JPH0716382B2 - Method for producing seaweed minerals - Google Patents
Method for producing seaweed mineralsInfo
- Publication number
- JPH0716382B2 JPH0716382B2 JP2120787A JP12078790A JPH0716382B2 JP H0716382 B2 JPH0716382 B2 JP H0716382B2 JP 2120787 A JP2120787 A JP 2120787A JP 12078790 A JP12078790 A JP 12078790A JP H0716382 B2 JPH0716382 B2 JP H0716382B2
- Authority
- JP
- Japan
- Prior art keywords
- seaweed
- mineral
- water
- extract
- minerals
- 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
Links
- 241001474374 Blennius Species 0.000 title claims description 45
- 229910052500 inorganic mineral Inorganic materials 0.000 title claims description 45
- 239000011707 mineral Substances 0.000 title claims description 45
- 238000004519 manufacturing process Methods 0.000 title claims description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 29
- 239000000284 extract Substances 0.000 claims description 16
- 150000003839 salts Chemical class 0.000 claims description 14
- 238000000605 extraction Methods 0.000 claims description 8
- 206010020772 Hypertension Diseases 0.000 claims description 7
- 238000003809 water extraction Methods 0.000 claims description 4
- 230000001631 hypertensive effect Effects 0.000 claims description 3
- 230000003449 preventive effect Effects 0.000 claims description 3
- 241001261506 Undaria pinnatifida Species 0.000 description 10
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 9
- 238000000034 method Methods 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- 238000012360 testing method Methods 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- 238000001035 drying Methods 0.000 description 6
- 230000036772 blood pressure Effects 0.000 description 5
- 235000013402 health food Nutrition 0.000 description 5
- 239000011734 sodium Substances 0.000 description 5
- 239000011780 sodium chloride Substances 0.000 description 5
- VPGRYOFKCNULNK-ACXQXYJUSA-N Deoxycorticosterone acetate Chemical compound C1CC2=CC(=O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H](C(=O)COC(=O)C)[C@@]1(C)CC2 VPGRYOFKCNULNK-ACXQXYJUSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- 238000010304 firing Methods 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 238000010521 absorption reaction Methods 0.000 description 3
- 230000002378 acidificating effect Effects 0.000 description 3
- KXGVEGMKQFWNSR-UHFFFAOYSA-N deoxycholic acid Natural products C1CC2CC(O)CCC2(C)C2C1C1CCC(C(CCC(O)=O)C)C1(C)C(O)C2 KXGVEGMKQFWNSR-UHFFFAOYSA-N 0.000 description 3
- 239000012153 distilled water Substances 0.000 description 3
- 239000003814 drug Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 241000512259 Ascophyllum nodosum Species 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- 241000700159 Rattus Species 0.000 description 2
- 235000019658 bitter taste Nutrition 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 235000001497 healthy food Nutrition 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 150000007522 mineralic acids Chemical class 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- WEXRUCMBJFQVBZ-UHFFFAOYSA-N pentobarbital Chemical compound CCCC(C)C1(CC)C(=O)NC(=O)NC1=O WEXRUCMBJFQVBZ-UHFFFAOYSA-N 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
- 206010002091 Anaesthesia Diseases 0.000 description 1
- 208000024172 Cardiovascular disease Diseases 0.000 description 1
- 241000282816 Giraffa camelopardalis Species 0.000 description 1
- 241001512709 Lessonia <stramenopiles> Species 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 238000002835 absorbance Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- 230000037005 anaesthesia Effects 0.000 description 1
- 239000006286 aqueous extract Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000004380 ashing Methods 0.000 description 1
- 235000019606 astringent taste Nutrition 0.000 description 1
- 239000004067 bulking agent Substances 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- ZESRJSPZRDMNHY-UHFFFAOYSA-N de-oxy corticosterone Natural products O=C1CCC2(C)C3CCC(C)(C(CC4)C(=O)CO)C4C3CCC2=C1 ZESRJSPZRDMNHY-UHFFFAOYSA-N 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 229940119740 deoxycorticosterone Drugs 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000013355 food flavoring agent Nutrition 0.000 description 1
- 235000011194 food seasoning agent Nutrition 0.000 description 1
- 235000003599 food sweetener Nutrition 0.000 description 1
- 241000411851 herbal medicine Species 0.000 description 1
- DKAGJZJALZXOOV-UHFFFAOYSA-N hydrate;hydrochloride Chemical compound O.Cl DKAGJZJALZXOOV-UHFFFAOYSA-N 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 210000003734 kidney Anatomy 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
- 235000011090 malic acid Nutrition 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000013059 nephrectomy Methods 0.000 description 1
- 210000001331 nose Anatomy 0.000 description 1
- 235000019645 odor Nutrition 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 229960001412 pentobarbital Drugs 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 235000019600 saltiness Nutrition 0.000 description 1
- 235000019643 salty taste Nutrition 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000010902 straw Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- 235000019640 taste Nutrition 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
Landscapes
- Medicines Containing Plant Substances (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
- Seasonings (AREA)
Description
【発明の詳細な説明】 [産業上の利用分野] 本発明は、食塩の代替調味料、健康食品、及び生薬等と
して有用な海藻ミネラルの製造方法に関する。特に、高
血圧予防効果を有する海藻ミネラルの製造方法に関す
る。TECHNICAL FIELD The present invention relates to a method for producing seaweed minerals useful as an alternative seasoning for salt, health foods, herbal medicines and the like. In particular, it relates to a method for producing a seaweed mineral having a hypertensive preventive effect.
[従来の技術] 海藻には健康上有用な各種ミネラルが多く含まれ、自体
健康食として広く供される。[Prior Art] Seaweed contains various minerals useful for health, and is widely used as a healthy food.
しかし従来、海藻を健康食として薬学的に調製したもの
は少ない。そのような中で、特公昭57−6899号公報に
は、海藻中のミネラルを含有する健康食品の製造法が開
示される。この方法に於いては、従来海藻より十分に抽
出されなかったCa、Mg、Fe、Zn等のミネラルを、酸性条
件下抽出する事により効果的に回収取得するものであ
る。However, conventionally, few seaweed have been pharmaceutically prepared as a healthy food. Under such circumstances, Japanese Patent Publication No. 57-6899 discloses a method for producing a health food containing minerals in seaweed. In this method, minerals such as Ca, Mg, Fe, and Zn that have not been sufficiently extracted from seaweed in the past are effectively collected and obtained by extracting them under acidic conditions.
しかし上記公報で製造される健康食品は、ミネラル水と
して調製した場合や、粉末化して再溶解した場合沈殿物
が生じ白濁し食用には適さないという問題を有する。更
に又、上記健康食品の品質は、海藻乾燥物を300〜550℃
で灰化した場合、その灰化条件(例えば、使用する焼成
機、処理する海藻乾燥物中の水分含量と脂肪含量、その
処理量、及びその処理時間等)に左右され易く、異臭な
どのない良好の品質のものを常に製造する事は困難であ
った。However, the health food produced in the above publication has a problem that when it is prepared as mineral water, or when it is pulverized and redissolved, a precipitate is generated and it becomes cloudy and is not suitable for food. Furthermore, the quality of the health foods is that seaweed dried products are 300-550 ° C.
When ashed with ash, it is easy to be affected by the ashing conditions (eg, baking machine used, water content and fat content in dried seaweed to be processed, the amount to be processed, and the processing time), and there is no offensive odor. It has always been difficult to produce good quality products.
[発明が解決しようとする課題] そこで本発明は、溶解度がよく、水に白濁せず、更に高
血圧予防効果を有する高品質の海藻ミネラルを廉価に製
造する事を、目的とする。[Problems to be Solved by the Invention] Accordingly, an object of the present invention is to inexpensively produce high-quality seaweed minerals that have good solubility, do not become cloudy in water, and have an effect of preventing hypertension.
[課題を解決するための手段] 上記目的を達成するため、海藻灰化物としてハンター白
度30以上のものを使用し、この灰化物からの各ミネラル
の水抽出をpH5〜14の条件下に行なえば、優れた功を奏
する事を見出し、本発明を成すに至った。[Means for Solving the Problems] In order to achieve the above object, use a seaweed ash having a Hunter whiteness of 30 or more, and perform water extraction of each mineral from this ash under pH 5 to 14 conditions. Therefore, they have found that they have an excellent effect, and have completed the present invention.
即ち本発明は、ハンター白度が30以上の海藻灰化物に対
し、pH5〜14の抽出条件下に水抽出を行ない、この水抽
出物を濃縮又は乾燥する事を特徴とする高血圧予防効果
を有する海藻ミネラルの製造方法を提供する。That is, the present invention, for the seaweed ash having a whiteness hunter of 30 or more, perform water extraction under extraction conditions of pH 5 to 14, and have a hypertensive preventive effect characterized by concentrating or drying this water extract. A method for producing seaweed minerals is provided.
本発明に使用する海藻種は、ワカメ、アラメ、根昆布、
ホンダワラ、アスコフィルム、ひじき、ツノマタ、キリ
ンサイ及びレッソニア等が挙げられる。本発明に於いて
は上記海藻の使用部位は特に限定されず、従来廃棄され
ていた未利用部位も使用出来る。即ち、例えばワカメの
芽株部、中助部及び葉上部、アラメの根部、根昆布の仮
根部等も使用出来、非常に経済的である。原料として
は、これらの乾燥品、具体的には水分3〜15%程度のも
のが好ましい。The seaweed species used in the present invention include wakame, arame, root kelp,
Examples include Honda straw, Asco film, hijiki, tsunomata, giraffe and Lessonia. In the present invention, the use part of the seaweed is not particularly limited, and an unused part which has been conventionally discarded can also be used. That is, for example, the sprout portion of Wakame seaweed, the middle part and the upper part of the leaf, the root portion of Arame seaweed, and the temporary root portion of root kelp can be used, which is very economical. As a raw material, these dried products, specifically, those having a water content of about 3 to 15% are preferable.
本発明の製造法に於いて、先ず上記海藻の乾燥品を焼成
灰化する。焼成は、灰化物のハンター白度が30以上とな
るように行なう。ハンター白度が30未満だと、得られる
海藻ミネラルは異臭を呈するので好ましくはない。その
ようなハンター白度が30以上となるような焼成条件とし
ては、処理する海藻乾燥品重量にも依るが、例えば400
〜600℃で2〜6時間が好ましい。In the production method of the present invention, first, the dried product of seaweed is calcined and ashed. Firing is performed so that the hunter whiteness of the ash is 30 or more. When the Hunter whiteness is less than 30, the obtained seaweed mineral has an offensive odor, which is not preferable. The firing conditions such that the hunter whiteness is 30 or more, depending on the seaweed dry product weight to be treated, for example 400
It is preferred that the temperature is up to 600 ° C for 2 to 6 hours.
又使用する焼成機としては、例えば電気炉、燃焼炉、焙
煎機等が挙げられる。Examples of the baking machine used include an electric furnace, a combustion furnace, and a roasting machine.
次いで、得られた灰化物を水抽出操作にかける。抽出溶
媒としては、例えば脱イオン水、蒸留水、水道水、有機
酸(例えば、クエン酸、コハク酸)および無機酸(例え
ば、塩酸)等の酸性水等が挙げられる。又抽出溶媒量は
特に限定されないが、例えば、灰化物1部につき4〜20
部である。抽出法は通常の方法でよく、例えば浸漬法等
が挙げられる。浸漬法の場合は、それは温浸でも冷浸で
も構わないが、一般に10〜40℃で1〜24時間行なうのが
好ましい。又浸漬中攪拌等を行うのが好ましい。Then, the obtained ash is subjected to a water extraction operation. Examples of the extraction solvent include deionized water, distilled water, tap water, acidic water such as organic acids (eg citric acid, succinic acid) and inorganic acids (eg hydrochloric acid). The amount of the extraction solvent is not particularly limited, but for example, 4 to 20 per 1 part of ash.
It is a department. The extraction method may be an ordinary method, and examples thereof include a dipping method. In the case of the dipping method, it may be hot-soaked or cold-soaked, but generally it is preferably carried out at 10 to 40 ° C for 1 to 24 hours. Further, it is preferable to perform stirring and the like during the immersion.
一般に上記抽出が進行すると次第に抽出液はアルカリ性
を強める(これは、抽出されるミネラルが一般にアルカ
リ性のためである。)。しかし本発明に於いては抽出液
のpHは、その抽出操作中、常に5〜14、好ましくは5〜
8の範囲に設定する。pHが5より小さいとCa、Mg、Fe、
Zn等のミネラルが過剰に抽出され、ミネラル水とした時
及び粉末化して再溶解した場合沈殿物が生じ、白濁し好
ましくない。上記pHの調整は、前述の有機酸、無機酸等
により行なう事が出来る。Generally, as the above extraction progresses, the extract gradually becomes more alkaline (because the extracted minerals are generally alkaline). However, in the present invention, the pH of the extract is always 5 to 14, preferably 5 to 5 during the extraction operation.
Set in the range of 8. If the pH is less than 5, Ca, Mg, Fe,
A mineral such as Zn is excessively extracted, and when it is made into mineral water or when it is pulverized and redissolved, a precipitate is generated and it becomes cloudy, which is not preferable. The pH can be adjusted with the above-mentioned organic acid, inorganic acid or the like.
その後、濾過、遠心分離等の公知の方法で上記水抽出液
を固形物より分離する。得られた水抽出液は、一般に透
明かやや褐色を呈する。即ち、例えば灰化物10gに蒸留
水40mlを加え1時間25℃で振とう抽出した水抽出液の分
光光度計による吸光値ΔO.D.(測定波長500nm、対照と
して水)は、一般に0.1以下である。又この抽出液100μ
を薄層板(シリカゲル60F−254)にスポットし、展開
溶媒(ブタノール:酢酸:水=4:1:5)で展開した場
合、Rf値約0.4及び0.7にはスポットは見られない。Then, the water extract is separated from the solid matter by a known method such as filtration or centrifugation. The resulting aqueous extract is generally transparent or slightly brown. That is, for example, the absorption value ΔO.D. (measurement wavelength: 500 nm, water as a control) of a water extract obtained by adding 40 ml of distilled water to 10 g of ash and extracting by shaking at 25 ° C. for 1 hour is generally 0.1 or less. is there. Also this extract 100μ
When spotted on a thin layer plate (silica gel 60F-254) and developed with a developing solvent (butanol: acetic acid: water = 4: 1: 5), no spot is seen at Rf values of about 0.4 and 0.7.
次いで、上記水抽出液を濃縮又は乾燥する。濃縮法とし
ては通常の方法でよく、例えば減圧濃縮、直火蒸発濃
縮、膜濃縮等により行なう事が出来る。濃縮の程度は特
に限定されず適宜選択してよい。又乾燥法も通常の方法
でよく、例えば減圧乾燥、噴霧乾燥、薄膜真空乾燥、直
火乾燥、常圧乾燥等により行なう事が出来る。乾燥品は
適宜粉砕等の加工処理を行なっても良い。Then, the water extract is concentrated or dried. The concentration method may be an ordinary method, for example, vacuum concentration, direct flame evaporation concentration, membrane concentration and the like. The degree of concentration is not particularly limited and may be appropriately selected. Also, the drying method may be an ordinary method, for example, reduced pressure drying, spray drying, thin film vacuum drying, open flame drying, atmospheric pressure drying and the like. The dried product may be appropriately subjected to processing such as crushing.
上記のようにして製造された本発明の海藻ミネラル濃縮
液若しくは乾燥物は、必要に応じ食品及び薬剤等に通常
添加されるもの、例えば賦形剤、甘味剤、増量剤、香
料、着色料、矯味剤及び品質改良剤等を加えても良い。The seaweed mineral concentrate or dried product of the present invention produced as described above is one that is usually added to foods and drugs as necessary, for example, an excipient, a sweetener, a bulking agent, a flavoring agent, a coloring agent, You may add a corrigent and a quality improving agent.
更に、食味を良好なものとするために、上記海藻ミネラ
ル濃縮液のpH、又は海藻ミネラル乾燥物1gを100mlの水
に溶かした水溶液のpHは、例えば5〜8になるように必
要に応じ調整するのが好ましい。この調整工程は、得ら
れる海藻ミネラルが上記pHとなるのであればいつ行なっ
ても良く、例えば上記水抽出液の分離後、或いは濃縮若
しくは乾燥後行なってもよい。調整法は特に限定され
ず、酸性物質(例えば塩酸水、クエン酸、リンゴ酸等)
を添加混合する事によって行なう事が出来る。但し、添
加に際しては、海藻ミネラル中の各ミネラル組成を可及
的に維持するように、添加量及び添加物を選択するのが
好ましい。Furthermore, in order to improve the eating quality, the pH of the above-mentioned seaweed mineral concentrate or the pH of an aqueous solution prepared by dissolving 1 g of the dried seaweed mineral in 100 ml of water is adjusted as necessary to be, for example, 5-8. Preferably. This adjusting step may be performed at any time as long as the obtained seaweed mineral has the above pH, for example, after separating the water extract, or after concentrating or drying. The preparation method is not particularly limited, and acidic substances (for example, hydrochloric acid water, citric acid, malic acid, etc.)
It can be performed by adding and mixing. However, upon addition, it is preferable to select the addition amount and additives so that each mineral composition in the seaweed mineral is maintained as much as possible.
上記のようにして得られる本発明の海藻ミネラルは、一
般にカリウムの方がナトリウムより多く含まれる。そし
て、より高血圧を有効に防止するためには、含有ナトリ
ウムと含有カリウムの比Na/Kは2以下が好ましい。その
為、例えば更に食塩等を必要に応じ加えて、Na/K比が2
以下となるように調整しても良い。この食塩の添加時期
は特に限定されず、いつ添加しても構わない。In the seaweed mineral of the present invention obtained as described above, potassium is generally contained in a larger amount than sodium. In order to prevent hypertension more effectively, the ratio Na / K of contained sodium and contained potassium is preferably 2 or less. For this reason, for example, add Na, etc. as needed to increase the Na / K ratio to 2
The adjustment may be made as follows. The timing of adding this salt is not particularly limited, and it may be added at any time.
[発明の効果] 本発明の製造法に於いては、従来未利用の海藻及び廃棄
されていた海藻部位を使用出来、非常に経済的である。[Effects of the Invention] In the production method of the present invention, previously unused seaweed and discarded seaweed parts can be used, which is very economical.
更に、本発明の製造法により得られた海藻ミネラルは循
環器系疾患の予防、特に高血圧予防に有用な薬効ミネラ
ル成分を多く含み、生薬として優れる。Furthermore, the seaweed mineral obtained by the production method of the present invention contains a large amount of medicinal mineral components useful for the prevention of cardiovascular diseases, particularly for preventing hypertension, and is excellent as a crude drug.
又、本発明の製造法により得られた海藻ミネラルは、苦
味や異臭が殆どなく、又ミネラル水としても白濁しない
ので、健康食品として、又食塩の代替物としても優れ
る。Further, the seaweed mineral obtained by the production method of the present invention has almost no bitterness or offensive odor, and does not become cloudy as mineral water, so that it is excellent as a health food or a substitute for salt.
[実施例] 以下、本発明を実施例で更に詳しく説明する。[Examples] Hereinafter, the present invention will be described in more detail with reference to Examples.
海藻ミネラルの調製 (実施例1) 西淡町(淡路島)で収穫されたワカメの芽株を天日で乾
燥後(水分12%)、この乾燥物1kgを電気炉(ヤマト科
学(株)製のDDR−22)に入れて500℃で3h焼成した。こ
の時の灰化物のハンター白度は32.1であった。この灰化
物1重量部に4重量部の蒸留水を加え、25℃で1時間振
とうした後、No.1濾紙で濾過して抽出液を得た。尚、得
られた抽出液の吸光値ΔO.D.(測定波長500nm、対照と
して水)は、0.022であった。又、この抽出液100μを
薄層板(ジカゲル60F−254)にスポットし、展開溶媒
(ブタノール:酢酸:水=4:1:5)で展開した場合、Rf
値約0.4及び0.7にはスポットは見られなかった。濾物に
対しても上記抽出操作を繰り返し行い、得られた抽出液
を始めの抽出液と併せ、塩酸でpHを7.0に調整後、エバ
ポレータで1/10体積程度にまで減圧濃縮した。濃縮液を
蒸発釜で煮つめて塩を析出させ、その塩をさらに150℃
で一晩乾燥し、最後に粉砕機で粉砕してパウダ状海藻ミ
ネラルを得た。Preparation of Seaweed Minerals (Example 1) Wakame sprouts harvested in Nishitan Town (Awaji Island) were dried in the sun (water content 12%), and 1 kg of this dried product was used in an electric furnace (Yamato Scientific Co., Ltd. DDR). -22) and baked at 500 ° C for 3 hours. Hunter whiteness of the ash at this time was 32.1. 4 parts by weight of distilled water was added to 1 part by weight of this ash, and the mixture was shaken at 25 ° C. for 1 hour and filtered with No. 1 filter paper to obtain an extract. The absorption value ΔO.D. (measurement wavelength: 500 nm, water as a control) of the obtained extract was 0.022. When 100 μl of this extract was spotted on a thin layer plate (Dikagel 60F-254) and developed with a developing solvent (butanol: acetic acid: water = 4: 1: 5), Rf
No spots were seen at values of 0.4 and 0.7. The above extraction operation was repeated on the residue, the obtained extract was combined with the first extract, the pH was adjusted to 7.0 with hydrochloric acid, and the mixture was concentrated under reduced pressure to about 1/10 volume with an evaporator. The concentrated liquid is boiled in an evaporator to precipitate salt, and the salt is further heated at 150 ° C.
The powdery seaweed mineral was obtained by pulverizing with a pulverizer at last.
(比較例1〜4) 表−1に示す焼成条件下に焼成を行った以外は、実施例
1と同様にして各海藻ミネラルを得た。尚各灰化物のハ
ンター白度、及び各抽出液の吸光値ΔO.D.と薄層板(TL
C)上のRf0.4及び0.7に於けるスポット結果も表−1に
示す。(Comparative Examples 1 to 4) Each seaweed mineral was obtained in the same manner as in Example 1 except that firing was performed under the firing conditions shown in Table 1. In addition, the Hunter whiteness of each ash, the absorption value ΔO.D. of each extract, and the thin plate (TL
The spot results for Rf 0.4 and 0.7 above C) are also shown in Table-1.
(海藻ミネラルの臭味試験) 上記実施例1及び比較例1〜4の各海藻ミネラル3gを薬
包紙上に載せ、パネラ8名がこれらを直接鼻で嗅いで、
異臭の強さを官能評価した。これらの結果を表−1に示
す。尚表−1中、「+++」はかなり強い臭い、「+
+」は中程度の臭い、「+」は謹かな臭い、「−」は無
臭をそれぞれ表す。(Seaweed Mineral Odor Test) 3 g of each seaweed mineral of Example 1 and Comparative Examples 1 to 4 was placed on a medicine wrapping paper, and eight panelists sniffed these directly with their noses.
A sensory evaluation of the strength of the offensive odor was made. The results are shown in Table-1. In Table-1, "+++" has a fairly strong odor, and "+"
“+” Means a moderate odor, “+” means a faint odor, and “−” means no odor.
表−1より明らかな様に、灰化物のハンター白度が30を
越えるか、抽出液の吸光度ΔO.D.が0.1を越えるか、薄
層クロマト板にスポットが見られた場合(Rf値、0.4、
0.7)は、その海藻ミネラルは異臭が感じられる。 As is clear from Table-1, if the Hunter whiteness of the ash is over 30, the absorbance ΔO.D. of the extract is over 0.1, or if spots are seen on the thin-layer chromatograph plate (Rf value, 0.4,
At 0.7), the seaweed mineral has a strange odor.
(薬理試験) 体重150〜200g、6週令のS.D.系雄性ラットの左腎をペ
ントバルビタール麻酔下で摘出した。腎摘出後、オリー
ブ油にけん濁したデオキシコルチコステロン(DOCA)を
30mg/kgの量で週一回皮下投与するとともに1%食塩含
有試料及び1%ワカメミネラル含有試料を自然摂取させ
た。尚、DOCA、1%NaCl含有試料及び1%ワカメミネラ
ル含有試料の投与法については、DOCAは2ヶ月間週一回
の割合で30mg/kgを皮下投与し、1%NaCl含有試料及び
1%ワカメミネラル含有試料はそれぞれ2ヶ月間連日経
口投与した。試験前、試験後1ケ月、及び試験後2ケ月
めのラットの血圧をテイルーカップ法(tail−cuff法)
により測定した。結果を下表に示す。(Pharmacological test) The left kidney of SD male rats aged 150 to 200 g and 6 weeks old was isolated under pentobarbital anesthesia. After nephrectomy, deoxycorticosterone (DOCA) suspended in olive oil was added.
The sample was subcutaneously administered once a week in an amount of 30 mg / kg, and the sample containing 1% salt and the sample containing 1% wakame mineral were naturally ingested. Regarding the administration method of DOCA, 1% NaCl-containing sample and 1% wakame mineral-containing sample, DOCA was subcutaneously administered at a rate of 30 mg / kg once a week for 2 months, and 1% NaCl-containing sample and 1% wakame Each of the mineral-containing samples was orally administered daily for 2 months. The blood pressure of the rat before the test, one month after the test, and the second month after the test was measured using the tail-cuff method.
It was measured by. The results are shown in the table below.
1%NaCl投与群は、対照群に比べ有意に血圧の上昇が認
められた。一方、1%ワカメミネラル投与群は、1ヶ月
では対照群と比較し有意な血圧上昇がみられなく、1%
NaCl投与1ケ月群(血圧:191.8±5.8mmHg)に1%ワカ
メミネラル投与により約10mmHgの降圧が認められた。 A significant increase in blood pressure was observed in the 1% NaCl administration group as compared with the control group. On the other hand, the 1% wakame mineral-administered group showed no significant increase in blood pressure at 1 month compared with the control group, and 1%
In the 1-month group administered with NaCl (blood pressure: 191.8 ± 5.8 mmHg), the blood pressure was reduced by about 10 mmHg by the administration of 1% wakame mineral.
このことからワカメミネラルが高血圧症の予防・治療に
有効であることが示唆された。This suggests that seaweed minerals are effective in the prevention and treatment of hypertension.
(食塩代替物としての使用性) 1.0%、1.5%及び2.0%の各濃度に調製した実施例1の
ワカメミネラル塩水の塩味が、それぞれ何%濃度の食塩
水に匹敵するかを、被試験者6名に食味試験した。これ
らの結果を第1図に示す。(Usability as a salt substitute) The test subjects were asked to determine what concentration of salty water of the wakame mineral salt water of Example 1 prepared to each concentration of 1.0%, 1.5% and 2.0% was equivalent to the salt water concentration. A taste test was conducted on 6 people. The results are shown in FIG.
第1図に示すように、1.0%、1.5%、及び2.0%濃度の
各ワカメミネラル塩水の塩味は、それぞれ約0.2〜0.6
%、約0.6〜1.0、及び約1.0〜1.5%濃度の食塩水と同等
である事が判った。従って本発明のワカメミネラルは、
食塩代替物として十分使用する事が出来、又過度な苦
み、渋み、異臭等もない。As shown in Fig. 1, the saltiness of each wakame mineral salt water of 1.0%, 1.5%, and 2.0% concentration is about 0.2 to 0.6.
%, About 0.6-1.0, and about 1.0-1.5% concentration of saline. Therefore, the seaweed mineral of the present invention,
It can be used well as a salt substitute and does not have excessive bitterness, astringency, or odor.
第1図は、本発明のワカメミネラル塩水と食塩水との塩
味に関する相関関係図を示す。FIG. 1 shows a correlation diagram regarding salty taste between seaweed mineral salt water of the present invention and salt water.
───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開 昭48−87046(JP,A) ─────────────────────────────────────────────────── ─── Continuation of the front page (56) References JP-A-48-87046 (JP, A)
Claims (2)
し、pH5〜14の抽出条件下に水抽出を行ない、この水抽
出物を濃縮又は乾燥する事を特徴とする高血圧予防効果
を有する海藻ミネラルの製造方法。1. A hypertensive preventive effect, characterized in that seaweed ash having a whiteness of hunter of 30 or more is subjected to water extraction under extraction conditions of pH 5 to 14 and the water extract is concentrated or dried. Method for producing seaweed minerals.
ネラルのpH調整工程、及び/又は海藻ミネラル中のNa/K
比が2以下となるように食塩の添加工程を含む請求項
(1)記載の海藻ミネラルの製造方法。2. The method for producing a seaweed mineral further comprises the step of adjusting the pH of the seaweed mineral, and / or Na / K in the seaweed mineral.
The method for producing a seaweed mineral according to claim 1, including a step of adding salt so that the ratio becomes 2 or less.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2120787A JPH0716382B2 (en) | 1990-05-10 | 1990-05-10 | Method for producing seaweed minerals |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2120787A JPH0716382B2 (en) | 1990-05-10 | 1990-05-10 | Method for producing seaweed minerals |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0416164A JPH0416164A (en) | 1992-01-21 |
JPH0716382B2 true JPH0716382B2 (en) | 1995-03-01 |
Family
ID=14794990
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2120787A Expired - Lifetime JPH0716382B2 (en) | 1990-05-10 | 1990-05-10 | Method for producing seaweed minerals |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0716382B2 (en) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3005950B2 (en) * | 1993-10-07 | 2000-02-07 | まるしげ上田株式会社 | Far infrared radiator |
JPH07255415A (en) * | 1994-03-25 | 1995-10-09 | Sangyo Gijutsu Kenkyusho:Kk | Functional salty taste composition |
JP2666179B2 (en) * | 1994-08-10 | 1997-10-22 | 財団法人韓國食品開發研究院 | Antihypertensive health food composition |
KR20040047487A (en) * | 2002-11-28 | 2004-06-05 | 김선재 | Preparation of Mineral and Salt from Sea-weed |
JP2004201568A (en) * | 2002-12-25 | 2004-07-22 | Shirako:Kk | Health food for ameliorating blood fluidity |
DE10355400A1 (en) * | 2003-11-25 | 2005-07-07 | Noack, Andreas, Dr. | Multicomponent mineral preparations and method for the preparation of multi-component mineral preparations |
JP7505831B2 (en) * | 2021-12-14 | 2024-06-25 | シード医療製薬株式会社 | Hypertension improving agent containing seaweed extract, and functional foods, quasi-drugs and medicines containing said hypertension improving agent |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS576899B2 (en) * | 1972-02-23 | 1982-02-08 | ||
JPS576899A (en) * | 1980-06-14 | 1982-01-13 | Victor Company Of Japan | Digital signal processor |
JPS5721301A (en) * | 1980-07-15 | 1982-02-04 | Katayama Chem Works Co Ltd | Agent for controlling sedentary marine life |
-
1990
- 1990-05-10 JP JP2120787A patent/JPH0716382B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
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JPH0416164A (en) | 1992-01-21 |
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