JP2720075B2 - Ruminant feed additives - Google Patents

Ruminant feed additives

Info

Publication number
JP2720075B2
JP2720075B2 JP1182291A JP18229189A JP2720075B2 JP 2720075 B2 JP2720075 B2 JP 2720075B2 JP 1182291 A JP1182291 A JP 1182291A JP 18229189 A JP18229189 A JP 18229189A JP 2720075 B2 JP2720075 B2 JP 2720075B2
Authority
JP
Japan
Prior art keywords
fatty acid
physiologically active
active substance
alkaline earth
earth metal
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 - Fee Related
Application number
JP1182291A
Other languages
Japanese (ja)
Other versions
JPH0347043A (en
Inventor
正毅 川島
秀志 田中
光紀 古田
治彦 下田
守男 二宮
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Miyoshi Oil and Fat Co Ltd
Original Assignee
Miyoshi Oil and Fat Co Ltd
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Filing date
Publication date
Application filed by Miyoshi Oil and Fat Co Ltd filed Critical Miyoshi Oil and Fat Co Ltd
Priority to JP1182291A priority Critical patent/JP2720075B2/en
Publication of JPH0347043A publication Critical patent/JPH0347043A/en
Application granted granted Critical
Publication of JP2720075B2 publication Critical patent/JP2720075B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は生理活性物質を含有する反すう動物用飼料添
加物に関する。さらに詳しくは、生理活性物質を反すう
動物に給与した場合、第1胃で分解されることなく第4
胃以降の消化器官で消化吸収される反すう動物用飼料添
加物に関する。
The present invention relates to a ruminant feed additive containing a physiologically active substance. More specifically, when a bioactive substance is supplied to a ruminant animal, the fourth substance is not decomposed in the rumen.
The present invention relates to a ruminant feed additive that is digested and absorbed in the digestive tract after the stomach.

〔従来の技術〕[Conventional technology]

反すう動物の健康を維持し、生長を促すために、生理
活性物質が用いられている。しかしながら、生理活性物
質を飼料に添加し反すう動物に経口投与すると、第1胃
内に有する微生物により、第1胃内において生理活性物
質が分解され、第4胃以降での有効な吸収が行われな
い。
BACKGROUND ART Bioactive substances are used to maintain the health of ruminants and promote their growth. However, when a bioactive substance is added to feed and administered orally to ruminants, the bioactive substance is degraded in the rumen by microorganisms in the rumen, and effective absorption is performed in the rumen and beyond. Absent.

反すう動物への生理活性物質の作用を高めるために
は、投与された生理活性物質が第1胃内を分解されるこ
となく通過し、第4胃以降の消化器官で吸収されること
が必要とされ、種々の方法が提案されている。
In order to enhance the action of the bioactive substance on ruminants, it is necessary that the administered bioactive substance passes through the rumen without being decomposed and is absorbed by the digestive organs after the abomasum. Various methods have been proposed.

例えば、第1胃内で不溶性の脂質、無機金属化合物、
高融点脂肪酸、あるいはその金属塩、高融点油脂、高融
点ロウ、セルロース誘導体、ポリビニル誘導体、アミン
を導入した高分子物質、キトサン等を保護剤として用
い、これら保護剤を生理活性物質と混合し造粒して飼料
添加剤とする方法(特開昭52−117780号、同60−168350
号)、あるいは保護剤と生理活性物質を混合し、造粒し
た後、表面を熱処理して被膜を形成し飼料添加物とする
方法(特開昭60−258111号、同60−258112号)、生理活
性物質を造粒後、常法に従ってその周囲に保護剤の被膜
を一重あるいは二重に形成し飼料添加物とする方法(特
開昭52−117780号、同58−175449号、同60−141242号、
同60−141243号、同61−37054号、同61−88844号、同64
−10947号、同64−13953号)等が知られている。
For example, lipids, inorganic metal compounds insoluble in the rumen,
A high melting point fatty acid or a metal salt thereof, a high melting point fat, a high melting point wax, a cellulose derivative, a polyvinyl derivative, a high molecular substance into which an amine is introduced, chitosan, etc. are used as a protective agent, and these protective agents are mixed with a physiologically active substance. A method of granulating into a feed additive (JP-A-52-117780, JP-A-60-168350)
Or a method in which a protective agent and a physiologically active substance are mixed and granulated, and the surface is heat-treated to form a film and used as a feed additive (JP-A-60-258111, JP-A-60-258112). After granulating a physiologically active substance, a method of forming a single or double coat of a protective agent therearound according to a conventional method to prepare a feed additive (JP-A-52-117780, JP-A-58-175449, JP-A-58-175449) No. 141242,
No. 60-141243, No. 61-37054, No. 61-88844, No. 64
Nos. -10947 and 64-13953) are known.

〔従来技術の問題点〕[Problems of the prior art]

しかしながら、従来知られているこれらの飼料添加物
は、第1胃における通過性、第4胃での消化吸収性に十
分な効果を発揮し難く、また製造費用も高いものであっ
た。
However, these conventionally known feed additives are difficult to exert a sufficient effect on the permeation in the rumen and the digestive absorption in the abomasum, and the production cost is high.

例えば生理活性物質と保護剤を混合し造粒する方法
は、一般に知られている転動造粒法、押し出し造粒法、
噴霧造粒法、粒動造粒法、圧縮造粒法等の造粒法により
粒子を製造するものであるが、特殊な造粒設備を必要と
し、製造コストが高くなること、保護剤の種類によって
さらに粘結剤等の第3成分を必要とし、生理活性物質の
濃度が希釈されること、そしてこれらの造粒法による粒
子は物理的強度が弱く、第1胃で崩壊し易い等の欠点が
ある。
For example, a method of mixing and granulating a physiologically active substance and a protective agent is generally known as a rolling granulation method, an extrusion granulation method,
Particles are produced by a granulation method such as spray granulation, dynamic granulation, or compression granulation.However, special granulation equipment is required, the production cost increases, and the type of protective agent is required. Disadvantages include the need for a third component, such as a binder, to dilute the concentration of the physiologically active substance, and the fact that the particles produced by these granulation methods have low physical strength and are easily disintegrated in the rumen. There is.

また被膜を形成する方法には、造粒工程と被膜形成工
程とより成り、これらに要する設備費用が高く、生成し
た粒子は第1胃の通過性が良くなっても第4胃以降での
消化吸収性が低下する等の欠点がある。
Further, the method of forming a film comprises a granulation step and a film formation step, which requires high equipment costs, and the generated particles are digested in the abomasum and beyond even if the ruminal permeability is improved. There are drawbacks such as reduced absorbency.

本発明は上記の点に着目しなされたもので、反すう動
物に経口投与した時、第1胃において生理活性物質が分
解されることがなく、第4胃以降の消化器官において良
好に消化吸収される反すう動物用飼料添加物を提供する
ことを目的とする。
The present invention has been made in view of the above points, and when orally administered to a ruminant animal, the physiologically active substance is not decomposed in the rumen and is well digested and absorbed in the digestive organs after the rumen. It is an object of the present invention to provide a ruminant feed additive for ruminants.

〔問題点を解決するための手段〕[Means for solving the problem]

本発明者らは上記課題を解決するため、鋭意研究を行
なった結果、生理活性物質を高級脂肪酸に溶解し、これ
を水中において金属塩化および粒状化することにより、
生理活性物質を高濃度に含む顆粒状の粒子が簡単な操作
と装置で得られ、得られた粒子は第1胃での通過性と第
4胃以降の消化器官での消化性にすぐれ、反すう動物用
飼料添加物に適することを見出し本発明に至った。
The present inventors have conducted intensive studies in order to solve the above-mentioned problems, and as a result of dissolving a physiologically active substance in a higher fatty acid, by metal salting and granulation in water,
Granular particles containing a high concentration of a physiologically active substance can be obtained with a simple operation and device, and the obtained particles have excellent permeability in the rumen and digestibility in the digestive organs after the abomasum and are ruminant. The present invention was found to be suitable as an animal feed additive and led to the present invention.

即ち、本発明は炭素数6〜22のアルキル基またはアル
ケニル基を有する高級脂肪酸に生理活性物質を溶解した
脂肪酸溶液を、アルカリ土類金属の酸化物、水酸化物ま
たは炭酸塩の少なくとも1種を溶解もしくは分散した水
溶液中に滴下し、粒状化するとともに脂肪酸を中和して
得られる、生理活性物質を含有する粒状の脂肪酸アルカ
リ土類金属塩を用いる反すう動物用飼料添加物である。
That is, the present invention provides a fatty acid solution obtained by dissolving a physiologically active substance in a higher fatty acid having an alkyl group or an alkenyl group having 6 to 22 carbon atoms, using at least one kind of alkaline earth metal oxide, hydroxide or carbonate. It is a ruminant animal feed additive using a granular fatty acid alkaline earth metal salt containing a physiologically active substance, which is obtained by dropping into a dissolved or dispersed aqueous solution, granulating and neutralizing the fatty acid.

本発明に用いる高級脂肪酸としては炭素数6〜22のア
ルキル基またはアルケニル基を有する脂肪酸が適する。
脂肪酸のアルキル基またはアルケニル基の炭素数が6未
満だと顆粒状の粒子を製造し難く、また22を超えると第
4胃以降の消化器官での消化吸収性が低下し好ましくな
い。
As the higher fatty acid used in the present invention, a fatty acid having an alkyl group or an alkenyl group having 6 to 22 carbon atoms is suitable.
If the alkyl group or alkenyl group of the fatty acid has less than 6 carbon atoms, it is difficult to produce granular particles, and if it has more than 22, the digestive and absorptive properties in the digestive organs after the abomasum decrease, which is not preferable.

上記高級脂肪酸の代表的なものとしてはカプロン酸、
カプリル酸、カプリン酸、ラウリン酸、ミリスチン酸、
パルミチン酸、ステアリン酸、アラキン酸、オレイン
酸、エライジン酸、リノール酸、リノレン酸、リシノー
ル酸、アラキドン酸、エイコサペンタエン酸、エルカ酸
等が挙げられ、これらの高級脂肪酸は単独でも、また2
種以上を混合したものであっても良い。2種以上混合し
た高級脂肪酸としては、動植物油脂、あるいはこれらの
動植物油脂を水素添加した水添硬化油脂等の油脂類を常
法に従って高圧分解あるいは酵素分解して得られる脂肪
酸が挙げられる。
Representative of the higher fatty acids are caproic acid,
Caprylic acid, capric acid, lauric acid, myristic acid,
Palmitic acid, stearic acid, arachinic acid, oleic acid, elaidic acid, linoleic acid, linolenic acid, ricinoleic acid, arachidonic acid, eicosapentaenoic acid, erucic acid, etc., and these higher fatty acids can be used alone or 2
A mixture of more than one species may be used. Examples of the higher fatty acid in which two or more kinds are mixed include fatty acids obtained by subjecting fats and oils such as animal and vegetable fats and oils such as hydrogenated hardened fats and hydrogenated animal and vegetable fats and oils to high pressure or enzymatic degradation according to a conventional method.

本発明に用いる生理活性物質としては、ビタミン類、
アミノ酸、リン脂質、脂質不ケン化物、生理活性を有す
る油脂、ミネラル等が挙げられる。例えばビタミン類と
しては、ビタミンA1、ビタミンA2、ビタミンA3、ビタミ
ンD2、ビタミンD3、ビタミンE、ビタミンK1、ビタミン
K2、ビタミンB1、ビタミンB2、ビタミンB6、ビタミンC
等及びこれらのパルミチン酸塩、酢酸塩等の誘導体が挙
げられる。
The physiologically active substance used in the present invention includes vitamins,
Examples include amino acids, phospholipids, unsaponifiable lipids, fats and oils having biological activity, and minerals. For example, as the vitamins, vitamin A 1, vitamin A 2, vitamin A 3, vitamin D 2, vitamin D 3, vitamin E, vitamin K 1, vitamin
K 2, vitamin B 1, vitamin B 2, vitamin B 6, vitamin C
And their derivatives such as palmitate and acetate.

アミノ酸としては、グリシン、アラニン、バリン、ロ
イシン、イソロイシン、セリン、トレオニン、システイ
ン、メチオニン、アスパラギン、グルタミン、リジン、
アルギニン、フェニルアラニン、チロシン、ヒスチジ
ン、トリプトファン、プロリン、オキシプロリン等が挙
げられる。
As amino acids, glycine, alanine, valine, leucine, isoleucine, serine, threonine, cysteine, methionine, asparagine, glutamine, lysine,
Arginine, phenylalanine, tyrosine, histidine, tryptophan, proline, oxyproline and the like.

リン脂質としては、ホスファチジルコリン、ホスファ
チジルエタノールアミン、ホスファチジルセリン、ホス
ファチジルイノシトール、ホスファチジン酸等のグリセ
ロリン脂質、スフィンゴエミリン、セラミドシリアチン
等のスフィンゴリン脂質、モノガラクトシルジグリセリ
ド、ジガラクトシルジグリセリド等の糖脂質が挙げられ
る。
Examples of the phospholipids include phosphatidylcholine, phosphatidylethanolamine, phosphatidylserine, phosphatidylinositol, glycerophospholipids such as phosphatidic acid, sphingomyelin, sphingolipids such as ceramide syratin, monogalactosyl diglyceride, and glycolipids such as digalactosyl diglyceride. .

脂質不ケン化物としては、コレステリン、デヒドロコ
レステリン、エルゴステリン、スチグマステリン、β−
シトステリン等のステリン、スクワレン、カロチノイド
等の脂肪族又は脂環式ポリエン類、キミルアルコール、
バチルアルコール、セラキルアルコール等とグリセリン
とのグリセリンエーテル類等が挙げられる。
Lipid unsaponifiable compounds include cholesterol, dehydrocholesterin, ergosterin, stigmasterin, β-
Sterins such as sitosterin, squalene, aliphatic or alicyclic polyenes such as carotenoids, chimyl alcohol,
Glycerin ethers of glycerin with batyl alcohol, serakyl alcohol, and the like are included.

生理活性を有する油脂類としては炭素数6〜12の中鎖
脂肪酸のトリグリセリド、魚油、ナッツ類の抽出油等が
挙げられる。
Examples of the physiologically active fats and oils include triglycerides of medium chain fatty acids having 6 to 12 carbon atoms, fish oils, and extracted oils of nuts.

これらの生理活性物質は、前記高級脂肪酸に溶解した
後、水中で粒状化反応を行うため、親油性を有すること
が好ましい。
It is preferable that these physiologically active substances have a lipophilic property because they dissolve in the higher fatty acid and then perform a granulation reaction in water.

また、生理活性物質の添加量は、前記高級脂肪酸の金
属塩99.9〜50重量%に対し0.1〜50重量%、より好まし
くは1〜20重量%である。生理活性物質の添加量が0.1
重量%未満ではその薬理効果が発現せず、また50重量%
を超えると第1胃内における高級脂肪酸の金属塩の保護
効果が薄れ、同胃内で分解され易くなり、好ましくな
い。
The addition amount of the physiologically active substance is 0.1 to 50% by weight, more preferably 1 to 20% by weight, based on 99.9 to 50% by weight of the metal salt of the higher fatty acid. 0.1 of bioactive substance added
If it is less than 50% by weight, its pharmacological effect is not exhibited, and 50% by weight
If the ratio exceeds the above range, the protective effect of the metal salt of higher fatty acid in the rumen is weakened, and it is easily decomposed in the rumen, which is not preferable.

本発明に用いるアルカリ土類金属の酸化物、水酸化物
または炭酸塩としては、マグネシウム、カルシウム、バ
リウム等のアルカリ土類金属の酸化物、水酸化物または
炭酸塩が挙げられ、これらの化合物から選ばれた少なく
とも1種が用いられる。
Examples of the alkaline earth metal oxide, hydroxide, or carbonate used in the present invention include magnesium, calcium, barium and other alkaline earth metal oxides, hydroxides, and carbonates. At least one selected one is used.

本発明の生理活性物質を含有する粒状の脂肪酸塩は、
前記高級脂肪酸、生理活性物質、およびアルカリ土類金
属の酸化物、水酸化物または炭酸塩を用いて水中で粒状
化して得られ、例えば次の様にして製造することができ
る。
Granular fatty acid salt containing the physiologically active substance of the present invention,
It is obtained by granulating in water using the above-mentioned higher fatty acid, physiologically active substance, and oxide, hydroxide or carbonate of alkaline earth metal, and can be produced, for example, as follows.

まず、高級脂肪酸に所定量の生理活性物質を溶解した
脂肪酸溶液を調製する。脂肪酸溶液の調製は、融点以上
に溶解した高級脂肪酸に生理活性物質を添加し混合する
か、高級脂肪酸に生理活性物質を添加した後、高級脂肪
酸の融点以上に加熱し混合して行うことができるが、一
般的に前者の方法が好ましい。必要に応じ、フレーバ
ー、酸化防止剤を配合する場合は、ここで加える。得ら
れた脂肪酸溶液をアルカリ土類金属の酸化物、水酸化物
または炭酸塩を溶解もしくは分散した水溶液に滴下し粒
状化を行うと共に、高級脂肪酸を中和して脂肪酸アルカ
リ土類金属塩とする。
First, a fatty acid solution in which a predetermined amount of a physiologically active substance is dissolved in a higher fatty acid is prepared. The preparation of the fatty acid solution can be performed by adding a physiologically active substance to the higher fatty acid dissolved above the melting point and mixing the mixture, or by adding the physiologically active substance to the higher fatty acid and then heating and mixing above the melting point of the higher fatty acid. However, the former method is generally preferred. Add flavors and antioxidants here if necessary. The obtained fatty acid solution is dropped into an aqueous solution in which an oxide, hydroxide or carbonate of an alkaline earth metal is dissolved or dispersed to perform granulation and neutralize the higher fatty acid to obtain a fatty acid alkaline earth metal salt. .

用いるアルカリ土類金属の酸化物、水酸化物または炭
酸塩の量は添加する高級脂肪酸に対し、1.0〜1.5モル当
量が好ましい。
The amount of the oxide, hydroxide or carbonate of the alkaline earth metal used is preferably 1.0 to 1.5 molar equivalents to the higher fatty acid to be added.

又得られる脂肪酸塩粒子の粒径は、該水溶液の撹拌速
度と、高級脂肪酸の該水溶液への滴下速度とにより変え
ることができ、本発明においては0.1〜5mmの粒径を有す
る脂肪酸塩粒子が得られるよう、これらの条件を調整す
ることが好ましい。
The particle size of the obtained fatty acid salt particles can be changed by the stirring speed of the aqueous solution and the dropping speed of the higher fatty acid to the aqueous solution.In the present invention, the fatty acid salt particles having a particle size of 0.1 to 5 mm are used. It is preferable to adjust these conditions so as to obtain.

高級脂肪酸を滴下した後、次に液温40〜90℃で0.1〜
3時間反応して高級脂肪酸をアルカリ土類金属塩化し、
必要に応じて乾燥及び粗大粒子あるいは微細粒子の分離
を行って反すう動物用飼料添加物に適した粒状の脂肪酸
塩を得る。
After dropping the higher fatty acid, then at a liquid temperature of 40-90 ° C, 0.1-
Reaction for 3 hours to convert higher fatty acid to alkaline earth metal,
If necessary, drying and separation of coarse particles or fine particles are performed to obtain granular fatty acid salts suitable for ruminant animal feed additives.

ここに得られる脂肪酸塩は、顆粒状の粒子であり、そ
の内部に生理活性物質を含有し、これを反すう動物に給
与した場合、第1胃においては生理活性物質が脂肪酸ア
ルカリ土類金属塩により保護されていて分解されること
がないので、第4胃以降の消化器官において生理活性物
質が消化吸収されて、その効果を発揮する。
The fatty acid salt obtained here is a granular particle, which contains a physiologically active substance inside, and when supplied to a ruminant, in the rumen, the physiologically active substance is converted into a fatty acid alkaline earth metal salt. Since it is protected and is not decomposed, the physiologically active substance is digested and absorbed in the digestive organs of the abomasum and thereafter, thereby exerting its effect.

本発明の生理活性物質を含有する脂肪酸アルカリ土類
金属塩は、単独でも、また必要に応じて通常用いられて
いる飼料等に配合して反すう動物に用いることができ
る。その使用量は反すう動物の種類、日令、飼料中への
配合比等によっても異なるが、通常、生理活性物質を含
有する脂肪酸アルカリ土類金属塩を1頭当たり200〜600
g/日が好ましい。
The alkaline earth metal salt of a fatty acid containing a physiologically active substance of the present invention can be used alone or, if necessary, in combination with a commonly used feed or the like for ruminants. The amount used varies depending on the type of ruminant, the age, the compounding ratio in the feed, etc., but usually 200 to 600 fatty acid alkaline earth metal salts containing a physiologically active substance per animal.
g / day is preferred.

以下実施例により本発明をさらに詳しく説明する。 Hereinafter, the present invention will be described in more detail with reference to examples.

〔実施例〕〔Example〕

実施例1 1のビーカーに水道水600mlと水酸化カルシウム40g
を入れ撹拌しながら70℃に加熱した。次に牛脂分解脂肪
酸(中和価204)270gを70℃に加熱し、これに大豆レシ
チン30gを加えて溶解した高級脂肪酸溶液を、上記水酸
化カルシウム水溶液に、攪拌下、徐々に適下し、適下
後、液温70℃で1時間反応した。反応終了後、濾過して
水を分離し、乾燥機を用いて濾過物を乾燥して、生理活
性物質を含有する脂肪酸カルシウム塩を得た。この脂肪
酸カルシウム塩は粒径0.5〜3mmの顆粒状の粒子であり、
6.8重量%のカルシウムと、30重量%の大豆レシチンを
含有し、酸価は0.8であった。
Example 1 600 ml of tap water and 40 g of calcium hydroxide were placed in one beaker.
And heated to 70 ° C. while stirring. Next, 270 g of tallow-decomposed fatty acid (neutralization value 204) was heated to 70 ° C., and 30 g of soybean lecithin was added thereto and dissolved. After adjustment, the reaction was carried out at a liquid temperature of 70 ° C. for 1 hour. After completion of the reaction, the mixture was filtered to separate water, and the filtrate was dried using a dryer to obtain a fatty acid calcium salt containing a physiologically active substance. This fatty acid calcium salt is a granular particle having a particle size of 0.5 to 3 mm,
It contained 6.8% by weight of calcium and 30% by weight of soy lecithin and had an acid value of 0.8.

得られた脂肪酸カルシウム塩を用いて、次に示す牛の
第1胃及び第4胃における溶解性試験を行い、その結果
を表−1に示す。
Using the obtained fatty acid calcium salt, a solubility test in the rumen and abomasum of cattle shown below was performed, and the results are shown in Table 1.

第1胃溶解性試験方法 生理活性物質を含有する粒状の脂肪酸塩1g、牛の第1
胃液に相当するpH7.0の緩衝液50mlを200mlの三角フラス
コに入れ、液温を40℃に保ちながら48時間振とうした。
振とう終了後、濾過し、濾液をヘキサンで抽出処理し、
抽出液中の生理活性物質濃度及び脂肪酸濃度をイアトロ
スキャン(イアトロンラボラトリーズ社製)で分析し
て、生理活性物質の溶出率(%)、及び脂肪酸塩の分解
率(%)を求めた。
Rumen solubility test method 1g granular fatty acid salt containing physiologically active substance
50 ml of a buffer solution having a pH of 7.0 corresponding to gastric juice was placed in a 200 ml Erlenmeyer flask, and shaken for 48 hours while maintaining the solution temperature at 40 ° C.
After shaking, the mixture was filtered, and the filtrate was extracted with hexane.
The concentration of the physiologically active substance and the concentration of the fatty acid in the extract were analyzed by Iatroscan (manufactured by Iatron Laboratories), and the elution rate (%) of the physiologically active substance and the decomposition rate (%) of the fatty acid salt were determined.

第4胃溶解性試験方法 生理活性物質を含有する粒状の脂肪酸塩1g、牛の第4
胃液に相当するpH2.0の緩衝液50mlを200mlの三角フラス
コに入れ、それを40℃に保ちながら5時間振とうした。
振とう後、前記と同様に濾過し、ヘキサンで抽出した
後、抽出液を分析し、生理活性物質の溶出率(%)と脂
肪酸塩の分解率(%)を求めた。
Abomasum Solubility Test Method 1g of granular fatty acid salt containing physiologically active substance
50 ml of a buffer solution having a pH of 2.0 corresponding to gastric juice was placed in a 200 ml Erlenmeyer flask, and shaken for 5 hours while maintaining the temperature at 40 ° C.
After shaking, filtration and extraction with hexane were performed in the same manner as described above, and the extract was analyzed to determine the elution rate (%) of the physiologically active substance and the decomposition rate (%) of the fatty acid salt.

実施例2〜4 表−1に示す高級脂肪酸A、生理活性物質Bおよびア
ルカリ土類金属酸化物、水酸化物または炭酸塩Cを分散
もしくは溶解した水溶液を用い、実施例1と同様に脂肪
酸溶液の調製、該脂肪酸溶液の粒状化反応および金属塩
化反応を行ない、生理活性物質を含有する粒状の脂肪酸
アルカリ土類金属塩を得、該脂肪酸塩の牛の第1胃及び
第4胃における溶解性試験を行った。
Examples 2 to 4 A fatty acid solution was used in the same manner as in Example 1 using an aqueous solution in which the higher fatty acid A, the physiologically active substance B, and the alkaline earth metal oxide, hydroxide or carbonate C shown in Table 1 were dispersed or dissolved. , A granulation reaction and a metal chloride reaction of the fatty acid solution to obtain a granular fatty acid alkaline earth metal salt containing a physiologically active substance, and the solubility of the fatty acid salt in the rumen and abomasum of cattle The test was performed.

各原料の配合比、得られた生理活性物質を含有する粒
状の脂肪酸アルカリ土類金属塩の組成及び溶解性試験結
果を表−1に示す。
Table 1 shows the compounding ratio of each raw material, the composition of the obtained alkaline earth metal salt of fatty acid containing the physiologically active substance, and the solubility test result.

比較例1 牛脂硬化油(mp60℃)50gに炭酸カルシウム200g、大
豆レシチン50gを加えて70℃に加熱して混合し、湿式双
軸型造粒機で造粒して、粒径0.3〜3mmの粒状物を得た。
Comparative Example 1 200 g of calcium carbonate and 50 g of soybean lecithin were added to 50 g of hardened tallow oil (mp 60 ° C.), mixed by heating to 70 ° C., and granulated by a wet twin-screw granulator to obtain a particle size of 0.3 to 3 mm. Granules were obtained.

得られた粒状物を用いて実施例1と同様に溶解性試験
を行い、その結果を表−1に示す。
A solubility test was carried out using the obtained granules in the same manner as in Example 1, and the results are shown in Table 1.

比較例2 牛脂硬化油(mp60℃)130gに、第3リン酸カルシウム
50g、メチオニン30g、ビタミンE30gを加えて、75℃に加
熱して溶解後、撹拌造粒機で造粒して、粒径0.1〜1mmの
粒状物を得た。
Comparative Example 2 Tribasic calcium phosphate was added to 130 g of hardened tallow oil (mp 60 ° C.)
50 g, methionine 30 g, and vitamin E 30 g were added, and the mixture was heated to 75 ° C. and dissolved, and then granulated with a stirring granulator to obtain granules having a particle size of 0.1 to 1 mm.

この粒状物100gに加熱溶融した牛脂硬化油(mp60℃)
20gを加えてコーティングし、粒径0.3〜3mmの粒状物を
得た。
Hardened beef tallow oil (mp60 ° C) heated and melted in 100g of this granular material
20 g was added for coating to obtain a granular material having a particle size of 0.3 to 3 mm.

得られた粒状物を用いて実施例1と同様に溶解性試験
を行い、その結果を表−1に示す。
A solubility test was carried out using the obtained granules in the same manner as in Example 1, and the results are shown in Table 1.

〔効果〕〔effect〕

以上説明したように本発明の反すう動物用飼料添加物
は、生理活性物質を高級脂肪酸に溶解し、これを水中に
おいてアルカリ土類金属塩化および粒状化して得られ
る、生理活性物質を高濃度に含有する粒状の脂肪酸アル
カリ土類金属塩を用いるもので、従来の飼料添加物と比
較して、簡単な操作および装置で製造することができる
と共に、反すう動物の第1胃での通過性と第4胃以降の
消化器官での消化性が良く、反すう動物へのエネルギー
源の供給、諸栄養素の消化吸収を促進し、反すう動物の
健康を保持し、体力を増強することができる等の効果を
発揮する。
As described above, the ruminant feed additive of the present invention is obtained by dissolving a physiologically active substance in a higher fatty acid, obtaining the alkaline earth metal salt and granulating the same in water, and containing a high concentration of the physiologically active substance. It uses a granular fatty acid alkaline earth metal salt that can be manufactured with simple operation and equipment as compared to conventional feed additives, and has a ruminant rumen permeability and a Good digestibility in the digestive tract after the stomach, providing an energy source to ruminants, promoting digestion and absorption of various nutrients, maintaining the ruminant's health, and enhancing its physical strength. I do.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 下田 治彦 東京都葛飾区堀切4丁目66番1号 ミヨ シ油脂株式会社内 (72)発明者 二宮 守男 東京都葛飾区堀切4丁目66番1号 ミヨ シ油脂株式会社内 (56)参考文献 特開 昭61−28351(JP,A) ──────────────────────────────────────────────────続 き Continued on the front page (72) Inventor Haruhiko Shimoda 4-66-1, Horikiri, Katsushika-ku, Tokyo Inside Miyoshi Oil & Fat Co., Ltd. (72) Inventor Morio Ninomiya 4-66-1, Horikiri, Katsushika-ku, Tokyo Miyo (56) References JP-A-61-28351 (JP, A)

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】炭素数6〜22のアルキル基またはアルケニ
ル基を有する高級脂肪酸に生理活性物質を溶解した脂肪
酸溶液を、アルカリ土類金属の酸化物、水酸化物または
炭酸塩の少なくとも1種を溶解もしくは分散した水溶液
に滴下し、粒状化するとともに脂肪酸を中和して得られ
る、生理活性物質を含有する粒状の脂肪酸アルカリ土類
金属塩を用いることを特徴とする反すう動物用飼料添加
物。
1. A fatty acid solution in which a physiologically active substance is dissolved in a higher fatty acid having an alkyl group or an alkenyl group having 6 to 22 carbon atoms, and at least one kind of alkaline earth metal oxide, hydroxide or carbonate. A ruminant animal feed additive comprising a granular fatty acid alkaline earth metal salt containing a physiologically active substance, which is obtained by dropping into a dissolved or dispersed aqueous solution, granulating and neutralizing a fatty acid.
JP1182291A 1989-07-14 1989-07-14 Ruminant feed additives Expired - Fee Related JP2720075B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1182291A JP2720075B2 (en) 1989-07-14 1989-07-14 Ruminant feed additives

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1182291A JP2720075B2 (en) 1989-07-14 1989-07-14 Ruminant feed additives

Publications (2)

Publication Number Publication Date
JPH0347043A JPH0347043A (en) 1991-02-28
JP2720075B2 true JP2720075B2 (en) 1998-02-25

Family

ID=16115715

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1182291A Expired - Fee Related JP2720075B2 (en) 1989-07-14 1989-07-14 Ruminant feed additives

Country Status (1)

Country Link
JP (1) JP2720075B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPWO2009139468A1 (en) * 2008-05-16 2011-09-22 出光興産株式会社 Coccidiosis control agent and feed containing the same
JP7093193B2 (en) * 2018-02-09 2022-06-29 太陽油脂株式会社 Vegetable oil saponified composition

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6128351A (en) * 1984-07-17 1986-02-08 Nippon Soda Co Ltd Preparation of feed additive for ruminant

Also Published As

Publication number Publication date
JPH0347043A (en) 1991-02-28

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