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Stable glucose oral solution for glucose tolerance test

A technology for oral solution and glucose, which is applied to preparations for in vivo experiments, compound screening/testing, pharmaceutical formulations, etc., can solve the problems of astringent taste, poor taste of sugar water, complex ingredients, etc. Convenient, high-performance results

Pending Publication Date: 2022-05-31
CHENGDU SHIBEIKANG BIOLOGICAL MEDICINE TECH CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The above methods of oral glucose tolerance test have the following disadvantages: first, high-concentration sugar water tastes bad, and has obvious sweet and greasy feeling, especially for pregnant women, it is easy to cause nausea and vomiting; second, the operability of the subjects is poor, For self-preparation, you need to bring a container and a stirring spoon, and the amount of water should not be controlled. It is very inconvenient to open multiple bottles of glucose injection for direct drinking; third, oral glucose tolerance beverages are food-grade beverages that implement general standards for beverages, and the quality requirements are low. , there is no control over the second type of genotoxic impurity 5-hydroxymethylfurfural; fourth, glucose injection generally adopts high-temperature sterilization process, and glucose is easily degraded under high temperature conditions to produce 5-hydroxymethylfurfural; while 5-hydroxymethylfurfural Furfural not only has neurotoxicity, can combine with human protein to produce accumulation poisoning, but also may polymerize and cause the color of the solution to turn yellow
[0004] Regarding 5-hydroxymethylfurfural, the prior art (IN299712B) discloses that the pH of the solution is adjusted to 6-8 by alkali, especially when the pH value is adjusted to 7, the production of the impurity can be significantly reduced; good or astringent
Regarding the taste problem, the prior art (CN110314243A, CN109568603A) adjusts the taste by adding vitamin C or sour agent, essence, etc. Although it can cover the taste to a certain extent or have a sour taste, it cannot solve the problem of oral solution stability
In addition, with regard to sterility, most of the glucose oral solutions reported in the prior art (CN109044966B, US7566463B2, CN113425675A) use bacteriostatic agents, but the composition is complex and the bacteriostatic effect is not ideal, and the complex additives also have the risk of toxicity to the human body
In addition, the oral glucose solution of the prior art has complex components, low glucose content, and no control of 5-hydroxymethylfurfural impurities and microorganisms, resulting in unstable quality

Method used

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  • Stable glucose oral solution for glucose tolerance test

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0075] Example 1: Sample 1

[0076] Prescription: 75g of anhydrous glucose, 0.65g of citric acid, 0.86g of sodium citrate, the mass ratio of citric acid to sodium citrate is 0.76, the volume of water is adjusted to 300ml, and the pH value of the solution is 4.5.

[0077] Preparation: (1) Dosing: Take 300ml of purified water, add the prescribed amount of citric acid and sodium citrate, mix well to obtain a buffer solution, and let it stand for 5-10 minutes; add the prescribed amount of anhydrous glucose to the buffer solution at 60 Under the condition of ℃, stir for 30 minutes at a speed of 700rpm to dissolve completely, mix well, and set aside; after the above solution is lowered to room temperature, add dilute phosphoric acid solution to the full volume, stir for 10 minutes, and mix well; use 20% sodium citrate solution or 20% citric acid solution to fine-tune the pH value of the solution to the target value, and mix well to obtain the medicinal solution; (2) Filtration and c...

Embodiment 2

[0078] Example 2: Sample 2

[0079] Prescription: 75g of anhydrous glucose, 2.83g of citric acid, 0.86g of sodium citrate, the mass ratio of citric acid to sodium citrate is 3.29, the volume of water is adjusted to 300ml, and the pH value of the solution is 3.0.

[0080] Preparation: (1) Dosing: Take 300ml of purified water, add the prescribed amount of citric acid and sodium citrate, mix well to obtain a buffer solution, and let it stand for 5-10 minutes; add the prescribed amount of anhydrous glucose to the buffer solution at 60 Under the condition of ℃, stir for 30min at a speed of 700rpm to dissolve completely, mix well, and set aside. After the above solution was lowered to room temperature, dilute phosphoric acid solution was added to make the volume to full volume, stirred for 10 minutes, and mixed evenly; the pH value of the solution was fine-tuned to the target value with 20% sodium citrate solution or 20% citric acid solution, and mixed evenly to obtain Liquid medic...

Embodiment 3

[0081] Example 3: Sample 3

[0082] Prescription: 75g of anhydrous glucose, 0.65g of citric acid, 1.63g of sodium citrate, the mass ratio of citric acid to sodium citrate is 0.40, the volume of water is adjusted to 300ml, and the pH value of the solution is 5.0.

[0083] Preparation: (1) Dosing: Take 300ml of purified water, add the prescribed amount of citric acid and sodium citrate, mix well to obtain a buffer solution, and let it stand for 5-10 minutes; add the prescribed amount of anhydrous glucose to the buffer solution at 60 Under the condition of ℃, stir for 30 minutes at a speed of 700rpm to dissolve completely, mix well, and set aside; after the above solution is cooled to room temperature, add dilute phosphoric acid solution to make up to full volume, stir for 10 minutes, and mix well. Use 20% sodium citrate solution or 20% citric acid solution to fine-tune the pH value of the solution to the target value, and mix well to obtain the medicinal solution; (2) Filtration...

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Abstract

The invention belongs to the field of pharmaceutical preparations, and particularly relates to a stable glucose oral solution for a glucose tolerance test as well as a preparation method and application thereof. The glucose oral solution comprises 75 g of anhydrous glucose and 0.5-5.0 g of a buffer pair, the volume of water is fixed to 150-350 ml, the ratio of acid and acid salt of the buffer pair is 0.40-3.30, and the pH value of the oral solution is 3.0-5.0. The glucose oral solution is convenient to take, good in taste, stable in property, especially beneficial to control of toxic impurity 5-hydroxymethylfurfural, basically free of impurities in 0 day, lower than 0.02% in impurity content in 30 days at high temperature, and controllable in quality.

Description

technical field [0001] The invention belongs to the field of pharmaceutical preparations, and in particular relates to a glucose oral solution for a glucose tolerance test and a preparation method and application thereof. Background technique [0002] With the rapid development of my country's economy and the continuous improvement of people's living standards, the number of diabetic patients has ranked first in the world, and the incidence of diabetes is showing a trend of increasing year by year and becoming younger. Oral glucose tolerance test (OGTT) is currently one of the important criteria for diagnosing type 2 diabetes and gestational diabetes. [0003] At present, there is no oral solution approved by the State Food and Drug Administration that can be produced by pharmaceutical companies and meets drug standards and is suitable for oral glucose tolerance tests for patients to use. At present, there are three main methods of clinical glucose tolerance test. The first...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): A61K49/00
CPCA61K49/0004
Inventor 聂昱易泽琴苏永文
Owner CHENGDU SHIBEIKANG BIOLOGICAL MEDICINE TECH CO LTD
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