JP2992737B2 - Extraction method of animal and plant extracts by disruption of frozen cell membrane - Google Patents

Extraction method of animal and plant extracts by disruption of frozen cell membrane

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Publication number
JP2992737B2
JP2992737B2 JP6179821A JP17982194A JP2992737B2 JP 2992737 B2 JP2992737 B2 JP 2992737B2 JP 6179821 A JP6179821 A JP 6179821A JP 17982194 A JP17982194 A JP 17982194A JP 2992737 B2 JP2992737 B2 JP 2992737B2
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JP
Japan
Prior art keywords
extract
animal
cell membrane
solvent
frozen
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.)
Expired - Lifetime
Application number
JP6179821A
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Japanese (ja)
Other versions
JPH0810503A (en
Inventor
隆文 石原
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.)
BIZEN KASEI KK
Original Assignee
BIZEN KASEI KK
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 BIZEN KASEI KK filed Critical BIZEN KASEI KK
Priority to JP6179821A priority Critical patent/JP2992737B2/en
Publication of JPH0810503A publication Critical patent/JPH0810503A/en
Application granted granted Critical
Publication of JP2992737B2 publication Critical patent/JP2992737B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】本発明は、凍結細胞膜破壊による
動植物エキスの抽出法に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for extracting an animal or plant extract by disrupting a frozen cell membrane.

【0002】[0002]

【従来技術と発明が解決すべき課題】動植物由来のエキ
スは、医薬、食品添加物、健康食品および化粧品などの
成分として広く用いられている。従来、そのようなエキ
スの製造法として、水等の適当な溶媒を用い、加熱およ
び/又は加圧下に抽出した後、溶媒を除去する方法が用
いられてきた。しかしながら、従来の方法では、原料に
含まれる目的成分を有効に抽出することができない場合
が多かった。従って、特定の原料から、可能な限り多量
の成分を抽出し、高純度のエキスを効率良く製造する方
法の開発が強く求められていた。
BACKGROUND ART Extracts derived from animals and plants are widely used as components of medicines, food additives, health foods and cosmetics. Heretofore, as a method for producing such an extract, a method has been used in which an appropriate solvent such as water is used, extraction is performed under heating and / or pressure, and then the solvent is removed. However, conventional methods often fail to effectively extract the target component contained in the raw material. Therefore, there has been a strong demand for the development of a method for extracting a component as much as possible from a specific raw material and efficiently producing a high-purity extract.

【0003】[0003]

【課題を解決するための手段】本発明者は、様々な原料
から、目的成分を効率良く抽出する方法を開発すること
を目的として鋭意、研究を重ねた結果、水分を含有する
動植物組織を、一旦、凍結して細胞膜を破壊した後、通
常の抽出溶媒を用いて、抽出し、濃縮することにより、
目的成分を含有するエキスを高収率で得ることができる
ことを見い出し本発明を完成するに至った。即ち、本発
明は、水分を含有する動植物(但し、 きのこを除く)
組織を、温度−15℃〜−20℃で細胞膜が破壊される
に十分な時間である少なくとも48時間処理した後、水
又はアルコール系溶媒で抽出し次いで抽出液から溶媒を
除去することを特徴とする凍結細胞膜破壊による動植物
エキスの抽出法を提供するものである。
Means for Solving the Problems The inventors of the present invention have conducted intensive studies for the purpose of developing a method for efficiently extracting a target component from various raw materials. Once frozen and disrupted the cell membrane, using a normal extraction solvent, extract and concentrate,
The present inventors have found that an extract containing the target component can be obtained in high yield, and have completed the present invention. That is, the present invention treats tissues of animals and plants containing water ( excluding mushrooms) at a temperature of −15 ° C. to −20 ° C. for at least 48 hours, which is a time sufficient for cell membranes to be destroyed. Another object of the present invention is to provide a method for extracting an animal or plant extract by destruction of a frozen cell membrane, which comprises extracting with an alcohol-based solvent and then removing the solvent from the extract.

【0004】本発明方法は、凍結時の水の体積膨張によ
る細胞膜破壊を利用して、細胞質に含有される目的成分
の溶出を促し、溶媒による抽出効率を高めることに成功
したものである。この方法は、水分を含有する、あらゆ
る動植物(きのこを除く)の組織に適用可能である。本
発明方法は、従って、牡蠣、鮪、鱈などの魚介、牛、豚
などの家畜、種々の薬草、ニンニクや大根などの野菜、
果実、茶などの潅木を含む、医薬、民間薬、調味料、健
康(機能性)食品、嗜好品などの原料となり得るものを
対照とする。即ち、本発明は、特定の原料の使用に限定
されるものではなく、あらゆる動植物(きのこを除く)
の組織を用いるエキスの製造に適用可能である。特に牡
蠣エキスおよび野菜エキスの製造に好適である。
The method of the present invention has succeeded in promoting the elution of a target component contained in the cytoplasm by utilizing the destruction of the cell membrane due to the volume expansion of water during freezing, and increasing the extraction efficiency with a solvent. The method is applicable to tissues of any animal or plant (excluding mushrooms) containing water. The method of the present invention, therefore, oysters, tuna, seafood such as cod, livestock such as cows, pigs, various herbs, vegetables such as garlic and radish,
Controls include those that can be raw materials for medicines, folk medicines, seasonings, health (functional) foods, and luxury items, including shrubs such as fruits and tea. That is, the present invention is not limited to the use of a specific raw material, but includes all animals and plants (excluding mushrooms).
It can be applied to the production of an extract using the tissue of the present invention. It is particularly suitable for producing oyster extracts and vegetable extracts.

【0005】本発明方法は、動植物組織を、そのまま、
あるいは適当な大きさの切片に切断した後、組織細胞内
の水分が完全に凍結し、細胞膜が破壊されるに十分な温
度で必要な時間、処理する即ち、必要に応じて、約1
mm〜5mmに切断した組織切片を、通常、温度−15
〜−25℃、好ましくは−15〜−20℃、より好まし
くは−20℃で原料が完全に凍結するまで凍結させる。
そのための時間は、原料の質および量によって様々であ
るが、通常、48時間又はそれ以上で十分である。次い
で、凍結した組織を親水性の溶媒、好ましくは水又はア
ルコール系溶媒で常法に従い抽出する。抽出の条件は、
用いる原料および溶媒によって適宜選択され、例えば、
常圧又は約400〜約500mmHg減圧下、もしくは
2.0気圧までの加圧下、低温、室温、加温あるいは加
熱潅流下、などの様々な条件を組み合わせて行う。適切
な条件は、個々の場合に、当業者の通常の知識に基づい
て容易に選択することができる。例えば、牡蠣むき身が
原料の場合、約−20℃で凍結し、抽出溶媒として水を
用いて、100℃で50〜80分、好ましくは60分
間、攪拌下ジャケット(蒸気圧力:2気圧)で加温抽出
する。次いで、抽出物をろ過し、減圧濃縮する。また、
大根、人参などの野菜類を用いる場合は、数mm,好ま
しくは約3mm厚さの切片にし、凍結させた後、1気圧
下、温度100℃で抽出する。次いで、ろ過、濃縮する
ことにより、エキスを得ることができる。
[0005] The method of the present invention comprises the steps of:
Alternatively, after cutting into sections of an appropriate size, the tissue is treated at a temperature sufficient for completely freezing the water in the tissue cells and destroying the cell membrane for a necessary time . That is, if necessary, about 1
A tissue section cut to a size of 5 mm to 5 mm is usually taken at a temperature of -15.
Freeze at -25 ° C, preferably -15-20 ° C, more preferably -20 ° C until the raw material is completely frozen.
The time for this depends on the quality and quantity of the raw materials, but usually 48 hours or more is sufficient. Next, the frozen tissue is extracted with a hydrophilic solvent, preferably water or an alcohol solvent, according to a conventional method. The conditions for extraction are
It is appropriately selected depending on the raw material and the solvent used, for example,
Various conditions such as normal pressure or reduced pressure of about 400 to about 500 mmHg, or pressurized pressure up to 2.0 atm, low temperature, room temperature, heated or heated perfusion are combined. Suitable conditions can in each case be readily selected on the basis of the ordinary knowledge of the person skilled in the art. For example, when the raw oyster is a raw material, it is frozen at about −20 ° C., and water is used as an extraction solvent at 100 ° C. for 50 to 80 minutes, preferably 60 minutes, with a jacket (steam pressure: 2 atm) under stirring. Extract hot. The extract is then filtered and concentrated under reduced pressure. Also,
When vegetables such as radishes and carrots are used, they are cut into slices having a thickness of several mm, preferably about 3 mm, frozen, and then extracted at 1 atm and a temperature of 100 ° C. Next, an extract can be obtained by filtration and concentration.

【0006】[0006]

【実施例】以下に実施例を挙げて本発明を説明するが、
これらは単なる例示にすぎず、本発明の範囲を制限する
ものではない。実施例1 牡蠣肉エキスの製造 牡牡蠣き身300kgを20kg入りのナイロン袋に分
割して入れ、容量18Lの鉄板亜鉛ビキ缶に入れて−2
0℃の冷凍庫内で、缶の中心の原料が完全に凍結するま
で48時間以上放置する。細胞膜が破壊された凍結牡蠣
原料(300kg)を水900Lを用い、撹拌下、抽出
釜(容量1500L;加熱蒸気圧力:2気圧;温度:1
00℃)により、撹拌下、60分間、加熱抽出する。抽
出後、目の粗いろ布でろ過した後、フィルタープレスで
再ろ過する。ろ液を真空式濃縮機にかけて濃度計(ブリ
ックス)で測定しながらエキス濃度35%まで濃縮す
る。これを瞬間殺菌装置に通して殺菌し、エキス製品を
得る(収量105kg)。100x[エキス製品量(k
g)xエキス濃度(%)]/原料(kg)で表されるエ
キス収率(%)を求め、12.25%を得た。これは3
00X0.1225=36.75kgの純度100%の
牡蠣エキスが得られたことを示している。即ち、本発明
方法による純品の牡蠣エキスの収率は12.25%、収
量は36.75kgであった。
EXAMPLES The present invention will be described below with reference to examples.
These are merely examples and do not limit the scope of the invention. Example 1 Production of Oyster Meat Extract 300 kg of oyster oyster meat was divided into 20 kg nylon bags and placed in a 18-liter zinc-plated iron-plate zinc can.
Leave in the freezer at 0 ° C. for 48 hours or more until the raw material in the center of the can is completely frozen. The frozen oyster raw material (300 kg) in which the cell membrane was destroyed was stirred with 900 L of water using an extraction pot (capacity: 1500 L; heating steam pressure: 2 atm; temperature: 1).
(00 ° C.) for 60 minutes with stirring. After the extraction, the mixture is filtered with a coarse filter cloth and then re-filtered with a filter press. The filtrate is concentrated in a vacuum concentrator to an extract concentration of 35% while measuring with a densitometer (Brix). This is sterilized by passing through an instant sterilizer to obtain an extract product (yield 105 kg). 100x [extract product amount (k
g) x extract concentration (%)] / extract yield (%) expressed as raw material (kg) was obtained to obtain 12.25%. This is 3
00X0.1225 = 36.75 kg of 100% pure oyster extract was obtained. That is, the yield of the pure oyster extract according to the method of the present invention was 12.25%, and the yield was 36.75 kg.

【0007】比較例1 牡蠣むき身300kgを用い、冷凍処理をしないことを
除いて、実施例1と同様の方法で抽出、ろ過、濃縮した
結果、純品エキスの収率は10.5%であった。この場
合の純品牡蠣エキスの収量は31.5kgであり、実施
例1に比較して、収率で1.75%、収率で5.25k
g少なかった。
Comparative Example 1 300 kg of oysters were extracted, filtered and concentrated in the same manner as in Example 1 except that the oysters were not frozen, and as a result, the yield of pure extract was 10.5%. Was. The yield of the pure oyster extract in this case was 31.5 kg, which was 1.75% in yield and 5.25 k in yield as compared with Example 1.
g less.

【0008】実施例2 野菜エキスの製造 生大根143kg、生大根葉69kg、生人参57k
g、生牛蒡28kg、生椎茸3kgを動力切断機で3m
m厚さに切断し、ナイロン袋に入れ、段ボール箱に詰
め、−20℃の冷凍庫内で、48時間以上放置する。次
いで、凍結原料(300kg)を水900Lにより、時
々、蒸気撹拌を行いながら、ジャケット加熱(温度:1
00℃)により、70分間抽出する。抽出後、実施例1
と同様、粗ろ過した後、フィルタープレスで再ろ過し、
真空式濃縮機を用いてブリックス20%まで濃縮し、瞬
間殺菌装置に通して殺菌することによりエキス製品を得
る(収量78kg)。実施例1と同様にして算出した純
品野菜エキスの収率は5.2%、収量は15.6kgで
あった。
Example 2 Production of vegetable extract 143 kg of fresh radish, 69 kg of fresh radish leaves, 57 k of fresh carrot
g, raw burdock 28 kg, raw shiitake 3 kg, 3 m
m, cut into a nylon bag, packed in a cardboard box, and left in a freezer at −20 ° C. for 48 hours or more. Then, the frozen material (300 kg) was heated with 900 L of water while jacket stirring (temperature: 1
(00 ° C.) for 70 minutes. After extraction, Example 1
As above, after coarse filtration, re-filter with a filter press,
The product is concentrated to 20% Brix using a vacuum concentrator, and sterilized by passing through an instant sterilizer to obtain an extract product (yield 78 kg). The yield of the pure vegetable extract calculated in the same manner as in Example 1 was 5.2%, and the yield was 15.6 kg.

【0009】比較例2 実施例2と同様の野菜原料300kgを、冷凍処理をし
ないことを除いて実施例2と同様の方法で抽出、ろ過、
濃縮した結果、純品野菜エキスの収率は4.5%、量は
13.5kgであり、実施例2に比較して、収率で0.
7%、収量で2.1kg少なかった。
Comparative Example 2 300 kg of the same vegetable material as in Example 2 was extracted, filtered, and processed in the same manner as in Example 2 except that the freezing treatment was not performed.
As a result of concentration, the yield of the pure vegetable extract was 4.5% and the amount was 13.5 kg, which was 0.1% in comparison with Example 2.
7%, 2.1 kg less in yield.

【0010】[0010]

【発明の効果】本発明方法によれば、従来の方法に比較
して極めて効率良く、動植物の組織から目的成分を含有
するエキスを得ることができ、資源の有効利用および経
費の節減が達成できる。
According to the method of the present invention, an extract containing the target component can be obtained from the tissues of animals and plants very efficiently as compared with the conventional method, and effective use of resources and reduction of costs can be achieved. .

Claims (3)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 水分を含有する動植物(但し、きのこを
除く)の組織を、温度−15℃〜−20℃で細胞膜が破
壊されるに十分な時間である少 なくとも48時間処理し
た後、水又はアルコール系溶媒で抽出し次いで抽出液か
ら溶媒を除去することを特徴とする凍結細胞膜破壊によ
る動植物エキスの抽出法。
1. An animal or plant containing water (however, mushrooms
Tissue excluded), after the cell membrane at a temperature -15 ° C. ~ - 20 ° C. was 48 hours even without least a time sufficient to be destroyed, and extracted with water or an alcoholic solvent then removing the solvent from the extract A method for extracting an animal or plant extract by destruction of a frozen cell membrane.
【請求項2】 溶媒が、水、メタノール、エタノール、
プロパノール又はこれらの任意の混合物である請求項1
記載の方法。
2. The method according to claim 1, wherein the solvent is water, methanol, ethanol,
2. The method according to claim 1, wherein said compound is propanol or any mixture thereof.
The described method.
【請求項3】 動植物の組織が、魚介、薬草、野菜およ
び畜肉から選択されるものの組織である請求項1〜2
いずれかに記載の方法。
3. A plant and animal tissues, fish, herbs, method according to any one of claims 21 to is of a tissue selected from vegetable and meat.
JP6179821A 1994-06-27 1994-06-27 Extraction method of animal and plant extracts by disruption of frozen cell membrane Expired - Lifetime JP2992737B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6179821A JP2992737B2 (en) 1994-06-27 1994-06-27 Extraction method of animal and plant extracts by disruption of frozen cell membrane

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6179821A JP2992737B2 (en) 1994-06-27 1994-06-27 Extraction method of animal and plant extracts by disruption of frozen cell membrane

Publications (2)

Publication Number Publication Date
JPH0810503A JPH0810503A (en) 1996-01-16
JP2992737B2 true JP2992737B2 (en) 1999-12-20

Family

ID=16072486

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
JP (1) JP2992737B2 (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6111096A (en) * 1997-10-31 2000-08-29 Bbi Bioseq, Inc. Nucleic acid isolation and purification
US8021967B2 (en) 2004-11-01 2011-09-20 California Institute Of Technology Nanoscale wicking methods and devices
JP5425518B2 (en) * 2009-04-28 2014-02-26 株式会社東洋高圧 High pressure ethanol extraction method
JP5465479B2 (en) 2009-07-17 2014-04-09 高砂香料工業株式会社 Onion extract and method for producing the same
JP5970672B2 (en) * 2010-05-21 2016-08-17 日本製粉株式会社 Method for obtaining extract from grape, method for producing food and method for producing cosmetics

Also Published As

Publication number Publication date
JPH0810503A (en) 1996-01-16

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