Use of luteolin in preparing anticomplement medicament
A technology of luteolin and anti-complement, which is applied to the new use of luteolin in the preparation of anti-complement medicine, and the field of anti-complement medicine, which can solve the problems such as the unseen anti-complement efficacy of luteolin.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0018] Embodiment 1 prepares luteolin
[0019] Houttuynia cordata, wild chrysanthemum, Capsicum chinensis, Peilan, and Caoguo five flavors of traditional Chinese medicine are compatible according to their composition ratio of 15:6:15:10:3, a total of 19.8Kg. Extract by cold immersion in 95% ethanol, filter, and recover the ethanol under reduced pressure until there is no alcohol smell to obtain 1Kg of ethanol extract. The ethanol extract was suspended in water, and extracted with equal volumes of petroleum ether, ethyl acetate, and n-butanol to obtain petroleum ether fraction (405 g), ethyl acetate fraction (200 g) and n-butanol fraction (100 g). The ethyl acetate fraction (190 g) was subjected to silica gel column chromatography, eluting with petroleum ether-acetone gradient. The fraction eluted with petroleum ether-acetone (8:2) was subjected to repeated silica gel column chromatography (petroleum ether-acetone 7:3), and then purified by Sephadex LH-20 (chloroform-methanol ...
Embodiment 2
[0021] Example 2 classical pathway complement inhibition test
[0022] Take guinea pig serum to VBS 2+ Buffer (barbital buffer, pH=7.4, containing 0.5mM Mg 2+ and 0.15mM Ca 2+ ) was diluted 1:80 as a source of complement for the classical pathway. Rabbit anti-sheep erythrocyte antibody in VBS 2+ The buffer was diluted 1:1000 as hemolysin; sheep red blood cells (SRBC) preserved in Alsever's solution were prepared as 2% SRBC. Precisely weigh 1mg of luteolin, add VBS 2+ The buffer was dissolved (adding 1% DMSO to aid dissolution), and diluted to 8 concentrations. 200 μL of luteolin solutions of different concentrations and 200 μL of 1:80 complement were pre-incubated at 37°C for 10 minutes, then 100 μL of hemolysin (1:1000) and 100 μL of 2% SRBC were added in sequence, and placed in a low-temperature high-speed centrifuge after 30 minutes in a water bath at 37°C , centrifuged at 5000rpm, 4°C for 10min. Take 200 μL of the supernatant from each tube in a 96-well plate, and m...
Embodiment 3
[0023] Example 3 Alternative Pathway Complement Inhibition Test
[0024] Serum was taken from healthy adult male volunteers and mixed with VBS-Mg-EGTA buffer (barbital buffer, pH=7.4, containing 5mM Mg 2+ and 8mM EGTA) diluted 1:10, as a source of complement for the alternative pathway. Rabbit red blood cells stored in 3.8% sodium citrate solution were prepared into 2% rabbit red blood cells with VBS-Mg-EGTA buffer solution. Precisely weigh 1 mg of luteolin, add VBS-Mg-EGTA buffer solution (1% DMSO is added to aid dissolution), and dilute to 8 concentrations. 150 μL of luteolin solutions of different concentrations and 150 μL of 1:10 complement were pre-incubated at 37°C for 10 minutes, then 200 μL of 2% rabbit red blood cells were added, and placed in a low-temperature high-speed centrifuge after 30 minutes in a water bath at 37°C. Centrifuge for 10 min. Take 200 μL of the supernatant from each tube in a 96-well plate, and measure the absorbance at 405 nm. At the same tim...
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