JPH0984552A - Calcium-containing composition excellent in absorbing property - Google Patents
Calcium-containing composition excellent in absorbing propertyInfo
- Publication number
- JPH0984552A JPH0984552A JP8007437A JP743796A JPH0984552A JP H0984552 A JPH0984552 A JP H0984552A JP 8007437 A JP8007437 A JP 8007437A JP 743796 A JP743796 A JP 743796A JP H0984552 A JPH0984552 A JP H0984552A
- Authority
- JP
- Japan
- Prior art keywords
- calcium
- sea urchin
- shell
- containing composition
- urchin shell
- 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
Links
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 title claims abstract description 92
- 239000011575 calcium Substances 0.000 title claims abstract description 89
- 229910052791 calcium Inorganic materials 0.000 title claims abstract description 89
- 239000000203 mixture Substances 0.000 title claims abstract description 44
- 241000257465 Echinoidea Species 0.000 claims abstract description 47
- 238000010304 firing Methods 0.000 claims description 8
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 abstract description 29
- 229910000019 calcium carbonate Inorganic materials 0.000 abstract description 11
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 abstract description 7
- 239000000292 calcium oxide Substances 0.000 abstract description 7
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 abstract description 7
- 235000013305 food Nutrition 0.000 abstract description 6
- 235000013372 meat Nutrition 0.000 abstract description 5
- 208000013038 Hypocalcemia Diseases 0.000 abstract description 4
- 230000000705 hypocalcaemia Effects 0.000 abstract description 4
- 239000012535 impurity Substances 0.000 abstract description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 4
- FNAQSUUGMSOBHW-UHFFFAOYSA-H calcium citrate Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O.[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O FNAQSUUGMSOBHW-UHFFFAOYSA-H 0.000 abstract description 2
- 239000001354 calcium citrate Substances 0.000 abstract description 2
- 235000013337 tricalcium citrate Nutrition 0.000 abstract description 2
- 229960005069 calcium Drugs 0.000 description 85
- 241000700159 Rattus Species 0.000 description 20
- 239000008280 blood Substances 0.000 description 16
- 210000004369 blood Anatomy 0.000 description 16
- 229960003563 calcium carbonate Drugs 0.000 description 9
- 238000010521 absorption reaction Methods 0.000 description 8
- 230000037213 diet Effects 0.000 description 8
- 235000005911 diet Nutrition 0.000 description 8
- 210000003608 fece Anatomy 0.000 description 7
- 239000002994 raw material Substances 0.000 description 7
- 238000001354 calcination Methods 0.000 description 5
- 239000002504 physiological saline solution Substances 0.000 description 5
- 210000002784 stomach Anatomy 0.000 description 5
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
- 230000037396 body weight Effects 0.000 description 4
- MKJXYGKVIBWPFZ-UHFFFAOYSA-L calcium lactate Chemical compound [Ca+2].CC(O)C([O-])=O.CC(O)C([O-])=O MKJXYGKVIBWPFZ-UHFFFAOYSA-L 0.000 description 4
- 239000001527 calcium lactate Substances 0.000 description 4
- 229960002401 calcium lactate Drugs 0.000 description 4
- 235000011086 calcium lactate Nutrition 0.000 description 4
- 210000000936 intestine Anatomy 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 3
- 241000237502 Ostreidae Species 0.000 description 3
- 239000001110 calcium chloride Substances 0.000 description 3
- 229910001628 calcium chloride Inorganic materials 0.000 description 3
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 3
- 239000000920 calcium hydroxide Substances 0.000 description 3
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 3
- 235000011116 calcium hydroxide Nutrition 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 230000029142 excretion Effects 0.000 description 3
- 235000013402 health food Nutrition 0.000 description 3
- 239000013642 negative control Substances 0.000 description 3
- 235000020636 oyster Nutrition 0.000 description 3
- 239000013641 positive control Substances 0.000 description 3
- 229940088417 precipitated calcium carbonate Drugs 0.000 description 3
- 208000013725 Chronic Kidney Disease-Mineral and Bone disease Diseases 0.000 description 2
- 241000238557 Decapoda Species 0.000 description 2
- 208000001132 Osteoporosis Diseases 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 235000010216 calcium carbonate Nutrition 0.000 description 2
- 239000001569 carbon dioxide Substances 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 230000037406 food intake Effects 0.000 description 2
- 210000001035 gastrointestinal tract Anatomy 0.000 description 2
- 239000010903 husk Substances 0.000 description 2
- 230000000968 intestinal effect Effects 0.000 description 2
- 239000008194 pharmaceutical composition Substances 0.000 description 2
- 201000006409 renal osteodystrophy Diseases 0.000 description 2
- 235000015170 shellfish Nutrition 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 206010002091 Anaesthesia Diseases 0.000 description 1
- 241000242757 Anthozoa Species 0.000 description 1
- 241000512259 Ascophyllum nodosum Species 0.000 description 1
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 1
- 235000014653 Carica parviflora Nutrition 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 241000238424 Crustacea Species 0.000 description 1
- 241000195493 Cryptophyta Species 0.000 description 1
- 239000004278 EU approved seasoning Substances 0.000 description 1
- 235000019738 Limestone Nutrition 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 241001261506 Undaria pinnatifida Species 0.000 description 1
- 229930003316 Vitamin D Natural products 0.000 description 1
- QYSXJUFSXHHAJI-XFEUOLMDSA-N Vitamin D3 Natural products C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)CCCC(C)C)=C/C=C1\C[C@@H](O)CCC1=C QYSXJUFSXHHAJI-XFEUOLMDSA-N 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 230000037005 anaesthesia Effects 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- 239000000648 calcium alginate Substances 0.000 description 1
- 235000010410 calcium alginate Nutrition 0.000 description 1
- 229960002681 calcium alginate Drugs 0.000 description 1
- 239000004227 calcium gluconate Substances 0.000 description 1
- 229960004494 calcium gluconate Drugs 0.000 description 1
- 235000013927 calcium gluconate Nutrition 0.000 description 1
- 229940095643 calcium hydroxide Drugs 0.000 description 1
- 229910001424 calcium ion Inorganic materials 0.000 description 1
- 239000001506 calcium phosphate Substances 0.000 description 1
- 229910000389 calcium phosphate Inorganic materials 0.000 description 1
- 229960001714 calcium phosphate Drugs 0.000 description 1
- 235000011010 calcium phosphates Nutrition 0.000 description 1
- OKHHGHGGPDJQHR-YMOPUZKJSA-L calcium;(2s,3s,4s,5s,6r)-6-[(2r,3s,4r,5s,6r)-2-carboxy-6-[(2r,3s,4r,5s,6r)-2-carboxylato-4,5,6-trihydroxyoxan-3-yl]oxy-4,5-dihydroxyoxan-3-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylate Chemical compound [Ca+2].O[C@@H]1[C@H](O)[C@H](O)O[C@@H](C([O-])=O)[C@H]1O[C@H]1[C@@H](O)[C@@H](O)[C@H](O[C@H]2[C@H]([C@@H](O)[C@H](O)[C@H](O2)C([O-])=O)O)[C@H](C(O)=O)O1 OKHHGHGGPDJQHR-YMOPUZKJSA-L 0.000 description 1
- NEEHYRZPVYRGPP-UHFFFAOYSA-L calcium;2,3,4,5,6-pentahydroxyhexanoate Chemical compound [Ca+2].OCC(O)C(O)C(O)C(O)C([O-])=O.OCC(O)C(O)C(O)C(O)C([O-])=O NEEHYRZPVYRGPP-UHFFFAOYSA-L 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000003651 drinking water Substances 0.000 description 1
- 235000020188 drinking water Nutrition 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 210000003278 egg shell Anatomy 0.000 description 1
- 235000011194 food seasoning agent Nutrition 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 235000016709 nutrition Nutrition 0.000 description 1
- 230000035764 nutrition Effects 0.000 description 1
- 210000001672 ovary Anatomy 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 210000002966 serum Anatomy 0.000 description 1
- 210000000813 small intestine Anatomy 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 235000019166 vitamin D Nutrition 0.000 description 1
- 239000011710 vitamin D Substances 0.000 description 1
- 150000003710 vitamin D derivatives Chemical class 0.000 description 1
- 229940046008 vitamin d Drugs 0.000 description 1
Landscapes
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Description
【０００１】[0001]
【発明の属する技術分野】本発明は、ウニ殻から得られ
る経口吸収性の良好なカルシウム含有組成物に関する。TECHNICAL FIELD The present invention relates to a calcium-containing composition obtained from sea urchin shells and having good oral absorbability.
【０００２】[0002]
【従来の技術及び課題】従来から、カルシウムの摂取不
足を補うため、種々のカルシウム製剤やカルシウムを有
効成分とする健康食品が提案されている。これらに用い
られるカルシウムは、一般に、石灰石や石灰乳などの鉱
物起源の炭酸カルシウム、リン酸カルシウム、水酸化カ
ルシウム、乳酸カルシウム、グルコン酸カルシウム等、
カキ殻、貝類、サンゴ等由来の貝カルシウム、カニ、エ
ビなどの甲殻類、コンブ、ヒジキ、ワカメなどの藻類、
哺乳動物などの骨、あるいは卵の殻などを原料としたも
のである。2. Description of the Related Art Conventionally, various calcium preparations and health foods containing calcium as an active ingredient have been proposed in order to make up for insufficient intake of calcium. Calcium used in these, generally, calcium carbonate, calcium phosphate, calcium hydroxide, calcium lactate, calcium gluconate, etc. of mineral origin such as limestone and lime milk,
Shellfish such as oyster shells, shellfish, corals, crustaceans such as crabs and shrimp, algae such as kelp, hijiki, wakame,
It is made from bones of mammals or egg shells.
【０００３】しかしながら、これらの原料を用いたカル
シウムは一般に吸収性が十分でない。しかも、カルシウ
ムは、ビタミンＤや蛋白質等と同時に摂取しないと、人
体への吸収率が極めて低く、それ単独での服用によって
は、人体における所要量のカルシウムを摂取することは
困難な状況にある。また、厚生省国民栄養調査によれ
ば、我国国民は平均して１日に５３１ｍｇしか摂取して
いない。この量は実に欧米諸国の半分以下のレベルであ
る。[0003] However, calcium using these raw materials generally has insufficient absorption. Moreover, if calcium is not taken at the same time as vitamin D or protein, the rate of absorption into the human body is extremely low, and it is difficult to take the required amount of calcium in the human body by taking it alone. According to the Ministry of Health and Welfare's National Nutrition Survey, Japanese people consume only 531 mg a day on average. This is actually less than half the level of Western countries.
【０００４】かかる事情に鑑み、本発明者らは、吸収性
の良好なカルシウム含有組成物を得るべく鋭意研究を重
ねた結果、原料として従来全く試みられていなかった、
しかも、全く利用されずに単に廃棄処分されていたウニ
殻を用い、これを焼成することによって、意外にも経口
吸収性に優れたカルシウム含有組成物が得られることを
見い出し、本発明を完成するに至った。In view of such circumstances, the present inventors have conducted intensive studies to obtain a calcium-containing composition having good absorbability, and as a result, no attempt has been made as a raw material in the past.
Moreover, it was discovered that a calcium-containing composition having excellent oral absorbability can be obtained unexpectedly by firing sea urchin shells that have been simply discarded without being used at all, and complete the present invention. Came to.
【０００５】[0005]
【課題を解決するための手段】すなわち、本発明はウニ
殻より得られるカルシウム含有組成物を提供するもので
ある。また、本出願は該組成物の製造方法、該組成物を
含有する食品、該組成物を含有する飼料、該組成物を含
有する医薬組成物を開示するものである。That is, the present invention provides a calcium-containing composition obtained from sea urchin shells. The present application also discloses a method for producing the composition, a food containing the composition, a feed containing the composition, and a pharmaceutical composition containing the composition.
【０００６】本発明のカルシウムの原料とするウニの種
類は特に限定されるものではなく、例えば、バフンウ
ニ、ムラサキウニ、エゾバフンウニ、アカウニ等を挙げ
ることができる。[0006] The type of sea urchin used as a raw material of calcium of the present invention is not particularly limited, and examples thereof include bahun sea urchin, murasaki sea urchin, ezoba fun sea urchin, and akauni sea urchin.
【０００７】本発明のカルシウム含有組成物を製造する
には、まず、ウニ殻の肉部分を取り除く。これは、例え
ば、ウニを分割し、卵巣または肉部分を取り除くことに
よって行うことができる。肉部分を取り除いた後、洗浄
する。洗浄は、通常水洗によって行うことができる。To produce the calcium-containing composition of the present invention, first, the meat portion of the sea urchin shell is removed. This can be done, for example, by splitting the sea urchin and removing the ovaries or meat parts. After removing the meat part, it is washed. Washing can be usually performed by washing with water.
【０００８】次いで、高温で焼成する。焼成温度は、好
ましくは５００〜１５００℃とする。焼成時間は、好ま
しくは０．５〜１．５時間とする。焼成の例としては、
例えば、焼成炉を用いる場合、好ましくは約１０００℃
で約１時間、真空炉を用いる場合、好ましくは約８００
℃で約１時間焼成する。Next, firing is performed at a high temperature. The firing temperature is preferably 500 to 1500 ° C. The firing time is preferably 0.5 to 1.5 hours. As an example of firing,
For example, when a firing furnace is used, it is preferably about 1000 ° C.
When using a vacuum furnace for about 1 hour, preferably about 800 hours
Bake at about 1 hour.
【０００９】かかる焼成により、ウニ殻に炭酸カルシウ
ムの形態で含まれていたカルシウムが酸化カルシウムの
形態に変換される。[0009] By such calcination, calcium contained in the sea urchin shell in the form of calcium carbonate is converted to the form of calcium oxide.
【００１０】焼成後、適宜、酸化カルシウムを炭酸カル
シウム、水酸化カルシウム、クエン酸カルシウム、アル
ギン酸カルシウム等の利用しやすい形態に変換すること
ができる。例えば、炭酸カルシウムへの変換は、酸化カ
ルシウムに炭酸ガスを与えることによって行われる。After calcination, the calcium oxide can be converted into an easily usable form such as calcium carbonate, calcium hydroxide, calcium citrate, calcium alginate or the like. For example, conversion to calcium carbonate is performed by giving carbon dioxide to calcium oxide.
【００１１】なお、本発明のウニ殻由来カルシウムは、
食用物質から得られるもので、毒性は問題とならない。The sea urchin shell-derived calcium of the present invention is
It is obtained from edible substances and toxicity is not a problem.
【００１２】次に、本発明のウニ殻を焼成して得られる
カルシウム含有組成物を含有してなる食品、飼料または
医薬組成物は、例えば、本発明のウニ殻を焼成して得ら
れるカルシウム含有組成物を、常法により、クエン酸、
その他の賦形剤などと共に配合し、錠剤または顆粒剤等
を製すること、あるいは溶解し、その他の調味剤等と共
に飲用水のような形態とすることができる。該カルシウ
ム含有組成物の配合量は適宜選択することができるが、
通常、食品等の全量に対して１０〜５０重量％程度であ
る。かくして、本発明のウニ殻由来カルシウムを配合し
た食品等を摂取させることによりカルシウムの良好な経
口吸収が得られる。Next, the food, feed or pharmaceutical composition containing the calcium-containing composition obtained by baking the sea urchin shell of the present invention includes, for example, the calcium-containing composition obtained by baking the sea urchin shell of the present invention. The composition, citric acid, by a conventional method,
It can be blended with other excipients to produce tablets or granules or the like, or can be dissolved and made into a form like drinking water together with other seasonings and the like. The blending amount of the calcium-containing composition can be appropriately selected,
Usually, it is about 10 to 50% by weight with respect to the total amount of food and the like. Thus, good oral absorption of calcium can be obtained by ingesting a food or the like containing the sea urchin shell-derived calcium of the present invention.
【００１３】[0013]
【発明の実施の形態】次に、実施例を挙げて本発明をさ
らに具体的に説明するが、本発明はこれに限定されるも
のではない。BEST MODE FOR CARRYING OUT THE INVENTION Next, the present invention will be described more specifically with reference to Examples, but the present invention is not limited thereto.
【００１４】［実施例１］バフンウニ及びムラサキウニ
の肉部分をヘラで取り除いた後、水洗した。このウニ殻
を焼成炉にて１０００℃で１時間焼成した。かかる焼成
によりウニ殻に炭酸カルシウムの形態で含まれていたカ
ルシウムが酸化カルシウムの形態に変換される。焼成
後、所定量の水を与え、撹拌反応させて水酸化カルシウ
ムの形態とした。この成分分析値を表１に掲げる。Example 1 After removing the meat portions of the sea urchin and sea urchin with a spatula, they were washed with water. The sea urchin shell was fired in a firing furnace at 1000 ° C. for 1 hour. By such calcination, calcium contained in the sea urchin shell in the form of calcium carbonate is converted to the form of calcium oxide. After the calcination, a predetermined amount of water was given and agitation reaction was performed to form calcium hydroxide. Table 1 shows the component analysis values.
【００１５】[0015]
【表１】 次に、本発明のウニ殻由来カルシウム含有組成物の特性
を、他の原料由来のカルシウム含有組成物と比較した。
比較した試料は、各原料を１０００℃で１時間焼成する
ことによって、各原料に炭酸カルシウム等の形態で含ま
れていたカルシウムを一度酸化カルシウムの形態とし、
更にこれらに炭酸ガスを与えて食餌として摂取可能な炭
酸カルシウムの形態に再度変換した上で比較した。結果
を表２に掲げる。[Table 1] Next, the characteristics of the sea urchin shell-derived calcium-containing composition of the present invention were compared with calcium-containing compositions derived from other raw materials.
The compared sample was prepared by calcining each raw material at 1000 ° C. for 1 hour to convert calcium contained in each raw material in the form of calcium carbonate or the like into calcium oxide once,
Furthermore, carbon dioxide was given to these to convert them again to the form of calcium carbonate that can be consumed as a diet, and then compared. The results are listed in Table 2.
【００１６】[0016]
【表２】 表２から明らかなごとく、ウニ殻由来のカルシウム含有
組成物は外観・味が良好で、不純物も無く、さらには、
歩留りも良い。[Table 2] As is clear from Table 2, the sea urchin shell-derived calcium-containing composition has a good appearance and taste, is free of impurities, and
Good yield.
【００１７】次に、本発明のウニ殻由来カルシウム含有
組成物を他の原料由来の他の形態のカルシウム含有物と
吸収性の比較を行った。Next, the absorbability of the sea urchin shell-derived calcium-containing composition of the present invention was compared with other forms of calcium-containing materials derived from other raw materials.
【００１８】比較試料としては、医薬品として使用され
る（６局）収載の炭酸カルシウム９８．５％以上の沈降
炭酸カルシウム、乳酸カルシウム（第１２改訂）、塩化
カルシウム（第１２改訂）を用いた。As comparative samples, precipitated calcium carbonate of 98.5% or more, calcium lactate (12th revision) and calcium chloride (12th revision), which are used as pharmaceuticals and listed in (6 stations), were used.
【００１９】吸収性については、ラットの腸管を使用し
てテストした。The absorbability was tested using rat intestinal tract.
【００２０】すなわち、ラット５匹を１グループとし、
麻酔した後、開腸し、小腸を結紮して腸大静脈を事前に
採血した後、２％沈降炭酸カルシウム、２％乳酸カルシ
ウム、２％塩化カルシウム、本発明の２％ウニ殻由来カ
ルシウムの、各々、ｐＨ２．０水溶液５ｍｌを腸内に注
入した。注入後、１０分間隔で、腸大静脈から採血し、
血清分離後総カルシウムイオン濃度を測定した。That is, five rats are grouped into one group,
After anesthesia, the intestine was opened, the small intestine was ligated and the intestinal vena cava was collected in advance, and then 2% precipitated calcium carbonate, 2% calcium lactate, 2% calcium chloride, and 2% sea urchin shell-derived calcium of the present invention were prepared. In each case, 5 ml of a pH 2.0 aqueous solution was injected into the intestine. Blood is collected from the intestinal vena cava at 10 minute intervals after injection,
After serum separation, the total calcium ion concentration was measured.
【００２１】本発明は２％ウニ殻由来カルシウム含有組
成物のｐＨ２．０水溶液５ｍｌを腸に注入すると、１０
分後には上昇を始め、３０分後には著しい増加が認めら
れた。驚くべきことに、最も多用されている沈降炭酸カ
ルシウムの８．５倍、塩化カルシウムの４倍、乳酸カル
シウムの３倍というイオン濃度が血液中から測定され
た。According to the present invention, when 5 ml of a pH 2.0 aqueous solution containing 2% sea urchin shell-derived calcium-containing composition is injected into the intestine, 10
An increase started after 30 minutes and a remarkable increase was observed after 30 minutes. Surprisingly, ionic concentrations of 8.5 times the most frequently used precipitated calcium carbonate, 4 times the calcium chloride, and 3 times the calcium lactate were measured in blood.
【００２２】［実施例２］本発明のウニ殻由来カルシウ
ム含有組成物を、副甲状腺摘出ラットに投与し、ウニ殻
由来カルシウム含有組成物の経口吸収性を、他の形態の
カルシウム含有物と比較した。なお、以下の「ウニ殻由
来カルシウム含有組成物」「カキ殻由来カルシウム含有
組成物」は実施例１のものと同一である。複数のラット
に副甲状腺摘出手術を行い、その後１５６時間にわたっ
て該ラットに低カルシウム食（通常のラット用の食餌に
カルシウムが０．１％しか含まれていないもの）を与え
て血中カルシウム濃度を低下させた。健康状態が正常で
あり、かつ十分血中カルシウム濃度が低下しているラッ
トを２４頭（雌雄同数）選別し、１群６頭ずつ（各雌雄
同数）４群にグループ分けした。その後いずれの群も絶
食を開始し、絶食開始から１２時間後にそれぞれ第１回
目の試料投与を行った。Example 2 A sea urchin shell-derived calcium-containing composition of the present invention was administered to parathyroidectomized rats, and the oral absorption of the sea urchin shell-derived calcium-containing composition was compared with that of other forms of calcium-containing material. did. The following “sea urchin shell-derived calcium-containing composition” and “oyster shell-derived calcium-containing composition” are the same as those in Example 1. Parathyroidectomy was performed on a number of rats, after which the rats were fed a low calcium diet (a diet for normal rats that contained only 0.1% calcium) for 156 hours to reduce blood calcium levels. Lowered. Twenty-four rats (equal number of males and females) having normal health and a sufficiently low blood calcium concentration were selected and grouped into four groups, each group comprising six rats (equal number of male and female). Thereafter, all groups started fasting, and the first sample administration was performed 12 hours after the start of fasting.
【００２３】その後、各群に以下の操作を行った。Thereafter, the following operation was performed on each group.
【００２４】 ネガティブ対照群：第１回目の試料投
与として生理食塩水２ｍｌを胃の中に注入した。その後
２４〜９６時間の間、前記低カルシウム食を摂取させ
た。Negative control group: 2 ml of physiological saline was injected into the stomach as the first sample administration. Thereafter, the low calcium diet was ingested for 24 to 96 hours.
【００２５】 ポジティブ対照群：第１回目の試料投
与として炭酸カルシウムを生理食塩水に溶解したもの
（カルシウム換算で６８．４ｍｇ／（１ｋｇラット体
重）を溶解したもの）２ｍｌを胃の中に注入した。その
後２４〜９６時間の間、前記低カルシウム食に炭酸カル
シウムを混合したもの（１日当りカルシウム換算で６
８．４ｍｇ／１ｋｇラット体重）を摂取させた。Positive control group: 2 ml of calcium carbonate dissolved in physiological saline (68.4 mg in calcium equivalent / (1 kg rat body weight) dissolved) was injected into the stomach as the first sample administration. . Thereafter, for 24 to 96 hours, a mixture of calcium carbonate and the low calcium diet (6 per day in terms of calcium).
8.4 mg / 1 kg rat body weight).
【００２６】 ウニ殻由来カルシウム群：第１回目の
試料投与としてウニ殻由来カルシウム含有組成物を生理
食塩水に溶解したもの（カルシウム換算で６８．４ｍｇ
／１ｋｇラット体重）を溶解したもの）２ｍｌを胃の中
に注入した。その後２４〜９６時間の間、前記低カルシ
ウム食にウニ殻由来カルシウム含有組成物を混合したも
の（１日当たりカルシウム換算で６８．４ｍｇ／１ｋｇ
ラット体重）を摂取させた。Sea urchin shell-derived calcium group: A sea urchin shell-derived calcium-containing composition dissolved in physiological saline as the first sample administration (68.4 mg in terms of calcium)
/ 1 kg rat body weight) was injected into the stomach. After that, for 24 to 96 hours, a mixture of the low calcium diet and the sea urchin shell-derived calcium-containing composition (68.4 mg / 1 kg in terms of calcium per day)
(Rat weight).
【００２７】 カキ殻由来カルシウム群：第１回目の
試料投与としてカキ殻由来カルシウム含有組成物を生理
食塩水に溶解したもの（カルシウム換算で６８．４ｍｇ
／（１ｋｇラット体重）を溶解したもの）２ｍｌを胃の
中に注入した。その後２４〜９６時間の間、前記低カル
シウム食にカキ殻由来カルシウム含有組成物を混合した
もの（１日当たりカルシウム換算で６８．４ｍｇ／１ｋ
ｇラット体重）を摂取させた。Oyster husk-derived calcium group: Oyster husk-derived calcium-containing composition dissolved in physiological saline as the first sample administration (68.4 mg in terms of calcium)
2 ml / (1 kg rat body weight) was injected into the stomach. After that, for 24 to 96 hours, a mixture of the low-calcium diet and the oyster shell-derived calcium-containing composition (68.4 mg / 1k in terms of calcium per day)
g rat weight).
【００２８】なお、上記４群とも、第１回目の試料投与
後６〜２４時間の間は、低カルシウム食を摂取させた。In all four groups, a low calcium diet was ingested for 6 to 24 hours after the first sample administration.
【００２９】上記４群とも、第１回目の試料投与直前、
その２４時間後、４８時間後、７２時間後、９６時間後
にそれぞれ採血を行い、血中カルシウム濃度を測定し
た。結果を図１に示す（図１では、第１回目の試料投与
の２４時間後を０時間として表示してある。ただし、２
４時間後の血中カルシウム濃度は、各群とも第１回目の
試料投与直前の血中カルシウム濃度と同じレベルまで下
がっていたことが確認されている）。この図から明らか
なように、血中カルシウム濃度の上昇は、ウニ殻由来カ
ルシウム群＞カキ殻由来カルシウム群＞ポジティブ対照
群＞ネガティブ対照群の順に高く、ウニ殻由来カルシウ
ム含有組成物を経口投与した場合、他の形態のカルシウ
ム含有物に比して、吸収が優れていることが判明した。In each of the above four groups, immediately before the first sample administration,
Blood was collected 24 hours, 48 hours, 72 hours, and 96 hours after that, and the calcium concentration in the blood was measured. The results are shown in FIG. 1 (in FIG. 1, 24 hours after the first sample administration is shown as 0 hour.
It has been confirmed that the blood calcium concentration after 4 hours had decreased to the same level as the blood calcium concentration immediately before the first sample administration in each group). As is clear from this figure, the increase in blood calcium concentration was higher in the order of sea urchin shell-derived calcium group> oyster shell-derived calcium group> positive control group> negative control group, and the sea urchin shell-derived calcium-containing composition was orally administered. In this case, it was found that the absorption was superior to other forms of calcium-containing material.
【００３０】また、上記４群とも、第１回目の試料投与
後２４時間にわたって各ラットの糞便を全量回収し、糞
便中に含まれているカルシウム量を測定した。結果を表
３に示す。In each of the above 4 groups, the total amount of feces of each rat was collected for 24 hours after the first administration of the sample, and the amount of calcium contained in the feces was measured. The results are shown in Table 3.
【００３１】[0031]
【表３】 この表から明らかなように、糞便中へのカルシウムの排
出は、ポジティブ対照群＞カキ殻由来カルシウム群＞ネ
ガティブ対照群＞ウニ殻由来カルシウム群の順で多かっ
た。ウニ殻由来カルシウム群の糞便中へのカルシウムの
排出が少ないことは、ウニ殻由来カルシウム含有組成物
を経口投与した場合、腸管から良好に吸収され、糞便中
には少量しか排出されないことを意味する。すなわち、
このことにより、ウニ殻由来カルシウム含有組成物を経
口投与した場合、他の形態のカルシウム含有物に比し
て、吸収が優れていることが確認された。一般に、ラッ
トが食餌を摂取してから糞便として排泄されるまでの時
間は約６時間程度と言われており、第１回目の試料投与
の際に生理食塩水とともに胃の中に注入された各試料は
腸で吸収されなければ、２４時間後までにはすべて糞便
中に排泄されると考えられる。[Table 3] As is clear from this table, the excretion of calcium into feces was higher in the order of positive control group> oyster shell-derived calcium group> negative control group> sea urchin shell-derived calcium group. The low excretion of calcium into the faeces of the sea urchin shell-derived calcium group means that when the sea urchin shell-derived calcium-containing composition is orally administered, it is well absorbed from the intestinal tract and only a small amount is excreted in the feces. . That is,
From this, it was confirmed that when the sea urchin shell-derived calcium-containing composition was orally administered, the absorption was superior to other forms of calcium-containing material. Generally, it is said that the time from the ingestion of a rat to the excretion of feces after ingestion of the food is about 6 hours, and each of the rats injected into the stomach together with physiological saline at the time of the first sample administration. If the sample is not absorbed in the intestine, it is believed that all will be excreted in feces by 24 hours.
【００３２】実施例１では正常なラットを、実施例２で
は血中カルシウム濃度の低い副甲状腺摘出ラットを用い
ているが、両実施例とも、本発明のウニ殻由来のカルシ
ウム含有組成物を経口投与した場合の優れたカルシウム
吸収性を定量的に示している。このことから、本発明の
ウニ殻由来カルシウム含有組成物は、低カルシウム血症
（hypocalcemia）、骨粗鬆症（osteoporosis）、腎性骨
形成異常症（renal osteodystrophy）等の、カルシウム
の供給を必要とする多くの疾病の治療または予防に有効
であることは明白である。また、実施例１で示したよう
に、本発明のウニ殻由来カルシウム含有組成物は、外
観、味が良好で、不純物が少ないことを考え合わせる
と、カルシウム供給を目的とする健康食品や飼料への配
合にも極めて適していることは明らかである。In Example 1, a normal rat was used, and in Example 2, a parathyroidectomized rat having a low blood calcium concentration was used. In both examples, the sea urchin shell-derived calcium-containing composition of the present invention was orally administered. It shows quantitatively the excellent calcium absorption when administered. For this reason, the sea urchin shell-derived calcium-containing composition of the present invention can be used for many calcium-requiring compositions such as hypocalcemia, hypocalcemia, osteoporosis, and renal osteodystrophy. It is clear that it is effective for the treatment or prevention of the disease of the present invention. Further, as shown in Example 1, the sea urchin shell-derived calcium-containing composition of the present invention has good appearance, taste, and few impurities, and is considered as a health food or feed intended for calcium supply. Obviously, it is also very suitable for the formulation of
【００３３】[0033]
【発明の効果】本発明により従来は廃棄されていたウニ
殻から、経口吸収性が優れるほか、味が良好で、不純物
が少なく、歩留りが良いカルシウム含有組成物が提供さ
れた。EFFECTS OF THE INVENTION The present invention provides a calcium-containing composition which is excellent in oral absorption from sea urchin shells that have been conventionally discarded, has a good taste, has few impurities, and has a good yield.
【００３４】該ウニ殻由来カルシウム含有組成物は、低
カルシウム血症、骨粗鬆症、腎性骨形成異常症等の、カ
ルシウムの供給を必要とする多くの疾病の治療または予
防に有効である。また、カルシウム供給を目的とする健
康食品や飼料への配合にも適している。The sea urchin shell-derived calcium-containing composition is effective for treating or preventing many diseases requiring calcium supply, such as hypocalcemia, osteoporosis, renal osteodystrophy. It is also suitable for incorporation into health foods and feeds for the purpose of supplying calcium.
【図１】 副甲状腺摘出ラットに各種カルシウム含有物
を経口投与したときの血中カルシウム濃度を示す図であ
る（第１回目の試料投与から２４時間後の血中カルシウ
ム濃度を基準（１００）とし、その後２４時間毎の各群
の血中カルシウム濃度を相対値で示した。なお、ここで
基準とした第１回目の試料投与から２４時間後の血中カ
ルシウム濃度は、各群とも第１回目の試料投与直前の血
中カルシウム濃度と同じレベルまで下がっていたことが
確認されている）。FIG. 1 is a graph showing the blood calcium concentration when various calcium-containing substances were orally administered to parathyroidectomized rats (using the blood calcium concentration 24 hours after the first sample administration as a reference (100)). The blood calcium concentration in each group was shown as a relative value every 24 hours thereafter, and the blood calcium concentration 24 hours after the first sample administration was used as the reference, and the blood calcium concentration in each group was the first time. It has been confirmed that the blood calcium level was decreased to the same level immediately before the administration of the sample).
Claims (2)
有組成物。1. A calcium-containing composition obtained by firing sea urchin shells.
徴とする請求項１記載のカルシウム含有組成物。2. The calcium-containing composition according to claim 1, which is fired at 500 to 1500 ° C.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP8007437A JPH0984552A (en) | 1993-07-16 | 1996-01-19 | Calcium-containing composition excellent in absorbing property |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP17650393 | 1993-07-16 | ||
| JP5-176503 | 1993-07-16 | ||
| JP8007437A JPH0984552A (en) | 1993-07-16 | 1996-01-19 | Calcium-containing composition excellent in absorbing property |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP6091694A Division JP2579593B2 (en) | 1993-07-16 | 1994-04-28 | Health food containing calcium-containing composition excellent in absorbability, drug containing the composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH0984552A true JPH0984552A (en) | 1997-03-31 |
Family
ID=26341730
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP8007437A Pending JPH0984552A (en) | 1993-07-16 | 1996-01-19 | Calcium-containing composition excellent in absorbing property |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0984552A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100449909B1 (en) * | 2001-08-29 | 2004-09-22 | 대한민국 | Antimicrobial composition containing the calcium powder of sea urchin integument |
| KR100782107B1 (en) * | 2006-01-24 | 2007-12-05 | 오재영 | Method for extract of calcium from echinoid shell |
-
1996
- 1996-01-19 JP JP8007437A patent/JPH0984552A/en active Pending
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100449909B1 (en) * | 2001-08-29 | 2004-09-22 | 대한민국 | Antimicrobial composition containing the calcium powder of sea urchin integument |
| KR100782107B1 (en) * | 2006-01-24 | 2007-12-05 | 오재영 | Method for extract of calcium from echinoid shell |
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