JPS6143978B2 - - Google Patents
Info
- Publication number
- JPS6143978B2 JPS6143978B2 JP57137414A JP13741482A JPS6143978B2 JP S6143978 B2 JPS6143978 B2 JP S6143978B2 JP 57137414 A JP57137414 A JP 57137414A JP 13741482 A JP13741482 A JP 13741482A JP S6143978 B2 JPS6143978 B2 JP S6143978B2
- Authority
- JP
- Japan
- Prior art keywords
- thiamine
- fatty acid
- acid ester
- coated
- salts
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
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- Feed For Specific Animals (AREA)
- Fodder In General (AREA)
Description
本発明は、養魚用チアミン又はチアミン塩類の
被覆製剤及びその製法に関する。
ハマチ、タイなどの飼育、養殖に用いられるカ
タクチイワシ、サンマ、サバ、イカナゴなどの生
餌に添加するチアミン製剤としては、1〜10倍量
の高級脂肪酸又はグリセリン脂肪酸エステルによ
つて被覆されたチアミン又はチアミン塩類を含有
する粒径100〜1000μの製剤が好評を得ている。
しかしこれらの製剤は、例えばチアミン塩酸塩
がその3倍量の牛脂硬化油で被覆された粒子でも
その粒径が100μ以下であつたり、平均粒径が200
μであつてもチアミン塩酸塩がその1倍量以下の
被覆剤で被覆された場合には、いずれも被覆効果
がほとんど認められなかつた。本発明者らはこの
製剤の改良について研究を進めた結果、前記の被
覆剤に少量の常温で固体のロウ状物質などを加え
ることにより、被覆剤の耐水性を改善することが
でき、またチアミン又はチアミン塩類との親和性
を高めるのに、脂肪酸エステル型又は燐脂質型の
界面活性剤がきわめて有効であることを発見し
た。
本発明は、チアミン又はチアミン塩類を高級脂
肪酸又はグリセリン脂肪酸エステルを主剤とし、
さらに脂肪酸エステル型又は燐脂質型の界面活性
剤を含有するコーテイング剤で被覆した養魚用チ
アミン被覆製剤である。
チアミン塩類としては、チアミンの塩酸塩、硝
酸塩、ラウリル硫酸塩、チオシアン酸塩、セチル
硫酸塩、1,5−ナフタリンジスルホン酸塩、
2,6−ナフタリンジスルホン酸塩、フタリン塩
などがあげられる。
高級脂肪酸としては、ラウリル酸、パルミチン
酸、ステアリン酸、ベヘニン酸など、グリセリン
脂肪酸エステルとしては、グリセリンのモノ、ジ
又はトリ脂肪酸エステルが用いられる。そして所
望によりその一部例えば1〜20%程度を、常温で
固体のロウ状物質例えばミツロウ、カルナウバロ
ウ、セラツク、高級アルコールなどで置きかえる
ことができる。
脂肪酸エステル型界面活性剤としては、蔗糖脂
肪酸エステル、プロピレングリコール脂肪酸エス
テル、ソルビタン脂肪酸エステル、ポリオキシエ
チレン脂肪酸エステル、ポリオキシエチレンソル
ビタン脂肪酸エステルなどが用いられ、燐脂質型
界面活性剤としては、ホスフアチジルコリン、ホ
スフアチジルエタノールアミン、ホスフアチジル
イノシトール、ホスフアチジン酸など、あるいは
通常レシチンという名称で市販されているこれら
の混合物などがあげられる。
被覆する方法としては、通常用いられる方法の
すべてが適用できる。例えば噴霧法、転動法、流
動層法、溶媒法、マイクロカプセルなどの造粒
法、被覆法があげられるが、大量生産が容易な噴
霧法が特に好ましい。チアミン又はチアミン塩類
の粉末は、粒径5〜100μ程度のものが好まし
く、製剤中の含量は10〜80%、出来上り製剤の粒
径は50〜1000μ程度が好ましい。
本発明の製剤を例えば噴霧法により製造するに
際しては、まずコーテイング剤の主剤としての高
級脂肪酸又はグリセリン脂肪酸エステルを加熱し
て溶融し、これに前記の界面活性剤を加えて混合
する。主剤と界面活性剤の混合比は1:0.01〜
0.2程度が好ましい。次いでチアミン又はその塩
類を添加し、均一に混合する。界面活性剤の添加
時間は、チアミン又はその塩類を添加したのちで
もよく、その改善効果は同等である。次いでこの
混合物を噴霧装置により30℃以下の室内に噴霧す
ると、粉末製剤が得られる。
実験例
粒径約30μ前後のチアミン硝酸塩を、必要量の
溶融した牛脂硬化油中に懸濁させ、全量の5%の
レシチンを加えたのちホモジナイザーで混合し、
混合物を回転円盤型噴霧装置により、30℃以下に
調整された室内に噴霧して製剤を得る。製剤中の
チアミン硝酸塩の含有量及び製剤の粒径が種々異
なるものを造り、それぞれカタクチイワシのミン
チにチアミンとして10mg/100gの割合に混合
し、30℃で1時間放置したのちチアミンの残存量
を測定すると、第1表のとおりである。この結果
から製剤の粒径の小さいものあるいはチアミン硝
酸塩が高含量でも良好な被覆効果を示すことが知
られる。
The present invention relates to a coated preparation of thiamine or thiamine salts for fish farming and a method for producing the same. Thiamin preparations added to live feed for anchovies, saury, mackerel, sand eel, etc. used for rearing and aquaculture of yellowtail, sea bream, etc., include thiamin or thiamin coated with 1 to 10 times the amount of higher fatty acids or glycerin fatty acid esters. Preparations containing thiamine salts with a particle size of 100 to 1000 microns have been well received. However, in these preparations, for example, even particles of thiamine hydrochloride coated with three times the amount of hydrogenated tallow oil have a particle size of 100μ or less, or have an average particle size of 200μ or less.
Even when μ, when thiamine hydrochloride was coated with a coating agent in an amount less than 1 times that amount, almost no coating effect was observed in any case. As a result of our research into improving this preparation, we found that by adding a small amount of a waxy substance that is solid at room temperature to the above-mentioned coating agent, we were able to improve the water resistance of the coating agent. It has also been discovered that fatty acid ester type or phospholipid type surfactants are extremely effective in increasing the affinity with thiamine salts. The present invention uses thiamine or thiamine salts as a main ingredient of higher fatty acids or glycerin fatty acid esters,
Furthermore, the present invention is a thiamin-coated preparation for fish farming coated with a coating agent containing a fatty acid ester type or phospholipid type surfactant. Thiamine salts include thiamine hydrochloride, nitrate, lauryl sulfate, thiocyanate, cetyl sulfate, 1,5-naphthalene disulfonate,
Examples include 2,6-naphthalene disulfonate and phthaline salt. Examples of higher fatty acids include lauric acid, palmitic acid, stearic acid, and behenic acid, and examples of glycerin fatty acid esters include mono-, di-, and tri-fatty acid esters of glycerin. If desired, a part of it, for example, about 1 to 20%, can be replaced with a waxy substance that is solid at room temperature, such as beeswax, carnauba wax, shellac, or higher alcohol. As the fatty acid ester type surfactant, sucrose fatty acid ester, propylene glycol fatty acid ester, sorbitan fatty acid ester, polyoxyethylene fatty acid ester, polyoxyethylene sorbitan fatty acid ester, etc. are used, and as the phospholipid type surfactant, phosphatide fatty acid ester is used. Examples include zircholine, phosphatidylethanolamine, phosphatidylinositol, phosphatidic acid, and mixtures of these commercially available under the name lecithin. As the coating method, all commonly used methods can be applied. Examples include a spraying method, a rolling method, a fluidized bed method, a solvent method, a granulation method such as a microcapsule method, and a coating method, but the spraying method is particularly preferred because it facilitates mass production. The powder of thiamine or thiamine salts preferably has a particle size of about 5 to 100 μm, the content in the preparation is preferably 10 to 80%, and the particle size of the finished preparation is preferably about 50 to 1000 μm. When producing the formulation of the present invention by, for example, a spraying method, first, the higher fatty acid or glycerin fatty acid ester as the main ingredient of the coating agent is heated and melted, and the above-mentioned surfactant is added and mixed. The mixing ratio of main agent and surfactant is 1:0.01~
Approximately 0.2 is preferable. Thiamine or its salts are then added and mixed uniformly. The surfactant may be added after the addition of thiamine or its salts, and the improvement effect is the same. This mixture is then sprayed into a room at 30° C. or below using a spray device to obtain a powder formulation. Experimental example Thiamine nitrate with a particle size of approximately 30μ is suspended in the required amount of melted hardened beef tallow oil, 5% of the total amount of lecithin is added, and then mixed with a homogenizer.
A preparation is obtained by spraying the mixture into a room controlled at 30°C or lower using a rotating disc type sprayer. Different formulations with different thiamin nitrate content and particle size were prepared, each was mixed with minced anchovies at a ratio of 10mg/100g of thiamine, and after being left at 30°C for 1 hour, the remaining amount of thiamine was measured. Then, Table 1 shows the result. From this result, it is known that even if the particle size of the preparation is small or the content of thiamine nitrate is high, it exhibits a good coating effect.
【表】
実施例 1
牛脂硬化油134Kgを75℃で加熱溶融し、これに
ミツロウ10Kg、カルナウバロウ10Kg及びレシチン
6Kgを加え、しばらく撹拌して溶解したのち、粒
径がほぼ50μ程度のチアミン硝酸塩40Kgをホモミ
キサーで撹拌しながら添加し、均一な懸濁液にす
る。この懸濁液を75℃に保持しながら、回転デイ
スク式噴霧機を用いて30℃の室内に噴霧すると、
粒径200〜300μの被覆チアミン製剤が得られる。
この製剤中のチアミン硝酸塩含有量は約20%で
ある。
実施例 2
牛脂硬化油70Kgを80℃で加熱溶融し、これにミ
ツロウ6Kg、カルナウバロウ7Kg、セラツク3Kg
及びレシチン4Kgを加え、撹拌して溶解したの
ち、平均粒径が約80μのチアミン硝酸塩110Kgを
ホモミキサーで撹拌しながら添加し、均一な懸濁
液にする。この懸濁液を80℃に保持しながら、回
転デイスク式噴霧機を用いて30℃の室内に噴霧す
ると、粒径200〜500μの被覆チアミン製剤が得ら
れる。この製剤中のチアミン硝酸塩含有量は約55
%である。
実施例 3
ステアリン酸960g及びステアリルアルコール
200gを75℃で加熱溶融し、これにソルビタンパ
ルミテート40gを加え、撹拌して溶解したのち、
平均粒径が約40μのチアミン硝酸塩800gを加
え、ホモミキサーで撹拌して均一な懸濁液にす
る。この懸濁液を回転デイスク式噴霧機を用いて
30℃の室内に噴霧すると、粒径150〜300μの被覆
チアミン製剤が得られる。この製剤中のチアミン
硝酸塩含有量は約40%である。
実施例 4
ニーダー中に牛脂極度硬化油1.16Kgを仕込み、
80℃で加熱溶融し、市販の蔗糖ステアリン酸エス
テル0.04Kgを加え、しばらく撹拌して同温度に保
持する。次いで60℃に加熱した平均粒径100μの
チアミン硝酸塩2.80Kgを加えて60rpmで撹拌し、
よく分散させる。この操作を20分間続けてチアミ
ン硝酸塩表面を硬化油で充分に濡らし、この分散
液を同一撹拌速度で3℃/分の冷却速度で冷却す
ると、平均粒径300μ、チアミン硝酸塩含有量約
70%の製剤が得られる。
応用例
漁獲直後の稚ダイ(体重平均約12.1g)を、2
×2×1mの生けす4個に各群約50尾ずつ入れた
4区を設けた。これを2日間投餌せずに餌育した
のち、ミンチしたカタクチイワシを与えた。比較
区には牛脂硬化油被覆のチアミン硝酸塩20%含有
製剤、そして本発明区1〜4にはそれぞれ実施例
1〜4の製剤を、いずれも乳糖でチアミン硝酸塩
として1%の配合製剤となるように希釈したの
ち、カタクチイワシのミンチ100g中にチアミン
硝酸塩含有量がいずれも約5mgになるように混合
して投与した。対照区には、チアミン硝酸塩約5
mgを乳糖で希釈して0.9gとしたものを、ミンチ
100gに混合して投与した。
前記の各中に対する投餌量は0〜5日は100
g、6〜15日は150g、16〜21日は200gとした。
投餌開始後0日、10日及び20日における体重の増
加率、ならびに漁獲直後及び20日後におけるチア
ミン含有量(筋肉中)を測定した結果を第2表に
示す。この結果から本発明の製剤は公知の被覆製
剤に比べて、被覆剤の量を著しく減じた場合でも
同等の効果を示し、タイの養殖において、カタク
チイワシの連続投餌による発育の遅れを大幅に防
止改善することが知られた。[Table] Example 1 134Kg of hardened beef tallow oil was heated and melted at 75℃, 10Kg of beeswax, 10Kg of carnauba wax and 6Kg of lecithin were added thereto, and after stirring and dissolving for a while, 40Kg of thiamine nitrate with a particle size of about 50μ was added. Add while stirring with a homomixer to make a homogeneous suspension. When this suspension is maintained at 75°C and sprayed into a room at 30°C using a rotating disc sprayer,
A coated thiamine preparation with a particle size of 200-300μ is obtained. Thiamine nitrate content in this formulation is approximately 20%. Example 2 Heat and melt 70 kg of hardened beef tallow oil at 80°C, add 6 kg of beeswax, 7 kg of carnauba wax, and 3 kg of shellac.
After adding 4 kg of lecithin and stirring to dissolve, 110 kg of thiamine nitrate having an average particle size of about 80 μm is added while stirring with a homomixer to form a uniform suspension. When this suspension is maintained at 80°C and sprayed into a room at 30°C using a rotary disk sprayer, a coated thiamine preparation with a particle size of 200 to 500μ is obtained. Thiamine nitrate content in this formulation is approximately 55
%. Example 3 960g stearic acid and stearyl alcohol
Heat and melt 200g at 75℃, add 40g of sorbitan palmitate, stir and dissolve, then
Add 800g of thiamine nitrate with an average particle size of about 40μ and stir with a homomixer to make a homogeneous suspension. This suspension is sprayed using a rotating disc sprayer.
When sprayed into a room at 30°C, a coated thiamine preparation with a particle size of 150-300μ is obtained. Thiamine nitrate content in this formulation is approximately 40%. Example 4 1.16 kg of extremely hardened beef tallow was placed in a kneader.
Heat and melt at 80°C, add 0.04 kg of commercially available sucrose stearate, stir for a while and maintain at the same temperature. Next, 2.80 kg of thiamine nitrate with an average particle size of 100 μ heated to 60°C was added and stirred at 60 rpm.
Distribute well. This operation was continued for 20 minutes to fully wet the surface of thiamine nitrate with hydrogenated oil, and this dispersion was cooled at a cooling rate of 3°C/min with the same stirring speed.The average particle size was 300μ, and the thiamine nitrate content was approximately
70% preparation is obtained. Application example: Young sea bream (average weight approximately 12.1 g) immediately after being caught are
Four plots were set up with approximately 50 fish in each group in four 2 x 1 m cages. After the animals were raised on food for two days without being fed, minced anchovies were fed. The comparison group contained a preparation containing 20% thiamine nitrate coated with hardened beef tallow oil, and the invention groups 1 to 4 contained the preparations of Examples 1 to 4, respectively, so that the formulation contained 1% thiamine nitrate in lactose. After diluting the mixture to 100 g of minced anchovy, the mixture was administered so that the thiamin nitrate content was approximately 5 mg. The control group contained thiamine nitrate approx.
diluted with lactose to make 0.9g, minced
It was mixed and administered to 100g. The feeding amount for each of the above is 100 for days 0 to 5.
g, 150g from 6th to 15th, and 200g from 16th to 21st.
Table 2 shows the results of measuring the rate of increase in body weight on days 0, 10, and 20 after the start of bait casting, as well as the thiamin content (in muscle) immediately after and 20 days after fishing. These results show that the formulation of the present invention has the same effect as known coating formulations even when the amount of coating agent is significantly reduced, and significantly prevents growth delays caused by continuous feeding of anchovies in Thai aquaculture. known to improve.
Claims (1)
はグリセリン脂肪酸エステルを主剤とし、さらに
脂肪酸エステル型又は燐脂質型の界面活性剤を含
有するコーテイング剤で被覆した養魚用チアミン
被覆製剤。 2 チアミン又はチアミン塩類を、高級脂肪酸又
はグリセリン脂肪酸エステルと常温で固体のロウ
状物質を主剤とし、さらに脂肪酸エステル型又は
燐脂質型の界面活性剤を含有するコーテイング剤
で被覆した養魚用チアミン被覆製剤。 3 チアミン又はチアミン塩類を、高級脂肪酸又
はグリセリン脂肪酸エステルを主剤とし、さらに
脂肪酸エステル型又は燐脂質型の界面活性剤を含
有するコーテイング剤で被覆することを特徴とす
る、養魚用チアミン被覆製剤の製法。[Scope of Claims] 1. A thiamin-coated preparation for fish farming, in which thiamine or thiamin salts are coated with a coating agent containing a higher fatty acid or a glycerin fatty acid ester as a main ingredient and a fatty acid ester type or phospholipid type surfactant. 2. A thiamine-coated preparation for fish farming in which thiamine or thiamin salts are coated with a coating agent containing a higher fatty acid or a glycerin fatty acid ester and a waxy substance that is solid at room temperature as the main ingredients, and a fatty acid ester-type or phospholipid-type surfactant. . 3. A method for producing a thiamine-coated preparation for fish farming, characterized by coating thiamine or thiamine salts with a coating agent containing a higher fatty acid or a glycerin fatty acid ester as a main ingredient and further containing a fatty acid ester type or phospholipid type surfactant. .
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP57137414A JPS5928441A (en) | 1982-08-09 | 1982-08-09 | Coated thiamine preparation for pisciculture and its preparation |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP57137414A JPS5928441A (en) | 1982-08-09 | 1982-08-09 | Coated thiamine preparation for pisciculture and its preparation |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5928441A JPS5928441A (en) | 1984-02-15 |
| JPS6143978B2 true JPS6143978B2 (en) | 1986-09-30 |
Family
ID=15198072
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP57137414A Granted JPS5928441A (en) | 1982-08-09 | 1982-08-09 | Coated thiamine preparation for pisciculture and its preparation |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5928441A (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5966844A (en) * | 1982-10-12 | 1984-04-16 | Riken Vitamin Co Ltd | Live bait feed composition for fish farming |
| KR900003228B1 (en) * | 1987-06-26 | 1990-05-11 | 김광철 | Microcomputer operation display device and its operation display method |
| CN120018778A (en) * | 2022-10-19 | 2025-05-16 | 花王株式会社 | Feed additive composition |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2228857B1 (en) * | 1973-05-09 | 1976-06-25 | Kloeckner Werke Ag | |
| JPS5013192A (en) * | 1973-06-06 | 1975-02-12 | ||
| JPS5337424A (en) * | 1976-09-17 | 1978-04-06 | Ricoh Co Ltd | Electrophotographic light sensitive material |
| JPS53127819A (en) * | 1977-04-12 | 1978-11-08 | Riken Vitamin Co Ltd | Stabilization of l-asocorbic acid and its salt |
| JPS5824104B2 (en) * | 1977-12-06 | 1983-05-19 | 博衛 小川 | fumaric acid preparations |
| JPS57115163A (en) * | 1981-01-05 | 1982-07-17 | Hiroe Ogawa | Method and agent for improving quality of fish-paste product |
-
1982
- 1982-08-09 JP JP57137414A patent/JPS5928441A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5928441A (en) | 1984-02-15 |
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