JP2929812B2 - Ruminant feed additive composition - Google Patents

Ruminant feed additive composition

Info

Publication number
JP2929812B2
JP2929812B2 JP3335073A JP33507391A JP2929812B2 JP 2929812 B2 JP2929812 B2 JP 2929812B2 JP 3335073 A JP3335073 A JP 3335073A JP 33507391 A JP33507391 A JP 33507391A JP 2929812 B2 JP2929812 B2 JP 2929812B2
Authority
JP
Japan
Prior art keywords
weight
substance
feed additive
lecithin
biologically active
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
JP3335073A
Other languages
Japanese (ja)
Other versions
JPH0523114A (en
Inventor
智 上田
俊 飯塚
晴雄 平馬
真 小澤
武 永井
弘之 佐藤
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.)
Ajinomoto Co Inc
Original Assignee
Ajinomoto Co Inc
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Ajinomoto Co Inc filed Critical Ajinomoto Co Inc
Priority to NO92920067A priority Critical patent/NO920067L/en
Priority to CA002059221A priority patent/CA2059221C/en
Priority to EP92100470A priority patent/EP0495441B1/en
Priority to DK92100470.1T priority patent/DK0495441T3/en
Priority to DE69204690T priority patent/DE69204690T2/en
Priority to US07/820,379 priority patent/US5227166A/en
Publication of JPH0523114A publication Critical patent/JPH0523114A/en
Priority to US08/045,099 priority patent/US5300297A/en
Application granted granted Critical
Publication of JP2929812B2 publication Critical patent/JP2929812B2/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】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】本発明は反すう動物用飼料添加組
成物に関する。さらに詳しくは、反すう動物の第1胃
(ルーメン)中では安定で、第4胃より下部の消化器官
で生物学的活性物質を放出する事を可能にする被覆組成
物で生物学的活性物質を被覆し、第4胃より下部の消化
器官で生物学的活性物質を消化させることを可能にした
反すう動物用飼料添加組成物に関する。
The present invention relates to a feed additive composition for ruminants. More specifically, the biologically active substance is coated with a coating composition that is stable in the rumen of the ruminant animal and allows the release of the biologically active substance in the digestive tract below the abomasum. The present invention relates to a ruminant feed additive composition which is coated and enables digestion of biologically active substances in the digestive tract below the abomasum.

【0002】[0002]

【従来の技術】牛や羊などの反すう動物ではアミノ酸、
ビタミン等の生物学的活性物質を直接経口投与すると、
第1胃中の微生物によって大部分が分解され、有効利用
されない。
2. Description of the Related Art In ruminants such as cows and sheep, amino acids,
Oral administration of biologically active substances such as vitamins directly
Most are degraded by microorganisms in the rumen and are not effectively used.

【0003】したがって、これら生物学的活性物質を、
第1胃中では微生物の分解から保護し、第4胃より下部
の消化器官で消化、吸収させるような反すう動物用のル
ーメンバイパス製剤は反すう動物用の飼料、栄養剤、動
物薬等の分野で重要である。
[0003] Therefore, these biologically active substances are
A ruminant bypass preparation for ruminants that protects against microbial degradation in the rumen and is digested and absorbed in the digestive tract below the abomasum is used in the fields of ruminant feed, nutrients, veterinary drugs, etc. is important.

【0004】生物学的活性物質を含有する反すう動物用
飼料添加物としては、脂肪酸、硬化動・植物油等で被覆
することが以前より提案されているが、これら油脂で被
覆された粒子は第1胃内の保護性は良いが、第4胃より
下部の消化器官で生物学的活性物質を溶出させることが
難しい。
[0004] As a ruminant feed additive containing a biologically active substance, coating with fatty acids, hardened animal and vegetable oils and the like has been proposed, but particles coated with these fats and oils are the first. While good protection in the stomach, it is difficult to elute biologically active substances in the digestive tract below the abomasum.

【0005】このため、油脂以外に溶出性を促進するた
めの物質を、保護する物質中に添加し、生物学的活性物
質を分散し粒状化する方法、保護物質により生物学的活
性物質を被覆する方法等が提案されている。
[0005] Therefore, a substance other than fats and oils for promoting dissolution is added to the substance to be protected, the biologically active substance is dispersed and granulated, and the biologically active substance is coated with the protective substance. A method of doing so has been proposed.

【0006】保護物質に生物学的活性物質を分散する方
法としては、例えば特開昭60−168351では生物
学的活性物質と、炭酸カルシウム20重量%以上、かつ
脂肪族モノカルボン酸、硬化した油脂等を10重量%以
上含有し造粒する方法を提案している。また、特開昭6
1−195653では脂肪族モノカルボン酸、硬化した
油脂等10重量%以上と塩酸より弱酸性な酸の不溶性塩
20重量%以上、50重量%以下からなる保護物質中に
生物学的活性物質を分散する方法を提案している。
As a method of dispersing a biologically active substance in a protective substance, for example, JP-A-60-168351 discloses a method of dispersing a biologically active substance, calcium carbonate at 20% by weight or more, an aliphatic monocarboxylic acid, and a hardened fat or oil. And the like are proposed in which 10% by weight or more is contained and granulation is carried out. In addition, Japanese Unexamined Patent Publication
In 1-195563, a biologically active substance is dispersed in a protective substance comprising 10% by weight or more of an aliphatic monocarboxylic acid, a hardened oil or the like, and 20% by weight or more and 50% by weight or less of an insoluble salt of an acid weakly acidic than hydrochloric acid. Suggest a way to do it.

【0007】生物学的活性物質を保護物質で被覆する方
法としては、例えば特開昭63−317053では脂肪
族モノカルボン酸、硬化した油とレシチンおよびグリセ
リン脂肪酸エステルからなる保護剤で生物学的活性物質
を被覆する方法を提案している。
As a method of coating a biologically active substance with a protective substance, for example, JP-A-63-317053 discloses a method of coating a biologically active substance with a protective agent comprising an aliphatic monocarboxylic acid, a hardened oil and lecithin and a glycerin fatty acid ester. A method of coating the material is proposed.

【0008】しかしながら、保護物質中に生物学的活性
物質を分散する方法では、粒子表面近傍に生物学的活性
物質が存在するため、保護性を重視するためには生物学
的活性物質の含有率をかなり下げる必要があり、水溶性
の生物学的活性物質では第1胃内の滞留時間が10数時
間〜数日間であることを考慮すると、十分に保護する事
が難しい。またレシチンおよびグリセリン脂肪酸エステ
ルと油脂からなる保護物質で被覆した場合、被覆層の強
度が不十分で保護性に問題が残る。また、レシチンおよ
びグリセリン脂肪酸エステルは油脂の乳化作用を期待し
たものではあるが、第4胃以降の消化器官を通過する時
間を考えると、溶出性が十分であるとはいえない。
However, in the method of dispersing a biologically active substance in a protective substance, the biologically active substance is present near the particle surface. It is difficult to sufficiently protect the water-soluble biologically active substance, considering that the residence time in the rumen is 10 to several hours to several days. Further, when coated with a protective substance consisting of lecithin and glycerin fatty acid ester and fats and oils, the strength of the coating layer is insufficient and a problem remains in the protective property. Although lecithin and glycerin fatty acid esters are expected to emulsify fats and oils, they cannot be said to have sufficient dissolution properties in view of the time required to pass through the digestive tract after the abomasum.

【0009】その他に第1胃と第4胃のpHの差を利用
するため、pH応答性の合成ポリマーで被覆する方法も
提案されているが、被覆に有機溶媒を使用すること、被
覆剤が高価になること、等を考慮すると、十分満足でき
る手段とは言えない。
In addition, in order to utilize the pH difference between the rumen and the abomasum, a method of coating with a pH-responsive synthetic polymer has also been proposed. In view of the fact that it becomes expensive, it cannot be said that this is a sufficiently satisfactory means.

【0010】[0010]

【本発明が解決しようとする課題】本発明が解決しよう
とする課題は、安全性、経済性を考慮した上で、生物学
的活性物質を反すう動物の第1胃内で安定に保護し、第
4胃以下の下部消化器官で効率よく消化吸収させる点に
ある。
The object of the present invention is to stably protect a biologically active substance in the rumen of a ruminant animal in consideration of safety and economy. The purpose is to efficiently digest and absorb the gastrointestinal tract below the abomasum.

【0011】[0011]

【課題を解決するための手段】本発明者等は上記の目的
を達成するため鋭意努力した結果、生物学的活性物質を
含有する核を、レシチンおよび中性では安定であるが、
酸性条件で可溶性の無機物質を含有する炭素原子数14
〜22個を有する直鎖または分枝状の飽和または不飽和
の脂肪族モノカルボン酸またはその塩、硬化した植物性
油脂、硬化した動物性油脂およびロウ、ワックスよりな
る群から選ばれた少なくとも1種の保護物質で被覆する
ことによって第1胃中での優れた保護性と第4胃以下の
下部消化器官中での優れた溶出性を兼ね備えることがで
きることを見いだし本発明を達成した。
The present inventors have made intensive efforts to achieve the above-mentioned object, and as a result, the nucleus containing the biologically active substance is stable in lecithin and neutral,
14 carbon atoms containing inorganic substances soluble under acidic conditions
At least one selected from the group consisting of linear or branched saturated or unsaturated aliphatic monocarboxylic acids or salts thereof having up to 22 carbon atoms, hardened vegetable oils, hardened animal oils and waxes, and waxes The present invention has been achieved by finding that by coating with various kinds of protective substances, it is possible to have both excellent protection in the rumen and excellent dissolution in the lower digestive tract below the abomasum.

【0012】即ち、本発明の要旨は、生物学的活性物質
を含有する核を、炭素原子数14〜22個を有する直鎖
または分枝状の飽和または不飽和の脂肪族モノカルボン
酸またはその塩、硬化した植物性油脂、硬化した動物性
油脂およびロウ、ワックスよりなる群から選ばれた少な
くとも1種の物質、レシチン、および中性では安定であ
るが、酸性条件で可溶性の無機物質の1種または2種以
上を含有する被覆組成物で被覆してなることを特徴とす
る反すう動物用飼料添加組成物である。
That is, the gist of the present invention is that a nucleus containing a biologically active substance comprises a linear or branched saturated or unsaturated aliphatic monocarboxylic acid having 14 to 22 carbon atoms, At least one substance selected from the group consisting of salts, hardened vegetable oils, hardened animal fats and waxes, and waxes, lecithin, and one of inorganic substances that are stable in neutral but soluble under acidic conditions. A feed additive composition for ruminants, which is coated with a coating composition containing at least one species.

【0013】本発明の反すう動物用飼料添加組成物は保
護物質中にレシチンおよび中性では安定であるが、酸性
条件で可溶性の無機物質を含有しているが、第4胃内が
酸性であることを利用した無機物質の作用による放出性
と、レシチンによる脂肪酸、硬化油脂等の乳化作用で、
第4胃より下部消化器官内で生物学的活性物質を放出さ
せる性質とを兼ね備えており、その相乗効果で溶出性を
良好にしている。また、無機塩の添加によって被覆層の
強度も大きくなっている。以下に本発明を詳細に説明す
る。
The ruminant feed additive composition of the present invention contains lecithin and a neutrally stable protective substance in a protective substance, but contains an inorganic substance soluble under acidic conditions, but is acidic in the abomasum. With the release property by the action of inorganic substances utilizing that and the emulsifying action of fatty acids, hardened fats etc. by lecithin,
It also has the property of releasing a biologically active substance in the lower digestive tract from the abomasum and has a good dissolution property due to its synergistic effect. Further, the strength of the coating layer is increased by the addition of the inorganic salt. Hereinafter, the present invention will be described in detail.

【0014】本発明において、生物学的活性物質として
は、周知の各種の栄養物やこれを含む飼料あるいは薬物
類、例えば、アミノ酸およびその誘導体、アミノ酸のヒ
ドロキシ同族化合物、タンパク質類、炭水化物類、ビタ
ミン類および獣医薬類から選ばれる1種または2種以上
の混合物が挙げられる。
In the present invention, the biologically active substance includes various known nutrients and feeds or drugs containing the same, for example, amino acids and their derivatives, hydroxy homologous compounds of amino acids, proteins, carbohydrates, vitamins. Or a mixture of two or more selected from the group and veterinary medicine.

【0015】具体的には、リジン、メチオニン、トリプ
トファン、スレオニン等のアミノ酸類;N−アシルアミ
ノ酸、N−ヒドロキシメチルメチオニンのカルシウム
塩、リジン塩酸塩等のアミノ酸誘導体;2−ヒドロキシ
−4−メチルメルカプト酪酸およびその塩等のアミノ酸
のヒドロキシ同族化合物;穀物粉末、羽毛粉末、魚粉等
の天然栄養物の粉末;カゼイン、トウモロコシタンパ
ク、馬鈴薯タンパク等のタンパク質;澱粉、ショ糖、ブ
ドウ糖等の炭水化物;ビタミンA、ビタミンA酢酸塩、
ビタミンAパルミチン酸塩、ビタミンB群、チアミン、
塩酸チアミン、リボフラビン、ニコチン酸、ニコチン酸
アミド、パントテン酸カルシウム、パントチン酸コリ
ン、塩酸ピリドキシン、塩化コリン、シアノコバラミ
ン、ビオチン、葉酸、p−アミノ安息香酸、ビタミンD
2、ビタミンD3、ビタミンE等のビタミン類およびそれ
に類する機能を有する物質;テトラサイクリン系、アミ
ノ配糖体系、マクロライド系、ポリエーテル系の抗生物
質、ネグフォン等の駆虫剤、ピペラジン等の虫下し、エ
ストロジェン、スチルベストロール、ヘキセストロー
ル、チロプロティン、ゴイトロジェン等のホルモン類が
使用される。
More specifically, amino acids such as lysine, methionine, tryptophan and threonine; amino acid derivatives such as N-acylamino acids, calcium salts of N-hydroxymethylmethionine and lysine hydrochloride; 2-hydroxy-4-methylmercapto Hydroxy homologous compounds of amino acids such as butyric acid and salts thereof; powders of natural nutrients such as cereal powder, feather powder, fish meal; proteins such as casein, corn protein, potato protein; carbohydrates such as starch, sucrose, glucose; , Vitamin A acetate,
Vitamin A palmitate, vitamin B group, thiamine,
Thiamine hydrochloride, riboflavin, nicotinic acid, nicotinamide, calcium pantothenate, choline pantoate, pyridoxine hydrochloride, choline chloride, cyanocobalamin, biotin, folic acid, p-aminobenzoic acid, vitamin D
2. Vitamins such as vitamin D3 and vitamin E and substances having functions similar thereto; tetracyclines, aminoglycosides, macrolides, polyether antibiotics, anthelmintics such as negphone, insecticides such as piperazine, estrogen Hormones such as stilbestrol, hexestrol, thyroprotein and goitrogen are used.

【0016】生物学的活性物質を含有する核の調製法に
特に制限はなく、必要に応じて増粘剤、賦形剤等を添加
し、通常の造粒法、例えば押し出し造粒法、流動造粒
法、撹拌造粒法等により粒状、好ましくは球形に近い粒
子を調製する。
The method for preparing the core containing the biologically active substance is not particularly limited, and if necessary, a thickener, an excipient, etc. may be added, and a conventional granulation method such as extrusion granulation, fluidization Granular, preferably nearly spherical, particles are prepared by a granulation method, a stirring granulation method or the like.

【0017】増粘剤としては、ヒドロキシプロピルセル
ロース、メチルセルロース、カルボキシメチルセルロー
スナトリウム等のセルロース誘導体、ポリビニルアルコ
ール、ポリビニルピロリドン等のビニル誘導体、アラビ
アゴム、グアガム、ポリアクリル酸ナトリウム等が使用
できる。
Examples of the thickener include cellulose derivatives such as hydroxypropylcellulose, methylcellulose and sodium carboxymethylcellulose, vinyl derivatives such as polyvinyl alcohol and polyvinylpyrrolidone, gum arabic, guar gum, sodium polyacrylate and the like.

【0018】賦形剤としては、澱粉、タンパク質、結晶
セルロース等を用いることができる。さらに必要であれ
ば、比重調整剤として、炭酸カルシウム、リン酸カルシ
ウム、タルク等を添加してもよい。
As the excipient, starch, protein, crystalline cellulose and the like can be used. If necessary, calcium carbonate, calcium phosphate, talc or the like may be added as a specific gravity adjuster.

【0019】前記生物学的活性物質を含有する核を被覆
する保護物質は、炭素原子数14〜22個を有する直鎖
または分枝状の飽和または不飽和の脂肪族モノカルボン
酸またはその塩、硬化した植物性油脂、硬化した動物性
油脂およびロウ、ワックスよりなる群から選ばれた少な
くとも1種の物質、レシチン、および中性では安定であ
るが、酸性条件で可溶性の無機物質の1種または2種以
上を含有する。
The protective substance for coating the nucleus containing the biologically active substance is a linear or branched saturated or unsaturated aliphatic monocarboxylic acid having 14 to 22 carbon atoms or a salt thereof, Hardened vegetable oils, hardened animal fats and waxes, at least one substance selected from the group consisting of waxes, lecithin, and one of inorganic substances that are stable in neutral but soluble under acidic conditions or Contains two or more.

【0020】脂肪族モノカルボン酸としては、ミリスチ
ン酸、パルミチン酸、ステアリン酸、オレイン酸、リノ
ール酸、ベヘニン酸等が使用でき、またそれらの塩でも
良い。硬化植物油としては、硬化パーム油、硬化大豆
油、硬化菜種油、硬化ひまし油等が、硬化動物油として
は、硬化牛脂、硬化豚脂等が、ロウ類としては、カルナ
バロウ、密ロウ等が、ワックス類としては、天然ワック
ス、合成ワックス、パラフィンワックス等が使用でき
る。
As the aliphatic monocarboxylic acid, myristic acid, palmitic acid, stearic acid, oleic acid, linoleic acid, behenic acid and the like can be used, and their salts may be used. As hardened vegetable oils, hardened palm oil, hardened soybean oil, hardened rapeseed oil, hardened castor oil, etc., as hardened animal oils, hardened tallow, hardened lard, etc., as waxes, carnauba wax, beeswax, etc., as waxes Can be natural wax, synthetic wax, paraffin wax or the like.

【0021】本発明に使用するレシチンは、必ずしも純
粋な物である必要はなく、ホスファチジルコリン、ホス
ファチジルエタノ−ルアミン、ホスファチジルイノシト
−ル等の混合物でよく、好ましくは大豆、卵黄などを原
料として製造された市販のレシチンが用いられる。
The lecithin used in the present invention does not necessarily have to be pure, but may be a mixture of phosphatidylcholine, phosphatidylethanolamine, phosphatidylinositol, etc., and is preferably produced using soybean, egg yolk or the like as a raw material. Commercially available lecithin is used.

【0022】中性では安定であるが、酸性条件で可溶性
の無機物質としては、炭酸マグネシウム、炭酸カルシウ
ム、リン酸カルシウム、ピロリン酸カルシウム等がある
が、炭酸マグネシウムや炭酸カルシウムのような炭酸塩
および、ピロリン酸のカルシウム塩がより好ましい。
Inorganic substances which are stable under neutral conditions but are soluble under acidic conditions include magnesium carbonate, calcium carbonate, calcium phosphate, calcium pyrophosphate and the like. Carbonates such as magnesium carbonate and calcium carbonate, and pyrophosphate Is more preferred.

【0023】本発明中の保護物質の組成は、全保護物質
中にレシチン0.1〜20重量%、中性で安定であり、
酸性条件で可溶性の無機物質0.1〜10重量%であ
り、好ましくはレシチン1〜10%、無機物質1〜10
%である。保護物質中のレシチン含量が20重量%を超
えると被覆層の強度が低下し第1胃中の保護性が低下す
る。レシチンが、0.1重量%に満たない場合には乳化
作用が不十分で第4胃より下部消化器官での溶出性が低
下する。中性で安定であり、酸性条件で可溶性の無機物
質が10重量%を超えると第1胃中の保護性が低下し、
0.1%に満たない場合には、第4胃内が酸性であるこ
とを利用した無機物質の作用が不十分である。
The composition of the protective substance in the present invention is 0.1 to 20% by weight of lecithin in the total protective substance, and is neutral and stable;
0.1 to 10% by weight of an inorganic substance soluble under acidic conditions, preferably 1 to 10% of lecithin and 1 to 10% of an inorganic substance.
%. If the lecithin content in the protective substance exceeds 20% by weight, the strength of the coating layer is reduced and the protective properties in the rumen are reduced. If the lecithin content is less than 0.1% by weight, the emulsifying action is insufficient and the dissolution in the lower digestive tract from the abomasum is reduced. Neutral and stable, when the amount of the inorganic substance soluble under acidic conditions exceeds 10% by weight, the protective property in the rumen decreases,
If it is less than 0.1%, the action of the inorganic substance utilizing the fact that the inside of the abomasum is acidic is insufficient.

【0024】本発明の反すう動物用飼料添加組成物は前
記生物学的活性物質を含有する核に前記保護物質を被覆
してなる事を特徴としている。
The ruminant feed additive composition of the present invention is characterized in that a core containing the biologically active substance is coated with the protective substance.

【0025】保護物質の被覆量に特に制限はなく、でき
るだけ少ない方が生物学的活性物質の含有率が大きくな
り望ましいが、第1胃内で生物学的活性物質を十分に保
護できる量が必要であり、通常は生物学的活性物質を含
有する核100重量部に対し10〜200重量部、好ま
しくは15〜150重量部を被覆する。
There is no particular limitation on the coating amount of the protective substance, and it is preferable that the coating amount of the protective substance is as small as possible because the content of the biologically active substance is large. However, an amount that can sufficiently protect the biologically active substance in the rumen is required. Usually, 10 to 200 parts by weight, preferably 15 to 150 parts by weight is coated with respect to 100 parts by weight of the core containing the biologically active substance.

【0026】被覆方法に特に制限はなく、通常の被覆方
法、例えば流動コーティング法、パンコーティング法、
溶融コーティング法等で被覆することができる。
There is no particular limitation on the coating method, and ordinary coating methods such as a fluid coating method, a pan coating method,
It can be coated by a melt coating method or the like.

【0027】以下に、本発明を実施例、及び比較例によ
り更に詳細に説明するが、本発明の範囲はこれらの実施
例に限定される物ではない。
Hereinafter, the present invention will be described in more detail with reference to Examples and Comparative Examples, but the scope of the present invention is not limited to these Examples.

【0028】[0028]

【実施例】反すう動物用飼料添加剤としての有用性は、
以下の方法で評価した。
EXAMPLES The usefulness of ruminant feed additives is as follows.
Evaluation was made by the following method.

【0029】第1胃内の保護性 調製した試料約2gを、200ml三角フラスコ中に投
入し、第1胃液に相当するMc Dougall緩衝液100ml
を注入して、39℃の温度下で48時間振盪した。振盪
終了後、生物学的活性物質の溶出量を分析し、第1胃の
保護性を算出した。
About 2 g of the prepared sample was put into a 200 ml Erlenmeyer flask, and 100 ml of Mc Dougall buffer solution corresponding to the rumen fluid was added.
And shaken at a temperature of 39 ° C. for 48 hours. After shaking, the amount of the biologically active substance eluted was analyzed to calculate the ruminal protection.

【0030】なお、生物学的活性物質として、実施例中
のアミノ酸の溶出量に関しては液体クロマトグラフィー
で分析を行った。
The amount of the amino acid eluted in the examples as a biologically active substance was analyzed by liquid chromatography.

【0031】*Mc Dougall緩衝液:水1000ml中に
以下の試薬を溶解した緩衝液。 炭酸水素ナトリウム :7.43g リン酸2ナトリウム・12水塩:7.00g 塩化ナトリウム :0.34g 塩化カリウム :0.43g 塩化マグネシウム・6水塩 :0.10g 塩化カルシウム :0.05g
* Mc Dougall buffer: a buffer obtained by dissolving the following reagents in 1000 ml of water. Sodium hydrogen carbonate: 7.43 g Disodium phosphate / 12 hydrate: 7.00 g Sodium chloride: 0.34 g Potassium chloride: 0.43 g Magnesium chloride / hexahydrate: 0.10 g Calcium chloride: 0.05 g

【0032】第4胃内の溶出性 保護性試験終了後、振盪したサンプルを回収し付着液を
洗浄後、さらに200ml三角フラスコに投入し、第4
胃液に相当するClark-Lubs緩衝液40mlを注入して、
39℃の温度下で3時間振盪した。振盪終了後、生物学
的活性物質の溶出量を分析し、第4胃の溶出性を算出し
た。
Dissolution in the abomasum After completion of the protection test, the shaken sample was recovered, and the adherent solution was washed, and then poured into a 200 ml Erlenmeyer flask.
Inject 40 ml of Clark-Lubs buffer equivalent to gastric juice,
Shake at a temperature of 39 ° C. for 3 hours. After the shaking, the elution amount of the biologically active substance was analyzed, and the elution property of the abomasum was calculated.

【0033】*Clark-Lubs緩衝液:水1000ml中に
以下の試薬を溶解した緩衝液 塩化カリウム:3.73g 塩酸 :2.1ml
* Clark-Lubs buffer: a buffer in which the following reagents are dissolved in 1000 ml of water: potassium chloride: 3.73 g hydrochloric acid: 2.1 ml

【0034】小腸内の溶出性 第4胃内の溶出性試験終了後、振盪したサンプルを回収
し、さらに200ml三角フラスコに投入し、小腸液に
相当する緩衝液100mlを注入して、39℃の温度下
で24時間振盪した。振盪終了後、生物学的活性物質の
溶出量を分析し、小腸の溶出性を算出した。
Dissolution property in small intestine After the dissolution test in the abomasum was completed, the shaken sample was collected, poured into a 200 ml Erlenmeyer flask, and 100 ml of a buffer solution corresponding to the small intestine fluid was injected. Shake at temperature for 24 hours. After completion of the shaking, the elution amount of the biologically active substance was analyzed, and the elution property of the small intestine was calculated.

【0035】[0035]

【実施例1】L−リジン塩酸塩325g、タルク17
2.5g、カルボキシメチルセルロースナトリウム2.
5g、水135gをニーダーに仕込み、混練した後、
1.5mmφの目開きのスクリーンを有する押し出し造
粒機を用いて円柱状の顆粒を得た。得られた顆粒を球形
化装置(マルメライザー、不二パウダル社製)を用いて
球形に近い顆粒とした。得られた球状顆粒を流動乾燥
し、L−リジン塩酸塩を含有する核を得た。
Example 1 325 g of L-lysine hydrochloride, talc 17
2.5 g, sodium carboxymethyl cellulose 2.
5 g and 135 g of water were charged into a kneader and kneaded.
Columnar granules were obtained using an extrusion granulator having a 1.5 mmφ aperture screen. The granules obtained were converted into granules having a near spherical shape using a sphering apparatus (Malmerizer, manufactured by Fuji Paudal). The obtained spherical granules were flow-dried to obtain a core containing L-lysine hydrochloride.

【0036】レシチン(和光純薬製大豆レシチン−食品
添加物−を使用、以下同様)5重量部、炭酸マグネシウ
ム5重量部を溶融した硬化牛脂90重量部に分散し、核
100重量部に対し、67重量部の割合で核に被覆した
(被覆率40%)。被覆は流動造粒コ−ティング装置
(ニュ−マルメライザ−、不二パウダル社製)を用い溶
融コ−ティングした。
5 parts by weight of lecithin (using soybean lecithin manufactured by Wako Pure Chemicals, a food additive, the same applies hereinafter) and 5 parts by weight of magnesium carbonate are dispersed in 90 parts by weight of molten hardened tallow, and 100 parts by weight of core The core was coated at a rate of 67 parts by weight (40% coverage). The coating was melt-coated using a fluidized-granulation coating device (New Melmizer, manufactured by Fuji Paudal).

【0037】この被覆粒子について上記評価試験を行っ
た結果、第1胃溶出率9%、第4胃溶出率39%、小腸
溶出率40%であった。
The coated particles were subjected to the above evaluation test. As a result, the ruminal dissolution rate was 9%, the abomasum dissolution rate was 39%, and the small intestine dissolution rate was 40%.

【0038】[0038]

【実施例2】中性で安定であり、酸性条件で可溶性の無
機物質として炭酸マグネシウムのかわりに炭酸カルシウ
ムを使用した以外は実施例1と同様に被覆粒子を調製し
た。
Example 2 Coated particles were prepared in the same manner as in Example 1 except that calcium carbonate was used instead of magnesium carbonate as an inorganic substance which was neutral, stable and soluble under acidic conditions.

【0039】この被覆粒子について上記評価試験を行っ
た結果、第1胃溶出率4%、第4胃溶出率46%、小腸
溶出率36%であった。
The coated particles were subjected to the above evaluation test. As a result, the ruminal dissolution rate was 4%, the abomasum dissolution rate was 46%, and the small intestine dissolution rate was 36%.

【0040】[0040]

【実施例3】保護物質の被覆を43重量部の割合で実施
した(被覆率30%)以外は実施例2と同様に被覆粒子
を調製した。
Example 3 Coated particles were prepared in the same manner as in Example 2, except that the coating of the protective substance was carried out at a rate of 43 parts by weight (coverage 30%).

【0041】この被覆粒子について上記評価試験を行っ
た結果、第1胃溶出率12%、第4胃溶出率20%、小
腸溶出率58%であった。
The coated particles were subjected to the above evaluation test. As a result, the ruminal dissolution rate was 12%, the abomasum dissolution rate was 20%, and the small intestine dissolution rate was 58%.

【0042】[0042]

【実施例4】保護物質として、硬化牛脂85重量部に対
し、レシチン10重量部、炭酸カルシウム5重量部含有
し、核100重量部に対し、保護物質の被覆を33重量
部の割合で実施した(被覆率25%)以外は実施例2と
同様に被覆粒子を調製した。
Example 4 As a protective substance, 10 parts by weight of lecithin and 5 parts by weight of calcium carbonate were contained with respect to 85 parts by weight of hardened tallow, and the protective substance was coated at a rate of 33 parts by weight with respect to 100 parts by weight of the core. Except for (coverage 25%), coated particles were prepared in the same manner as in Example 2.

【0043】この被覆粒子について上記評価試験を行っ
た結果、第1胃溶出率19%、第4胃溶出率46%、小
腸溶出率32%であった。
The coated particles were subjected to the above evaluation test. As a result, the ruminal dissolution rate was 19%, the abomasum dissolution rate was 46%, and the small intestine dissolution rate was 32%.

【0044】[0044]

【実施例5】保護物質として、硬化牛脂88重量部に対
し、レシチン2重量部、炭酸カルシウム10重量部含有
し、核100重量部に対し、保護物質の被覆を25重量
部の割合で実施した(被覆率20%)以外は実施例2と
同様に被覆粒子を調製した。
Example 5 As a protective substance, 2 parts by weight of lecithin and 10 parts by weight of calcium carbonate were contained in 88 parts by weight of hardened beef tallow, and a coating of 25 parts by weight was applied to 100 parts by weight of cores. Except for (20% coverage), coated particles were prepared in the same manner as in Example 2.

【0045】この被覆粒子について上記評価試験を行っ
た結果、第1胃溶出率14%、第4胃溶出率31%、小
腸溶出率35%であった。
The coated particles were subjected to the above evaluation test. As a result, the ruminal dissolution rate was 14%, the abomasum dissolution rate was 31%, and the small intestine dissolution rate was 35%.

【0046】[0046]

【実施例6】中性で安定であり、酸性条件で可溶性の無
機物質として炭酸カルシウムのかわりにピロリン酸カル
シウムを使用した以外は実施例1と同様に被覆粒子を調
製した。
Example 6 Coated particles were prepared in the same manner as in Example 1, except that calcium pyrophosphate was used instead of calcium carbonate as an inorganic substance which was neutral, stable and soluble under acidic conditions.

【0047】この被覆粒子について上記評価試験を行っ
た結果、第1胃溶出率7%、第4胃溶出率49%、小腸
溶出率32%であった。
The coated particles were subjected to the above evaluation test. As a result, the ruminal dissolution rate was 7%, the abomasum dissolution rate was 49%, and the small intestine dissolution rate was 32%.

【0048】[0048]

【実施例7】D,L−メチオニン375g、タルク12
0g、カルボキシメチルセルロースナトリウム5g、水
150gをニーダーに仕込み、混練した後、1.5mm
φの目開きのスクリーンを有する押し出し造粒機を用い
て円柱状の顆粒を得た。得られた顆粒を球形化装置(マ
ルメライザー、不二パウダル社製)を用いて球形に近い
顆粒とした。得られた球状顆粒を流動乾燥し、D,L−
メチオニンを含有する核を得た。
Example 7 D, L-methionine (375 g), talc 12
0 g, sodium carboxymethylcellulose 5 g, and water 150 g were charged into a kneader, kneaded, and then mixed with 1.5 mm.
Cylindrical granules were obtained using an extrusion granulator having a screen with a mesh opening of φ. The granules obtained were converted into granules having a near spherical shape using a sphering apparatus (Malmerizer, manufactured by Fuji Paudal). The obtained spherical granules are flow-dried, and D, L-
A core containing methionine was obtained.

【0049】硬化牛脂90重量部に対し、レシチン5重
量部、炭酸マグネシウム5重量部含有する保護物質を溶
融し、核100重量部に対し、43重量部の割合で核に
被覆した(被覆率30%)。
A protective substance containing 5 parts by weight of lecithin and 5 parts by weight of magnesium carbonate was melted with respect to 90 parts by weight of hardened tallow, and the core was coated at a ratio of 43 parts by weight with respect to 100 parts by weight of the core (coating ratio: 30). %).

【0050】この被覆粒子について上記評価試験を行っ
た結果、第1胃溶出率17%、第4胃溶出率20%、小
腸溶出率60%であった。
The above particles were subjected to the above evaluation test. As a result, the ruminal dissolution rate was 17%, the abomasum dissolution rate was 20%, and the small intestine dissolution rate was 60%.

【0051】[0051]

【実施例8】中性で安定であり、酸性条件で可溶性の無
機物質として炭酸マグネシウムのかわりに炭酸カルシウ
ムを使用した以外は実施例7と同様に被覆粒子を調製し
た。
Example 8 Coated particles were prepared in the same manner as in Example 7, except that calcium carbonate was used instead of magnesium carbonate as an inorganic substance which was neutral, stable and soluble under acidic conditions.

【0052】この被覆粒子について上記評価試験を行っ
た結果、第1胃溶出率15%、第4胃溶出率26%、小
腸溶出率59%であった。
The above particles were subjected to the above evaluation test. As a result, the ruminal dissolution rate was 15%, the abomasum dissolution rate was 26%, and the small intestine dissolution rate was 59%.

【0053】[0053]

【実施例9】保護物質として、硬化牛脂88重量部に対
し、レシチン10重量部、炭酸カルシウム2重量部含有
し、核100重量部に対し、保護物質の被覆を33重量
部の割合で実施した(被覆率25%)以外は実施例8と
同様に被覆粒子を調製した。
Example 9 As a protective substance, 10 parts by weight of lecithin and 2 parts by weight of calcium carbonate were contained with respect to 88 parts by weight of hardened tallow, and the protective substance was coated at a rate of 33 parts by weight with respect to 100 parts by weight of the core. Coated particles were prepared in the same manner as in Example 8, except that the coating ratio was 25%.

【0054】この被覆粒子について上記評価試験を行っ
た結果、第1胃溶出率21%、第4胃溶出率38%、小
腸溶出率37%であった。
The coated particles were subjected to the above evaluation test. As a result, the ruminal dissolution rate was 21%, the abomasum dissolution rate was 38%, and the small intestine dissolution rate was 37%.

【0055】[0055]

【比較例1】硬化牛脂90重量部に対し、炭酸カルシウ
ム10重量部含有する保護物質を使用した以外は実施例
1と同様に被覆粒子を調製した。この被覆粒子について
上記評価試験を行った結果、第1胃溶出率5%、第4胃
溶出率15%、小腸溶出率16%であった。
Comparative Example 1 Coated particles were prepared in the same manner as in Example 1 except that a protective substance containing 10 parts by weight of calcium carbonate was used for 90 parts by weight of hardened tallow. As a result of performing the above-described evaluation test on the coated particles, the ruminal dissolution rate was 5%, the abomasum dissolution rate was 15%, and the small intestine dissolution rate was 16%.

【0056】[0056]

【比較例2】硬化牛脂70重量部に対し、レシチン30
重量部含有する保護物質を使用した以外は実施例3と同
様に被覆粒子を調製した。この被覆粒子について上記評
価試験を行った結果、第1胃溶出率71%、第4胃溶出
率27%、小腸溶出率1%であった。
Comparative Example 2 Lecithin 30 was added to 70 parts by weight of hardened tallow.
Coated particles were prepared in the same manner as in Example 3, except that the protective substance contained in parts by weight was used. As a result of performing the above-described evaluation test on the coated particles, the ruminal dissolution rate was 71%, the abomasum dissolution rate was 27%, and the small intestine dissolution rate was 1%.

【0057】[0057]

【比較例3】硬化牛脂70重量部に対し、炭酸カルシウ
ム30重量部含有する保護物質を使用した以外は実施例
8と同様に被覆粒子を調製した。この被覆粒子について
上記評価試験を行った結果、第1胃溶出率82%、第4
胃溶出率10%、小腸溶出率3%であった。
Comparative Example 3 Coated particles were prepared in the same manner as in Example 8, except that a protective substance containing 30 parts by weight of calcium carbonate was used for 70 parts by weight of hardened tallow. As a result of performing the above evaluation test on the coated particles, the ruminal dissolution rate was 82%,
The gastric dissolution rate was 10% and the small intestine dissolution rate was 3%.

【0058】以上の結果を表1、表2にまとめた。本発
明の飼料添加組成物は従来の組成物に比べ、第1胃中の
保護性、第4胃より下部消化器官での溶出性に優れた効
果を有することがわかる。
The above results are summarized in Tables 1 and 2. It can be seen that the feed additive composition of the present invention has superior effects on the protection in the rumen and the dissolution in the lower digestive tract from the abomasum compared to the conventional composition.

【0059】[0059]

【表1】 [Table 1]

【0060】[0060]

【表2】 [Table 2]

【0061】[0061]

【発明の効果】以上説明したように、生物学的活性物質
を含有する核を、炭素原子数14〜22個を有する直鎖
または分枝状の飽和または不飽和の脂肪族モノカルボン
酸またはその塩、硬化した植物性油脂、硬化した動物性
油脂およびロウ、ワックスよりなる群から選ばれた少な
くとも1種の物質、レシチン、および中性では安定であ
るが、酸性条件で可溶性の無機物質の1種または2種以
上を含有する被覆組成物で被覆することにより、従来の
技術に比べ、第1胃中の保護性、第4胃より下部消化器
官での溶出性に優れた効果を有する反すう動物用飼料添
加組成物が得られた。
As described above, a nucleus containing a biologically active substance is composed of a linear or branched saturated or unsaturated aliphatic monocarboxylic acid having 14 to 22 carbon atoms or a monocyclic or branched aliphatic monocarboxylic acid. At least one substance selected from the group consisting of salts, hardened vegetable oils, hardened animal fats and waxes, and waxes, lecithin, and one of inorganic substances that are stable in neutral but soluble under acidic conditions. A ruminant animal having an effect of being superior in protection in the rumen and dissolution in the lower digestive tract from the abomasum compared to the prior art by being coated with a coating composition containing one or more species. A feed additive composition for use was obtained.

【0062】本発明は、生物学的活性物質が反すう動物
に有効に吸収されることを可能にした飼料添加物を提供
するものであり、産業上の意義は極めて大きい。
The present invention provides a feed additive which enables a biologically active substance to be effectively absorbed by ruminants, and is of great industrial significance.

フロントページの続き (72)発明者 永井 武 神奈川県川崎市川崎区鈴木町1−1 味 の素株式会社 中央研究所内 (72)発明者 佐藤 弘之 神奈川県川崎市川崎区鈴木町1−1 味 の素株式会社 中央研究所内 審査官 長井 啓子 (56)参考文献 特開 昭63−317053(JP,A) (58)調査した分野(Int.Cl.6,DB名) A23K 1/16,1/18 Continued on the front page (72) Inventor Takeshi Nagai 1-1 Suzukicho, Kawasaki-ku, Kawasaki-shi, Kanagawa Prefecture Ajinomoto Co., Inc. (72) Inventor Hiroyuki Sato 1-1 Suzukicho, Kawasaki-ku, Kawasaki-shi, Kanagawa Ajino Keiko Nagai, Examiner, Central Research Laboratory, Motoo Corporation (56) References JP-A-63-317053 (JP, A) (58) Fields investigated (Int. Cl. 6 , DB name) A23K 1 / 16,1 / 18

Claims (5)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】生物学的活性物質を含有する核を、炭素原
子数14〜22個を有する直鎖または分枝状の飽和また
は不飽和の脂肪族モノカルボン酸またはその塩、硬化し
た植物性油脂、硬化した動物性油脂およびロウ、ワック
スよりなる群から選ばれた少なくとも1種の物質、レシ
チン、および中性では安定であるが、酸性条件で可溶性
の無機物質の1種または2種以上を含有する被覆組成物
で被覆してなることを特徴とする反すう動物用飼料添加
組成物。
1. A nucleus containing a biologically active substance comprising a linear or branched saturated or unsaturated aliphatic monocarboxylic acid having 14 to 22 carbon atoms or a salt thereof, and a hardened vegetable. At least one substance selected from the group consisting of fats and oils, hardened animal fats and waxes, and waxes, lecithin, and one or more inorganic substances that are stable in neutral but soluble under acidic conditions. A feed additive composition for ruminants, which is coated with a coating composition containing the composition.
【請求項2】該被覆組成物中に、レシチンを0.1〜2
0重量%、中性では安定であるが、酸性条件で可溶性の
無機物質を0.1〜10重量%含む請求項1記載の反す
う動物用飼料添加組成物。
2. The composition according to claim 1, wherein lecithin is contained in an amount of 0.1 to 2 lecithin.
The ruminant feed additive composition according to claim 1, wherein the composition contains 0.1 to 10% by weight of 0% by weight and 0.1 to 10% by weight of an inorganic substance which is stable under neutral conditions but soluble under acidic conditions.
【請求項3】中性では安定であるが、酸性条件で可溶性
の無機物質が、炭酸塩であることを特徴とする請求項1
記載の反すう動物用飼料添加組成物。
3. The inorganic substance which is stable under neutral conditions but soluble under acidic conditions is carbonate.
A feed additive composition for ruminants as described in the above.
【請求項4】中性では安定であるが、酸性条件で可溶性
の無機物質が、ピロリン酸のカルシウム塩であることを
特徴とする請求項1記載の反すう動物用飼料添加組成
物。
4. The ruminant feed additive composition according to claim 1, wherein the inorganic substance which is stable under neutral conditions but soluble under acidic conditions is a calcium salt of pyrophosphate.
【請求項5】請求項1〜4記載の反すう動物用飼料添加
組成物を含有する飼料。
5. A feed containing the ruminant feed additive composition according to claim 1.
JP3335073A 1991-01-14 1991-12-18 Ruminant feed additive composition Expired - Fee Related JP2929812B2 (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
NO92920067A NO920067L (en) 1991-01-14 1992-01-06 FORADDITIVE FOR DRUGS
EP92100470A EP0495441B1 (en) 1991-01-14 1992-01-13 Feed additive for ruminants
DK92100470.1T DK0495441T3 (en) 1991-01-14 1992-01-13 Feed additive for ruminants
DE69204690T DE69204690T2 (en) 1991-01-14 1992-01-13 Feed additives for ruminants.
CA002059221A CA2059221C (en) 1991-01-14 1992-01-13 Feed additive for ruminants
US07/820,379 US5227166A (en) 1991-01-14 1992-01-14 Feed additive for ruminants
US08/045,099 US5300297A (en) 1991-01-14 1993-04-12 Feed additive for ruminants

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP3-70265 1991-01-14
JP7026591 1991-01-14

Publications (2)

Publication Number Publication Date
JPH0523114A JPH0523114A (en) 1993-02-02
JP2929812B2 true JP2929812B2 (en) 1999-08-03

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
JP3335073A Expired - Fee Related JP2929812B2 (en) 1991-01-14 1991-12-18 Ruminant feed additive composition

Country Status (1)

Country Link
JP (1) JP2929812B2 (en)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4017227B2 (en) * 1998-01-20 2007-12-05 白石カルシウム株式会社 Pelletized fatty acid-containing mixed feed granulated product and method for producing the same
US6797291B2 (en) * 2002-01-09 2004-09-28 Balchem Corporation Stable hygroscopic compositions and methods for stabilizing hygroscopic ingredients
EP1741347A4 (en) 2004-04-30 2009-09-23 Bio Science Co Ltd Feed additive composition for ruminant, feed containing the same and process for producing feed additive composition for ruminant
PL2077076T3 (en) 2006-10-04 2017-05-31 Ajinomoto Co., Inc. Feed additive composition for ruminants and method of producing the same
JP2011125217A (en) 2008-04-03 2011-06-30 Ajinomoto Co Inc Ruminant feed additive composition containing acidic or neutral amino acid, and method for producing the same
NZ587090A (en) 2008-04-03 2012-10-26 Ajinomoto Kk Feed additive composition for ruminants and method of producing the same
IT201700021852A1 (en) * 2017-02-27 2018-08-27 Bioscreen Tech S R L RELEASED COMPOSITION OF PHYSIOLOGICALLY ACTIVE SUBSTANCES AND PROCESS FOR ITS PREPARATION
IT201700021879A1 (en) 2017-02-27 2018-08-27 Bioscreen Tech S R L RELEASED COMPOSITION OF PHYSIOLOGICALLY ACTIVE SUBSTANCES AND PROCESS FOR ITS PREPARATION
CN111885923A (en) 2018-03-29 2020-11-03 味之素株式会社 Feed additive composition for ruminant

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