JP6202570B2 - Fish anesthetic agent, method for producing the same, and method for determining the expiration date of the fish anesthetic agent - Google Patents

Fish anesthetic agent, method for producing the same, and method for determining the expiration date of the fish anesthetic agent Download PDF

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JP6202570B2
JP6202570B2 JP2013263686A JP2013263686A JP6202570B2 JP 6202570 B2 JP6202570 B2 JP 6202570B2 JP 2013263686 A JP2013263686 A JP 2013263686A JP 2013263686 A JP2013263686 A JP 2013263686A JP 6202570 B2 JP6202570 B2 JP 6202570B2
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研一 渡邉
研一 渡邉
創 松原
創 松原
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Tokyo University of Agriculture
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    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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    • Y02A40/00Adaptation technologies in agriculture, forestry, livestock or agroalimentary production
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Description

本発明は、魚類用麻酔剤及びその製造方法並びに該魚類用麻酔剤の使用期限を判別する方法に関する。   The present invention relates to a fish anesthetic, a method for producing the same, and a method for determining the expiration date of the fish anesthetic.

魚類養殖や栽培漁業の現場では、ワクチン接種、歯切り、標識装着、各種の測定などの用途で麻酔剤が使用されている。従来、魚類用麻酔剤としては、動物用医薬品として承認されているFA100(主成分・オイゲノール)が使用されているが、高価という欠点がある。また、FA100は、使用する際に麻酔液が濁り、液表面に泡が発生して魚が観察しづらいことや、麻酔後に死亡する魚の個体が発生するケースが多いこと、独特の臭いがあること等の理由から必ずしも良い麻酔剤とは言えない。   In the field of fish farming and cultivating fisheries, anesthetics are used for vaccination, chopping, labeling, and various measurements. Conventionally, FA100 (main component / eugenol), which has been approved as a veterinary drug, has been used as an anesthetic for fish. In addition, the FA100 has an anesthetic liquid that becomes turbid when used, bubbles appear on the liquid surface, making it difficult to observe the fish, and there are many cases of fish that die after anesthesia, and there is a unique smell. For such reasons, it is not necessarily a good anesthetic.

また、動物用医薬品として未承認である学術的試薬の2−フェノキシエタノールは、ニジマスやマダイに対する麻酔効果が報告されており、FA100よりも廉価である。しかしながら、2−フェノキシエタノールは、動物用医薬品として未承認であることや食品添加物に指定されていないことなど、食の安全性の観点から問題がある。   In addition, 2-phenoxyethanol, an academic reagent that has not been approved as a veterinary drug, has been reported to have an anesthetic effect on rainbow trout and red sea bream, and is less expensive than FA100. However, 2-phenoxyethanol has problems from the viewpoint of food safety such as being unapproved as a veterinary drug and not being designated as a food additive.

一方、炭酸ガスは、魚類に対して麻酔効果を有することが広く知られている。従来、炭酸ガスを麻酔剤として使用する場合は、炭酸ガスボンベを用いて炭酸ガスを水中に通気する方法や水中に炭酸水素ナトリウムと酢酸を規定量添加することで炭酸ガスを発生させる方法で麻酔が行われている。しかしながら、これらの方法は、ボンベの用意や、炭酸水素ナトリウムや酢酸を計量して別々に保管するなどの手間がかかり、簡便な方法とは言えない。   On the other hand, it is widely known that carbon dioxide has an anesthetic effect on fish. Conventionally, when carbon dioxide is used as an anesthetic, anesthesia is achieved by a method of venting carbon dioxide into water using a carbon dioxide cylinder or a method of generating carbon dioxide by adding a prescribed amount of sodium bicarbonate and acetic acid into water. Has been done. However, these methods are not a simple method because it takes time and effort to prepare a cylinder and to measure and store sodium bicarbonate and acetic acid separately.

このような背景から、本発明者は、食の安全性を十分に確保すると共に、従来の麻酔剤よりも使用しやすく、かつ、低コストの魚類用麻酔剤として、炭酸水素ナトリウム由来の炭酸ガスを利用した固形状の魚類用麻酔剤に関する技術を提案した(特許文献1)。   From such a background, the present inventor has ensured sufficient food safety, is easier to use than conventional anesthetics, and is a low-cost fish anesthetic agent. A technique related to a solid fish anesthetic using the above has been proposed (Patent Document 1).

特許第4831409号公報Japanese Patent No. 4831409

しかしながら、炭酸水素ナトリウム由来の炭酸ガスを利用した固形状の魚類用麻酔剤は、保管中に空気中などの水分を吸湿すると麻酔の有効成分である炭酸ガスを放出するため、該吸湿した魚類用麻酔剤を麻酔剤として使用しても麻酔効果が得られないが、該魚類用麻酔剤が吸湿することによって麻酔効果が消失したものであるかどうかを判別することが困難であった。そのため、炭酸水素ナトリウム由来の炭酸ガスを利用した固形状の魚類用麻酔剤を使用する際に、該魚類用麻酔剤が保管中に空気中などの水分を吸湿することで麻酔効果が消失したものであるかどうかを簡単に判別できることが望まれていた。   However, solid fish anesthetics using carbonic acid gas derived from sodium bicarbonate release carbon dioxide, which is an active ingredient for anesthesia, when moisture in the air is absorbed during storage. Although an anesthetic is not obtained even if an anesthetic is used as an anesthetic, it is difficult to determine whether the anesthetic is lost due to moisture absorption by the fish anesthetic. Therefore, when using a solid fish anesthetic using carbonic acid gas derived from sodium hydrogen carbonate, the anesthetic for the fish has lost its anesthetic effect by absorbing moisture in the air during storage. It was desired to be able to easily determine whether or not.

そこで、本発明の目的は、炭酸水素ナトリウム由来の炭酸ガスを利用した固形状の魚類用麻酔剤が保管中に空気中などの水分を吸湿することで麻酔効果が消失したかどうかを簡単に判別することができる固形状魚類用麻酔剤及びその製造方法並びに該固形状魚類用麻酔剤の使用期限を判別する方法に関する技術を提供することにある。   Therefore, the object of the present invention is to easily determine whether or not the solid fish anesthetic using carbonic acid gas derived from sodium hydrogen carbonate has absorbed the moisture in the air during storage and the anesthetic effect has disappeared. An object of the present invention is to provide a technique relating to a solid fish anesthetic, a method for producing the same, and a method for determining the expiration date of the solid fish anesthetic.

本発明者らが鋭意検討した結果、炭酸水素ナトリウム由来の炭酸ガスを利用した固形状の魚類用麻酔剤の表面の一部分に食品用添加物である水溶性色素を含有させ、該固形状魚類用麻酔剤の表面に存在する水溶性色素の色調変化を肉眼で観察することで該固形状魚類用麻酔剤の麻酔効果が消失したかどうかを簡単に判別することができるとの知見を得た。   As a result of intensive studies by the present inventors, a water-soluble pigment that is a food additive is contained in a part of the surface of a solid fish anesthetic using carbonic acid gas derived from sodium hydrogen carbonate, and the solid fish It was found that it was possible to easily determine whether or not the anesthetic effect of the solid fish anesthetic was lost by observing the color change of the water-soluble pigment present on the surface of the anesthetic with the naked eye.

本発明はかかる知見に基づきなされたものであり、水溶性色素の色調変化によって使用期限を判別することのできる炭酸水素ナトリウム由来の炭酸ガスを利用した固形状の魚類用麻酔剤であって、炭酸水素ナトリウムと、有機酸と、食品添加物である水溶性色素とを含有し、該水溶性色素の色調変化が肉眼で観察できるように該魚類用麻酔剤の表面の一部分に該水溶性色素が存在することを特徴とする、固形状魚類用麻酔剤を提供するものである。   The present invention has been made on the basis of such findings, and is a solid fish anesthetic using carbonic acid gas derived from sodium hydrogen carbonate that can determine the expiration date by changing the color tone of a water-soluble dye. It contains sodium hydride, an organic acid, and a water-soluble pigment that is a food additive, and the water-soluble pigment is partly on the surface of the fish anesthetic so that the color change of the water-soluble pigment can be observed with the naked eye. The present invention provides an anesthetic agent for solid fish characterized in that it exists.

また、本発明は、水溶性色素の色調変化によって使用期限を判別することのできる炭酸水素ナトリウム由来の炭酸ガスを利用した固形状の魚類用麻酔剤の製造方法であって、炭酸水素ナトリウムと有機酸とを含有する混合物を調製する工程と、前記混合物に該魚類用麻酔剤の表面の一部分に存在するように食品添加物である水溶性色素を添加する工程と、前記水溶性色素が添加された炭酸水素ナトリウムを固形状に成型する工程と、を有する固形状魚類用麻酔剤の製造方法を提供するものである。   The present invention also relates to a method for producing a solid fish anesthetic agent using carbonic acid gas derived from sodium hydrogen carbonate, the expiration date of which can be determined by changing the color tone of a water-soluble dye, comprising sodium bicarbonate and organic A step of preparing a mixture containing an acid, a step of adding a water-soluble dye as a food additive to the mixture so as to be present on a part of the surface of the fish anesthetic agent, and the addition of the water-soluble dye A method for producing a solid fish anesthetic agent, comprising the step of molding sodium bicarbonate into a solid form.

さらに、本発明は、上述の固形状魚類用麻酔剤の使用期限を判別する方法であって、該魚類用麻酔剤の表面の一部に食品用添加物である水溶性色素を含有させ、該固形状魚類用麻酔剤が水分を吸湿することによって該水溶性色素が滲み、該水溶性色素の色調が低下又は消失することに基づいて使用期限を判別することを特徴とする、固形状魚類用麻酔剤の使用期限の判別方法を提供するものである。   Furthermore, the present invention is a method for determining the expiration date of the above-mentioned solid fish anesthetic agent, comprising a water-soluble dye as a food additive in part of the surface of the fish anesthetic agent, The solid fish anesthetic agent absorbs moisture, so that the water-soluble pigment oozes out, and the expiration date is determined based on the color tone of the water-soluble pigment being lowered or disappeared. A method for determining the expiration date of an anesthetic is provided.

本発明の固形状魚類用麻酔剤及びその製造方法並びに該固形状魚類用麻酔剤の使用期限を判別する方法によれば、該固形状魚類用麻酔剤が保管中に空気中などの水分を吸湿することによって該固形状魚類用麻酔剤の表面に存在する水溶性色素の色調が変化し、該固形状魚類用麻酔剤の麻酔効果が消失したことを簡単に判別することができる効果が得られる。   According to the solid fish anesthetic agent of the present invention, a method for producing the same, and a method for determining the expiration date of the solid fish anesthetic agent, the solid fish anesthetic agent absorbs moisture such as air during storage. As a result, the color tone of the water-soluble pigment present on the surface of the solid fish anesthetic agent is changed, and the effect that the anesthetic effect of the solid fish anesthetic agent is lost can be easily determined. .

多湿条件下で保持した固形状魚類用麻酔剤に含有するコチニール色素(0.064重量%)の色調変化を示す図である。It is a figure which shows the color tone change of the cochineal pigment | dye (0.064 weight%) contained in the solid fish anesthetic agent hold | maintained on the humid conditions. 多湿条件下で保持した固形状魚類用麻酔剤に含有するコチニール色素(0.043重量%)の色調変化を示す図である。It is a figure which shows the color tone change of the cochineal pigment | dye (0.043 weight%) contained in the solid fish anesthetic agent hold | maintained on the humid conditions. 多湿条件下で保持した固形状魚類用麻酔剤に含有するコチニール色素(0.034重量%)の色調変化を示す図である。It is a figure which shows the color tone change of the cochineal pigment | dye (0.034 weight%) contained in the solid fish anesthetic agent hold | maintained on the humid conditions. 多湿条件下で保持した固形状魚類用麻酔剤に含有するコチニール色素(0.015重量%)の色調変化を示す図である。It is a figure which shows the color tone change of the cochineal pigment | dye (0.015 weight%) contained in the solid fish anesthetic agent hold | maintained on the humid conditions. 多湿条件下で保持した固形状魚類用麻酔剤に含有するコチニール色素(0.0088重量%)の色調変化を示す図である。It is a figure which shows the color change of the cochineal pigment | dye (0.0088 weight%) contained in the solid fish anesthetic agent hold | maintained on the humid conditions. 多湿条件下で保持した固形状魚類用麻酔剤に含有するコチニール色素(0.0008重量%)の色調変化を示す図である。It is a figure which shows the color change of the cochineal pigment | dye (0.0008 weight%) contained in the solid fish anesthetic agent hold | maintained on the humid conditions. 多湿条件下で保持した固形状魚類用麻酔剤に含有するクチナシ黄色色素(0.05重量%)の色調変化を示す図である。It is a figure which shows the color tone change of gardenia yellow pigment | dye (0.05 weight%) contained in the solid fish anesthetic agent hold | maintained on the humid conditions. 多湿条件下で保持した固形状魚類用麻酔剤に含有するスピルリナ青色色素(0.049重量%)の色調変化を示す図である。It is a figure which shows the color tone change of Spirulina blue pigment | dye (0.049 weight%) contained in the solid fish anesthetic agent hold | maintained on the humid conditions. 多湿条件下で保持した固形状魚類用麻酔剤に含有するクチナシ緑色色素(0.045重量%)の色調変化を示す図である。It is a figure which shows the color tone change of gardenia green pigment | dye (0.045 weight%) contained in the solid fish anesthetic agent hold | maintained on the humid conditions.

本発明の実施形態おける固形状魚類用麻酔剤について説明する。本実施形態に係る固形状魚類用麻酔剤は、炭酸水素ナトリウムと、有機酸と、食品添加物である水溶性色素とを含有し、該水溶性色素の色調変化が肉眼で観察できるように該固形状魚類用麻酔剤の表面の一部分に該水溶性色素が存在するものである。   The solid fish anesthetic agent in the embodiment of the present invention will be described. The solid fish anesthetic agent according to the present embodiment contains sodium hydrogen carbonate, an organic acid, and a water-soluble pigment that is a food additive, and the color change of the water-soluble pigment can be observed with the naked eye. The water-soluble pigment is present on a part of the surface of the solid fish anesthetic.

前記炭酸水素ナトリウムは、食の安全性の観点から、食品や医薬品に使用されているものが好ましい。また、本発明の効果が妨げられなければ、炭酸水素ナトリウムと共に炭酸ナトリウムや炭酸カルシウムなどの炭酸塩を併用することができる。   From the viewpoint of food safety, the sodium bicarbonate is preferably used in foods and pharmaceuticals. Moreover, if the effect of this invention is not prevented, carbonates, such as sodium carbonate and a calcium carbonate, can be used together with sodium hydrogencarbonate.

前記水溶性色素は、食の安全性の観点から、食品添加物として認められたものであればよく、例えば、ベニコウジ赤色色素、クチナシ赤色色素、コチニール色素、ラック色素、アカビート色素、アントシアニン色素、クチナシ青色色素、スピルリナ青色色素、アナトー色素、クチナシ黄色色素、ベニバナ黄色色素、ウコン色素、ベニコウジ黄色色素などを挙げることができる。なかでも、コチニ―ル色素は、pH
によって色が変化するpH指示機能も有するため、固形状魚類用麻酔剤を投入する浴槽内が、魚類に対する麻酔効果が十分発現するpHになっているか否かを目視で確認することが可能となるので、特に好ましい色素である。
The water-soluble dyes may be those recognized as food additives from the viewpoint of food safety. For example, Benikouji red dye, gardenia red dye, cochineal dye, lac dye, red beet dye, anthocyanin dye, gardenia Examples thereof include a blue pigment, a spirulina blue pigment, an anato pigment, a gardenia yellow pigment, a safflower yellow pigment, a turmeric pigment, and a Benikouji yellow pigment. Of these, cochineal dyes are
Since it also has a pH indication function that changes color depending on the condition, it is possible to visually check whether or not the inside of the bathtub into which the solid fish anesthetic is introduced has a pH at which the anesthetic effect on the fish is sufficiently expressed. Therefore, it is a particularly preferable dye.

一方、油溶性色素及び不溶性色素については、これら色素を用いて調製した固形状魚類用麻酔剤が空気中などの水分を吸湿しても、吸湿した水分中に該色素が溶け込まないため、該固形状魚類用麻酔剤の表面に存在する色素は滲むことなく、該色素の色調の低下又は消失は観察されない。そのため、油溶性色素及び不溶性色素は、本実施形態の固形状魚類用麻酔剤の麻酔効果が消失したものであるかどうかを判別することができないため、使用することができない。   On the other hand, for oil-soluble dyes and insoluble dyes, even if the solid fish anesthetic prepared using these dyes absorbs moisture such as air, the dye does not dissolve in the absorbed moisture. The pigment present on the surface of the shape fish anesthetic agent does not bleed, and no decrease or disappearance of the color of the pigment is observed. Therefore, oil-soluble pigments and insoluble pigments cannot be used because it cannot be determined whether the anesthetic effect of the solid fish anesthetic agent of this embodiment has been lost.

前記水溶性色素の含有量は、本発明の効果が得られれば特に制限はないが、該水溶性色素の色調を肉眼で観察する観点から、0.0088重量%〜0.064重量%が好ましく、0.033重量%〜0.064重量%がさらに好ましい。   The content of the water-soluble dye is not particularly limited as long as the effects of the present invention can be obtained. However, from the viewpoint of observing the color tone of the water-soluble dye with the naked eye, 0.0088% by weight to 0.064% by weight is preferable. 0.033 wt% to 0.064 wt% is more preferable.

本実施形態の魚類用麻酔剤は、炭酸ガスの発生を促進して発泡させるために、有機酸を添加する。   The fish anesthetic agent of the present embodiment is added with an organic acid in order to promote generation of carbon dioxide gas and cause foaming.

前記有機酸は、本発明の目的及び効果が得られれば特に限定されず、コハク酸、クエン酸、フマル酸、マレイン酸、リンゴ酸、酒石酸などを挙げることができるが、食の安全性の観点から、食品や医薬品に使用されているものが好ましく、また、魚類に対する麻酔効果の観点から、コハク酸を用いることが好ましい。なお、本実施形態の魚類用麻酔剤では、麻酔剤としての効力に影響しない限り、2種類以上の有機酸を併用しても差し支えない。   The organic acid is not particularly limited as long as the objects and effects of the present invention can be obtained, and examples thereof include succinic acid, citric acid, fumaric acid, maleic acid, malic acid, and tartaric acid. Therefore, those used in foods and pharmaceuticals are preferable, and succinic acid is preferably used from the viewpoint of anesthetic effects on fish. In the fish anesthetic of this embodiment, two or more organic acids may be used in combination as long as the effect as an anesthetic is not affected.

また、前記炭酸水素ナトリウムと前記コハク酸の重量比は、魚類に対する麻酔効果の観点から、4:6〜6:4が好ましい。   Moreover, the weight ratio of the sodium hydrogen carbonate and the succinic acid is preferably 4: 6 to 6: 4 from the viewpoint of an anesthetic effect on fish.

本実施形態の魚類用麻酔剤は、固形化を促進するために、固形化促進剤を添加することができる。   In order to promote solidification, the fish anesthetic agent of this embodiment can add a solidification accelerator.

前記固形化促進剤は、食の安全性の観点から、食用グリセリンや無水エタノールが好ましい。   The solidification accelerator is preferably edible glycerin or absolute ethanol from the viewpoint of food safety.

前記食用グリセリンの添加量は、固形化を促進する観点から、炭酸水素ナトリウム等の原材料の重量に対して2.5〜15重量%が好ましい。   The amount of the edible glycerin added is preferably 2.5 to 15% by weight with respect to the weight of the raw material such as sodium hydrogencarbonate from the viewpoint of promoting solidification.

前記無水エタノールの添加量は、固形化を促進する観点から、炭酸水素ナトリウム等の原材料の重量に対して10〜20重量%が好ましい。   From the viewpoint of promoting solidification, the amount of the absolute ethanol added is preferably 10 to 20% by weight based on the weight of the raw material such as sodium hydrogen carbonate.

本実施形態の固形状魚類用麻酔剤は、前記水溶性色素の色調変化が肉眼で観察できるように該固形状魚類用麻酔剤の表面の一部分に該水溶性色素を含有する。これにより、該固形状魚類用麻酔剤が空気中などの水分を吸湿した場合、吸湿した水分に該水溶性色素が滲むことで該色素の色調が低下又は消失するため、該色素の色調変化を肉眼で観察することで該固形状魚類用麻酔剤が吸湿し、該固形状魚類用麻酔剤の麻酔効果が消失したかどうかを判別することができる。   The solid fish anesthetic agent of the present embodiment contains the water soluble pigment in a part of the surface of the solid fish anesthetic agent so that the color change of the water soluble pigment can be observed with the naked eye. As a result, when the solid fish anesthetic absorbs moisture such as in the air, the color tone of the pigment decreases or disappears due to the water-soluble pigment oozing into the moisture that has been absorbed. By observing with the naked eye, it is possible to determine whether the solid fish anesthetic absorbs moisture and the anesthetic effect of the solid fish anesthetic disappears.

なお、固形状魚類用麻酔剤の表面全体に水溶性色素が存在する場合は、該固形状魚類用麻酔剤が空気中などの水分を吸湿しても、吸湿した水分に該水溶性色素が滲むことで該色素の色調の低下又は消失を観察することができないため、該固形状魚類用麻酔剤が吸湿することによって麻酔効果が消失したかどうかを判別することができない。   In addition, when a water-soluble dye is present on the entire surface of the solid fish anesthetic agent, even if the solid fish anesthetic agent absorbs moisture such as in the air, the water-soluble dye oozes into the absorbed moisture. Therefore, it cannot be observed whether the color tone of the pigment is lowered or disappeared, and thus it cannot be determined whether or not the anesthetic effect has disappeared by absorbing the solid fish anesthetic.

本実施形態の固形状魚類用麻酔剤は、本発明の目的及び効果を妨げなければ、他の素材や食品添加物などを含有することができる。   The solid fish anesthetic agent of the present embodiment can contain other materials, food additives and the like as long as the object and effect of the present invention are not hindered.

本願実施形態の固形状魚類用麻酔剤の使用方法は、該固形状魚類用麻酔剤を水槽中の水に溶解し、ここに麻酔対象の魚類を収容するか、あるいは、麻酔対象の魚類を収容してある水槽中の水に本魚類用麻酔剤を溶解することで、麻酔対象の魚類に麻酔をかけることができる。   The method for using the solid fish anesthetic according to the embodiment of the present invention is to dissolve the solid fish anesthetic in water in a water tank and accommodate the fish to be anesthetized or accommodate the fish to be anesthetized. The fish to be anesthetized can be anesthetized by dissolving the fish anesthetic agent in the water in the water tank.

なお、本発明の固形状魚類用麻酔剤を使用すると、該固形状魚類用麻酔剤が水溶性色素を含有していることから、該固形状魚類用麻酔剤を投入した水槽中の水が該水溶性色素によって着色するが、特に問題はない。また、本発明の固形状魚類用麻酔剤を水槽中の水に投入すると炭酸ガスの気泡が生ずるが、該炭酸ガスの気泡が水面に達すると消失し、該気泡が水面に残留しないため、水槽中の魚類の観察を妨げない。   When the solid fish anesthetic agent of the present invention is used, since the solid fish anesthetic agent contains a water-soluble pigment, the water in the tank containing the solid fish anesthetic agent is Although it is colored with a water-soluble dye, there is no particular problem. Also, when the solid fish anesthetic agent of the present invention is poured into the water in the water tank, carbon dioxide bubbles are generated, but when the carbon dioxide gas bubbles reach the water surface, the bubbles disappear, and the bubbles do not remain on the water surface. Does not interfere with the observation of fish inside.

本実施形態の固形状魚類用麻酔剤は、魚の種類を問わず、あらゆる魚類に対する麻酔剤として使用することができ、例えば、アメマス、ウグイ、フクドジョウ、ゼブラフィッシュ、プラティ、メダカ、ニシキゴイ、マゴイ、ティラピア、シマアジ、カンパチ、マダイ、トラフグ、ブリ、ヒラメ、メバル、クロソイ、ニジマス、ギンザケ、アユ、ウナギを挙げることができる。   The solid fish anesthetic agent of the present embodiment can be used as an anesthetic agent for any fish regardless of the type of fish. , Striped horse mackerel, amberjack, red sea bream, yellowtail, flounder, rockfish, blackfish, rainbow trout, coho salmon, sweetfish, eel.

次に、本発明の実施形態における固形状魚類用麻酔剤の製造方法について説明する。本実施形態に係る固形状魚類用麻酔剤の製造方法は、炭酸水素ナトリウムと有機酸とを含有する混合物を調製する工程と、前記混合物に該魚類用麻酔剤の表面の一部分に存在するように食品添加物である水溶性色素を添加する工程と、前記水溶性色素が添加された炭酸水素ナトリウムを固形状に成型する工程とを有するものである。   Next, the manufacturing method of the solid fish anesthetic agent in embodiment of this invention is demonstrated. The method for producing a solid fish anesthetic according to the present embodiment includes a step of preparing a mixture containing sodium hydrogen carbonate and an organic acid, and the mixture is present on a part of the surface of the fish anesthetic. It has the process of adding the water-soluble pigment | dye which is a food additive, and the process of shape | molding the sodium hydrogencarbonate to which the said water-soluble pigment | dye was added to solid form.

本実施形態において、まず始めに、炭酸水素ナトリウムとコハク酸とを混合し、炭酸水素ナトリウムとコハク酸とを含有する混合物を調製する。   In this embodiment, first, sodium hydrogen carbonate and succinic acid are mixed to prepare a mixture containing sodium hydrogen carbonate and succinic acid.

前記炭酸水素ナトリウムは、食の安全性の観点から、食品や医薬品に使用されているものが好ましい。また、本発明の効果が妨げられなければ、炭酸水素ナトリウムと共に炭酸ナトリウムや炭酸カルシウムなどの炭酸塩を併用することができる。   From the viewpoint of food safety, the sodium bicarbonate is preferably used in foods and pharmaceuticals. Moreover, if the effect of this invention is not prevented, carbonates, such as sodium carbonate and a calcium carbonate, can be used together with sodium hydrogencarbonate.

前記有機酸は、本発明の効果が得られれば特に限定されず、コハク酸、クエン酸、フマル酸、マレイン酸、リンゴ酸、酒石酸などを挙げることができるが、食の安全性の観点から、食品や医薬品に使用されているものが好ましく、また、魚類に対する麻酔効果の観点から、コハク酸を用いることが好ましい。なお、本実施形態の魚類用麻酔剤では、麻酔剤としての効力に影響しない限り、2種類以上の有機酸を併用しても差し支えない。   The organic acid is not particularly limited as long as the effect of the present invention can be obtained, and can include succinic acid, citric acid, fumaric acid, maleic acid, malic acid, tartaric acid, etc., from the viewpoint of food safety, Those used in foods and pharmaceuticals are preferred, and succinic acid is preferably used from the viewpoint of anesthetic effects on fish. In the fish anesthetic of this embodiment, two or more organic acids may be used in combination as long as the effect as an anesthetic is not affected.

前記炭酸水素ナトリウムと前記コハク酸の重量比は、魚類に対する麻酔効果の観点から、4:6〜6:4が好ましい。   The weight ratio of the sodium bicarbonate and the succinic acid is preferably 4: 6 to 6: 4 from the viewpoint of an anesthetic effect on fish.

次に、前記混合物に、食品添加物である水溶性色素を成型加工後に魚類用麻酔剤の表面の一部分に存在するように添加する。   Next, a water-soluble pigment, which is a food additive, is added to the mixture so as to be present on a part of the surface of the fish anesthetic after molding.

前記食品添加物を添加する方法は、成型加工後の固形状魚類用麻酔剤の表面の一部分に水溶性色素が存在すれば特に限定されず、例えば、成型加工に用いる容器内にあらかじめ所定量の水溶性色素を入れ、そこに炭酸水素ナトリウムと有機酸との混合物を投入した後、これを成型加工することで固形状魚類用麻酔剤の表面の一部分に水溶性色素を含有させる方法や、成型加工に使用する前記混合物の一部をとり、ここに所定量の水溶性色素を添加した後、よく混合し、この水溶性色素を含有する混合物を成型加工に用いる容器内に入れ、ここに残りの混合物を投入した後、成型加工することで固形状魚類用麻酔剤の表面の一部分に水溶性色素を含有させる方法などが挙げられる。   The method of adding the food additive is not particularly limited as long as a water-soluble pigment is present on a part of the surface of the solid fish anesthetic agent after molding, and for example, a predetermined amount of the food additive is previously contained in a container used for molding. Put water-soluble dye, put a mixture of sodium hydrogen carbonate and organic acid into it, and then mold and process it to make it part of the surface of the solid fish anesthetic agent, Take a part of the mixture used for processing, add a predetermined amount of water-soluble dye here, mix well, put the mixture containing this water-soluble dye into a container used for molding processing, and leave it here The method of making a part of the surface of the solid fish anesthetic agent contain a water-soluble pigment | dye by carrying out the shaping | molding process after throwing in the mixture of these is mentioned.

なお、固形状魚類用麻酔剤の表面全体に水溶性色素が存在するように添加した場合は、調製された固形状魚類用麻酔剤が空気中などの水分を吸湿しても、吸湿した水分に該水溶性色素が滲むことで該色素の色調の低下又は消失を観察することができないため、該固形状魚類用麻酔剤が吸湿することによって麻酔効果が消失したかどうかを判別することができない。   If the solid fish anesthetic is added so that the water-soluble pigment is present on the entire surface, the prepared solid fish anesthetic will absorb moisture in the air, etc. Since the decrease or disappearance of the color tone of the dye cannot be observed due to bleeding of the water-soluble dye, it cannot be determined whether or not the anesthetic effect has disappeared due to moisture absorption by the solid fish anesthetic.

前記水溶性色素は、上述の通り、食品添加物として認められたものであればよく、例えば、ベニコウジ赤色色素、クチナシ赤色色素、コチニール色素、ラック色素、アカビート色素、アントシアニン色素、クチナシ青色色素、スピルリナ青色色素、アナトー色素、クチナシ黄色色素、ベニバナ黄色色素、ウコン色素、ベニコウジ黄色色素などを挙げることができる。これら水溶性色素の中でも、pH指示機能も有するコチニ―ル色素が特に好ましいことはすでに述べたとおりである。   As described above, the water-soluble dye may be any one recognized as a food additive. For example, Benikouji red dye, gardenia red dye, cochineal dye, lac dye, red beet dye, anthocyanin dye, gardenia blue dye, spirulina A blue pigment, an anato pigment, a gardenia yellow pigment, a safflower yellow pigment, a turmeric pigment, a Benikouji yellow pigment and the like can be mentioned. Among these water-soluble dyes, as described above, a cotinyl dye having a pH indicating function is particularly preferable.

一方、油溶性色素及び不溶性色素については、これら色素を用いて調製した固形状魚類用麻酔剤が空気中などの水分を吸湿しても、吸湿した水分中に該色素が溶け込まないため、該固形状魚類用麻酔剤の表面に存在する色素は滲むことなく、該色素の色調の低下又は消失は観察されない。そのため、油溶性色素及び不溶性色素は、本実施形態の固形状魚類用麻酔剤の麻酔効果が消失したものであるかどうかを判別することができないため、使用することができない。   On the other hand, for oil-soluble dyes and insoluble dyes, even if the solid fish anesthetic prepared using these dyes absorbs moisture such as air, the dye does not dissolve in the absorbed moisture. The pigment present on the surface of the shape fish anesthetic agent does not bleed, and no decrease or disappearance of the color of the pigment is observed. Therefore, oil-soluble pigments and insoluble pigments cannot be used because it cannot be determined whether the anesthetic effect of the solid fish anesthetic agent of this embodiment has been lost.

前記水溶性色素の含有量は、本発明の効果が得られれば特に制限はないが、該水溶性色素の色調を肉眼で観察する観点から、0.0088重量%〜0.064重量%が好ましく、0.033重量%〜0.064重量%がさらに好ましい。   The content of the water-soluble dye is not particularly limited as long as the effects of the present invention can be obtained. However, from the viewpoint of observing the color tone of the water-soluble dye with the naked eye, 0.0088% by weight to 0.064% by weight is preferable. 0.033 wt% to 0.064 wt% is more preferable.

また、本実施形態の魚類用麻酔剤に固形化を促進するための固形化促進剤を添加することができる。   Moreover, the solidification promoter for accelerating solidification can be added to the fish anesthetic agent of this embodiment.

前記固形化促進剤は、食の安全性の観点から、食用グリセリンや無水エタノールが好ましい。   The solidification accelerator is preferably edible glycerin or absolute ethanol from the viewpoint of food safety.

前記食用グリセリンの添加量は、固形化を促進する観点から、炭酸水素ナトリウム等の原材料の重量に対して2.5〜15重量%が好ましい。   The amount of the edible glycerin added is preferably 2.5 to 15% by weight with respect to the weight of the raw material such as sodium hydrogencarbonate from the viewpoint of promoting solidification.

前記無水エタノールの添加量は、固形化を促進する観点から、炭酸水素ナトリウム等の原材料の重量に対して10〜20重量%が好ましい。   From the viewpoint of promoting solidification, the amount of the absolute ethanol added is preferably 10 to 20% by weight based on the weight of the raw material such as sodium hydrogen carbonate.

さらに、本発明の目的及び効果を妨げなければ、前記混合物に他の素材や食品添加物などを添加することができる。   Furthermore, other materials and food additives can be added to the mixture as long as the objects and effects of the present invention are not hindered.

次いで、上記で調製した水溶性色素が添加された混合物を固形状に成型する。   Next, the mixture prepared by adding the water-soluble pigment prepared above is molded into a solid form.

前記成型方法は、本発明の目的及び効果が得られればに特に制限されず、例えば、成型容器に原材料を入れて成型し、これを乾燥することで固形状にする方法や、プレス機を用いて成型容器に入れた原材料に高い圧力を加圧することで固形状する方法などが挙げられる。   The molding method is not particularly limited as long as the objects and effects of the present invention can be obtained. For example, a raw material is placed in a molding container and molded, and then dried to form a solid, or a press is used. For example, a method of solidifying the raw material placed in the molding container by applying a high pressure to the raw material is included.

本実施形態において、原材料に固形化促進剤が含有しない場合、プレス機を用いて原材料を1cmあたり1592ポンド以上の圧力で加圧する。 In this embodiment, when the raw material does not contain a solidification accelerator, the raw material is pressurized at a pressure of 1592 pounds or more per cm 2 using a press.

このような工程を経て、水溶性色素の色調変化によって使用期限を判別することのできる炭酸水素ナトリウム由来の炭酸ガスを利用した固形状の魚類用麻酔剤を得ることができる。   Through such a process, a solid fish anesthetic agent using carbonic acid gas derived from sodium hydrogen carbonate, the expiration date of which can be determined by the color change of the water-soluble pigment, can be obtained.

次に、本発明の実施形態における固形状魚類用麻酔剤の使用期限を判別する方法について説明する。本実施形態に係る固形状魚類用麻酔剤の使用期限を判別する方法は、上述の固形状魚類用麻酔剤の表面の一部分に存在する水溶性色素が空気中などの水分を吸湿することによって該水溶性色素が滲み、該水溶性色素の色調が低下又は消失したことに基づいて使用期限を判別するものである。   Next, a method for determining the expiration date of the solid fish anesthetic in the embodiment of the present invention will be described. The method for determining the expiration date of the solid fish anesthetic according to the present embodiment is such that the water-soluble pigment present on a part of the surface of the solid fish anesthetic absorbs moisture such as in the air. The expiration date is discriminated based on the fact that the water-soluble dye is blurred and the color tone of the water-soluble dye is lowered or disappeared.

前記固形状魚類用麻酔剤は、上述のとおりに調製した炭酸水素ナトリウムと、食品添加物である水溶性色素とを含有し、該水溶性色素の色調変化が肉眼で観察できるように該固形状魚類用麻酔剤の表面の一部分に該水溶性色素が存在するものである。   The solid fish anesthetic contains sodium bicarbonate prepared as described above and a water-soluble pigment that is a food additive, and the solid fish so that the color change of the water-soluble pigment can be observed with the naked eye. The water-soluble pigment is present on a part of the surface of the fish anesthetic.

本実施形態において、前記水溶性色素の色調変化は、前記固形状魚類用麻酔剤の表面の一部分に存在する水溶性色素の色調を肉眼で観察し、該色素が滲むことによって該色素の色調の低下又は消失を判別する。このとき、前記水溶性色素が滲むことで色調が低下又は消失していれば、前記固形状魚類用麻酔剤が吸湿したことを示し、吸湿によって固形状魚類用麻酔剤から麻酔の有効成分である炭酸ガスが放出されたために麻酔効果が消失して該固形状魚類麻酔剤の使用期限が徒過したことを簡単に判別できる。   In the present embodiment, the color tone of the water-soluble pigment is changed by observing the color tone of the water-soluble pigment present on a part of the surface of the solid fish anesthetic agent with the naked eye, Determine decrease or disappearance. At this time, if the color tone decreases or disappears due to bleeding of the water-soluble pigment, it indicates that the solid fish anesthetic agent has absorbed moisture, and is an active ingredient for anesthesia from the solid fish anesthetic agent by moisture absorption. It can be easily determined that the anesthetic effect has disappeared due to the release of carbon dioxide gas and the expiration date for use of the solid fish anesthetic has passed.

1.固形状魚類用麻酔剤の調製
(1)固形化促進剤を用いて成型加工した固形状魚類用麻酔剤
炭酸水素ナトリウムとコハク酸とを重量比で1:1となるようにそれぞれ計量し、これを乳鉢で混合した後、この混合物に対して食用グリセリン2.5重量%を加えて混練し、混練物を調製した。
1. Preparation of solid fish anesthesia (1) Solid fish anesthesia molded with solidification accelerator Sodium bicarbonate and succinic acid were weighed at a weight ratio of 1: 1, respectively. After mixing with a mortar, 2.5% by weight of edible glycerin was added to the mixture and kneaded to prepare a kneaded product.

一方、上記と同様に、炭酸水素ナトリウムとコハク酸とを重量比で1:1となるようにそれぞれ計量して調製した混合物に、該混合物に対して固形化促進剤である食用グリセリンを2.5重量%加えて混練した。この混練物に食品添加物である水溶性色素(コチニール色素、クチナシ黄色色素、スピルリナ青色色素又はクチナシ緑色色素)を該混練物に対して0.1重量%〜8重量%加えて混合することで水溶性色素含有混練物を調製した。   On the other hand, in the same manner as described above, edible glycerin, which is a solidification accelerator, is added to a mixture prepared by measuring sodium bicarbonate and succinic acid so as to have a weight ratio of 1: 1. 5% by weight was added and kneaded. A water-soluble pigment (cochineal pigment, gardenia yellow pigment, spirulina blue pigment or gardenia green pigment), which is a food additive, is added to the kneaded mixture in an amount of 0.1 to 8% by weight and mixed. A water-soluble dye-containing kneaded material was prepared.

上記で調製した水溶性色素0.1重量%〜6重量%を含む水溶性色素含有混練物0.1gを計量し、これを固形状に成型加工するための成型容器内に入れた後、上記で調製した水溶性色素を含まない混練物約12gを加えて押し固め、これを60℃の乾燥機内で24時間保持することで固形状魚類用麻酔剤を調製した。   After weighing 0.1 g of the water-soluble dye-containing kneaded material containing 0.1% to 6% by weight of the water-soluble dye prepared above, and putting it in a molding container for molding into a solid state, About 12 g of the kneaded material containing no water-soluble pigment prepared in step 1 was added and pressed, and this was kept in a dryer at 60 ° C. for 24 hours to prepare a solid fish anesthetic.

(2)プレス機を用いて成型加工した固形状魚類用麻酔剤
炭酸水素ナトリウムとコハク酸とを重量比で1:1となるようにそれぞれ計量し、これを乳鉢で混合することで混合物を調製した。
(2) Solid fish anesthesia molded using a press machine Sodium bicarbonate and succinic acid are weighed to a weight ratio of 1: 1, and mixed in a mortar to prepare a mixture. did.

一方、上記と同様に、炭酸水素ナトリウムとコハク酸とを重量比で1:1となるようにそれぞれ計量した混合物に、該混合物に食品添加物であるコチニール色素(水溶性色素)を6重量%加えて混合することでコチニール色素含有混合物を調製した。   On the other hand, in the same manner as described above, sodium bicarbonate and succinic acid were each weighed to have a weight ratio of 1: 1, and then 6% by weight of cochineal dye (water-soluble dye) as a food additive was added to the mixture. In addition, a cochineal dye-containing mixture was prepared by mixing.

上記で調製した混合物約12gをプレス機の成型容器(直径40mmの円形状容器)に入れ、これを1cmあたり398〜1592ポンドの圧力で1分間加圧することで固形状に成型した。次いで、この固形状に成型された混合物の表面の一部分に上記で調製したコチニール色素含有混合物0.1gを添加し、再度、1cmあたり398〜1592ポンドの圧力で1分間加圧することで固形状魚類用麻酔剤を調製した。 About 12 g of the mixture prepared above was put into a molding container (a circular container having a diameter of 40 mm) of a press machine, and this was molded into a solid form by pressurizing at a pressure of 398 to 1592 pounds per 1 cm 2 . Next, 0.1 g of the cochineal dye-containing mixture prepared above is added to a part of the surface of the solid-shaped mixture, and the mixture is pressed again at a pressure of 398 to 1592 pounds per cm 2 for 1 minute. A fish anesthetic was prepared.

2.吸湿による色調変化及び麻酔効果について
上記1.(1)で調製した各種固形状魚類用麻酔剤(実施例1〜9)を温度35℃、湿度80%以上の恒温器内で4日間保持した後、該固形状魚類用麻酔剤の表面に存在する水溶性色素の色調変化及び該固形状魚類用麻酔剤の麻酔効果について調べた。
2. About color change and anesthetic effect by moisture absorption After holding the various solid fish anesthetics (Examples 1 to 9) prepared in (1) for 4 days in a thermostat having a temperature of 35 ° C. and a humidity of 80% or more, the surface of the solid fish anesthetic agent is applied. The change in color tone of the water-soluble pigments present and the anesthetic effect of the solid fish anesthetic were investigated.

すなわち、固形状魚類用麻酔剤の表面に存在する水溶性色素の色調変化は、湿度80%以上の恒温器で保持する前の吸湿していない固形状魚類用麻酔剤の表面に存在する水溶性色素の色調(0日後)と、湿度80%以上の恒温器に4日間保持することで吸湿させた固形状魚類用麻酔剤の表面に存在する水溶性色素の色調(4日後)を比較することで水溶性色素の色調の低下又は消失を評価した。   In other words, the color change of the water-soluble pigment present on the surface of the solid fish anesthetic agent is caused by the water-soluble pigment present on the surface of the solid fish anesthetic agent that has not absorbed moisture before being held in a thermostat having a humidity of 80% or more. To compare the color tone of the dye (after 0 days) and the color tone of the water-soluble dye (after 4 days) present on the surface of the solid fish anesthetic that has been absorbed by holding it in a thermostat with a humidity of 80% or more for 4 days The decrease or disappearance of the color tone of the water-soluble dye was evaluated.

一方、固形状魚類用麻酔剤の魚類に対する麻酔効果は、水温が25℃の海水20Lに濃度が1.6g/Lとなるように湿度80%以上の恒温器に4日間保持することで吸湿させた魚類用麻酔剤を溶解し、これに25℃の海水で飼育されたフグ(約20g/個体)5尾を投入し、フグを投入した時点から麻酔に懸るまでの時間を計測することで調べた。なお、フグが麻酔に懸ったかどうかについては、フグの鰭の動きなどを肉眼で観察し、横転、呼吸が緩慢になり、鰭の動きが停止した時点で麻酔に懸ったと判断した。また、対照は、乾燥条件下で保持することで吸湿していない固形状魚類用麻酔剤を用いた。   On the other hand, the anesthetic effect on fish of the solid fish anesthetic agent is to absorb moisture by holding it in a thermostat of 80% humidity or higher for 4 days in 20 L of seawater with a water temperature of 25 ° C. so that the concentration is 1.6 g / L. The fish anesthesia was dissolved, and 5 puffer fish (approximately 20 g / individual) reared in seawater at 25 ° C. were added to the fish. It was. Whether or not puffer fish was anesthetized was determined by observing the puffer's spear movements with the naked eye, and when he fell and the breathing slowed down and the sputum movement stopped, it was judged that he was engaged in anesthesia. Moreover, the control | contrast used the anesthetic agent for solid fish which is not moisture-absorbing by hold | maintaining under dry conditions.

図1〜9に示すように、湿度80%以上の恒温器に4日間保持することで吸湿させた魚類用麻酔剤の表面に存在する水溶性色素の色調(4日後)は、吸湿していない場合(0日後)と比べ、全ての場合において固形状魚類用麻酔剤の表面に存在する水溶性色素が滲み、その色調が低下又は消失していた。   As shown in FIGS. 1-9, the color tone (after 4 days) of the water-soluble pigment present on the surface of the fish anesthetic that was absorbed by holding it in a thermostat having a humidity of 80% or more for 4 days does not absorb moisture. Compared with the case (after 0 day), in all cases, the water-soluble pigment present on the surface of the solid fish anesthetic was soaked and the color tone was lowered or disappeared.

また、湿度80%以上の恒温器に4日間保持した固形状魚類用麻酔剤を用いて、フグが麻酔にかかるかどうかを調べたところ、全ての場合において、フグに麻酔が懸からなかったのに対し、乾燥条件下で保持することで吸湿していない固形状魚類用麻酔剤を用いた場合には、フグが麻酔に懸かった。   In addition, using a solid fish anesthetic kept in a thermostat with a humidity of 80% or more for 4 days, it was investigated whether or not the puffer fish was anesthetized. In all cases, the pufferfish was not anesthetized. On the other hand, when a solid fish anesthetic that did not absorb moisture by holding under dry conditions was used, Fugu was engaged in anesthesia.

このように、固形状魚類用麻酔剤の表面に存在する水溶性色素の色調が低下又は消失したものを使用した場合は、魚類に対して麻酔効果が得られなかったことから、固形状魚類用麻酔剤の表面に存在する水溶性色素の色調変化を肉眼で観察することによって該固形状魚類用麻酔剤が魚類に対して麻酔効果を有するかどうかを判別できることが分かった。   In this way, when using a water-soluble pigment whose color tone is reduced or eliminated on the surface of the solid fish anesthetic agent, an anesthetic effect could not be obtained for the fish. It was found that whether or not the solid fish anesthetic has an anesthetic effect on the fish can be determined by observing the color change of the water-soluble pigment present on the surface of the anesthetic with the naked eye.

3.固形化促進剤を用いて成型加工した固形状魚類用麻酔剤の麻酔効果
(1)トラフグ
水温が17.5〜27.5℃の海水20Lに、上記1.(1)で調製した実施例2のコチニール色素の色調が変化していない固形状魚類用麻酔剤の濃度が0.1〜8g/Lとなるように溶解し、これに平均120g/個体のトラフグ5尾を投入し、トラフグを投入した時点からトラフグが麻酔に懸るまでの時間を計測した。なお、トラフグが麻酔に懸ったかどうかについて、トラフグの鰭の動きなどを肉眼で観察し、横転、呼吸が緩慢になり、鰭の動きが停止した時点で麻酔に懸ったと判断した。また、固形状魚類用麻酔剤を投入してから完全に溶けるまでの時間を計数した。さらに、固形状魚類用麻酔剤を投入する前後の海水のpHを測定した。
3. Anesthetic effect of solid fish anesthesia molded using a solidification accelerator (1) Troughfish In 20 L of seawater having a water temperature of 17.5 to 27.5 ° C. The concentration of the solid fish anesthetic agent of Example 2 prepared in (1) in which the color tone of the cochineal pigment is not changed is dissolved to be 0.1 to 8 g / L, and an average of 120 g / individual troughfish Five fish were introduced, and the time from when the trough was introduced until the trough was engaged in anesthesia was measured. In addition, as to whether or not the trough puffer took anesthesia, the movement of the puffer's spider was observed with the naked eye, and it was judged that he took the anesthesia when the rollover and respiration became slow and the wandering movement stopped. In addition, the time from when the solid fish anesthetic was added until completely dissolved was counted. Furthermore, the pH of the seawater before and after feeding the solid fish anesthetic was measured.

表3に示したように、トラフグは、水温が17.5〜27.5℃のすべての場合において、固形状魚類用麻酔剤の濃度が1g/L以上で麻酔に懸ることが分かった。一方、固形状魚類用麻酔剤の濃度が0.7g/L以下の濃度ではいずれの海水温度においても麻酔に懸らなかった。   As shown in Table 3, in all cases where the water temperature was 17.5 to 27.5 ° C., it was found that trough puffer was anesthetized when the concentration of the solid fish anesthetic was 1 g / L or more. On the other hand, when the concentration of the solid fish anesthetic was 0.7 g / L or less, it was not affected by anesthesia at any seawater temperature.

(2)アメマス
水温が1〜20℃の淡水又は海水20Lに、上記1.(1)で調製した実施例2のコチニール色素の色調が変化していない固形状魚類用麻酔剤の濃度が0.1〜8g/Lとなるように溶解し、これに1〜20℃の淡水又は海水で飼育された約230g/個体のアメマス5尾を投入し、アメマスを投入した時点からアメマスが麻酔に懸るまでの時間を計測した。なお、アメマスが麻酔に懸ったかどうかについて、アメマスの鰭の動きなどを肉眼で観察し、横転、呼吸が緩慢になり、鰭の動きが停止した時点で麻酔に懸ったと判断した。また、固形状魚類用麻酔剤を淡水又は海水に投入してから完全に溶けるまでの時間を計数した。さらに、固形状魚類用麻酔剤を投入する前後の淡水又は海水のpHを測定した。
(2) American trout Fresh water or seawater with a water temperature of 1 to 20 ° C. The solid fish anesthetic agent of Example 2 prepared in (1) in which the color tone of the cochineal pigment is not changed is dissolved in a concentration of 0.1 to 8 g / L, and fresh water at 1 to 20 ° C. is dissolved therein. Alternatively, about 230 g / individual American trout bred in seawater was introduced, and the time from when the American trout was put into the anesthet was measured. In addition, it was judged whether or not the American trout was engaged in anesthesia by visually observing the movement of the trout of the American trout with the naked eye, and the rollover and breathing became slow, and the movement of the sputum stopped. In addition, the time from when the solid fish anesthetic was added to fresh water or seawater until completely dissolved was counted. Furthermore, the pH of fresh water or seawater before and after the solid fish anesthetic was added was measured.

表4に示したように、淡水で飼育したアメマスは、水温が1〜20℃のすべての場合において、固形状魚類用麻酔剤の濃度が2g/L以上で麻酔に懸ることが分かった。一方、水温が1℃の場合は、固形状魚類用麻酔剤の濃度が1g/Lでも麻酔に懸ったが、0.1g/Lでは麻酔に懸らなかった。   As shown in Table 4, it was found that American trout bred in fresh water was subjected to anesthesia when the concentration of the solid fish anesthetic was 2 g / L or higher in all cases where the water temperature was 1 to 20 ° C. On the other hand, when the water temperature was 1 ° C., the anesthesia was applied even when the concentration of the solid fish anesthetic was 1 g / L, but the anesthesia was not applied when the concentration was 0.1 g / L.

一方、表5に示したように、海水で飼育したアメマスは、水温が1〜20℃のすべての場合において、固形状魚類用麻酔剤の濃度が2g/L以上で麻酔に懸ることが分かった。また、水温が10及び20℃の場合は、魚類用麻酔剤の濃度が1g/Lでも麻酔に懸ったが、0.1g/Lでは麻酔に懸らなかった。   On the other hand, as shown in Table 5, it was found that American trout bred in seawater is subject to anesthesia when the concentration of the solid fish anesthetic is 2 g / L or higher in all cases where the water temperature is 1 to 20 ° C. . Further, when the water temperature was 10 and 20 ° C., the anesthesia agent for fish was used for anesthesia even when the concentration was 1 g / L, but the anesthesia was not used for 0.1 g / L.

(3)ウグイ
水温が1〜30℃の淡水又は海水20Lに、上記1.(1)で調製した実施例2のコチニール色素の色調が変化していない固形状魚類用麻酔剤の濃度が0.1〜8g/Lとなるように溶解し、これに1〜30℃の淡水又は海水で飼育された約160g/個体のウグイ5尾を投入し、ウグイを投入した時点からウグイが麻酔に懸るまでの時間を計測した。なお、ウグイが麻酔に懸ったかどうかについて、ウグイの鰭の動きなどを肉眼で観察し、横転、呼吸が緩慢になり、鰭の動きが停止した時点で麻酔に懸ったと判断した。また、固形状魚類用麻酔剤を淡水又は海水に投入してから完全に溶けるまでの時間を計数した。さらに、固形状魚類用麻酔剤を投入する前後の淡水又は海水のpHを測定した。
(3) Ugui In the fresh water or seawater 20L of water temperature 1-30 degreeC, said 1. It melt | dissolved so that the density | concentration of the solid fish anesthetic for which the color tone of the cochineal pigment | dye of Example 2 prepared in (1) may not change is 0.1-8 g / L, and it is 1-30 degreeC fresh water to this. Alternatively, about 160 g / individual eels raised in seawater were introduced, and the time from when the ugly was introduced until the ugly was anesthetized was measured. In addition, it was judged whether or not Ugui was engaged in anesthesia by observing the movement of the Ugui's heel with the naked eye. In addition, the time from when the solid fish anesthetic was added to fresh water or seawater until completely dissolved was counted. Furthermore, the pH of fresh water or seawater before and after the solid fish anesthetic was added was measured.

表6に示したように、淡水で飼育したウグイは、水温が1〜30℃のすべての場合において、固形状魚類用麻酔剤の濃度が4g/L以上で麻酔に懸ることが分かった。一方、水温が1℃の場合は、固形状魚類用麻酔剤の濃度が2g/L及び1g/Lでも麻酔に懸ったが、0.1g/Lの濃度では麻酔に懸らなかった。なお、本実施例でも、固形状魚類用麻酔剤の投入前後のpHの変化を水中に投入した固形状魚類用麻酔剤の色を観察することで、目視によって容易に確認することができた。   As shown in Table 6, it was found that the Japanese goose bred in fresh water hangs on anesthesia when the concentration of the solid fish anesthetic is 4 g / L or higher in all cases where the water temperature is 1 to 30 ° C. On the other hand, when the water temperature was 1 ° C., the anesthesia for solid fish was 2 g / L and 1 g / L, but it was not anesthetized at the concentration of 0.1 g / L. Also in this example, the change in pH before and after the solid fish anesthetic was added could be easily confirmed visually by observing the color of the solid fish anesthetic added to the water.

一方、表7に示したように、海水で飼育したウグイは、水温が1〜30℃のすべての場合において、固形状魚類用麻酔剤の濃度が4g/L以上で麻酔に懸ることが分かった。また、水温が1℃の場合は、固形状魚類用麻酔剤の濃度が2g/Lでも麻酔に懸ったが、1g/Lの濃度では麻酔に懸らなかった。   On the other hand, as shown in Table 7, it was found that the Japanese sea bream bred in seawater hangs under anesthesia when the concentration of the solid fish anesthetic is 4 g / L or higher in all cases where the water temperature is 1 to 30 ° C. . Moreover, when the water temperature was 1 ° C., the anesthesia was applied even when the concentration of the solid fish anesthetic was 2 g / L, but the anesthesia was not applied at the concentration of 1 g / L.

(4)フクドジョウ
水温が1〜20℃の淡水20Lに、上記1.(1)で調製した実施例2のコチニール色素の色調が変化していない固形状魚類用麻酔剤の濃度が1〜8g/Lとなるように溶解し、これに1〜20℃の淡水で飼育された約6g/個体のフクドジョウ5尾を投入し、フクドジョウを投入した時点からフクドジョウが麻酔に懸るまでの時間を計測した。なお、フクドジョウが麻酔に懸ったかどうかについて、フクドジョウの鰭の動きなどを肉眼で観察し、横転、呼吸が緩慢になり、鰭の動きが停止した時点で麻酔に懸ったと判断した。また、固形状魚類用麻酔剤を淡水に投入してから完全に溶けるまでの時間を計数した。さらに、固形状魚類用麻酔剤を投入する前後の淡水のpHを測定した。
(4) Fukudojo In 20L of fresh water having a water temperature of 1 to 20 ° C, the above 1. Dissolve so that the concentration of the solid fish anesthetic agent of Example 2 prepared in (1), in which the color tone of the cochineal pigment does not change, is 1 to 8 g / L, and is kept in fresh water at 1 to 20 ° C. About 5 g / individual Fukudojo was added, and the time from when the Fukudojo was put in until Fukudojo was engaged in anesthesia was measured. Whether or not Fukudojo was involved in anesthesia was observed with the naked eye, such as the movements of Fukudojo's sputum, and it was determined that he was engaged in anesthesia when the rollover and breathing slowed and the movement of the spider stopped. In addition, the time from when the solid fish anesthetic was added to fresh water until completely dissolved was counted. Further, the pH of fresh water before and after the solid fish anesthetic was added was measured.

表8に示したように、淡水で飼育したフクドジョウは、水温が1〜20℃のすべての場合において、固形状魚類用麻酔剤の濃度が2g/L以上で麻酔に懸ることが分かった。一方、固形状魚類用麻酔剤の濃度が1g/Lの濃度では麻酔に懸らなかった。   As shown in Table 8, it was found that fukudojo bred in fresh water was subjected to anesthesia at a solid fish anesthetic concentration of 2 g / L or more in all cases where the water temperature was 1 to 20 ° C. On the other hand, anesthesia for solid fish was not affected by anesthesia at a concentration of 1 g / L.

(5)ゼブラフィッシュ
水温が20〜30℃の淡水20Lに、上記1.(1)で調製した実施例2のコチニール色素の色調が変化していない固形状魚類用麻酔剤の濃度が1〜10g/Lとなるように溶解し、これに20〜30℃の淡水で飼育された約0.25g/個体のゼブラフィッシュ5尾を投入し、ゼブラフィッシュを投入した時点からゼブラフィッシュが麻酔に懸るまでの時間を計測した。なお、ゼブラフィッシュが麻酔に懸ったかどうかについて、ゼブラフィッシュの鰭の動きなどを肉眼で観察し、横転、呼吸が緩慢になり、鰭の動きが停止した時点で麻酔に懸ったと判断した。また、固形状魚類用麻酔剤を淡水に投入してから完全に溶けるまでの時間を計数した。さらに、固形状魚類用麻酔剤を投入する前後の淡水のpHを測定した。
(5) Zebrafish To 20 L of fresh water having a water temperature of 20 to 30 ° C., the above 1. Dissolve so that the concentration of the solid fish anesthetic agent of Example 2 prepared in (1) in which the color tone of the cochineal pigment does not change is 1 to 10 g / L, and breed in fresh water at 20 to 30 ° C. Five zebrafish of about 0.25 g / individual were put in, and the time from when the zebrafish was put into the zebrafish was put into anesthesia was measured. In addition, as to whether or not the zebrafish was involved in anesthesia, the movements of the zebrafish spears were observed with the naked eye, and it was judged that they were engaged in anesthesia when the rollover and breathing slowed and the wrinkle movement stopped. In addition, the time from when the solid fish anesthetic was added to fresh water until completely dissolved was counted. Further, the pH of fresh water before and after the solid fish anesthetic was added was measured.

表9に示したように、淡水で飼育したゼブラフィッシュは、水温が20〜30℃のすべての場合において、固形状魚類用麻酔剤の濃度が4g/L以上で麻酔に懸ることが分かった。一方、水温が30℃の場合は、固形状魚類用麻酔剤の濃度が2g/Lでも麻酔に懸ったが、1g/Lの濃度では麻酔に懸らなかった。   As shown in Table 9, it was found that zebrafish bred in fresh water were subjected to anesthesia when the concentration of the solid fish anesthetic was 4 g / L or higher in all cases where the water temperature was 20-30 ° C. On the other hand, when the water temperature was 30 ° C., anesthesia was applied even when the concentration of the solid fish anesthetic was 2 g / L, but the anesthesia was not applied at the concentration of 1 g / L.

(6)プラティ
水温が20〜30℃の淡水20Lに、上記1.(1)で調製した実施例2のコチニール色素の色調が変化していない固形状魚類用麻酔剤の濃度が2〜10g/Lとなるように溶解し、これに20〜30℃の淡水で飼育された約0.4g/個体のプラティ5尾を投入し、プラティを投入した時点からプラティが麻酔に懸るまでの時間を計測した。なお、プラティが麻酔に懸ったかどうかについて、プラティの鰭の動きなどを肉眼で観察し、横転、呼吸が緩慢になり、鰭の動きが停止した時点で麻酔に懸ったと判断した。また、固形状魚類用麻酔剤を淡水に投入してから完全に溶けるまでの時間を計数した。さらに、固形状魚類用麻酔剤を投入する前後の淡水のpHを測定した。
(6) Platy To 20 L of fresh water having a water temperature of 20 to 30 ° C., the above 1. Dissolve so that the concentration of the solid fish anesthetic agent of Example 2 prepared in (1) in which the color tone of the cochineal pigment does not change is 2 to 10 g / L, and breed in fresh water at 20 to 30 ° C. About 5 g of the platies of about 0.4 g / individual were put in, and the time from when the platies were put into place until the platies got into anesthesia was measured. As to whether or not Prati was involved in anesthesia, the movement of Plati's sputum was observed with the naked eye, and it was judged that he was engaged in anesthesia when the rollover and breathing slowed and the movement of the sputum stopped. In addition, the time from when the solid fish anesthetic was added to fresh water until completely dissolved was counted. Further, the pH of fresh water before and after the solid fish anesthetic was added was measured.

表10に示したように、淡水で飼育したプラティは、水温が20〜30℃のすべての場合において、固形状魚類用麻酔剤の濃度が4g/L以上で麻酔に懸ることが分かった。一方、固形状魚類用麻酔剤の濃度が2g/Lでは麻酔に懸らなかった。   As shown in Table 10, it was found that the platters bred in fresh water were subjected to anesthesia when the concentration of the solid fish anesthetic was 4 g / L or higher in all cases where the water temperature was 20-30 ° C. On the other hand, when the concentration of the solid fish anesthetic was 2 g / L, anesthesia was not affected.

(7)メダカ
水温が10〜30℃の淡水20Lに、上記1.(1)で調製した実施例2のコチニール色素の色調が変化していない固形状魚類用麻酔剤の濃度が1〜10g/Lとなるように溶解し、これに10〜30℃の淡水で飼育された約0.23g/個体のメダカ5尾を投入し、メダカを投入した時点からメダカが麻酔に懸るまでの時間を計測した。なお、メダカが麻酔に懸ったかどうかについて、メダカの鰭の動きなどを肉眼で観察し、横転、呼吸が緩慢になり、鰭の動きが停止した時点で麻酔に懸ったと判断した。また、固形状魚類用麻酔剤を淡水に投入してから完全に溶けるまでの時間を計数した。さらに、固形状魚類用麻酔剤を投入する前後の淡水のpHを測定した。
(7) Medaka To 20 L of fresh water having a water temperature of 10 to 30 ° C., the above 1. Dissolve so that the concentration of the solid fish anesthetic agent of Example 2 prepared in (1) in which the color tone of the cochineal pigment does not change is 1 to 10 g / L, and keep it in fresh water at 10 to 30 ° C. Five medaka fish of about 0.23 g / individual were put in, and the time from when the medaka was put in until the medaka was engaged in anesthesia was measured. As to whether or not the medaka was involved in anesthesia, the movement of the medaka moth was observed with the naked eye, and it was judged that the medaka was engaged in anesthesia when the rollover and breathing slowed and the heel movement stopped. In addition, the time from when the solid fish anesthetic was added to fresh water until completely dissolved was counted. Further, the pH of fresh water before and after the solid fish anesthetic was added was measured.

表11に示したように、淡水で飼育したメダカは、水温が10〜30℃のすべての場合において、固形状魚類用麻酔剤の濃度が4g/L以上で麻酔に懸ることが分かった。一方、水温が10℃の場合は、固形状魚類用麻酔剤の濃度が2g/Lでも麻酔に懸ったが、1g/Lの濃度では麻酔に懸らなかった。   As shown in Table 11, it was found that the medaka bred in fresh water was subjected to anesthesia when the concentration of the solid fish anesthetic was 4 g / L or higher in all cases where the water temperature was 10 to 30 ° C. On the other hand, when the water temperature was 10 ° C., the anesthesia was applied even when the concentration of the solid fish anesthetic was 2 g / L, but the anesthesia was not applied at the concentration of 1 g / L.

(8)ニシキゴイ
水温が5〜30℃の淡水20Lに、上記1.(1)で調製した実施例2のコチニール色素の色調が変化していない固形状魚類用麻酔剤の濃度が1〜20g/Lとなるように溶解し、これに5〜30℃の淡水で飼育された約27g/個体のニシキゴイ5尾を投入し、ニシキゴイを投入した時点からニシキゴイが麻酔に懸るまでの時間を計測した。なお、ニシキゴイが麻酔に懸ったかどうかについて、ニシキゴイの鰭の動きなどを肉眼で観察し、横転、呼吸が緩慢になり、鰭の動きが停止した時点で麻酔に懸ったと判断した。また、固形状魚類用麻酔剤を淡水に投入してから完全に溶けるまでの時間を計数した。さらに、固形状魚類用麻酔剤を投入する前後の淡水のpHを測定した。
(8) Nishikigoi To 20 L of fresh water having a water temperature of 5 to 30 ° C. Dissolved so that the concentration of the solid fish anesthetic agent of Example 2 prepared in (1) in which the color tone of the cochineal pigment was not changed is 1 to 20 g / L, and was bred in fresh water at 5 to 30 ° C. Approximately 27 g / individual Nishikigoi was injected, and the time from when the Nishikigoi was introduced until it became anesthetized was measured. Whether or not Nishikigoi was involved in anesthesia was observed with the naked eye, such as the movements of Nishikigoi's sputum, and it was determined that he was engaged in anesthesia when the rollover and breathing slowed and the movement of the spider stopped. In addition, the time from when the solid fish anesthetic was added to fresh water until completely dissolved was counted. Further, the pH of fresh water before and after the solid fish anesthetic was added was measured.

表12に示したように、淡水で飼育したニシキゴイは、水温が20〜30℃のすべての場合において、固形状魚類用麻酔剤の濃度が5g/L以上で麻酔に懸ることが分かった。一方、固形状魚類用麻酔剤の濃度が1g/Lでは麻酔に懸らなかった。   As shown in Table 12, it was found that the Nishikigoi bred in fresh water hangs on anesthesia at a solid fish anesthetic concentration of 5 g / L or higher in all cases where the water temperature is 20-30 ° C. On the other hand, when the concentration of the solid fish anesthetic was 1 g / L, anesthesia was not affected.

(9)マゴイ
水温が5〜30℃の淡水20Lに、上記1.(1)で調製した実施例2のコチニール色素の色調が変化していない固形状魚類用麻酔剤の濃度が1〜20g/Lとなるように溶解し、これに5〜30℃の淡水で飼育された約26g/個体のマゴイ5尾を投入し、マゴイを投入した時点からマゴイが麻酔に懸るまでの時間を計測した。なお、マゴイが麻酔に懸ったかどうかについて、マゴイの鰭の動きなどを肉眼で観察し、横転、呼吸が緩慢になり、鰭の動きが停止した時点で麻酔に懸ったと判断した。また、固形状魚類用麻酔剤を淡水に投入してから完全に溶けるまでの時間を計数した。さらに、固形状魚類用麻酔剤を投入する前後の淡水のpHを測定した。
(9) Magoi To 20L of fresh water having a water temperature of 5 to 30 ° C, the above 1. Dissolved so that the concentration of the solid fish anesthetic agent of Example 2 prepared in (1) in which the color tone of the cochineal pigment was not changed is 1 to 20 g / L, and was bred in fresh water at 5 to 30 ° C. Approximately 5Og / individual Magoi of about 26g were introduced, and the time from when Magoi was introduced until Magoi was engaged in anesthesia was measured. As for whether Magoi was involved in anesthesia, the movement of Magoi's spider was observed with the naked eye, and it was judged that he was engaged in anesthesia when the rollover and breathing slowed and the movement of the spider stopped. In addition, the time from when the solid fish anesthetic was added to fresh water until completely dissolved was counted. Further, the pH of fresh water before and after the solid fish anesthetic was added was measured.

表13に示したように、淡水で飼育したマゴイは、水温が20〜30℃のすべての場合において、固形状魚類用麻酔剤の濃度が5g/L以上で麻酔に懸ることが分かった。一方、固形状魚類用麻酔剤の濃度が1g/Lの濃度では麻酔に懸らなかった。   As shown in Table 13, Magoi raised in fresh water was found to be anesthetized when the concentration of the solid fish anesthetic was 5 g / L or higher in all cases where the water temperature was 20-30 ° C. On the other hand, anesthesia for solid fish was not affected by anesthesia at a concentration of 1 g / L.

(10)ティラピア
水温が20〜30℃の淡水20Lに、上記1.(1)で調製した実施例2のコチニール色素の色調が変化していない固形状魚類用麻酔剤の濃度が1〜20g/Lとなるように溶解し、これに20〜30℃の淡水で飼育された約29g/個体のティラピア5尾を投入し、ティラピアを投入した時点からティラピアが麻酔に懸るまでの時間を計測した。なお、ティラピアが麻酔に懸ったかどうかについて、ティラピアの鰭の動きなどを肉眼で観察し、横転、呼吸が緩慢になり、鰭の動きが停止した時点で麻酔に懸ったと判断した。また、固形状魚類用麻酔剤を淡水に投入してから完全に溶けるまでの時間を計数した。さらに、固形状魚類用麻酔剤を投入する前後の淡水のpHを測定した。
(10) Tilapia To 20 L of fresh water having a water temperature of 20 to 30 ° C. Dissolve so that the concentration of the solid fish anesthetic agent of Example 2 in which the color tone of the cochineal pigment of Example 2 prepared in (1) does not change is 1 to 20 g / L, and is bred in fresh water at 20 to 30 ° C. 5 tilapia of about 29 g / individual were introduced, and the time from when tilapia was introduced until tilapia was engaged in anesthesia was measured. As to whether or not Tilapia was involved in anesthesia, we observed the movement of Tilapia's sputum with the naked eye and judged that he was engaged in anesthesia when the rollover and breathing slowed and the movement of the spear stopped. In addition, the time from when the solid fish anesthetic was added to fresh water until completely dissolved was counted. Further, the pH of fresh water before and after the solid fish anesthetic was added was measured.

表14に示したように、淡水で飼育したティラピアは、水温が20〜30℃のすべての場合において、固形状魚類用麻酔剤の濃度が5g/L以上で麻酔に懸ることが分かった。一方、固形状魚類用麻酔剤の濃度が1g/Lの濃度では麻酔に懸らなかった。   As shown in Table 14, tilapia bred in fresh water was found to be anesthetized when the concentration of the solid fish anesthetic was 5 g / L or higher in all cases where the water temperature was 20-30 ° C. On the other hand, anesthesia for solid fish was not affected by anesthesia at a concentration of 1 g / L.

(11)ニジマス
水温が1〜20℃の淡水又は海水20Lに、上記1.(1)で調製した実施例2のコチニール色素の色調が変化していない固形状魚類用麻酔剤の濃度が0.1〜8g/Lとなるように溶解し、これに1〜20℃の淡水又は海水で飼育された約159g/個体のニジマス5尾を投入し、ニジマスを投入した時点からニジマスが麻酔に懸るまでの時間を計測した。なお、ニジマスが麻酔に懸ったかどうかについて、ニジマスの鰭の動きを肉眼で観察し、鰭の動きが停止した時点で麻酔に懸ったと判断した。また、固形状魚類用麻酔剤を淡水に投入してから完全に溶けるまでの時間を計数した。さらに、固形状魚類用麻酔剤を投入する前後の淡水のpHを測定した。
(11) Rainbow trout To fresh water or seawater 20 L with a water temperature of 1 to 20 ° C., the above 1. The solid fish anesthetic agent of Example 2 prepared in (1) in which the color tone of the cochineal pigment is not changed is dissolved in a concentration of 0.1 to 8 g / L, and fresh water at 1 to 20 ° C. is dissolved therein. Alternatively, about 159 g / individual rainbow trout bred in seawater were introduced, and the time from when the rainbow trout was introduced until the rainbow trout became anesthetized was measured. Whether or not rainbow trout was involved in anesthesia, the movement of the rainbow trout moth was observed with the naked eye, and it was determined that the rainbow trout was engaged in anesthesia when the movement of the moth stopped. In addition, the time from when the solid fish anesthetic was added to fresh water until completely dissolved was counted. Further, the pH of fresh water before and after the solid fish anesthetic was added was measured.

表15に示したように、淡水で飼育したニジマスは、水温が1〜20℃のすべての場合において、固形状魚類用麻酔剤の濃度が1g/L以上で麻酔に懸ることが分かった。一方、固形状魚類用麻酔剤の濃度が0.1g/Lの濃度では麻酔に懸らなかった。
As shown in Table 15, rainbow trout bred in fresh water was found to be anesthetized when the concentration of the solid fish anesthetic was 1 g / L or higher in all cases where the water temperature was 1 to 20 ° C. On the other hand, the anesthesia agent for solid fish was not affected by anesthesia at a concentration of 0.1 g / L.

一方、表16に示したように、海水で飼育したニジマスは、水温が1〜20℃のすべての場合において、固形状魚類用麻酔剤の濃度が1g/L以上で麻酔に懸ることが分かった。一方、固形状魚類用麻酔剤の濃度が0.1g/Lの濃度では麻酔に懸らなかった。
On the other hand, as shown in Table 16, rainbow trout bred in seawater was found to be anesthetized when the concentration of the solid fish anesthetic was 1 g / L or higher in all cases where the water temperature was 1 to 20 ° C. . On the other hand, the anesthesia agent for solid fish was not affected by anesthesia at a concentration of 0.1 g / L.

水温が10℃の淡水又は汽水(2/3海水pH8.06のもの又は1/3海水海水pH7.92のもの)20Lに、上記1.(1)で調製した実施例2のコチニール色素の色調が変化していない固形状魚類用麻酔剤の濃度が0.1〜8g/Lとなるように溶解し、これに10℃の淡水又は汽水(2/3海水pH8.06のもの又は1/3海水海水pH7.92のもの)で飼育された約159g/個体のニジマス5尾を投入し、ニジマスを投入した時点からニジマスが麻酔に懸るまでの時間を計測した。なお、ニジマスが麻酔に懸ったかどうかについて、ニジマスの鰭の動きなどを肉眼で観察し、横転、呼吸が緩慢になり、鰭の動きが停止した時点で麻酔に懸ったと判断した。また、固形状魚類用麻酔剤を投入してから完全に溶けるまでの時間を計数した。さらに、固形状魚類用麻酔剤を投入する前後のpHを測定した。   To 20 L of fresh water or brackish water (having 2/3 seawater pH 8.06 or 1/3 seawater seawater pH 7.92) having a water temperature of 10 ° C. It melt | dissolved so that the density | concentration of the solid fish anesthetic for which the color tone of the cochineal pigment | dye of Example 2 prepared in (1) may not change is 0.1-8 g / L, and it is 10 degreeC fresh water or brackish water. 5 rainbow trouts of about 159g / individual bred in (2/3 seawater pH 8.06 or 1/3 seawater seawater pH 7.92) are introduced, and from the time when the rainbow trout is put into the anesthesia Was measured. Whether or not rainbow trout was involved in anesthesia, the movement of the rainbow trout spider was observed with the naked eye. In addition, the time from when the solid fish anesthetic was added until completely dissolved was counted. Furthermore, the pH before and after the solid fish anesthetic was added was measured.

表17に示したように、pHをアルカリ性にして汽水で飼育したニジマスは、それらを麻酔にかけると、pHを中性にして汽水で飼育したニジマスと比較して、麻酔剤が懸りにくくなる傾向が認められた。同様に、pHをアルカリ性にして淡水で飼育したニジマスは、それらを麻酔にかけると、pHを中性にして淡水で飼育したニジマスと比較して、麻酔剤が懸りにくくなる傾向が認められた。このことから、酸性状態では麻酔に懸りやすく、海水(pH8付近)を中性(pH7付近)にすると、さらに短い時間で麻酔に懸ると推察された。   As shown in Table 17, rainbow trout bred with brackish water with an alkaline pH, when they are subjected to anesthesia, the anesthetic is less likely to hang than rainbow trout bred with brackish water with a neutral pH. Was recognized. Similarly, rainbow trout bred in fresh water with an alkaline pH was found to be less susceptible to anesthetics when subjected to anesthesia than rainbow trout bred in fresh water with a neutral pH. From this, it was inferred that anesthesia can be easily affected in an acidic state, and if seawater (around pH 8) is neutral (around pH 7), anesthesia is expected in a shorter time.

なお、上述の各実験においては、固形状魚類用麻酔剤の投入前後の水のpH変化の状況を水中に投入した固形状魚類用麻酔剤の色の変化を目視により観察することによっても、容易に確認することができた。   In each of the above-mentioned experiments, it is also easy to visually observe the color change of the solid fish anesthetic added to the water before and after the addition of the solid fish anesthetic. I was able to confirm.

4.プレス機を用いて成型加工した固形状魚類用麻酔剤の麻酔効果
水温が20〜30℃の海水20Lに、上記1.(2)で調製した実施例10のプレス機を用いて成型加工したコチニール色素の色調が変化していない固形状魚類用麻酔剤の濃度が0.4〜1.0g/Lとなるように溶解し、これに24℃の淡水で飼育された約1.2g/固体(全長31mm)のマダイ5尾を投入し、マダイを投入した時点からマダイが麻酔に懸るまでの時間を計測した。なお、マダイが麻酔に懸ったかどうかについて、マダイの鰭の動きなどを肉眼で観察し、横転、呼吸が緩慢になり、鰭の動きが停止した時点で麻酔に懸ったと判断した。一方、対照として、上記1.(1)で調製した固形化促進剤を用いて成型加工したコチニール色素の色調が変化していない魚類用麻酔剤(実施例2)についても同様に調べた。
4). Anesthetic effect of solid fish anesthesia molded and processed using a press machine. Dissolve so that the concentration of the solid fish anesthetic agent that is not changed in color tone of the cochineal pigment molded using the press machine of Example 10 prepared in (2) is 0.4 to 1.0 g / L. Then, about 1.2 g / solid (total length: 31 mm) of red sea bream raised in fresh water at 24 ° C. was added thereto, and the time from when the red sea bream was placed until the red sea bream took anesthesia was measured. As to whether or not the red sea bream took anesthesia, the movement of the red sea bream was observed with the naked eye. On the other hand, as a control, 1. The fish anesthetic (Example 2) in which the color tone of the cochineal pigment molded using the solidification accelerator prepared in (1) did not change was also examined in the same manner.

表18に示したように、プレス機によって成型加工した固形状魚類用麻酔剤は、固形化促進剤によって成型加工した固形状魚類用麻酔剤と同様の麻酔効果が得られた。このように、プレス機による加圧によって成型加工した固形化魚類用麻酔剤及び固形化促進剤によって成型加工した固形状魚類用麻酔剤ともに魚類に対して同様の麻酔効果が得られ、成型加工方法に関わらず固形状魚類用麻酔剤が魚類に対して麻酔効果を有することが分かった。   As shown in Table 18, the anesthetic for solid fish molded by a press machine had the same anesthetic effect as the anesthetic for solid fish molded by a solidification accelerator. In this way, the same anesthetic effect can be obtained for fish both with an anesthetic for solidified fish molded by pressing with a press machine and an anesthetic for solid fish molded with a solidification accelerator. Regardless, it was found that the solid fish anesthetic has an anesthetic effect on the fish.

Claims (10)

水溶性色素の色調変化によって使用期限を判別することのできる炭酸水素ナトリウム由来の炭酸ガスを利用した固形状の魚類用麻酔剤であって、
炭酸水素ナトリウムと、有機酸と、食品添加物である水溶性色素とを含有し、
該水溶性色素の色調変化が肉眼で観察できるように該魚類用麻酔剤の表面の一部分に該水溶性色素が存在することを特徴とする、
固形状魚類用麻酔剤。
A solid fish anesthetic using carbonic acid gas derived from sodium bicarbonate that can determine the expiration date based on the color change of the water-soluble dye,
Contains sodium hydrogen carbonate, organic acids, and water-soluble pigments that are food additives,
The water-soluble dye is present on a part of the surface of the fish anesthetic so that the color change of the water-soluble dye can be observed with the naked eye,
An anesthetic for solid fish.
前記水溶性色素が、コチニール色素、クチナシ黄色色素、スピルリナ青色色素、クチナシ緑色色素からなる群から選ばれる1種の水溶性色素である、
請求項1に記載の固形状魚類用麻酔剤。
The water-soluble dye is one water-soluble dye selected from the group consisting of a cochineal dye, a gardenia yellow dye, a spirulina blue dye, and a gardenia green dye.
The anesthetic for solid fish according to claim 1.
前記水溶性色素の含有量が、0.0088重量%〜0.064重量%である、
請求項1又は2に記載の固形状魚類用麻酔剤。
The content of the water-soluble dye is 0.0088 wt% to 0.064 wt%,
The anesthetic for solid fish according to claim 1 or 2.
前記有機酸が、コハク酸である、
請求項1〜4のいずれか1項に記載の固形状魚類用麻酔剤。
The organic acid is succinic acid,
The anesthetic for solid fish according to any one of claims 1 to 4.
さらに、固形化促進剤を含有することを特徴とする、
請求項1〜4のいずれか1項に記載の固形状魚類用麻酔剤。
Further, characterized by containing a solidification accelerator,
The anesthetic for solid fish according to any one of claims 1 to 4.
前記固形化促進剤が食用グリセリン又は無水エタノールである、
請求項5に記載の固形状魚類用麻酔剤。
The solidification accelerator is edible glycerin or absolute ethanol,
The solid fish anesthetic agent according to claim 5.
前記魚類が、アメマス、ウグイ、フクドジョウ、ゼブラフィッシュ、プラティ、メダカ、ニシキゴイ、マゴイ、ティラピア、シマアジ、カンパチ、マダイ、トラフグ、ブリ、ヒラメ、メバル、クロソイ、ニジマス、ギンザケ、アユ、ウナギである、
請求項1〜6のいずれか1項に記載の固形状魚類用麻酔剤。
The fish are American trout, cormorant, fukudojo, zebrafish, prati, medaka, nishikigoi, magoi, tilapia, striped mackerel, amberjack, red sea bream, trough, yellowtail, flounder, rockfish, crocodile, rainbow trout, coho salmon, sweetfish, eel,
The anesthetic for solid fish according to any one of claims 1 to 6.
水溶性色素の色調変化によって使用期限を判別することのできる炭酸水素ナトリウム由来の炭酸ガスを利用した固形状の魚類用麻酔剤の製造方法であって、
炭酸水素ナトリウムと有機酸とを含有する混合物を調製する工程と、
前記混合物に該魚類用麻酔剤の表面の一部分に存在するように食品添加物である水溶性色素を添加する工程と、
前記水溶性色素が添加された炭酸水素ナトリウムを固形状に成型する工程と、
を有する固形状魚類用麻酔剤の製造方法。
A method for producing a solid fish anesthetic agent using carbon dioxide gas derived from sodium hydrogen carbonate that can determine the expiration date by changing the color tone of a water-soluble pigment,
Preparing a mixture containing sodium bicarbonate and an organic acid;
Adding a water-soluble dye, which is a food additive, to be present on a part of the surface of the fish anesthetic agent in the mixture;
Molding the sodium bicarbonate to which the water-soluble dye is added into a solid state;
The manufacturing method of the anesthetic for solid fish which has this.
前記成型工程が、プレス機によって1cmあたり1592ポンド以上の圧力で加圧される、
請求項8に記載の固形状魚類用麻酔剤の製造方法。
The molding process is pressurized by a press at a pressure of 1592 pounds per cm 2 or more,
The manufacturing method of the anesthetic for solid fishes of Claim 8.
請求項1〜7のいずれか1項に記載の固形状魚類用麻酔剤の使用期限を判別する方法であって、
該固形状魚類用麻酔剤の表面の一部分に存在する水溶性色素が水分を吸湿することによって該水溶性色素が滲み、該水溶性色素の色調が低下又は消失することに基づいて使用期限を判別することを特徴とする、
固形状魚類用麻酔剤の使用期限を判別する方法。
A method for determining the expiration date of the solid fish anesthetic according to any one of claims 1 to 7,
The water-soluble dye present on a part of the surface of the solid fish anesthetic agent absorbs moisture, so that the water-soluble dye oozes out and the expiration date is determined based on the decrease or disappearance of the color of the water-soluble dye. It is characterized by
A method for determining the expiration date of a solid fish anesthetic.
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