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Preparation method of pancreatin

A technology of pancreatin and pancreas, which is applied in the direction of pancreatin, can solve the problems of large consumption of organic solvents, unfavorable penetration of activators and extracts, and large amount of waste liquid, so as to improve the activation rate and extraction rate, and increase the activation rate and extraction rate, the effect of increasing permeability

Active Publication Date: 2017-11-10
江苏麦德森制药有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

(1) This patent directly uses thawed fresh pancreas or duodenum as raw material, which is activated and extracted after shaving and refining. At this time, the pancreas slurry contains a lot of water, so it is directly activated and extracted. Extraction requires a large amount of activator and extraction solvent, which increases production costs; (2) The pancreas slurry contains a large amount of oil because it has not been degreased. At this time, the activator and extraction solution are directly added for extraction. The existence of oil is not conducive to The penetration of the activator and the extract affects the extraction efficiency, and it is not conducive to the low-temperature extraction to protect the activity of trypsin; (3) the organic solvent acetone is used as the extraction solvent and the precipitation solvent when the trypsin is precipitated, and the patent is still extracted. After the trypsin is degreased with an organic solvent (acetone), the consumption of the organic solvent is large, and the organic solvent will inevitably affect the activity of the trypsin, and the amount of waste liquid is large; (4) the trypsin product in this patent The main index components trypsin activity is only about 3500u / g, pancreatic amylase activity is only about 100000u / g, pancreatic lipase activity is only about 42000u / g, the activity is low

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment approach 1

[0023] (1) Fresh and frozen raw materials: Take 5kg of frozen pancreas;

[0024] (2) Freeze-drying of flakes: flake the fresh frozen pancreas with a pancreas planer, and dry them with a freeze dryer until the water content is less than 8%;

[0025] (3) Grinding: Grinding the freeze-dried pancreas into freeze-dried pancreas powder;

[0026] (4) Degreasing: add 1 L of acetone pre-cooled at 0-5°C to the freeze-dried pancreas powder, defat twice, and then filter and dry to obtain the freeze-dried pancreas powder.

[0027] (5) Activation and extraction: add 20g of CaCl to the freeze-dried powder of defatted pancreas 2 As an activator, add 5 L of acetic acid aqueous solution with a pH of 3 as an extraction solvent, and stir and extract at 0-5°C for 6 hours to obtain an extract;

[0028] (6) Precipitation: After the extract is refrigerated and centrifuged at 0~5°C, take the supernatant, and add 2.5kg of solid ammonium sulfate to the supernatant for salting out (at this time, the sa...

Embodiment approach 2

[0032] (1) Fresh and frozen raw materials: Take 5kg of frozen duodenum;

[0033] (2) Freeze-drying of flakes: flake the fresh-frozen duodenum with a pancreas planer, and dry it with a freeze dryer until the water content is less than 8%;

[0034] (3) Grinding: Grinding the freeze-dried duodenum into freeze-dried duodenum powder;

[0035] (4) Degreasing: Add 2 L of acetone pre-cooled at 0-5°C to the lyophilized duodenum powder, defat 3 times, filter and dry to obtain the lyophilized duodenum powder.

[0036] (5) Activation and extraction: Add 25g of CaCl to the lyophilized powder from duodenum 2 As an activator, add 6L of acetic acid aqueous solution with a pH of 3.5 as an extraction solvent, stir and extract at 0-5°C for 4 hours to obtain an extract;

[0037] (6) Precipitation: After the extract is refrigerated and centrifuged at 0~5°C, take the supernatant, and add 3kg of solid ammonium sulfate to the supernatant for salting out (at this time, the saturation of solid sodium...

Embodiment approach 3

[0041] (1) Fresh and frozen raw materials: 5kg of frozen pancreas and duodenum;

[0042](2) Freeze-drying of flakes: flake the fresh-frozen pancreas and duodenum with a pancreas planer, and dry them with a freeze dryer until the water content is less than 8%;

[0043] (3) Grinding: Grinding the freeze-dried pancreas and duodenum into freeze-dried powder;

[0044] (4) Degreasing: add 1.5 L of acetone pre-cooled at 0-5°C to the lyophilized powder, defat three times, filter and dry to obtain the degreased lyophilized powder.

[0045] (5) Activation and extraction: add 10g of CaCl to the defatted freeze-dried powder 2 As an activator, add 4L of acetic acid aqueous solution with a pH of 4 as an extraction solvent, and stir and extract at 0-5°C for 5 hours to obtain an extract;

[0046] (6) Precipitation: After the extract is refrigerated and centrifuged at 0~5°C, take the supernatant, and add 2kg of solid ammonium sulfate to the supernatant for salting out (at this time, the satu...

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PUM

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Abstract

The invention relates to the field of biological medicines, and discloses a preparation method of pancreatin. The preparation method comprises the following steps: taking freshly frozen raw materials, namely, freshly frozen pancreas and / or duodenum; carrying out slicing and freeze-drying, namely, slicing the freshly frozen raw materials, and drying the slices by adopting a freeze-drying machine till the water content in the raw materials is less than 8%; carrying out grinding for obtaining powder, namely, grinding the freeze-dried raw materials into freeze-dried powder; carrying out degreasing, namely, degreasing the freeze-dried powder, and carrying out draining to obtain degreased freeze-dried powder; carrying out activating and extracting, namely, adding an activating agent and an extracting solvent into the degreased freeze-dried powder, carrying out stirring for extracting at 0-5 DEG C for 3-6 h, thus obtaining an extracted solution; and carrying out precipitating, namely, carrying out freeze centrifugation on the extracted solution at 0-5 DEG C, taking the supernate, carrying out salting-out, and carrying out separating to obtain pancreatin sediment; carrying out squeezing and drying, namely, squeezing the pancreatin sediment till the pancreatin sediment is block-shaped, thus obtaining pancreatin blocks; drying the pancreatin blocks, and grinding the dried pancreatin blocks to obtain pancreatin powder. According to the preparation method of pancreatin, the yield of the pancreatin product is relatively high, the consumption of the solvent is greatly reduced, the activity of trypsin, amylopsin and pancrelipase in the prepared pancreatin is relatively high, and the yield of pancreatin is relatively high.

Description

technical field [0001] The invention relates to the field of biomedicine, in particular to a preparation method of pancreatin. Background technique [0002] Pancreatin is a digestive drug recorded in the pharmacopoeias of various countries. It is a mixture of various enzymes extracted from animal pancreas. The main components are trypsin, pancreatic lipase and pancreatic amylase. Pancreatin is mainly used for indigestion, loss of appetite, and digestive disorders caused by liver and pancreatic diseases. It is also suitable for congenital pancreatic insufficiency, abdominal surgery, and pancreatic insufficiency caused by traumatic pancreatectomy. In addition, pancreatin contains a variety of active substances, which can be used as basic raw materials to extract a variety of biochemical drugs, such as pancreatic kininogen, elastase, asparaginase, chymotrypsin, carboxypeptidase, etc., which have great industrial value . [0003] At present, pancreatin is mainly produced throu...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12N9/94
CPCC12N9/94
Inventor 刘榜惠
Owner 江苏麦德森制药有限公司
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