Unlock instant, AI-driven research and patent intelligence for your innovation.

Application of triacetyl glucal in preparation of antiviral drug

A technology of antiviral drugs and glucal sugar, which is applied in antiviral agents, pharmaceutical formulas, medical preparations containing active ingredients, etc.

Active Publication Date: 2014-08-20
SUZHOU HARMONY BIOTECH
View PDF3 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, there are no relevant reports so far on the application of triacetylglucose in hypoglycemic, antiviral and antitumor aspects.

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
  • Application of triacetyl glucal in preparation of antiviral drug
  • Application of triacetyl glucal in preparation of antiviral drug
  • Application of triacetyl glucal in preparation of antiviral drug

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0020] Effects of triacetylglucenose on diabetic mice induced by alloxan

[0021] Test protocol: Take Kunming mice, fast for 12 hours, inject 80mg / kg of alloxan into the tail vein, measure blood glucose after 3 days, take blood glucose above 11.2-22.4mmol / L and randomly divide them into model control group and triacetylglucene In the sugar group, another 10 rats were taken as the normal control group, and the normal saline was injected into the tail vein at 0.2 ral / mouse. There were 10 rats in each group. The triacetyl glucenose group was given intragastrically, once a day, with doses of 125 and 250 mg / kg body weight respectively; the model control group and the normal control group were given sterilized distilled water. After 14 days of continuous administration, blood was collected from the tail vein for blood glucose measurement, and the weight of the mice, drinking water and feed consumption on the day of blood collection were recorded.

[0022] The effect of triacetylglucenos...

Embodiment 2

[0031] Antiviral activity of triacetyl glucenose

[0032] Strains: Dog kidney cells (MDCK) and parainfluenza virus type 1 (HVJ) cells and toxicity test to MDCK cells

[0033] The triacetyl glucenose was prepared with distilled water into a 20 mg / mL medicinal solution, filtered and sterilized, and diluted with cell maintenance solution to different concentrations. Digest the MDCK cells in the flask, inoculate them in a 96-well cell culture plate, culture for 2 days in a 37°C, 5% CO2 incubator, remove the original culture medium after growing into a monolayer of cells, and add 100 μL of the medicinal solution of different dilution concentrations, and Set up a cell control with only 100μL of maintenance solution, set 4 replicate holes for each concentration, and place them in the incubator to continue culturing. Observe the cytopathic effect (CPE) of the drug with an inverted microscope every day, with "-" indicating 0% CPE , "+" means 1% to 25% CPE, ++ means 25% to 50% CPE, +++ mean...

Embodiment 3

[0040] In Vitro Screening Test of Anti-tumor Biological Activity of Triacetyl Glucenose

[0041] Screening method: Tetrazolium salt (Methyl-Thiazol-Tetrozlium, MTT reduction method)

[0042] Sulforhodamine B (sulforhodamine B, SRB) protein beam color method.

[0043] Cell lines: BEL-7402 human liver cancer, P338 mouse leukemia, A-549 human lung adenocarcinoma

[0044] Action time: 72 hours

[0045] Result evaluation: invalid: 10 -5 mol / L<85%;

[0046] Weak effect: 10 -5 mol / L≥85% or 10 -6 mol / L>50%;

[0047] Powerful: 10 -6 mol / L≥85% or 10 -7 mol / L>50%.

[0048] The result of the table below shows the inhibitory rate of triacetyl glucenose on tumor cell growth%

[0049] Note: The administration group in the table below is the administration of triacetyl glucenose.

[0050]

[0051]

[0052]

[0053] According to the above test results, triacetylglucenose has strong effects on BEL-7402 human liver cancer, P338 mouse leukemia, and A-549 human lung adenocarcinoma.

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 provides application of triacetyl glucal in the preparation of drugs and particularly provides application of triacetyl glucal in the preparation of a hypoglycemic, antiviral or antitumor drug. According to the application, shown by the determination of animals or MIC (Minimal Inhibitory Concentration), triacetyl glucal has hypoglycemic, antiviral or antitumor actions. According to the application, the drug is prepared from triacetyl glucal serving as an active ingredient, and a conventional pharmaceutical excipient by conventional methods and is of oral tablets, capsules, oral liquid or granules or percutaneous absorption injections or patches. Triacetyl glucal has a high practical value in the field of medicines.

Description

[0001] This patent application is a divisional application of Patent Application No. 201010232434.6, the name of the invention: the application of triacetylglucenose in the preparation of medicines. Technical field [0002] The present invention relates to medicinal chemistry. Specifically, it relates to the application of triacetyl glucenose in the preparation of medicines. In particular, it relates to the application of triacetylglucenose in the preparation of blood sugar lowering, antiviral and antitumor drugs. Background technique [0003] Glycochemistry and glycobiology have now become frontiers and hotspots in life sciences. Sugars not only serve as energy sources or structural components, but also perform extremely important biological functions. The oligosaccharides in sugar complexes are information molecules in the body, which play an important role in the occurrence, development and prognosis of human diseases, and are also an important class of therapeutic drugs. [00...

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
Patent Type & Authority Patents(China)
IPC IPC(8): A61K31/7024A61P31/12A61P31/16
Inventor 冒华
Owner SUZHOU HARMONY BIOTECH