CN103483303A - Proanthocyanidin extraction method - Google Patents

Proanthocyanidin extraction method Download PDF

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Publication number
CN103483303A
CN103483303A CN201210202895.8A CN201210202895A CN103483303A CN 103483303 A CN103483303 A CN 103483303A CN 201210202895 A CN201210202895 A CN 201210202895A CN 103483303 A CN103483303 A CN 103483303A
Authority
CN
China
Prior art keywords
pycnogenols
extracting method
starting material
ethanolic solution
aqueous ethanolic
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
CN201210202895.8A
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Chinese (zh)
Inventor
王永江
杨志祥
毛建卫
朱银邦
邵云东
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.)
Zhejiang Lover Health Science and Technology Development Co Ltd
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Zhejiang Lover Health Science and Technology Development 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 Zhejiang Lover Health Science and Technology Development Co Ltd filed Critical Zhejiang Lover Health Science and Technology Development Co Ltd
Priority to CN201210202895.8A priority Critical patent/CN103483303A/en
Publication of CN103483303A publication Critical patent/CN103483303A/en
Pending legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D311/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
    • C07D311/02Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D311/04Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
    • C07D311/58Benzo[b]pyrans, not hydrogenated in the carbocyclic ring other than with oxygen or sulphur atoms in position 2 or 4
    • C07D311/60Benzo[b]pyrans, not hydrogenated in the carbocyclic ring other than with oxygen or sulphur atoms in position 2 or 4 with aryl radicals attached in position 2
    • C07D311/62Benzo[b]pyrans, not hydrogenated in the carbocyclic ring other than with oxygen or sulphur atoms in position 2 or 4 with aryl radicals attached in position 2 with oxygen atoms directly attached in position 3, e.g. anthocyanidins

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Extraction Or Liquid Replacement (AREA)

Abstract

The invention discloses a proanthocyanidin extraction method. The method is characterized in that proanthocyanidin is extracted through a diafiltration process under the ultrasonic effect in a container provided with an ultrasonic generating device, is further purified, and is dried to obtain a powdery product.

Description

A kind of extracting method of pycnogenols
Technical field
The present invention relates to a kind of extracting method of pycnogenols.
Background technology
The pycnogenols polyphenolic substance general name that to be a class formed by catechin or the l-Epicatechol condensation of different quantities, nonpoisonous and tasteless, there is powerful anti-oxidant activity and radical scavenging activity, there is hypotensive, reducing blood-fat, prevent arteriosclerosis, the effect such as anticancer, anti-ageing and beauty treatment, be used in disease treatment, healthcare products and cosmetic field, become the natural plant extracts that liked by the various countries people.Therefore people more and more pay attention to the research of pycnogenols, and finding the new starting material that are rich in pycnogenols is two study hotspots with the method that is suitable for industrialization extraction, detection pycnogenols.
At present, the extraction process about pycnogenols mainly contains soxhlet extraction, heat reflow method, ultrasonic extraction and supercritical extraction.Although soxhlet extraction has high extraction yield, is not suitable for suitability for industrialized production; The heat reflow method industrialized producing technology is simple, but the destruction that heating easily causes effective constituent, yield is also not as good as soxhlet extraction; Ultrasonic extraction has short advantage of time, but yield is also not as good as soxhlet extraction; Although supercritical extraction has the advantages such as environmental friendliness, product be easily separated, energy consumption is higher.
Summary of the invention
The object of the present invention is to provide a kind of extracting method of pycnogenols, in order to realize this purpose, the present invention has adopted following concrete technological step:
(1) will join containing the starting material of pycnogenols in the container that ultrasonic generator (0-400W) is housed of certain capacity;
(2) 10-20min under ul-trasonic irradiation, adopt the diafiltration method that the aqueous ethanolic solution of 20%-80% ratio is passed through to starting material by certain flow rate;
(3) reaction gained mixture is through concentrating, be drying to obtain target product.
As a kind of improvement, described container is equipped with ultrasonic generator.
As a kind of improvement, described diafiltration method is to carry out under ultrasonication.
As a kind of improvement, after purifying, also comprise that freeze-drying makes the step of powdered product.
The beneficial effect that the present invention has is:
(1) diafiltration method is extracted pycnogenols, and easy and simple to handle saving time, reduced cost;
(2) use ultrasonic wave auxiliary, greatly accelerated extraction rate, efficiency of pcr product also is improved;
(3) use aqueous ethanolic solution safe, nontoxic, that be easy to get to make solvent, convenient operation and processing, ethanol easily reclaims use.
Embodiment
Below by specific embodiment, the invention will be further described:
Under embodiment 1 ultrasonic wave is auxiliary, extract pycnogenols in Cortex Pini in ethanol current hydrodynamic
In the 50mL container, add a certain amount of Cortex Pini, the pillar 20min that flows through under the 300W ul-trasonic irradiation of the aqueous ethanolic solution with 80%, collect extracting solution, and concentrated, freeze-drying obtains powder, and the pycnogenols extraction yield is 97%.
Under embodiment 2 ultrasonic wave are auxiliary, in ethanol current hydrodynamic, extract Proanthocyanidins from Grape Seeds
In the 50mL container, add a certain amount of Semen Vitis viniferae, the pillar 15min that flows through under the 250W ul-trasonic irradiation of the aqueous ethanolic solution with 65%, collect extracting solution, and concentrated, freeze-drying obtains powder, and the pycnogenols extraction yield is 89%.
Under embodiment 3 ultrasonic wave are auxiliary, extract pycnogenols in purple sweet potato in ethanol current hydrodynamic
In the 50mL container, add a certain amount of Semen Vitis viniferae, the pillar 10min that flows through under the 200W ul-trasonic irradiation of the aqueous ethanolic solution with 35%, collect extracting solution, and concentrated, freeze-drying obtains powder, and the pycnogenols extraction yield is 0.9%.
Under embodiment 4 ultrasonic wave are auxiliary, extract pycnogenols in Testa arachidis hypogaeae in ethanol current hydrodynamic
In the 50mL container, add a certain amount of Semen Vitis viniferae, the pillar 10min that flows through under the 200W ul-trasonic irradiation of the aqueous ethanolic solution with 50%, collect extracting solution, and concentrated, freeze-drying obtains powder, and the pycnogenols extraction yield is 12%
Under embodiment 5 ultrasonic wave are auxiliary, extract pycnogenols in rapeseed hull in ethanol current hydrodynamic
In the 50mL container, add a certain amount of Semen Vitis viniferae, the pillar 20min that flows through under the 300W ul-trasonic irradiation of the aqueous ethanolic solution with 75%, collect extracting solution, and concentrated, freeze-drying obtains powder, and the pycnogenols extraction yield is 2.6%
Finally, it is also to be noted that, what more than enumerate is only specific embodiments of the invention.Obviously, the invention is not restricted to above examples of implementation, many distortion can also be arranged.All distortion that those of ordinary skill in the art can directly derive or associate from content disclosed by the invention, all should think protection scope of the present invention.

Claims (5)

1. the extracting method of a pycnogenols, is characterized in that, comprises the following steps:
(1) will join containing the starting material of pycnogenols in the container that ultrasonic generator (0-400W) is housed of certain capacity;
(2) 10-20min under ul-trasonic irradiation, adopt the diafiltration method that the aqueous ethanolic solution of 20%-80% ratio is passed through to starting material by certain flow rate;
(3) reaction gained mixture is through concentrating, be drying to obtain target product.
2. the extracting method of pycnogenols according to claim 1, is characterized in that, starting material can be all solids shape materials containing pycnogenols.
3. the extracting method of pycnogenols according to claim 1, is characterized in that, described percolating device has ultrasonic generating function.
4. the extracting method of pycnogenols according to claim 1, is characterized in that, adopts the diafiltration method that a certain proportion of aqueous ethanolic solution is extracted by starting material by certain flow rate.
5. the extracting method of pycnogenols according to claim 1, is characterized in that, after purifying, also comprises that freeze-drying makes the step of powdered product.
CN201210202895.8A 2012-06-13 2012-06-13 Proanthocyanidin extraction method Pending CN103483303A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201210202895.8A CN103483303A (en) 2012-06-13 2012-06-13 Proanthocyanidin extraction method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201210202895.8A CN103483303A (en) 2012-06-13 2012-06-13 Proanthocyanidin extraction method

Publications (1)

Publication Number Publication Date
CN103483303A true CN103483303A (en) 2014-01-01

Family

ID=49823952

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201210202895.8A Pending CN103483303A (en) 2012-06-13 2012-06-13 Proanthocyanidin extraction method

Country Status (1)

Country Link
CN (1) CN103483303A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111518860A (en) * 2020-05-09 2020-08-11 浙江天草生物科技股份有限公司 Preparation method of cowberry fruit extract

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111518860A (en) * 2020-05-09 2020-08-11 浙江天草生物科技股份有限公司 Preparation method of cowberry fruit extract

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Application publication date: 20140101