CN106831454A - A kind of ephedrine extraction method - Google Patents

A kind of ephedrine extraction method Download PDF

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Publication number
CN106831454A
CN106831454A CN201510876975.5A CN201510876975A CN106831454A CN 106831454 A CN106831454 A CN 106831454A CN 201510876975 A CN201510876975 A CN 201510876975A CN 106831454 A CN106831454 A CN 106831454A
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CN
China
Prior art keywords
ephedrine
extraction method
filter
ephedra
distilled water
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN201510876975.5A
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Chinese (zh)
Inventor
吴健民
尹丹
贺莲
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kamp Pharmaceuticals Co Ltd
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Kamp Pharmaceuticals Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Kamp Pharmaceuticals Co Ltd filed Critical Kamp Pharmaceuticals Co Ltd
Priority to CN201510876975.5A priority Critical patent/CN106831454A/en
Publication of CN106831454A publication Critical patent/CN106831454A/en
Pending legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C213/00Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton
    • C07C213/10Separation; Purification; Stabilisation; Use of additives

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

The invention discloses a kind of ephedrine extraction method, using half bionical-biological enzyme extracting method, the shortcomings of overcoming half biomimetic method Extracting temperature be high at ambient pressure, be difficult to separating-purifying, the addition of enzyme is conducive to leaching and the bioconversion of active material, on the premise of original composition is not destroyed, the ephedrine inside Chinese ephedra is more effectively extracted.

Description

A kind of ephedrine extraction method
Technical field
The invention belongs to pharmaceutical technology field, and in particular to be a kind of ephedrine extraction method.
Background technology
Chinese ephedra, Latin literary fame:Ephedra sinica Stapf, Ephedraceae, Ephedra herbaceous plant.For diseases caused by external factors wind Cold, fever with aversion to cold is opened facilitaing lung gas, dispersing wind and cold and is relievingd asthma.Alkaloid enriches, and is the Main Resources for extracting ephedrine.Chinese ephedra Alkali, 1. can prevent bronchial asthma attack and alleviate mild asthma breaking-out, not good to acute severe asthma breaking-out effect.2. it is used for Low blood pressure and chronic hypotension disease that subarachnoid anesthesia or caudal anaesthesia cause.3. the nose that treatment a variety of causes causes is sticked The nasal obstruction that film is congested, swelling causes.
There are patent literature, a kind of extraction process of ephedrine(CN201210489938)Carried using alkalization, dimethylbenzene Take, oxalic acid extraction technique, extract high-purity ephedrine.Wherein the organic solvent pollution such as dimethylbenzene weight, high cost.The present invention The environment absorbed through gastrointestinal transit using half bionical-biological enzyme extraction method simulation oral drugs, selects Suitable cellulases pair Chinese medicine is pre-processed, and destroys vegetable drug cell membrane, and energy is more environmentally friendly, more effectively extract ephedrine.
Semi-bionic extraction (abbreviation SBE) is the new method for proposing in recent years.It is the angle from biopharmacy, will be whole Body drug research method is combined with molecular medicine organon, the environment that simulation oral drugs absorb through gastrointestinal transit, using work Property instruct under guiding separation method;It is a kind of new extraction process of the formulation design being administered orally through alimentary canal.Half bionical- Biological enzyme extraction method is that first selection Suitable cellulases are pre-processed to Chinese medicine, to destroy vegetable drug cell membrane.The method gram The shortcomings of having taken half biomimetic method Extracting temperature is high at ambient pressure, be difficult to separating-purifying, the addition of enzyme is conducive to the leaching of active material Go out and bioconversion, be conducive to human body to absorb active material.
The content of the invention
The invention provides a kind of accurate, reliable, stabilization ephedrine extraction method.
For achieving the above object, a kind of ephedrine extraction method of the invention, concrete scheme is:
A kind of ephedrine extraction method of the present invention, it is characterised in that its extracting method is:
1. extract for the first time:Ephedra is placed in flask, plus 4 ~ 8 times of distilled water(pH=1.5~2.5), 1 ~ 2h is heated to reflux, Filtering;
2. extract for second:To being added in filter residue, biology enzyme is appropriate, 40 ~ 50 DEG C of 1 ~ 2h of hydrolysis, filtering;
3. third time is extracted:Added plus 2 ~ 6 times of distilled water in filter residue(pH=7.0~8.5), 1 ~ 2h is heated to reflux, filter;Merge Three filtrates of extraction, are drying to obtain.
A kind of ephedrine extraction method of the present invention, step 2. the biology enzyme species be cellulase, alphalise starch One or more combination in enzyme, pectase, 1,4 beta-glucanase, lipase.
A kind of ephedrine extraction method of the present invention, 3. the drying temperature is 70 ~ 105 DEG C to step.
Specific embodiment
Example below is only to further illustrate the present invention, scope that the invention is not limited in any way.
Embodiment 1
Ephedra is placed in flask, plus 5 times of distilled water(pH=2.0), 1.5h is heated to reflux, filter;To adding 1% in filter residue Cellulase(In terms of Chinese ephedra quality), 45 DEG C of hydrolysis 2h, filtering;Added plus 4 times of distilled water in filter residue(pH=7.5), heat back Stream 1.5h, filtering;Merging filtrate, is drying to obtain.
Embodiment 2
Ephedra is placed in flask, plus 6 times of distilled water(pH=2.0), 1.5h is heated to reflux, filter;To adding 1% in filter residue AMS(In terms of Chinese ephedra quality), 50 DEG C of hydrolysis 2h, filtering;Added plus 6 times of distilled water in filter residue(pH=7.5), heat back Stream 1.5h, filtering;Merging filtrate, is drying to obtain.
Embodiment 3
Ephedra is placed in flask, plus 7 times of distilled water(pH=2.5), 1.5h is heated to reflux, filter;To adding 1% in filter residue Cellulase and 1% AMS 1:1 mixing(In terms of Chinese ephedra quality), 45 DEG C of hydrolysis 2h, filtering;Add plus distill in filter residue 4 times of water(pH=8.0), 1h is heated to reflux, filter;Merging filtrate, is drying to obtain.
Embodiment 4
The purity and yield of the ephedrine that the extraction process of comparative example 1,2,3 is extracted, as a result show what embodiment 1,2,3 was extracted Ephedrine purity and yield are higher, but the ephedrine purity and yield of the extraction of mixed biologic enzyme are optimal, as a result see the table below.

Claims (3)

1. a kind of ephedrine extraction method, it is characterised in that the ephedrine extraction method and step is:
1. Ephedra is placed in flask, plus 4 ~ 8 times of distilled water(pH=1.5~2.5), 1 ~ 2h is heated to reflux, filter;
2. to adding biology enzyme appropriate in filter residue, 40 ~ 50 DEG C of 1 ~ 2h of hydrolysis are filtered;
3. added plus 2 ~ 6 times of distilled water in filter residue(pH=7.0~8.5), 1 ~ 2h is heated to reflux, filter;
Merge 1. 2. 3. filtrate, be drying to obtain.
2. a kind of ephedrine extraction method according to claim 1, it is characterised in that the species of the step 2. biology enzyme It is one or more combination in cellulase, AMS, pectase, 1,4 beta-glucanase, lipase.
3. a kind of ephedrine extraction method according to claim 1, it is characterised in that 3. the drying temperature is 70 to step ~105℃。
CN201510876975.5A 2015-12-03 2015-12-03 A kind of ephedrine extraction method Pending CN106831454A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201510876975.5A CN106831454A (en) 2015-12-03 2015-12-03 A kind of ephedrine extraction method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201510876975.5A CN106831454A (en) 2015-12-03 2015-12-03 A kind of ephedrine extraction method

Publications (1)

Publication Number Publication Date
CN106831454A true CN106831454A (en) 2017-06-13

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Family Applications (1)

Application Number Title Priority Date Filing Date
CN201510876975.5A Pending CN106831454A (en) 2015-12-03 2015-12-03 A kind of ephedrine extraction method

Country Status (1)

Country Link
CN (1) CN106831454A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107892652A (en) * 2017-11-07 2018-04-10 何本科 A kind of extracting method of ephedrine
CN109692248A (en) * 2017-10-24 2019-04-30 汉寿康运医药科技有限公司 A kind of vine tea total flavone extracting method
CN109692232A (en) * 2017-10-23 2019-04-30 康普药业股份有限公司 A kind of extracting method of Aguiyangxue granules

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109692232A (en) * 2017-10-23 2019-04-30 康普药业股份有限公司 A kind of extracting method of Aguiyangxue granules
CN109692248A (en) * 2017-10-24 2019-04-30 汉寿康运医药科技有限公司 A kind of vine tea total flavone extracting method
CN107892652A (en) * 2017-11-07 2018-04-10 何本科 A kind of extracting method of ephedrine

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Application publication date: 20170613

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