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JPS597685B2 - Method for manufacturing vitamin preparations - Google Patents
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JPS597685B2 - Method for manufacturing vitamin preparations - Google Patents

Method for manufacturing vitamin preparations

Info

Publication number
JPS597685B2
JPS597685B2 JP53123337A JP12333778A JPS597685B2 JP S597685 B2 JPS597685 B2 JP S597685B2 JP 53123337 A JP53123337 A JP 53123337A JP 12333778 A JP12333778 A JP 12333778A JP S597685 B2 JPS597685 B2 JP S597685B2
Authority
JP
Japan
Prior art keywords
vitamin
parts
fatty acid
oil
hydrogenated
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
Application number
JP53123337A
Other languages
Japanese (ja)
Other versions
JPS5549313A (en
Inventor
良吾 上原
哲夫 小柳
秀彦 中野
貞雄 近藤
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.)
Takeda Pharmaceutical Co Ltd
Original Assignee
Takeda Chemical Industries Ltd
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 Takeda Chemical Industries Ltd filed Critical Takeda Chemical Industries Ltd
Priority to JP53123337A priority Critical patent/JPS597685B2/en
Publication of JPS5549313A publication Critical patent/JPS5549313A/en
Publication of JPS597685B2 publication Critical patent/JPS597685B2/en
Expired legal-status Critical Current

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  • Medicinal Preparation (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Description

【発明の詳細な説明】 本発明は安定なビタミン製剤の製造法に関する。[Detailed description of the invention] The present invention relates to a method for producing stable vitamin formulations.

さらに詳し《は(A)ビタミンK類、葉酸、ビタミンB
12の1種または2種以上またはそれらをうすめた散剤
(以後これらを総称して芯物質と呼ぷ:?、(B)融点
40〜90℃の油脂と(C)レシチン、グリセリン脂肪
酸モノエステル、シヨ糖脂肪酸エステルの1種または2
種以上との溶融物に混合して被覆粉末化することを特徴
とするビタミン製剤の製造法に関するものである。
For further details, see (A) Vitamin K, folic acid, vitamin B
Powders of one or more of 12 or diluted thereof (hereinafter collectively referred to as core substances), (B) fats and oils with a melting point of 40 to 90°C, (C) lecithin, glycerin fatty acid monoester, One or two sucrose fatty acid esters
The present invention relates to a method for producing a vitamin preparation, which is characterized in that it is mixed in a melt with at least one seed and then coated and powdered.

ここで言うビタミンK類とは、天然に存在するK1、K
2とその同族体およびK3、K4、K5、K6、K7と
そのエステルまたは亜硫酸塩付加物である。
The vitamin K mentioned here refers to naturally occurring K1, K
2 and its homologues, and K3, K4, K5, K6, K7 and their esters or sulfite adducts.

ビタミンK類は動物の栄養上欠くことのできないもので
、血液の凝固因子として知られており、医薬品、動物用
薬品または飼料添加物として、また一部食品の保存料と
しても用いられている。
BACKGROUND OF THE INVENTION Vitamin K is essential for animal nutrition, is known as a blood coagulation factor, and is used as a pharmaceutical, animal drug, feed additive, and as a preservative for some foods.

また飼料用には、安定化されたK3剤としてメナジオン
亜硫酸水素ナトリウム(以後MSB と呼ぶ)およびメ
ナジオン亜硫酸水素ジメチルピリミジノール(以後MP
B と呼ぶ)などが広く用いられているが、飼料中、特
にペレット中安定性についてはなお十分でない製剤もあ
る。
For feed use, stabilized K3 agents include menadione sodium bisulfite (hereinafter referred to as MSB) and menadione bisulfite dimethylpyrimidinol (hereinafter referred to as MP).
B) are widely used, but some formulations still have insufficient stability in feed, especially in pellets.

K類は一般に光に対して敏感、不安定で容易に分解され
る。
Class K is generally sensitive to light, unstable and easily decomposed.

K1は空気および酸には比較的安定であるが、強アルカ
リには不安定で、また日光によって分解される。
K1 is relatively stable to air and acids, but unstable to strong alkalis and decomposed by sunlight.

K3は高湿、ミネラルおよび高温によって分解が促進さ
れる。
The decomposition of K3 is accelerated by high humidity, minerals and high temperature.

またこのものは皮膚、粘膜、呼吸器などを刺激する作用
がある。
This substance also has the effect of irritating the skin, mucous membranes, and respiratory system.

葉酸は化学的にはプテロイルグルタミン酸として知られ
ているもので、フォール酸、フォーラミンとも呼ばれて
おり、栄養性貧血に関係のある因子として知られている
Folic acid is chemically known as pteroylglutamic acid, and is also called foliic acid or foramin, and is known as a factor related to nutritional anemia.

葉酸は光線に対して敏感で、室内光などの弱い光で徐々
に、,直射日光または紫外線によって急速に分解される
Folic acid is sensitive to light and is degraded gradually by weak light such as indoor light, and rapidly by direct sunlight or ultraviolet light.

また酸(pH6.0以下)や亜硫酸塩およびその他の酸
化還元剤によって容易に分解される。
It is also easily decomposed by acids (pH 6.0 or less), sulfites, and other redox agents.

ビタミンB1はシアノコバラミンとも呼ばれており、抗
貧血因子として知られている。
Vitamin B1 is also called cyanocobalamin and is known as an anti-anemia factor.

ビタミンB12は弱い多酸性塩基である。Vitamin B12 is a weak polyacid base.

吸湿性を有し高湿下では不安定となる,,また強い光に
長?間さらすと分解する。
It has hygroscopic properties and becomes unstable under high humidity, and is also sensitive to strong light. It will decompose if left for a while.

pH4.5〜5.0で最も安定であるが、強酸性または
アルカリ性で長時間放置すると酸アミドの加水分解をは
じめとする種々の分解反応がおこる。
Although it is most stable at pH 4.5 to 5.0, if it is left for a long time in strongly acidic or alkaline conditions, various decomposition reactions including hydrolysis of acid amide will occur.

以上のように湿度、温度、光、ミネラル、pH1酸化還
元剤などがビタミンK類、葉酸およびビタミンB1の安
定性に著しい影響を与える。
As described above, humidity, temperature, light, minerals, pH 1 redox agents, etc. have a significant effect on the stability of vitamin K, folic acid, and vitamin B1.

そこでビタミンK類、葉酸およびビタミンB1。So vitamin K, folic acid and vitamin B1.

を安定化させるには、これら因子との接触を断つことが
有効であるので、硬化油などを利用し硬化油などとビタ
ミン類との間の親和性を増すように油溶性の乳化剤を導
入し、最適の組み合せを見出すよう鋭意試験を重ねた結
果本発明を完成したものである。
In order to stabilize vitamins, it is effective to cut off contact with these factors, so we use hydrogenated oil and introduce an oil-soluble emulsifier to increase the affinity between the hydrogenated oil and vitamins. The present invention was completed as a result of extensive testing to find the optimal combination.

すなわち、本発明は(A)芯物質を、(B)融点40〜
90℃の油脂と(’C)レシチン、グリセリン脂肪酸モ
ノエステル、シヨ糖脂肪酸酸エステルの1種または2種
以上との溶融物に混合して被覆粉末化するビタミン製剤
の製造法に係わるものである。
That is, the present invention uses (A) a core material, (B) a melting point of 40 to
This relates to a method for producing a vitamin preparation in which the mixture is mixed into a melt of 90°C oil and fat and one or more of ('C) lecithin, glycerin fatty acid monoester, and sucrose fatty acid acid ester, and then coated and powdered. .

本発明に言う融点40〜90℃の油脂とは特に限定され
るものではないが、硬化牛脂、硬化ラード、硬化魚油、
硬化鯨油、硬化鶏脂、硬化・ぐーム油、硬化菜種油、硬
化大豆油、硬化ヤシ油、硬化ヒマシ油などで、これらは
1種もしくは2種以上を混合して用いることができる。
The fats and oils with a melting point of 40 to 90°C referred to in the present invention are not particularly limited, but include hydrogenated beef tallow, hydrogenated lard, hydrogenated fish oil,
Hydrogenated whale oil, hydrogenated chicken fat, hydrogenated gum oil, hydrogenated rapeseed oil, hydrogenated soybean oil, hydrogenated coconut oil, hydrogenated castor oil, etc. may be used alone or in combination of two or more.

またこれらの油脂の1部をグリセリン脂肪酸ジエステル
に置きかえることもできる。
Moreover, a part of these fats and oils can also be replaced with glycerol fatty acid diester.

本発明に言うグリセリン脂肪酸モノエステルは炭素数8
〜22の脂肪酸のモノエステルであれば飽和でも不飽和
でもかまわない。
The glycerin fatty acid monoester referred to in the present invention has 8 carbon atoms.
As long as it is a monoester of ~22 fatty acids, it may be saturated or unsaturated.

たとえばグリセリンモノステアレート、モノオレエート
、モノラウレートなどが汎用される。
For example, glycerin monostearate, monooleate, monolaurate, etc. are commonly used.

また、シヨ糖脂肪酸エステルは低HLB(1〜6)のも
のが本発明の目的には好ましい。
Furthermore, sucrose fatty acid esters with low HLB (1 to 6) are preferable for the purpose of the present invention.

本発明の被覆剤中のレシチン、グリセリン脂肪酸モノエ
ステル、シヨ糖脂肪酸エステルの1種を使用する場合の
量は油脂1重量部に対して0.1〜1重量部、レシチン
、グリセリン脂肪酸モノエステル、シヨ糖脂肪酸エステ
ルの2種以上併用の場合も同じく、油脂1重量部に対し
て合計量で0.1〜1重量部が好ましい。
When one of lecithin, glycerin fatty acid monoester, and sucrose fatty acid ester is used in the coating material of the present invention, the amount is 0.1 to 1 part by weight per 1 part by weight of oil and fat; lecithin, glycerin fatty acid monoester, Similarly, when two or more types of sucrose fatty acid esters are used in combination, the total amount is preferably 0.1 to 1 part by weight per 1 part by weight of oil or fat.

芯物質1重量部に対して本発明の被覆剤は1〜200重
量部の範囲で使用する。
The coating agent of the present invention is used in an amount of 1 to 200 parts by weight per 1 part by weight of the core material.

本発明の被覆剤溶融物に芯物質を添加した混合物は分散
または溶解状態は良好であり、分散または溶解安定性も
良い。
The mixture of the present invention, in which a core material is added to the coating melt, has a good dispersion or dissolution state and good dispersion or dissolution stability.

ここで、他のビタミン類を同時に混合することも出来る
Here, other vitamins can also be mixed at the same time.

この混合物な粉末化する際の手段として、たとえば回転
円盤型噴霧装置により35℃以下に調整された室内に噴
霧すると、粒子径約50〜800μの粉粒状の製品が得
られる。
As a means for pulverizing this mixture, for example, by spraying it into a room controlled at 35° C. or lower using a rotating disc type sprayer, a powdery product with a particle size of about 50 to 800 μm can be obtained.

粉末化の手段については、上記の方法に限定されること
なく適宜な方法で粉末化することができる。
The means for pulverization is not limited to the above-mentioned method, but can be pulverized by any appropriate method.

芯物質に対して被覆剤が1重量部以下の場合には被覆剤
溶融物に芯物質を分散または溶解させて得られる懸濁液
の粘度が非常に高くなり、噴霧や微粒化、造粒化するこ
とが困難となり、目的とする被覆粒子が得られない。
If the amount of coating material is less than 1 part by weight based on the core material, the viscosity of the suspension obtained by dispersing or dissolving the core material in the molten coating material will be very high, making it difficult to spray, atomize, or granulate. This makes it difficult to obtain the desired coated particles.

また200重量部以上になると被覆剤を増した効果がそ
の保存安定性において認められず、またビタミン類の単
位当りのコストも犬となり好ましくない。
Moreover, if the amount exceeds 200 parts by weight, the effect of increasing the coating agent will not be recognized in terms of storage stability, and the cost per unit of vitamins will be too high, which is not preferable.

本発明の被覆方法によりビタミン類の安定性は著しく改
善されるため、粉末状のビタミン混合物、ビタミン・ミ
ネラル混合物、配合飼料などにおいて、本発明品の利用
価値は犬である。
Since the stability of vitamins is significantly improved by the coating method of the present invention, the product of the present invention is useful for dogs in powdered vitamin mixtures, vitamin/mineral mixtures, mixed feeds, and the like.

またビタミンK3は取扱いに際し、皮膚、粘膜、呼吸器
などを刺激することがあるが、本法により被覆粉末化さ
れたものは安全である。
Furthermore, vitamin K3 may irritate the skin, mucous membranes, respiratory organs, etc. when handled, but it is safe when coated and powdered using this method.

以下実施例、実1験例により説明するが、本発明はこれ
らの例に限定されるものではない。
The present invention will be explained below using examples and experimental examples, but the present invention is not limited to these examples.

なお特に記載がない場合、部は重量部のことを示す。Note that unless otherwise specified, parts refer to parts by weight.

実施例 1 融点61℃の硬化牛脂60部、レシチン10部よりなる
被覆剤を溶融し、温度70〜90℃に保った中にMPB
結晶(又はMSB結晶、葉酸結晶、ビタミンB12粉末
(10%倍散粉末)を夫々単独で)30部を加え、均一
に攪拌混合しながら回転円盤型噴霧装置にて35℃以下
の室内に噴霧してそれぞれ50〜300μのMPB,M
SB、葉酸、ビタミンB12の被覆粒子を得た。
Example 1 A coating consisting of 60 parts of hardened beef tallow with a melting point of 61°C and 10 parts of lecithin was melted and MPB was poured into the mixture while keeping the temperature at 70 to 90°C.
Add 30 parts of crystals (or MSB crystals, folic acid crystals, and vitamin B12 powder (10% triturated powder) each individually), and while stirring and mixing uniformly, spray into a room at 35°C or lower with a rotating disc sprayer. MPB, M of 50 to 300μ each
Coated particles of SB, folic acid, and vitamin B12 were obtained.

実施例 2 融点69℃の硬化大豆油60部、レシチン10部、グリ
セリンモノステアレート10部よりなる被覆剤を溶融し
、温度75〜100℃に保った中にMSB結晶20部を
加え、均一に攪拌混合しながらノズル型噴霧装置にて3
5℃以下の室内に噴?して70〜500μの被覆粒子を
得た。
Example 2 A coating material consisting of 60 parts of hydrogenated soybean oil with a melting point of 69°C, 10 parts of lecithin, and 10 parts of glycerin monostearate was melted, and 20 parts of MSB crystals were added to the mixture while maintaining the temperature at 75 to 100°C, and the mixture was uniformly mixed. 3 using a nozzle type sprayer while stirring and mixing.
Spraying indoors at temperatures below 5℃? Coated particles of 70 to 500 μm were obtained.

実施例 3 融点63℃の硬化菜種油50部、シヨ糖脂肪酸エステル
(第一工業製薬製DKSF−50 、HLB6)14部
よりなる被覆剤を溶融し、温度70〜90℃に保った中
にMPB結晶20部、葉酸結晶8部、ビタミンB12結
晶8部を加え、均一に攪拌混合しながら実施例1と同様
にして50〜400μの被覆粒子を得た。
Example 3 A coating material consisting of 50 parts of hydrogenated rapeseed oil with a melting point of 63°C and 14 parts of sucrose fatty acid ester (DKSF-50, HLB6, manufactured by Daiichi Kogyo Seiyaku) was melted, and MPB crystals were placed in the mixture kept at a temperature of 70 to 90°C. 20 parts, 8 parts of folic acid crystals, and 8 parts of vitamin B12 crystals were added thereto, and coated particles of 50 to 400 μm in size were obtained in the same manner as in Example 1 while stirring and mixing uniformly.

実施例 4 融点61℃の硬化・牛脂55部、レシチン5部、シヨ糖
脂肪酸エステル(菱糖製S−370、HLB 2〜3
)15部、グリセリンモノオレエート10部よりなる被
覆剤を溶融し、温度70〜90℃に保った中にMPB結
晶15部を加え、均一に攪拌混合しながら実施例2と同
様にして70〜500μの被覆粒子を得た。
Example 4 Hardened beef tallow with a melting point of 61°C, 5 parts of lecithin, sucrose fatty acid ester (S-370 manufactured by Hishito Co., Ltd., HLB 2-3
) and 10 parts of glycerin monooleate were melted, 15 parts of MPB crystals were added to the mixture kept at a temperature of 70 to 90°C, and the mixture was heated in the same manner as in Example 2 while stirring and mixing uniformly. Coated particles of 500μ were obtained.

実施例 5 融点59℃の硬化パーム油20部、融点60℃の硬化鶏
脂40部、シヨ糖脂肪酸エステル(第一工業製薬製DK
SF−10、HLBI)10部、グリセリンモノラウレ
ート10部よりなる被覆剤を溶融し、温度70〜90℃
に保った中にMSB結晶20部、葉酸結晶8部を加え均
一に攪拌混合しながら実施例1と同様にして60〜40
0μの被覆粒子を得た。
Example 5 20 parts of hydrogenated palm oil with a melting point of 59°C, 40 parts of hardened chicken fat with a melting point of 60°C, sucrose fatty acid ester (DK manufactured by Daiichi Kogyo Seiyaku Co., Ltd.)
A coating material consisting of 10 parts of SF-10, HLBI) and 10 parts of glycerin monolaurate was melted and heated to a temperature of 70 to 90°C.
20 parts of MSB crystals and 8 parts of folic acid crystals were added in the same manner as in Example 1 while stirring and mixing uniformly.
Coated particles of 0μ were obtained.

実施例 6 融点60℃の硬化鶏脂80部、グリセリンモノベヘネ−
}10部、レシチン10部よりなる被覆剤を溶融し、温
度70〜90℃に保った中にビタミンB1結晶0.5部
を加え、均一に攪拌混合しながら実施例1と同様にして
70〜600μの被覆粒子を得た。
Example 6 80 parts of cured chicken fat with a melting point of 60°C, glycerin monobehenene
}10 parts of lecithin was melted, 0.5 parts of vitamin B1 crystals were added to the mixture kept at a temperature of 70 to 90°C, and the same procedure as in Example 1 was carried out while stirring and mixing uniformly. Coated particles of 600μ were obtained.

試験例 実施例、被覆前のビタミン粉末及び実施例1と同様の方
法にて硬化牛脂のみを被覆剤として製造した比較例につ
いて下記の条件にて安定性試験を行った。
Test Examples Stability tests were conducted under the following conditions for Examples, vitamin powder before coating, and Comparative Examples prepared using only hardened beef tallow as a coating agent in the same manner as in Example 1.

(1)試料 プレミックス;市販の鶏用プレミックス 飼料;市販のブロイラー用飼料 上記の試料に(2)の濃度になるよう各ビタミンを添加
し均一に混合する。
(1) Sample premix; Commercially available premix feed for chickens; Commercially available broiler feed Each vitamin is added to the above sample to achieve the concentration shown in (2) and mixed uniformly.

(2) ビタミン類の濃度 MSB : 5 0 ppm MPB ; 5 0 ppm 葉酸:20ppm ビタミンB ;20ppm 12 なお2種以上のビタミン類を併用する場合も前記濃度に
なるよう調製した。
(2) Concentration of vitamins MSB: 50 ppm MPB: 50 ppm Folic acid: 20 ppm Vitamin B: 20 ppm 12 In addition, when two or more vitamins were used together, they were adjusted to the above concentrations.

(3)安定度試験条件 100ml容の褐色ガラスびん中に試料50グを入れ密
封し、下記条件にて8週間経過後、各ビタミン含量を測
定した。
(3) Stability test conditions 50 grams of a sample was placed in a 100 ml brown glass bottle and sealed, and after 8 weeks under the following conditions, the content of each vitamin was measured.

プレミックス;40°C 飼料;30℃ (4)ビタミン類の定量方法 MSB : E.Leerbeckら( Acta A
gricul −turae S candinavi
ca 2 5 ( 1 9 7 5 ) )の方法(D
NP比色法)に準ずる。
Premix; 40°C Feed; 30°C (4) Method for quantifying vitamins MSB: E. Leerbeck et al. (Acta A
gricul-turae S candinavi
ca25 (1975)) method (D
(NP colorimetric method).

MPB ;同上 葉酸.A,0.A.C■に準ずる ビタミンB12;U.S.PXIXに準ずる以上の結果
から、本発明の方法で被覆したビタミン類は比較例と対
比してわかるように、特に安定性の悪い飼料中でも格段
に優れている。
MPB; folic acid as above. A, 0. A. Vitamin B12 according to C■; U. S. From the above results, which are similar to those of PXIX, the vitamins coated by the method of the present invention are significantly superior even in particularly unstable feeds, as can be seen in comparison with the comparative example.

Claims (1)

【特許請求の範囲】[Claims] 1 (A)ビタミンK類、葉酸、ビタミンB12の1
種または2種以上を、(B)融点40〜90℃の油脂と
(C)レシチン、グリセリン脂肪酸モノエステル、シヨ
糖脂肪酸エステルの1種または2種以上との溶融物に混
合して被覆粉末化することを特徴とする安定なビタミン
製剤の製造法。
1 (A) Vitamin K, folic acid, vitamin B12 1
The seed or two or more are mixed into a melt of (B) an oil or fat with a melting point of 40 to 90°C and (C) one or more of lecithin, glycerin fatty acid monoester, and sucrose fatty acid ester to form a coated powder. A method for producing a stable vitamin preparation characterized by:
JP53123337A 1978-10-06 1978-10-06 Method for manufacturing vitamin preparations Expired JPS597685B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP53123337A JPS597685B2 (en) 1978-10-06 1978-10-06 Method for manufacturing vitamin preparations

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP53123337A JPS597685B2 (en) 1978-10-06 1978-10-06 Method for manufacturing vitamin preparations

Publications (2)

Publication Number Publication Date
JPS5549313A JPS5549313A (en) 1980-04-09
JPS597685B2 true JPS597685B2 (en) 1984-02-20

Family

ID=14858059

Family Applications (1)

Application Number Title Priority Date Filing Date
JP53123337A Expired JPS597685B2 (en) 1978-10-06 1978-10-06 Method for manufacturing vitamin preparations

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JP (1) JPS597685B2 (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58109761U (en) * 1982-01-22 1983-07-26 ミノルタ株式会社 Toner scattering prevention device
IT1191608B (en) * 1985-02-01 1988-03-23 Zambon Spa PHARMACEUTICAL COMPOSITION AND PHARMACEUTICAL FORMS THAT CONTAIN IT
US6265391B1 (en) 1995-10-17 2001-07-24 Upsher-Smith Laboratories, Inc. Method for preventing peripheral nerve damage
ES2187380A1 (en) * 2001-11-16 2003-06-01 Sanchez Juan Balufo Improvements on products intended for human or animal consumption
ITFI20020043A1 (en) * 2002-03-08 2003-09-08 Fernando Cantini A LIPID PRODUCT BASED ON MONOGLYCERIDES AND DIGLYCERIDES OF ACIDOOLEIC, TRIGLYCERIDES RANDOMIZED AND GLYCEROL, FOR ANIMAL FEEDING
DE102007012644A1 (en) 2007-03-16 2008-09-18 Bayer Healthcare Ag Stabilization of vitamin B12

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6013208B2 (en) * 1976-07-09 1985-04-05 株式会社日立製作所 Arithmetic control method for multiprocessing equipment

Also Published As

Publication number Publication date
JPS5549313A (en) 1980-04-09

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