / mL, 8.187mg / mL, 10.23mg / mL. According to 1.3 chromatographic conditions sample introduction analysis, obtain total saponin standard substance high performance liquid chromatography (see image 3 ); With the logarithm of peak area (A) as ordinate, the logarithm of concentration (C) as abscissa, carry out linear regression, regression equation is lnA=1.6271lnC+3.2131(R 2 =0.9983) (see Figure 8 ).
[0057] 1.2. Preparation of the solution to be tested: same as step 1.2 of "Example...
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