Eureka AIR delivers breakthrough ideas for toughest innovation challenges, trusted by R&D personnel around the world.

Preparation for panaxoside-Rd aqueous solution of propylene glycol and new application thereof in inflammation resistance, immune suppression and organ transplant rejection resistance

A technology of ginsenoside and propylene glycol, which is applied in anti-inflammatory agents, plant raw materials, medical preparations of non-active ingredients, etc., and can solve the problem of low content of ginsenoside-Rd

Inactive Publication Date: 2010-07-07
LANZHOU UNIVERSITY +1
View PDF0 Cites 7 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0009]In addition, due to the low content of ginsenoside-Rd in the original ginsenoside-Rd injection, its application is currently limited to the treatment of acute ischemic stroke

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
  • Preparation for panaxoside-Rd aqueous solution of propylene glycol and new application thereof in inflammation resistance, immune suppression and organ transplant rejection resistance
  • Preparation for panaxoside-Rd aqueous solution of propylene glycol and new application thereof in inflammation resistance, immune suppression and organ transplant rejection resistance
  • Preparation for panaxoside-Rd aqueous solution of propylene glycol and new application thereof in inflammation resistance, immune suppression and organ transplant rejection resistance

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0088] Embodiment 1. The formula research of the low concentration ginsenoside-Rd solution of propylene glycol dissolving

[0089] Objective: To adjust the concentration of propylene glycol so that ginsenoside-Rd can be completely dissolved, in order to obtain a true solution, so as to ensure the safety of clinical medication.

[0090] Method: select different volume ratio (20 volume %, 30 volume %, 40 volume %, 50 volume %, 55 volume %, 60 volume %, 75 volume % and 100 volume %) propylene glycol aqueous solution as solvent, with 10mg / ml and 5mg Add ginsenoside-Rd at the content of / ml to determine the propylene glycol concentration that can fully dissolve ginsenoside-Rd. After obtaining the true solution, examine the dissolution state of the medicinal solution under freezing or refrigerated conditions. The available preparations are diluted with water for injection and then added to 250ml of normal saline for mixing or directly diluted with normal saline to investigate the d...

Embodiment 2

[0140] Embodiment 2. The impact of high concentration propylene glycol on the solubility of high concentration ginsenoside-Rd

[0141] Objective: To increase the concentration of propylene glycol, increase the content of ginsenoside-Rd in turn, and investigate the effect of the concentration of propylene glycol on the solubility of ginsenoside-Rd.

[0142]Method: select propylene glycol with a concentration ≥ 50% by volume, add ginsenoside-Rd with different contents (20mg / ml, 25mg / ml, 50mg / ml, 75mg / ml) respectively [dissolve ginsenoside-Rd powder with pure propylene glycol before Add quantitative water (Method B)]. Place it at room temperature for several days, put the sample in a good solution state in refrigerator or freezer, observe the solution state, and detect its Tyndall phenomenon.

[0143] 1. material (with embodiment 1)

[0144] 2. Method

[0145] Propylene glycol with a concentration ≥ 50% by volume is selected, and ginsenoside-Rd is added and dissolved at differ...

Embodiment 3

[0163] Example 3. Effect of Ginsenoside-Rd on Inflammation

[0164] In this experiment, carrageenan was used as an acute inflammation inducer, and it was injected subcutaneously in the foot of mice and rats to induce rat and mouse foot swelling models to observe the effect of ginsenoside-Rd on inflammation.

[0165] 1. Animals

[0166] 120 Kunming mice, half male and half female, clean grade, weighing 18-22 g, were purchased from the Experimental Animal Center of Lanzhou University, license number: SCXK (Gan) 20050007; 96 Wistar rats, half male and half male, SPF grade, Body weight 180-220g, purchased from the Scientific Research and Experiment Center of Gansu College of Traditional Chinese Medicine, license number: SCXK (Gan) 20040006.

[0167] 2. Drugs

[0168] 2.1 Ginsenoside-Rd: provided by Guangdong Tahoe Bio-Pharmaceutical Co., Ltd., product batch number: 980303, dissolved in 55% propylene glycol to prepare a solution of corresponding concentration one day before use. ...

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 relates to preparation for panaxoside-Rd aqueous solution of propylene glycol and new application thereof in inflammation resistance, immune suppression and organ transplant rejection resistance. The invention provides panaxoside-Rd solution and a preparation method thereof. The solution is formed by dissolving the panaxoside-Rd in propylene glycol aqueous solution containing 50 to 100 volume percent of propylene glycol, and the content of the panaxoside-Rd is 1 to 100 mg / ml, wherein the volume percentage of the propylene glycol is based on the total volume of the aqueous solution of propylene glycol. The invention further provides a medicinal composition containing the solution of the invention and a preparation method thereof, and application of the panaxoside-Rd or the panaxoside-Rd solution of the invention in preparing a medicament for inflammation resistance, immune suppression and / or organ transplant rejection resistance.

Description

technical field [0001] The invention relates to the technical field of pharmaceutical preparations, more specifically, to a ginsenoside-Rd propylene glycol aqueous solution with high solubility and stability, its preparation, preparation method and application. Background technique [0002] Ginsenoside-Rd is a monomeric compound obtained by multi-step separation from the traditional Chinese medicine Araliaceae plant Panax notoginseng, and belongs to protopanaxadiol type saponin. Its Chinese chemical name is 20-(S)-protopanaxadiol-3[O-β-D-glucopyranose (1→2)-β-D-glucopyranoside]-20-O-β- D-Glucopyranoside, the English chemical name is 20(S)-Protopanaxadiol 3-O-[β-D-glucopyranosyl(1→2)-β-D-glucopyranosyl]-20-O-β-glucopyranoside, chemical structure as follows: [0003] [0004] Ginsenoside-Rd is white to light yellow powder, odorless, easily soluble in methanol, ethanol, propylene glycol, n-butanol and hot water; soluble in acetone, chloroform and water. The main physical ...

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): A61K31/704A61K9/08A61P29/00A61P37/06
CPCA61K9/08A61K31/704A61K47/10A61K36/258A61P9/00A61P19/02A61P19/08A61P29/00A61P37/06A61P43/00
Inventor 王莉王丽花吴勇杰余剑桥梁健仪E.王范富林
Owner LANZHOU UNIVERSITY
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Eureka Blog
Learn More
PatSnap group products