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Aqueous formulation

A water-based preparation, selected technology, applied in directions such as non-central analgesics, anti-inflammatory agents, aerosol delivery, etc., can solve problems such as the disclosure and enlightenment of solutions without anti-inflammatory sprays, and achieve a good feeling of taking, The effect of ensuring the circulation process and sufficient stability

Active Publication Date: 2022-02-18
DAIYA SEIYAKU +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] However, there is no disclosure or suggestion about long-term storage stability, and a solution for an anti-inflammatory spray containing sodium azulenesulfonate that has a good feeling of taking and can be taken for a long time

Method used

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  • Aqueous formulation
  • Aqueous formulation
  • Aqueous formulation

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0069] Dissolve 0.2 g of sodium azulene sulfonate in purified water, and dilute to 100 mL. 5 mL of this liquid was put into a volumetric flask, and 15 g of various sugar alcohols were further added as additives, shaken well, and then the volume was adjusted to 50 mL with purified water. This liquid was subdivided into three sample bottles of about 15 cc each, and used as a test liquid. Then, the absorbance of the prepared test solution was measured, and then stored at 60°C for 7 days to measure the absorbance, and the residual rate was calculated based on the decrease in absorbance at the start and after the accelerated test.

[0070] The results are shown in Table 1.

[0071] Table 1

[0072] (w / v%)

[0073]

[0074] From the results in Table 1, it is clear that the stability of sodium azulene sulfonate is significantly deteriorated when sugar alcohol is blended into sodium azulene sulfonate.

Embodiment 2

[0076] Dissolve 0.2 g of sodium azulene sulfonate in purified water, and dilute to 100 mL. After adding 5 mL of this liquid to a volumetric flask, a predetermined amount of maltitol was added and shaken well, and then the volume was adjusted to 50 mL with purified water. This liquid was subdivided into three sample bottles of about 15 cc each, and used as a test liquid. Then, the absorbance of the prepared test solution was measured, and then stored at 60°C for 7 days to measure the absorbance, and the residual rate was calculated based on the decrease in absorbance at the start and after the accelerated test. The results are shown in Table 2.

[0077] Table 2

[0078] (w / v%)

[0079] Example example 1 Example 2 Example 3 Example 4 Example 5 Example 6 Example 7 Example 8 Example 9 Example 10 Example 11 Example 12 Example 13 Sodium azulene sulfonate 0.02 0.02 0.02 0.02 0.02 0.02 0.02 0.02 0.02 0.02 0.02 0.02 0.02 Malt...

Embodiment 3

[0082] Dissolve 0.2 g of sodium azulene sulfonate in purified water, and dilute to 100 mL. 5 mL of this liquid was put into a volumetric flask, and a predetermined amount of specified additives (glycerin and alcohol (ethanol)) was added and shaken well, then purified water was added, and the volume was adjusted to about 80% of 50 mL. Then, a pH regulator was added to adjust the pH to a range of 7.0±0.5, and then the volume was adjusted to 50 mL. This liquid was subdivided into 3 sample bottles of about 15 ㏄ each and used as a test liquid. Then, the absorbance of the prepared test solution was measured, and then stored at 60°C for 7 days to measure the absorbance, and the residual rate was calculated based on the decrease in absorbance at the beginning and after completion of the severe test. The results are shown in Table 3.

[0083] table 3

[0084] (w / v%)

[0085]

[0086] From the results of Table 1 and Table 3, it is clear that adding glycerin or ethanol to sodium a...

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Abstract

To provide an aqueous solution of sodium azulenesulfonate capable of ensuring sufficient stability against light, heat, and oxygen and having a good feeling of ingestion.

Description

technical field [0001] The present invention relates to novel aqueous formulations containing sodium azulene sulfonate. Background technique [0002] It is known that sodium azulene sulfonate exists in the form of 1 / 2 hydrate or monohydrate, and sodium azulene sulfonate is easily decomposed by light, heat, oxygen, etc., resulting in a decrease in content and a change in the unique taste of azulene sulfonate , color fading and other problems, resulting in instability (Non-Patent Document 1). In order to stabilize it, the method of stabilizing by mix|blending a nonionic surfactant and alcohol, for example (patent documents 1-5), etc. are proposed. [0003] However, there is no disclosure or suggestion regarding long-term storage stability and a solution for an anti-inflammatory spray containing sodium azulenesulfonate that has a good feeling of taking and can be taken for a long time. [0004] [Prior art literature] [0005] [Patent Document] [0006] [Patent Document 1] J...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): A61K9/08A61K31/185A61K47/26A61K9/12A61P11/04A61P1/02A61P29/00
CPCA61K47/26A61K9/006A61K9/08A61K31/185
Inventor 守金大藏
Owner DAIYA SEIYAKU
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