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Preparation method of colloidal bismuth pectin

A technology of colloidal bismuth pectin and pectin is applied in the directions of pharmaceutical formulations, medical preparations containing active ingredients, antibacterial drugs, etc., to avoid the yellowing of bismuth alkali and increase the safety of medication.

Active Publication Date: 2020-06-02
SHANXI ZHENDONG ANTE BIOPHARMACEUTICAL CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Although the current Pharmacopoeia has not stipulated the requirement to detect sorbitol and bismuth sorbitol in c

Method used

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  • Preparation method of colloidal bismuth pectin

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0036] Weigh 10g of bismuth nitrate pentahydrate, add it into 7.8ml of sorbitol liquid and stir evenly. Add 20ml of purified water and continue stirring for 1.5h until it becomes a clear liquid.

[0037] Under stirring, add lye to the above clear liquid drop by drop. When the pH=5.0, the clear liquid starts to become turbid. Continue to drop the lye to produce white flocculent precipitates. When the pH=7.0, the white precipitates are completely separated out. Add 7.5ml of lye.

[0038] Continue to add 100ml of purified water, stir for 5min, and let stand for 2h to separate layers. Aspirate the supernatant, add 100ml of purified water to the white precipitate in the lower layer, stir, let it stand for 2 hours, remove the supernatant, and obtain a white paste-like bismuth base.

[0039] Add 20g of citrus pectin into 200ml of water, stir and heat to 95°C to dissolve evenly, cool down to room temperature, add 7.5ml of lye, stir for 0.5h to disperse evenly, and prepare pectin glu...

Embodiment 2

[0046] Weigh 10g bismuth nitrate pentahydrate, add it into 4.5ml sorbitol liquid and stir evenly. Add 20ml of purified water and continue to stir for 1h until it becomes a clear liquid.

[0047] Under stirring, add lye to the above clear liquid drop by drop. When the pH=5.0, the clear liquid starts to become turbid. Continue to drop the lye to produce white flocculent precipitates. When the pH=7.0, the white precipitates are completely separated out. Add 7.3ml of lye.

[0048] Continue to add 100ml of purified water, stir for 5min, and let stand for 2h to separate layers. Aspirate the supernatant, add 100ml of purified water to the white precipitate in the lower layer, stir, let it stand for 2 hours, remove the supernatant, and obtain a white paste-like bismuth base.

[0049] Add 20g of sunflower pectin into 200ml of water, stir and heat to 80°C to dissolve evenly, cool down to room temperature, add 7.5ml of lye, stir for 0.5h to disperse evenly, and prepare pectin glue, pH=...

Embodiment 3

[0056] Weigh 10g bismuth nitrate pentahydrate, add it into 5.8ml sorbitol liquid and stir evenly. Add 20ml of purified water and continue to stir for 1h until it becomes a clear liquid.

[0057] Under stirring, add lye to the above clear liquid drop by drop. When the pH=5.0, the clear liquid starts to become turbid. Continue to drop the lye to produce white flocculent precipitates. When the pH=7.0, the white precipitates are completely separated out. Add 7.5ml of lye.

[0058] Continue to add 100ml of purified water, stir for 5min, and let stand for 2h to separate layers. Aspirate the supernatant, add 100ml of purified water to the white precipitate in the lower layer, stir, let it stand for 2 hours, remove the supernatant, and obtain a white paste-like bismuth base.

[0059] Add 20g of apple pectin to 200ml of water, stir and heat to 60°C to dissolve evenly, cool down to room temperature, add 7.5ml of lye, stir for 0.5h to disperse evenly, and prepare pectin glue, pH=7.0. ...

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Abstract

The invention discloses a preparation method of colloidal bismuth pectin. The method includes: adding bismuth nitrate into a sorbitol aqueous solution for dissolving, adjusting the pH value of the solution to 7-8 by using a potassium hydroxide solution, conducting standing to separate a precipitate, and fully washing the precipitate with water to obtain a pasty bismuth alkali precipitate; and adding pectin mucilage into the bismuth alkali precipitate, then adding a potassium hydroxide solution, and carrying out salt forming reaction to prepare colloidal bismuth pectin, firstly adding a potassium hydroxide-ethanol solution, carrying out centrifugation for dewatering, then adding ethanol, carrying out stirring washing, carrying out centrifugation to remove the solution, and performing dryingto obtain a colloidal bismuth pectin finished product. According to the preparation method, the bismuth alkali precipitate and pectin mucilage are subjected to reaction, so that the problem that a cosolvent sorbitol serving as an additional impurity remains too much in a colloidal bismuth pectin finished product is solved, the content of sorbitol in the prepared colloidal bismuth pectin finishedproduct is less than 3.5%, and the content of free bismuth is less than 0.8%.

Description

technical field [0001] The invention belongs to the technical field of colloidal bismuth pectin preparation, relates to a preparation method of colloidal bismuth pectin, in particular to a preparation method of colloidal bismuth pectin capable of effectively removing cosolvent sorbitol. Background technique [0002] Colloidal bismuth pectin and its capsules are the first drugs produced by Taiyuan Hongxing Pharmaceutical Factory, the predecessor of Shanxi Zhendong Ante Biopharmaceutical Co., Ltd. The drug was first approved by the former Ministry of Health in July 1992 to be produced and launched by Taiyuan Hongxing Pharmaceutical Factory. [0003] Colloidal bismuth pectin is a new bismuth salt compound formed by replacing inorganic acid radicals (subnitrate, metaaluminate) and small molecular organic acid radicals (subcitrate) with natural polymer pectin. Compared with other bismuth preparations such as traditional bismuth subgallate, bismuth subnitrate, bismuth salicylate,...

Claims

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Application Information

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IPC IPC(8): C08B37/06A61K31/732A61P1/04A61P31/04
CPCC08B37/0045A61K33/245A61P1/04A61P31/04
Inventor 李安平徐强强高宁王旭文刘艳之
Owner SHANXI ZHENDONG ANTE BIOPHARMACEUTICAL CO LTD