JP2003250488A - Food composition and method for producing the same - Google Patents

Food composition and method for producing the same

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Publication number
JP2003250488A
JP2003250488A JP2002050945A JP2002050945A JP2003250488A JP 2003250488 A JP2003250488 A JP 2003250488A JP 2002050945 A JP2002050945 A JP 2002050945A JP 2002050945 A JP2002050945 A JP 2002050945A JP 2003250488 A JP2003250488 A JP 2003250488A
Authority
JP
Japan
Prior art keywords
powder
tablet
yeast
calcium
dietary fiber
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.)
Granted
Application number
JP2002050945A
Other languages
Japanese (ja)
Other versions
JP4143312B2 (en
Inventor
Takamitsu Ueto
隆充 植戸
Yoshimitsu Takai
良充 高井
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.)
Fancl Corp
Original Assignee
Fancl Corp
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Publication of JP2003250488A publication Critical patent/JP2003250488A/en
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Publication of JP4143312B2 publication Critical patent/JP4143312B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Coloring Foods And Improving Nutritive Qualities (AREA)
  • Jellies, Jams, And Syrups (AREA)
  • Formation And Processing Of Food Products (AREA)

Abstract

<P>PROBLEM TO BE SOLVED: To provide a powder-containing tablet capable of preventing a low hardness tablet and the abrasion, breaking, chipping, etc., of the tablet occurring in the tablet highly incorporated with a substance having a very low forming property such as beer yeast powder, and excellent in stability as a product. <P>SOLUTION: This powder-containing tablet is characterized by containing one kind or more selected from a group consisting of beer yeast powder, mineral yeast powder, hem iron powder, chitosan powder, a protein powder, royal jelly powder and a plant powder, and an edible soluble fiber by 0.01-50.00 pt.wt. The method for producing the powder-containing tablet is characterized by granulating one king or more selected from a group consisting of beer yeast powder, mineral yeast powder, hem iron powder, chitosan powder, a protein powder, royal jelly powder and a plant powder by using an aqueous solution of the edible soluble fiber and tableting. <P>COPYRIGHT: (C)2003,JPO

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【発明が属する技術分野】本発明は、ビール酵母粉末の
ような粉末活性成分を高含有する錠剤、およびその製造
方法に関する。
TECHNICAL FIELD The present invention relates to a tablet having a high content of a powdered active ingredient such as brewer's yeast powder, and a method for producing the same.

【0002】[0002]

【従来の技術】ビール酵母粉末に含有されている栄養成
分を効率良く摂取するためには、一日当たりに摂取する
量は非常に多くなることから、ビール酵母粉末を含む錠
剤には、成形助剤として配合するべき添加剤の配合量を
できる限り少なくする必要性がある。
2. Description of the Related Art In order to efficiently ingest the nutritional components contained in brewer's yeast powder, the amount taken per day is very large. It is necessary to reduce the compounding amount of the additive to be compounded as.

【0003】しかしながら、ビール酵母粉末を高含有さ
せた錠剤を製造する場合、その成形性が非常に悪いた
め、適切な錠剤硬度が得られず、錠剤の摩損、割れ、欠
け等が生じることが問題視されている。
However, when a tablet containing a large amount of brewer's yeast powder is produced, its moldability is very poor, so that an appropriate tablet hardness cannot be obtained and abrasion, cracking, chipping, etc. of the tablet occur. Is being watched.

【0004】このような問題を解決する先行技術として
は、特開昭55−162984号が知られているが、軽
質無水珪酸、珪酸アルミニウム、水酸化アルミニウムお
よびメタ珪酸アルミン酸マグネシウム等の食品添加物と
して許可されていない添加剤が必須となるため、汎用性
に乏しい。
JP-A-55-162984 is known as a prior art for solving such a problem, but it is a food additive such as light anhydrous silicic acid, aluminum silicate, aluminum hydroxide and magnesium aluminometasilicate. As an additive that is not permitted as above is essential, it lacks versatility.

【0005】また、関連する技術としては、特開昭61
−231966号があるが、ビール酵母粉末の含有量が
10〜40重量%と低い。同様にして、特公平05−7
5373、特公平06−29190、特開昭63−21
1224号、特開平07−324033号、特開平10
−225285号、特開2000−178662号等が
知られているが、錠剤の硬度を高める技術とは目的が異
なる。また、特開2001−342129号に関して
は、硬化油脂の滑沢剤を添加しなくてはならない。
As a related technique, Japanese Patent Laid-Open No. Sho 61-61
However, the content of brewer's yeast powder is as low as 10 to 40% by weight. In a similar manner
5373, Japanese Patent Publication No. 06-29190, JP-A-63-21
1224, JP 07-324033 A, JP 10
No. 225285 and Japanese Patent Application Laid-Open No. 2000-178662 are known, but their purpose is different from the technique for increasing the hardness of tablets. Further, as for JP-A-2001-342129, a lubricant for hardened oil and fat must be added.

【0006】[0006]

【発明が解決しようとする課題】本発明は、ビール酵母
粉末のような粉末を高含有し、しかも錠剤として満足で
きる硬度を有する錠剤、およびその製造方法を提供する
ことを目的とする。
SUMMARY OF THE INVENTION It is an object of the present invention to provide a tablet having a high content of powder such as brewer's yeast powder and having satisfactory hardness as a tablet, and a method for producing the tablet.

【0007】[0007]

【課題を解決するための手段】本発明者は、ビール酵母
粉末のような粉末を高含有する錠剤を製造する際に、可
溶性食物繊維、更には必要に応じてカルシウム素材を配
合することによって、ビール酵母粉末のような粉末を高
含有する錠剤の錠剤硬度を高めることができ、製品とし
ての安定性に優れた粉末高含有錠剤が得られることを見
出し、本発明に至った。本発明は、ビール酵母粉末のよ
うな粉末を高含有する錠剤、およびその製造方法を提供
することを目的とする。
Means for Solving the Problems When the present invention produces tablets containing a large amount of powder such as brewer's yeast powder, by adding soluble dietary fiber and, if necessary, a calcium material, The present inventors have found that the tablet hardness of a tablet containing a large amount of powder such as brewer's yeast powder can be increased, and that a tablet containing a large amount of powder having excellent stability as a product can be obtained, which led to the present invention. An object of the present invention is to provide a tablet having a high content of powder such as brewer's yeast powder, and a method for producing the same.

【0008】即ち、本発明は、 1.ビール酵母粉末、ミネラル酵母粉末、ヘム鉄粉末、
キトサン粉末、プロテイン粉末、ローヤルゼリー粉末、
及び植物粉末からなる群から選択される1種以上、並び
に可溶性食物繊維を含むことを特徴とする粉末含有錠
剤、 2.ビール酵母粉末、ミネラル酵母粉末、ヘム鉄粉末、
キトサン粉末、プロテイン粉末、ローヤルゼリー粉末、
及び植物粉末からなる群から選択される1種以上を5
0.00〜99.99質量部含む事を特徴とする1記載
の粉末含有錠剤、 3.可溶性食物繊維を0.01〜50.00質量部含む
ことを特徴とする1記載の粉末含有錠剤、 4.可溶性食物繊維水溶液を用いてビール酵母粉末、ミ
ネラル酵母粉末、ヘム鉄粉末、キトサン粉末、プロテイ
ン粉末、ローヤルゼリー粉末、及び植物粉末からなる群
から選択される1種以上を造粒し、打錠することを特徴
とする粉末含有錠剤の製造方法、 5.ビール酵母粉末、ミネラル酵母粉末、ヘム鉄粉末、
キトサン粉末、プロテイン粉末、ローヤルゼリー粉末、
及び植物粉末からなる群から選択される1種以上、可溶
性食物繊維、及びカルシウム素材を含むことを特徴とす
るビール酵母粉末含有錠剤、 6.配合する可溶性食物繊維が0.01〜50.00質
量部、カルシウム素材が0.10〜49.99質量部で
あることを特徴とする5記載の粉末含有錠剤、 7.可溶性食物繊維水溶液を用いてビール酵母粉末、ミ
ネラル酵母粉末、ヘム鉄粉末、キトサン粉末、プロテイ
ン粉末、ローヤルゼリー粉末、及び植物粉末からなる群
から選択される1種以上を造粒し、カルシウム素材を配
合して打錠することを特徴とする粉末含有錠剤の製造方
法、及び 8.4または7記載の製造方法によって得られる粉末含
有錠剤、に関する。
That is, the present invention is as follows: Beer yeast powder, mineral yeast powder, heme iron powder,
Chitosan powder, protein powder, royal jelly powder,
1. A powder-containing tablet comprising one or more kinds selected from the group consisting of: and vegetable powder, and soluble dietary fiber; Beer yeast powder, mineral yeast powder, heme iron powder,
Chitosan powder, protein powder, royal jelly powder,
And at least one selected from the group consisting of plant powder and 5
2. The powder-containing tablet according to 1, wherein the tablet contains 0.00 to 99.99 parts by mass. 3. The powder-containing tablet according to 1, characterized in that it contains 0.01 to 50.00 parts by mass of soluble dietary fiber. Granulating and tableting one or more selected from the group consisting of beer yeast powder, mineral yeast powder, heme iron powder, chitosan powder, protein powder, royal jelly powder, and plant powder using an aqueous soluble dietary fiber solution. 4. A method for producing a powder-containing tablet, which is characterized by: Beer yeast powder, mineral yeast powder, heme iron powder,
Chitosan powder, protein powder, royal jelly powder,
And at least one selected from the group consisting of vegetable powder, soluble dietary fiber, and a calcium material, and a brewer's yeast powder-containing tablet, 6. 6. The powder-containing tablet according to 5, wherein the soluble dietary fiber to be blended is 0.01 to 50.00 parts by mass and the calcium material is 0.10 to 49.99 parts by mass. Beer yeast powder, mineral yeast powder, heme iron powder, chitosan powder, protein powder, royal jelly powder, and one or more selected from the group consisting of plant powder are granulated using an aqueous soluble dietary fiber solution, and a calcium material is blended. The present invention relates to a method for producing a powder-containing tablet, which is characterized by being compressed into tablets, and a powder-containing tablet obtained by the production method according to 8.4 or 7.

【0009】[0009]

【発明の実施の形態】以下に本発明を詳細に説明する。
錠剤に含有させる粉末として、ビール酵母粉末、亜鉛酵
母、マグネシウム酵母、鉄酵母、セレン酵母、クロム酵
母、マンガン酵母、銅酵母、モリブデン酵母、ヨウ素酵
母のような、ミネラルが酵母の菌体内に取り込まれてい
るミネラル酵母粉末や、ヘモグロビンを酵素処理した
後、限外濾過もしくは等電点沈殿を行い、乾燥して得ら
れるヘム鉄粉末、キトサン粉末、プロテイン粉末、ロー
ヤルゼリー粉末、緑茶粉末、ケール粉末、大麦若葉粉末
のような植物粉末等の活性成分を使用することができ
る。
BEST MODE FOR CARRYING OUT THE INVENTION The present invention is described in detail below.
As powder to be contained in the tablet, minerals are incorporated into the yeast cells, such as brewer's yeast powder, zinc yeast, magnesium yeast, iron yeast, selenium yeast, chromium yeast, manganese yeast, copper yeast, molybdenum yeast, and iodine yeast. Heme iron powder, chitosan powder, protein powder, royal jelly powder, green tea powder, kale powder, barley obtained by enzymatic treatment of mineral yeast powder and hemoglobin, followed by ultrafiltration or isoelectric precipitation, and drying. Active ingredients such as plant powders such as young leaf powder can be used.

【0010】このような粉末活性成分は、錠剤中50質
量%以上配合することができる。特に、粉末活性成分と
して、1日当たりの摂取量が多いビール酵母粉末を用い
ると、添加剤の配合量を少なくすることができ、大摂取
量に適した優れた錠剤を得ることができる。ビール酵母
粉末は、錠剤中に50質量%以上、好ましくは70質量
%以上、特に好ましくは90質量%以上配合させる。
Such a powdered active ingredient can be incorporated in a tablet in an amount of 50% by mass or more. In particular, when brewer's yeast powder, which has a large daily intake, is used as the powder active ingredient, the amount of the additive compounded can be reduced, and an excellent tablet suitable for a large intake can be obtained. The beer yeast powder is mixed in the tablet in an amount of 50% by mass or more, preferably 70% by mass or more, and particularly preferably 90% by mass or more.

【0011】ビール酵母粉末は、一般的にビールを主発
酵させる際に加え、回収された生酵母を篩過、脱苦味洗
浄、遠心分離、水洗、ドラム乾燥、粉砕、篩過して得ら
れる酵母のことで、その製造方法に依らず、市販品を使
用することができる。
The brewer's yeast powder is generally obtained when the beer is mainly fermented, and the raw yeast recovered is sieved, debittered, washed, centrifuged, washed with water, drum-dried, crushed and sieved. Therefore, a commercially available product can be used regardless of the manufacturing method.

【0012】本発明における可溶性食物繊維としては、
グアーガム、キサンタンガム、ローカストビーンガム、
トラガントガム、カラヤガム、アラビアガム、ゼラチ
ン、プルラン等の天然物由来の可溶性食物繊維を挙げる
ことができ、特にグアーガムの使用が望ましい。
As the soluble dietary fiber in the present invention,
Guar gum, xanthan gum, locust bean gum,
Examples thereof include soluble dietary fibers derived from natural products such as tragacanth gum, karaya gum, gum arabic, gelatin and pullulan, and it is particularly preferable to use guar gum.

【0013】カルシウム素材としては、例えばドロマイ
ト、卵殻カルシウム、帆立貝殻カルシウム、カキ貝殻カ
ルシウム、珊瑚カルシウム、ウニ殻カルシウム、石化海
藻カルシウム、真珠カルシウム、牛骨カルシウム、魚骨
粉カルシウム、魚鱗片カルシウム、ミルクカルシウム等
の焼成カルシウム、あるいは未焼成カルシウム等の天然
カルシウム高含有物、または、炭酸カルシウム、リン酸
カルシウム、乳酸カルシウム、グルコン酸カルシウム、
クエン酸カルシウム、塩化カルシウム等のカルシウム塩
を挙げることができ、食品で使用可能なすべての市販品
を使用することができる。本発明では、上記カルシウム
素材を単独あるいは2種以上併用することができる。
Examples of the calcium material include dolomite, egg shell calcium, scallop shell calcium, oyster shell calcium, coral calcium, sea urchin shell calcium, petrified seaweed calcium, pearl calcium, beef bone calcium, fish bone meal calcium, fish scale calcium, milk calcium. Calcined calcium such as, or high natural calcium content such as uncalcined calcium, or calcium carbonate, calcium phosphate, calcium lactate, calcium gluconate,
Examples thereof include calcium salts such as calcium citrate and calcium chloride, and all commercially available food products can be used. In the present invention, the above calcium materials can be used alone or in combination of two or more kinds.

【0014】天然カルシウム高含有物の一般的な製造方
法は、原料の選別、粗粉砕、篩別、加熱殺菌等の後、所
定の粒度になるように粉砕するという一連の流れになっ
ている。例えばドロマイトは、ドロマイト原石を粗砕、
加熱殺菌した後、粉砕して得られるものである。卵殻カ
ルシウムの一般的な製造方法は、原料の選別、粗粉砕、
篩別した後、例えば100℃で加熱殺菌し、所定の粒度
になるように粉砕して製造される。また、一般的に珊瑚
カルシウムは、まずコーラルサンドまたは珊瑚化石を採
取し、水洗いした後異物を除去し、次に例えば100℃
以上で加熱して殺菌および乾燥を行った後、所定の粒度
になるように粉砕する方法で製造される。
A general method for producing a natural calcium-enriched product is a series of processes in which raw materials are selected, coarsely crushed, sieved, heat sterilized, and then crushed to a predetermined particle size. Dolomite, for example, roughly crushes rough dolomite,
It is obtained by heat sterilization and crushing. The general method of producing egg shell calcium is to select raw materials, coarsely crush,
After sieving, it is sterilized by heating, for example, at 100 ° C., and pulverized to have a predetermined particle size. In general, for coral calcium, first, coral sand or coral fossil is collected, washed with water and then foreign matter is removed, and then, for example, 100 ° C.
After being heated and sterilized and dried as described above, it is manufactured by a method of pulverizing to a predetermined particle size.

【0015】次にカルシウム塩のうち、例えば炭酸カル
シウムは、石灰石を焼成して得られる酸化カルシウムを
水と反応させて水酸化カルシウムとし、これに炭酸ガス
を通じてコロイド性または、軽質炭酸カルシウムを得る
方法、または塩化カルシウム溶液に炭酸ナトリウム溶液
を反応させて沈降炭酸カルシウムとする方法、あるいは
天然石灰石を微粉砕の上、重質炭酸カルシウムとする方
法がある。さらに、炭酸カルシウムまたは酸化カルシウ
ムを種々の酸性溶液と反応させて得られるカルシウム塩
がある。例えば乳酸カルシウムは、一般的に乳酸発酵の
途中で、中和剤として炭酸カルシウムを加えて粗乳酸カ
ルシウムを得、それを精製する方法か、合成乳酸に炭酸
カルシウムを加える方法で製造される。
Next, of the calcium salts, for example, calcium carbonate is a method in which calcium oxide obtained by calcining limestone is reacted with water to form calcium hydroxide, and carbon dioxide is passed through this to obtain colloidal or light calcium carbonate. Alternatively, there is a method of reacting a calcium carbonate solution with a sodium carbonate solution to obtain precipitated calcium carbonate, or a method of pulverizing natural limestone to obtain heavy calcium carbonate. Further, there are calcium salts obtained by reacting calcium carbonate or calcium oxide with various acidic solutions. For example, calcium lactate is generally produced by adding calcium carbonate as a neutralizing agent to obtain crude calcium lactate during the lactic acid fermentation and purifying it, or by adding calcium carbonate to synthetic lactic acid.

【0016】本発明における可溶性食物繊維の配合量と
しては、0.01〜50.00質量%、好ましくは0.
01〜30.0質量%、特に好ましくは0.01〜2
0.0質量%である。可溶性食物繊維の配合量が50.
0質量%を越えると、その分ビール酵母粉末のような粉
末活性成分の含有量が減るため、その結果、一日の摂取
量を多くしなければならなくなり、摂取者への負担が大
きくなる。また、可溶性食物繊維の配合量が0.01質
量%に満たないと、適切な錠剤硬度が得られず、錠剤の
摩損、割れ、欠け等が生じることがあるため、上記範囲
内であることが望ましい。
The amount of soluble dietary fiber used in the present invention is 0.01 to 50.00% by mass, preferably 0.1.
01 to 30.0% by mass, particularly preferably 0.01 to 2
It is 0.0 mass%. The soluble fiber content is 50.
When it exceeds 0% by mass, the content of the powdered active ingredient such as brewer's yeast powder is reduced correspondingly, and as a result, the daily intake must be increased and the burden on the ingestor becomes large. If the amount of soluble dietary fiber is less than 0.01% by mass, appropriate tablet hardness may not be obtained, and tablets may be worn out, cracked, chipped, etc. desirable.

【0017】可溶性食物繊維は、粉末活性成分に対し
て、0.0001〜1質量部、好ましくは、0.001
〜0.3質量部添加することができる。
The soluble dietary fiber is 0.0001 to 1 part by mass, preferably 0.001 part by weight, based on the powdered active ingredient.
~ 0.3 parts by mass can be added.

【0018】同様にして、本発明におけるカルシウム素
材の配合量としては、0.10〜49.99質量%、好
ましくは0.50〜20.00質量%、特に好ましくは
1.00〜10.00質量%である。カルシウム素材の
配合量が49.99質量%を越えると、その分ビール酵
母粉末の含有量が減るため、その結果、一日の摂取量を
多くしなければならなくなり、摂取者への負担が大きく
なる。また、カルシウム素材の配合量が0.10質量%
に満たないと、適切な錠剤硬度が得られず、錠剤の摩
損、割れ、欠け等が生じることがあるため、上記範囲内
であることが望ましい。
Similarly, the blending amount of the calcium material in the present invention is 0.10 to 49.99 mass%, preferably 0.50 to 20.00 mass%, and particularly preferably 1.00 to 10.00. It is% by mass. When the content of calcium material exceeds 49.99% by mass, the content of brewer's yeast powder decreases accordingly, and as a result, the daily intake has to be increased, and the burden on the ingestor is large. Become. In addition, the compounding amount of calcium material is 0.10 mass%
If it is less than the above range, an appropriate tablet hardness cannot be obtained, and the tablet may be worn out, cracked, chipped, or the like, so that it is preferably within the above range.

【0019】カルシウム素材は、粉末活性成分に対し
て、0.0001〜2.0質量部、好ましくは、0.0
01〜1.0質量部添加することができる。
The calcium material is 0.0001 to 2.0 parts by mass, preferably 0.0
01 to 1.0 parts by mass can be added.

【0020】本発明においては、製造性を高める目的
で、可溶性食物繊維、およびカルシウム素材の他に、不
活性成分を含有させることもできる。このような不活性
成分としては、デキストリン、小麦澱粉、米澱粉、とう
もろこし澱粉、馬鈴薯澱粉、α化澱粉、部分α化澱粉、
乳糖、麦芽糖、還元乳糖、還元麦芽糖、ソルビトール、
マンニトール、エリスリトール、キシリトール、白糖、
ブドウ糖、寒天、大豆食物繊維、結晶セルロース、メチ
ルセルロース、エチルセルロース、低置換度ヒドロキシ
プロピルセルロース、ヒドロキシプロピルメチルセルロ
ースフタレート、ヒドロキシプロピルメチルセルロース
アセテートサクシネート、カルボキシメチルエチルセル
ロース、酢酸フタル酸セルロース、ヒドロキシエチルセ
ルロース、ヒドロキシプロピルスターチ、ポリビニルピ
ロリドン、カルメロース、カルメロースカルシウム、カ
ルメロースナトリウム、クロスカルメロースナトリウ
ム、カルボキシメチルスターチナトリウム、植物硬化
油、植物油脂末、カルナウバロウ、カカオ脂末、ショ糖
脂肪酸エステル、ステアリン酸、ステアリン酸マグネシ
ウム、ステアリン酸アルミニウム、ステアリン酸カルシ
ウム、二酸化ケイ素、タルク、ケイ酸アルミニウム、リ
ン酸水素カルシウム等を挙げることができる。
In the present invention, an inactive component may be contained in addition to the soluble dietary fiber and the calcium material for the purpose of enhancing the productivity. Such inactive ingredients include dextrin, wheat starch, rice starch, corn starch, potato starch, pregelatinized starch, partially pregelatinized starch,
Lactose, maltose, reduced lactose, reduced maltose, sorbitol,
Mannitol, erythritol, xylitol, white sugar,
Glucose, agar, soybean dietary fiber, crystalline cellulose, methyl cellulose, ethyl cellulose, low-substituted hydroxypropyl cellulose, hydroxypropyl methyl cellulose phthalate, hydroxypropyl methyl cellulose acetate succinate, carboxymethyl ethyl cellulose, cellulose acetate phthalate, hydroxyethyl cellulose, hydroxypropyl starch, Polyvinylpyrrolidone, carmellose, carmellose calcium, carmellose sodium, croscarmellose sodium, sodium carboxymethyl starch, hardened vegetable oil, vegetable oil powder, carnauba wax, cacao oil powder, sucrose fatty acid ester, stearic acid, magnesium stearate, stearin Aluminum acid, calcium stearate, silicon dioxide, It can be given torque, aluminum silicate, calcium hydrogen phosphate, and the like.

【0021】また、本発明に依れば、ビール酵母粉末の
他に、例えば、亜鉛酵母、マグネシウム酵母、鉄酵母、
セレン酵母、クロム酵母、マンガン酵母、銅酵母、モリ
ブデン酵母、ヨウ素酵母のような、ミネラルが酵母の菌
体内に取り込まれているミネラル酵母粉末や、ヘモグロ
ビンを酵素処理した後、限外濾過もしくは等電点沈澱を
行い、乾燥して得られるヘム鉄粉末、キトサン粉末、プ
ロテイン粉末、ローヤルゼリー粉末、植物粉末として、
緑茶粉末、ケール粉末、大麦若葉粉末等の活性成分を高
含有させた錠剤を製造する際にも、錠剤低硬度、摩損、
割れ、欠け等を防止することができる。
Further, according to the present invention, in addition to brewer's yeast powder, for example, zinc yeast, magnesium yeast, iron yeast,
Mineral yeast powder, such as selenium yeast, chrome yeast, manganese yeast, copper yeast, molybdenum yeast, and iodine yeast, in which minerals are incorporated into yeast cells, and hemoglobin are treated with an enzyme, followed by ultrafiltration or isoelectricity. As heme iron powder, chitosan powder, protein powder, royal jelly powder, and plant powder obtained by performing point precipitation and drying,
Even when producing tablets containing a high content of active ingredients such as green tea powder, kale powder, and barley young leaf powder, low tablet hardness, abrasion,
It is possible to prevent cracks and chips.

【0022】本発明の錠剤は、その形状および重量に左
右されることはなく、これらは一般的な製造方法に準じ
て製造される。
The tablet of the present invention does not depend on its shape and weight and is manufactured according to a general manufacturing method.

【0023】例えば、粉末活性成分と前記可溶性食物繊
維を混合したものを常法に従って圧縮成形して錠剤とす
るか、または、粉末活性成分を適当な方法で顆粒状とし
た後、前記可溶性食物繊維、更には必要に応じてカルシ
ウム素材を加え、常法に従って圧縮成型して錠剤とする
か、粉末活性成分を前記可溶性食物繊維によって顆粒状
とした後、必要に応じて前記カルシウム素材または前記
不活性成分等を加え、常法に従って圧縮成型して錠剤と
することができる。前記カルシウム素材および前記不活
性成分は混合する際に加えても、粉末活性成分を顆粒状
にする際に使用しても良く、その場合、前記カルシウム
素材および前記不活性成分は2種以上併用してもかまわ
ない。なお、可溶性食物繊維を溶かした溶液を用いて粉
末活性成分を顆粒化した後、カルシウム素材を加え、圧
縮成形したときに、特に高い硬度が得られる。また、打
錠適性を向上させる目的で、打錠前に適切な粒子径にな
るように、粉砕、または篩過等を施す場合もある。前記
粉末活性成分は2種以上併用してもかまわない。
For example, a mixture of a powdered active ingredient and the soluble dietary fiber is compression-molded according to a conventional method to give a tablet, or the powdered active ingredient is granulated by an appropriate method and then the soluble dietary fiber is prepared. Further, if necessary, a calcium material is added, and compression molding is performed according to a conventional method to give tablets, or the powdered active ingredient is granulated with the soluble dietary fiber, and then the calcium material or the inactive material is added as necessary. The ingredients and the like can be added, and the mixture can be compression molded into tablets according to a conventional method. The calcium material and the inactive ingredient may be added during mixing, or may be used when the powdered active ingredient is granulated. In that case, two or more kinds of the calcium ingredient and the inactive ingredient are used in combination. It doesn't matter. It should be noted that particularly high hardness is obtained when the powdered active ingredient is granulated using a solution in which soluble dietary fiber is dissolved, and then a calcium material is added and compression molding is performed. Further, for the purpose of improving tableting suitability, crushing or sieving may be performed before tableting so as to obtain an appropriate particle size. The powdered active ingredients may be used in combination of two or more kinds.

【0024】以下、顆粒の製造方法について説明する。
造粒工程における、結合剤の使用方法としては、粉末活
性成分、または必要に応じて前記可溶性食物繊維、また
は前記カルシウム素材を加えた混合物に対し、水やエタ
ノール水溶液を結合液として添加する方法がある。使用
するエタノール水溶液のエタノール濃度は、粉末それぞ
れの吸湿性、平均粒子径、嵩比重等によって調節するこ
とができる。必要に応じて、前記可溶性食物繊維を溶か
し込んだ粘性の高い溶液を結合液として使用するか、前
記不活性成分を溶かし込んだ粘性の高い溶液を結合液と
して使用するか、もしくは、前記可溶性食物繊維と前記
不活性成分の混合物を溶かし込んだ粘性の高い溶液を結
合液として使用することによって、造粒工程の作業時間
の効率化を図ることができる。
The method for producing granules will be described below.
As a method of using the binder in the granulation step, a method of adding water or an aqueous ethanol solution as a binding solution to a powder active ingredient, or the soluble dietary fiber as required, or a mixture to which the calcium material is added, is used. is there. The ethanol concentration of the aqueous ethanol solution to be used can be adjusted by the hygroscopicity of each powder, the average particle size, the bulk specific gravity and the like. If necessary, a highly viscous solution containing the soluble dietary fiber is used as a binding solution, a highly viscous solution containing the inactive ingredient is used as a binding solution, or the soluble food is used. By using a highly viscous solution in which a mixture of the fiber and the above-mentioned inactive component is dissolved as the binding solution, the working time of the granulation step can be made efficient.

【0025】造粒方法としては、湿式造粒法が適当で、
具体的には流動層造粒法、攪拌造粒法、押し出し造粒
法、破砕造粒法、転動造粒法等が有効である。流動層造
粒法では、流動層造粒装置の中で、流動化された粉体に
結合液を噴霧して造粒する。攪拌造粒法では、結合液を
添加しながら、混合槽内で攪拌羽を高速度で回転させる
ことにより、粉体の混合、練合、造粒が密閉構造の中で
同時に行われる。押し出し造粒法では、結合液の添加に
よって練合された湿潤塊をスクリュー式やバスケット式
等の方法で、適当な大きさのスクリーンから強制的に押
し出すことによって造粒する。破砕造粒法では、結合液
の添加によって練合された湿潤塊を造粒機の回転刃でせ
ん断、摩砕し、その遠心力によって外周のスクリーンか
らはじき出すことにより造粒する。転動造粒法では、回
転するローターの遠心力によって外壁部に寄せられた原
料粉体が、スリットから吹き上げられる空気によって転
動し、この時スプレーガンから噴霧される結合液によっ
て、雪だるま式に粒径の均一な球形顆粒を成長させてい
くことにより造粒する。
As a granulation method, a wet granulation method is suitable,
Specifically, the fluidized bed granulation method, the stirring granulation method, the extrusion granulation method, the crushing granulation method, the rolling granulation method and the like are effective. In the fluidized bed granulation method, the fluidized powder is granulated by spraying the binding liquid onto the fluidized powder in a fluidized bed granulator. In the stirring granulation method, powder is mixed, kneaded and granulated simultaneously in a closed structure by rotating a stirring blade at a high speed in a mixing tank while adding a binding solution. In the extrusion granulation method, the wet mass kneaded by adding the binding solution is forcedly extruded from a screen of an appropriate size by a screw type or basket type method to perform granulation. In the crushing and granulating method, the wet mass kneaded by adding the binding solution is sheared and ground by a rotary blade of a granulator, and the centrifugal force ejects it from the outer peripheral screen for granulation. In the rolling granulation method, the raw material powder that has been drawn to the outer wall by the centrifugal force of the rotating rotor rolls by the air blown up from the slit, and at this time the binding liquid sprayed from the spray gun creates a snowball type. Granulation is performed by growing spherical granules having a uniform particle size.

【0026】造粒物の乾燥方法は、熱風加熱型(棚乾
燥、真空棚乾燥、流動層乾燥)、伝導伝熱型(平鍋型・
棚段箱型、ドラム型等)や凍結乾燥の様ないずれの方法
も使用することができる。熱風加熱型では、材料と熱風
を直接接触させ、同時に蒸発水分を持ち去らせる。伝導
伝熱型では、伝熱壁を通して材料を間接的に加熱させ
る。凍結乾燥では、材料を−10℃〜−40℃で凍結さ
せておき、次に高真空下(2〜0.1Torr)で加温する
ことによって、水を昇華させて除去する。
The granules can be dried by hot air heating type (shelf drying, vacuum shelf drying, fluidized bed drying), conduction heat transfer type (flat pan type,
Any method such as a shelf box type, a drum type) or freeze-drying can be used. In the hot air heating type, the material and hot air are brought into direct contact with each other, and at the same time, the evaporated water is removed. In the conductive heat transfer type, the material is indirectly heated through the heat transfer wall. In freeze-drying, the material is frozen at -10 ° C to -40 ° C and then warmed under high vacuum (2-0.1 Torr) to sublime and remove water.

【0027】本発明により得られる粉末含有錠剤は、粉
末活性成分を50重量%以上のように高含有させても、
適切な硬度となり、多量に含有させることが要求される
粉末活性成分の錠剤として適切である。ビール酵母粉末
等の成形性が非常に悪い物質を高含有させた錠剤に起こ
る、錠剤低硬度、錠剤の摩損、割れ、欠け等を防止する
ことができ、製品としての安定性に優れた錠剤が得られ
る。
The powder-containing tablet obtained according to the present invention contains the powdered active ingredient as high as 50% by weight or more,
It is suitable as a tablet of a powdered active ingredient which has an appropriate hardness and is required to be contained in a large amount. It is possible to prevent tablet low hardness, tablet abrasion, cracking, chipping, etc. that occur in tablets containing a substance with extremely poor moldability such as brewer's yeast powder, and a tablet with excellent stability as a product can get.

【0028】以下に本発明の実施例を示すが、本発明は
これらのみに限定されるものではない。
Examples of the present invention will be shown below, but the present invention is not limited thereto.

【0029】[実施例1]ビール酵母粉末4.50kg
及びグアーガム0.25kgを流動層造粒機(パウレッ
ク社製)に投入し、流動させながら水2.00kgを噴
霧した後、乾燥減量が5%以下になるように80℃にて
20〜30分間の乾燥を行った。乾燥後、結晶セルロー
ス0.25kgを混合し、篩(16メッシュ)で整粒し
た後、打錠を行った。(打錠機:ロータリー打錠機、回
転数:30回転、錠剤重量:300mg、打錠圧力:20
00kg)
Example 1 Beer yeast powder 4.50 kg
And 0.25 kg of guar gum were put into a fluidized bed granulator (manufactured by Paulec), and 2.00 kg of water was sprayed while flowing, and then the weight loss on drying was 5% or less at 80 ° C. for 20 to 30 minutes. Was dried. After drying, 0.25 kg of crystalline cellulose was mixed and sized with a sieve (16 mesh), followed by tableting. (Tabletting machine: rotary tableting machine, rotation speed: 30 rotations, tablet weight: 300 mg, tableting pressure: 20
00kg)

【0030】[実施例2]ビール酵母粉末4.50kg
を流動層造粒機(パウレック社製)に投入し、流動させ
ながら0.5%グアーガム水溶液2.00kgを噴霧し
た後、乾燥減量が5%以下になるように80℃にて20
〜30分間の乾燥を行った。乾燥後、結晶セルロース
0.49kgを混合し、篩(16メッシュ)で整粒した
後、打錠を行った。(打錠機:ロータリー打錠機、回転
数:30回転、錠剤重量:300mg、打錠圧力:200
0kg)
Example 2 Beer yeast powder 4.50 kg
Was poured into a fluidized bed granulator (manufactured by Powrex) and sprayed with 2.00 kg of a 0.5% guar gum aqueous solution while being fluidized, and then 20% at 20 ° C. so that the loss on drying was 5% or less.
Dry for -30 minutes. After drying, 0.49 kg of crystalline cellulose was mixed and sized with a sieve (16 mesh), followed by tableting. (Tabletting machine: rotary tableting machine, rotation speed: 30 rotations, tablet weight: 300 mg, tableting pressure: 200
0kg)

【0031】[実施例3]ビール酵母粉末4.50kg
を流動層造粒機(パウレック社製)に投入し、流動させ
ながら0.5%グアーガム水溶液2.00kgを噴霧し
た後、乾燥減量が5%以下になるように80℃にて20
〜30分間の乾燥を行った。乾燥後、卵殻カルシウム
0.49kgを混合し、篩(16メッシュ)で整粒した
後、打錠を行った。(打錠機:ロータリー打錠機、回転
数:30回転、錠剤重量:300mg、打錠圧力:200
0kg)
Example 3 Beer yeast powder 4.50 kg
Was poured into a fluidized bed granulator (manufactured by Powrex) and sprayed with 2.00 kg of a 0.5% guar gum aqueous solution while being fluidized, and then 20% at 20 ° C. so that the loss on drying was 5% or less.
Dry for -30 minutes. After drying, 0.49 kg of eggshell calcium was mixed, and the mixture was sized with a sieve (16 mesh) and then tableted. (Tabletting machine: rotary tableting machine, rotation speed: 30 rotations, tablet weight: 300 mg, tableting pressure: 200
0kg)

【0032】[比較例1]グアーガムの代わりにデキス
トリンを用いること以外は、実施例1と同様にして錠剤
を製造した。
Comparative Example 1 Tablets were produced in the same manner as in Example 1 except that dextrin was used instead of guar gum.

【0033】[比較例2]0.5%グアーガム水溶液の
代わりに、0.5%デキストリン水溶液を用いること以
外は、実施例2と同様にして錠剤を製造した。
Comparative Example 2 Tablets were produced in the same manner as in Example 2 except that 0.5% dextrin aqueous solution was used instead of 0.5% guar gum aqueous solution.

【0034】[比較例3]0.5%グアーガム水溶液の
代わりに、5.0%デキストリン水溶液を用いること以
外は、実施例2と同様にして錠剤を製造した。
[Comparative Example 3] Tablets were produced in the same manner as in Example 2 except that a 5.0% dextrin aqueous solution was used instead of the 0.5% guar gum aqueous solution.

【0035】上記実施例1、2、3、および比較例1、
2、3の錠剤をそれぞれ10錠とり、錠剤硬度を測定し
た。
Examples 1, 2, 3 and Comparative Example 1,
Ten tablets of a few tablets were taken and the tablet hardness was measured.

【0036】また、上記実施例1、2、3、および比較
例1、2、3の錠剤をそれぞれ20錠とり、錠剤摩損度
試験機に入れ、25rpmの回転速度で、10分間の摩
損度試験を行った。その結果を表1に示す。
Further, 20 tablets each of the above-mentioned Examples 1, 2 and 3 and Comparative Examples 1, 2 and 3 were taken and placed in a tablet friability tester and subjected to a friability test for 10 minutes at a rotation speed of 25 rpm. I went. The results are shown in Table 1.

【0037】[0037]

【表1】 [Table 1]

【0038】表1の通り、実施例1、実施例2、および
実施例3では、錠剤硬度が充分得られ、摩損度(初期重
量に対する減少質量の重量百分率)が低く、錠剤の割
れ、欠け等は認められなかった。
As shown in Table 1, in Examples 1, 2 and 3, sufficient tablet hardness was obtained, friability (weight percentage of the reduced mass relative to the initial weight) was low, and tablets were cracked or chipped. Was not recognized.

【0039】一方、比較例1、比較例2、および比較例
3においては、錠剤硬度は低く、摩損度は高かった。
On the other hand, in Comparative Example 1, Comparative Example 2 and Comparative Example 3, the tablet hardness was low and the friability was high.

【0040】[0040]

【発明の効果】本発明に依れば、例えばビール酵母粉末
のような成形性が非常に悪い物質を高含有させた錠剤に
起こる、錠剤低硬度、錠剤の摩損、割れ、欠け等を防止
することができ、製品としての安定性に優れた粉末高含
有錠剤を得ることができる。
EFFECTS OF THE INVENTION According to the present invention, it is possible to prevent low tablet hardness, tablet abrasion, cracking, chipping and the like which occur in tablets containing a high content of a substance having extremely poor moldability such as brewer's yeast powder. It is possible to obtain a powder-rich tablet having excellent stability as a product.

フロントページの続き Fターム(参考) 4B018 LE01 MD04 MD33 MD41 MD47 MD77 MD81 ME02 MF08 4B041 LD06 LE01 LH07 LH09 LH17 LK02 LK33 LK40 LK42 LP12 4B048 PE02 PE03 PN01 PN06 PS01 PS02 Continued front page    F term (reference) 4B018 LE01 MD04 MD33 MD41 MD47                       MD77 MD81 ME02 MF08                 4B041 LD06 LE01 LH07 LH09 LH17                       LK02 LK33 LK40 LK42 LP12                 4B048 PE02 PE03 PN01 PN06 PS01                       PS02

Claims (8)

【特許請求の範囲】[Claims] 【請求項1】 ビール酵母粉末、ミネラル酵母粉末、ヘ
ム鉄粉末、キトサン粉末、プロテイン粉末、ローヤルゼ
リー粉末、及び植物粉末からなる群から選択される1種
以上、並びに可溶性食物繊維を含むことを特徴とする粉
末含有錠剤。
1. A beer yeast powder, a mineral yeast powder, a heme iron powder, a chitosan powder, a protein powder, a royal jelly powder, and one or more kinds selected from the group consisting of a plant powder, and a soluble dietary fiber. Powder containing tablets.
【請求項2】 ビール酵母粉末、ミネラル酵母粉末、ヘ
ム鉄粉末、キトサン粉末、プロテイン粉末、ローヤルゼ
リー粉末、及び植物粉末からなる群から選択される1種
以上を50.00〜99.99質量部含むことを特徴と
する請求項1記載の粉末含有錠剤。
2. 50.00-99.99 parts by mass of at least one selected from the group consisting of beer yeast powder, mineral yeast powder, heme iron powder, chitosan powder, protein powder, royal jelly powder, and plant powder. The powder-containing tablet according to claim 1, wherein:
【請求項3】 可溶性食物繊維を0.01〜50.00
質量部含むことを特徴とする請求項1記載の粉末含有錠
剤。
3. Soluble dietary fiber 0.01 to 50.00
The powder-containing tablet according to claim 1, wherein the powder-containing tablet comprises a mass part.
【請求項4】 可溶性食物繊維水溶液を用いてビール酵
母粉末、ミネラル酵母粉末、ヘム鉄粉末、キトサン粉
末、プロテイン粉末、ローヤルゼリー粉末、及び植物粉
末からなる群から選択される1種以上を造粒し、打錠す
ることを特徴とする粉末含有錠剤の製造方法。
4. A beer yeast powder, a mineral yeast powder, a heme iron powder, a chitosan powder, a protein powder, a royal jelly powder, and one or more kinds selected from the group consisting of plant powders are granulated using an aqueous soluble dietary fiber solution. A method for producing a powder-containing tablet, which comprises tableting.
【請求項5】 ビール酵母粉末、ミネラル酵母粉末、ヘ
ム鉄粉末、キトサン粉末、プロテイン粉末、ローヤルゼ
リー粉末、及び植物粉末からなる群から選択される1種
以上、可溶性食物繊維、及びカルシウム素材を含むこと
を特徴とする粉末含有錠剤。
5. A beer yeast powder, a mineral yeast powder, a heme iron powder, a chitosan powder, a protein powder, a royal jelly powder, and one or more kinds selected from the group consisting of a plant powder, a soluble dietary fiber, and a calcium material. A powder-containing tablet characterized by:
【請求項6】 配合する可溶性食物繊維が0.01〜5
0.00質量部、カルシウム素材が0.10〜49.9
9質量部であることを特徴とする請求項5記載の粉末含
有錠剤。
6. The soluble dietary fiber blended is from 0.01 to 5
0.00 parts by mass, 0.10 to 49.9 of calcium material
The powder-containing tablet according to claim 5, which is 9 parts by mass.
【請求項7】 可溶性食物繊維水溶液を用いてビール酵
母粉末、ミネラル酵母粉末、ヘム鉄粉末、キトサン粉
末、プロテイン粉末、ローヤルゼリー粉末、及び植物粉
末からなる群から選択される1種以上を造粒し、カルシ
ウム素材を配合して打錠することを特徴とする粉末含有
錠剤の製造方法。
7. A soluble dietary fiber aqueous solution is used to granulate at least one selected from the group consisting of beer yeast powder, mineral yeast powder, heme iron powder, chitosan powder, protein powder, royal jelly powder, and plant powder. A method for producing a powder-containing tablet, which comprises blending a calcium material and tableting.
【請求項8】 請求項4、または7記載の製造方法によ
って得られる粉末含有錠剤。
8. A powder-containing tablet obtained by the method according to claim 4 or 7.
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CN114177206A (en) * 2021-12-09 2022-03-15 北京中蜜科技发展有限公司 Royal jelly core-spun tablet and preparation method thereof
CN114668055A (en) * 2022-04-12 2022-06-28 广州合和昌茶业科技有限公司 Auxiliary material composition for tea fermentation and fermentation method thereof

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CN114177206A (en) * 2021-12-09 2022-03-15 北京中蜜科技发展有限公司 Royal jelly core-spun tablet and preparation method thereof
CN114668055A (en) * 2022-04-12 2022-06-28 广州合和昌茶业科技有限公司 Auxiliary material composition for tea fermentation and fermentation method thereof

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