Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Applications of compound F-A in preparation of products for preventing and/or treating heart injuries

A heart injury, F-A technology, applied in the field of medical use of flavonoids, can solve problems such as side effects, patient prognosis and adverse effects on rehabilitation, cardiotoxicity, etc.

Active Publication Date: 2021-02-02
HUZHOU TEACHERS COLLEGE
View PDF1 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0002] At present, many drugs will cause side effects of cardiotoxicity during treatment, especially in the chemotherapy of malignant tumors, the cytostatics used will cause severe cardiotoxicity, which has a negative impact on the prognosis and rehabilitation of patients

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Applications of compound F-A in preparation of products for preventing and/or treating heart injuries
  • Applications of compound F-A in preparation of products for preventing and/or treating heart injuries
  • Applications of compound F-A in preparation of products for preventing and/or treating heart injuries

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0040] The therapeutic effect of embodiment 1 compound F-A on doxorubicin-induced cardiotoxicity

[0041] Rabbit test method for doxorubicin-induced cardiomyopathy (this experiment complies with relevant ethical regulations):

[0042] (1) Test with two sexes of rabbits whose initial body weight is 2.3 ± 0.2kg, group a is untreated animals (for control animals, n=8), group b is animals treated with doxorubicin (+ replace test substance with placebo, n=8), group c is doxorubicin and test substance treated animals (n=8), test substance is flavonoids F-A, F-B, F-C, respectively c1, c2 , Group c3.

[0043] (2) Groups b and c administered intravenously twice a week with doxorubicin, 1 mg / kg each time, for a total of 4 weeks, and group c took orally administered the test substance 20 mg / kg body weight per day, starting from the first day of doxorubicin treatment To start, feed the feed at the same time.

[0044] (3) After 4 weeks, separate the heart and weigh it, and detect the co...

Embodiment 2

[0051] Therapeutic Effect of Example 2 Compound F-A on Doxorubicin-induced Cardiotoxicity

[0052] Inhibition of cardiomyocyte apoptosis in the H9c2 cardiotoxicity model:

[0053] (1) After incubating H9c2 cells with different concentrations of flavonoids F-A, F-B, and F-C for 24 hours, the toxic effects of flavonoids on cardiomyocytes were evaluated by MTT colorimetry. H9c2 cells were incubated with flavonoids for 1 hour before adding 2.5 After cultured with μM DOX for 24 hours, MTT colorimetric method was used to screen the activity of flavonoids on doxorubicin (DOX)-induced cardiomyocyte apoptosis, and determine the optimal concentration range.

[0054] (2) After treating H9c2 cardiomyocytes with different seabuckthorn flavonoids for 1 hour, treat them with 2.5 μM DOX for 24 hours, then extract the protein, lyse, scrape, collect the cell lysate, centrifuge at 12000 g for 15 minutes, collect the supernatant and discard the precipitate, - Store at 80°C, and use BCA method to...

Embodiment 3

[0061] Embodiment 3 contains the tablet of flavonoid compound

[0062] The following ingredients are produced for each tablet:

[0063]

[0064] The above-mentioned components were mixed according to the stated dosage, granulated, blended and compressed into tablets to prepare 250 mg tablets.

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention discloses applications of a compound F-A in preparation of products for preventing and / or treating heart injuries. Activity study is performed on the compound F-A; that the compound F-Acan reduce the ratio of the heart to the weight is verified; cardiomyocyte fibrosis can be inhibited by reducing the content of hydroxyproline, so that the proliferation of cardiac extracellular matrix can be inhibited, and apoptosis induced by cardiotoxicity effects can be obviously inhibited as well; H9c2 cardiotoxicity effects can be relieved by lowering the expression level of p-JNK and / or Cleaved-Caspase-3, so that the effects of preventing and / or treating cardiomyocyte toxicity can be realized; and the compound can be used to prepare drugs for preventing and / or treating diseases relatedto heart injuries.

Description

technical field [0001] The invention relates to the field of medical application of flavonoids, in particular to the application of flavonoids F-A. Background technique [0002] At present, many drugs will cause side effects of cardiotoxicity during treatment, especially in the chemotherapy of malignant tumors, the cytostatics used will cause severe cardiotoxicity, which has a negative impact on the prognosis and rehabilitation of patients. [0003] According to reports, anthracyclines are generally cardiotoxic, and these drugs are widely used in clinic because of their good antitumor activity. Taking doxorubicin (DOX), the most widely used and most successful anthracycline antineoplastic drug, as an example, its accumulation and dose-dependent cardiomyocyte toxicity are the main problems that have plagued the practice of cancer treatment from drug development to clinical use. , manifested in its therapeutic dose greater than 550mg / m 2 The incidence of congestive heart fai...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
IPC IPC(8): A61K31/7048A61P9/00
CPCA61K31/7048A61P9/00
Inventor 周文娜王洪伦欧阳健胡娜
Owner HUZHOU TEACHERS COLLEGE
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

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