JP2612001B2 - Granules containing useful intestinal bacteria and method for producing the same - Google Patents

Granules containing useful intestinal bacteria and method for producing the same

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Publication number
JP2612001B2
JP2612001B2 JP62221756A JP22175687A JP2612001B2 JP 2612001 B2 JP2612001 B2 JP 2612001B2 JP 62221756 A JP62221756 A JP 62221756A JP 22175687 A JP22175687 A JP 22175687A JP 2612001 B2 JP2612001 B2 JP 2612001B2
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JP
Japan
Prior art keywords
bacteria
granules
useful
enteric bacteria
shellac
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 - Lifetime
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JP62221756A
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Japanese (ja)
Other versions
JPS6466124A (en
Inventor
誠一 梅田
泰弘 野口
正子 星野
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Freund Corp
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Freund Corp
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Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、健康食品あるいは医薬に適用して有効な腸
内有用細菌含有顆粒およびその製造方法に関するもので
ある。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a granule containing useful intestinal bacteria which is effective when applied to health foods or medicines, and a method for producing the same.

〔従来の技術〕[Conventional technology]

人間の腸内には多数の細菌類が常在しており、それら
の活動が人間の腸管内の物質の化学反応に関与し、腸の
機能、ひいては人間の健康状態に大きな影響を及ぼすこ
とはよく知られている。
Numerous bacteria are resident in the human intestine, and their activities are involved in the chemical reactions of substances in the human intestinal tract, and have a significant effect on intestinal function and, consequently, human health. well known.

これら細菌類のうち、ビヒダス菌や乳酸菌は、これら
自体は有害な作用を有せず、これらが腸内で繁殖すると
他の有害な作用を有する細菌類の繁殖が抑制され、この
有害細菌類が原因となる腸内異常醗酵などによる有害な
産生物の発生が防止されることから、健康の維持にとっ
て上記ビヒダス菌や乳酸菌を腸内に増殖させることが望
ましいこととされている。
Among these bacteria, bihidobacteria and lactic acid bacteria do not have a harmful effect by themselves, and when they proliferate in the intestine, the proliferation of other harmful bacteria is suppressed. Since the generation of harmful products due to abnormal intestinal fermentation or the like is prevented, it is considered that it is desirable to grow the above-mentioned bacteria and lactic acid bacteria in the intestine for maintaining health.

ところで、人間は、乳児期においては母乳からN−ア
セチルグルコサミンなどを主とするアミノ糖類、いわゆ
るビヒダス・ファクターと呼ばれる成分の供給を受けて
いるために腸内にビヒダス菌や乳酸菌が増殖され、腸内
細菌の90%以上がこれらの有用細菌で占められる結果、
腸内に極めて良好な細菌叢が形成されているといわれて
いる。
By the way, humans are supplied with amino sugars such as N-acetylglucosamine from mother's milk, a component called so-called behidas factor, during infancy. As a result, more than 90% of the endogenous bacteria are occupied by these useful bacteria,
It is said that extremely good bacterial flora is formed in the intestine.

ところが、成長して母乳を摂取しなくなるのに伴って
ビヒダス・ファクターの供給が減少すると、上記腸内有
用細菌が減少して細菌叢が劣化するため、腸内有用細菌
を経口投与することによって細菌叢を改善することが試
みられており、これを目的とする乳酸菌含有錠剤やビヒ
ダス菌含有飲食品などが市販されている。
However, when the supply of bihidas factor decreases with the growth and cessation of ingestion of breast milk, the useful intestinal bacteria decrease and the bacterial flora deteriorates. Attempts have been made to improve the flora, and tablets and lactic acid bacteria-containing tablets and foods and beverages containing bihidobacteria for the purpose are commercially available.

〔発明が解決しようとする問題点〕[Problems to be solved by the invention]

一般に、乳酸菌やビヒダス菌などの腸内有用細菌を錠
剤や飲食品などに含有させて経口投与すると、胃液によ
って相当量の生菌が死滅することから、有効量を確保す
るには生菌を高濃度に含有させる必要があり、例えば、
ビヒダス菌においては、1g中に1×1010個程度の生菌濃
度が必要になるとされている。
Generally, when useful enteric bacteria such as lactic acid bacteria and Viridus bacteria are orally administered in tablets and foods and drinks, a considerable amount of viable bacteria will be killed by gastric juice. Concentration must be included, for example,
It is said that a concentration of about 1 × 10 10 viable bacteria per gram is required for behydobacteria.

ところが、上記従来の乳酸菌錠剤やビヒダス菌含有飲
料品は、高濃度の生菌を安定に保存することが困難であ
るという欠点がある。
However, the conventional lactic acid bacterium tablets and behidas bacterium-containing beverages have a drawback that it is difficult to stably store high-concentration viable bacteria.

すなわち、錠剤の場合においては、錠剤化工程で強い
圧力や熱が加わるために、殆どの生菌が死滅してしまう
という問題がある。
That is, in the case of tablets, there is a problem that most viable bacteria are killed because strong pressure or heat is applied in the tableting process.

一方、水分を含む飲食品の場合には、水分によって飲
食品中の生菌が活動するために、栄養分がないと死滅し
てしまうという問題があり、これを防止するために生菌
の他に生菌の栄養分を配合した飲食品も提供されている
が、これによって飲食品中の生菌の濃度が低下してしま
うという問題や、生菌の活動により産生される乳酸など
によって生菌が死滅するなどの問題が生じ、いずれにし
ても、これらの飲食品中に高濃度の生菌を長期間保存さ
せるのは困難である。
On the other hand, in the case of foods and drinks containing water, the live bacteria in the food and drink are activated by the water, and there is a problem that they die when there is no nutrient. Foods and drinks containing nutrients of live bacteria are also provided, but this reduces the concentration of live bacteria in food and drink, and kills live bacteria due to lactic acid produced by the activity of live bacteria In any case, it is difficult to store a high concentration of viable bacteria in these foods and drinks for a long period of time.

さらに、腸内有用細菌を含有する固定状の食品とし
て、粉末状の食品や、いわゆるソフト顆粒と称される食
品が提供されているが、粉末状の食品は、その形状が食
品として不適当であり、気軽に食するには不便であると
いう欠点がある。
Further, powdered foods and foods called so-called soft granules are provided as fixed foods containing useful intestinal bacteria, but powdered foods are not suitable as foods. There is a disadvantage that it is inconvenient to eat casually.

また、ソフト顆粒は、顆粒状の呈味料などと粉末状の
菌とを混合したものであるが、生菌を高濃度に含有させ
ようとすれば必然的に粉末に近いものとなるため、上記
粉末状の食品と同様の欠点を有している。
In addition, soft granules are a mixture of powdered bacteria and a granular taste, etc., but if it is going to contain viable bacteria at a high concentration, it will inevitably be close to powder. It has the same disadvantages as the powdered food.

しかも、これらの固定状の食品は、いずれも製造工程
で圧力や熱を加えたり、結合剤の溶剤として水を使用し
たりするため、前記錠剤同様、生菌濃度が低下してしま
うという問題がある。
In addition, since these fixed foods are all subjected to pressure or heat during the manufacturing process, or water is used as a solvent for the binder, there is a problem that the concentration of viable bacteria is reduced as in the case of the tablets. is there.

このようにして、生菌を高濃度に保存することがで
き、しかも服用し易い腸内有用細菌含有製品は、未だ提
供されていないのが現状である。
In this way, a product containing useful intestinal bacteria that can store viable bacteria at a high concentration and is easy to take has not yet been provided.

本発明は、上記問題点に着目してなされたものであ
り、その目的は、健康食品あるいは医薬に用いて有効な
腸内有用細菌含有顆粒およびその製造方法を提供するこ
とにある。
The present invention has been made in view of the above problems, and an object of the present invention is to provide useful enteric bacteria-containing granules effective for use in health foods or medicines and a method for producing the same.

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

本発明による腸内有用細菌含有顆粒は、腸内有用細菌
またはこの腸内有用細菌を担持せしめた粉末をシェラッ
クを結合剤として造粒したものである。
The granules containing useful enteric bacteria according to the present invention are obtained by granulating useful enteric bacteria or a powder carrying the useful enteric bacteria using shellac as a binder.

本発明において利用しうる腸内有用細菌としては、B.
bifidum,B.longum,B.adolescentis,B.breve,B.infantis
などのビヒダス菌(Bifidobacterium);L.acidophilus,
L.lactis,L.casei,L.bulgaricusなどの乳酸稈菌(Lacto
bacillus);あるいはStreptococcus lactisなどを例示
することができる。
Examples of useful intestinal bacteria that can be used in the present invention include B.
bifidum, B.longum, B.adolescentis, B.breve, B.infantis
Bifidobacterium; L. acidophilus,
Lacto culm bacteria such as L.lactis, L.casei, L.bulgaricus (Lacto
bacillus); or Streptococcus lactis.

これらの細菌は、菌末として、あるいは脱脂粉乳、澱
粉などに担持せしめた粉末として用いられるが、顆粒中
に含有される細菌類は、一種類であっても多種類を混合
したものであってもよい。
These bacteria are used as fungal powder or powder supported on skim milk powder, starch, etc., and the bacteria contained in the granules may be one kind or a mixture of many kinds. Is also good.

上記細菌を含有する顆粒を造粒する際の結合剤として
シェラックを用いると、細菌の保存安定性が特異的に向
上することは、本発明者によって見出されたものであ
り、可食性結合剤として従来より使用されているゼイ
ン、シクロデキストリン、澱粉、フラクトオリゴ糖、キ
サンタンガム、ローカストビーンガムなどの天然ガムや
ポリ酢酸ビニル樹脂などを用いた場合には、理由は不明
であるが、腸内有用細菌の保存安定性は著しく低下す
る。
When shellac is used as a binder when granulating the above-mentioned bacteria-containing granules, the storage stability of the bacteria is specifically improved, which has been found by the present inventors, and is an edible binder. When using natural gums such as zein, cyclodextrin, starch, fructooligosaccharides, xanthan gum, locust bean gum, and polyvinyl acetate resin as conventionally used, the reason is unknown, but useful intestinal bacteria Storage stability is significantly reduced.

また、上記シェラックを結合剤として顆粒を造粒する
際、結合剤の溶液中に水分が含有されていると、細菌を
死滅させる原因となるが、本発明においては、シェラッ
クの無水エタノール溶液が使用されるため、細菌を死滅
させる虞れはない。
Further, when granules are granulated using the above shellac as a binder, if water is contained in a solution of the binder, the bacteria may be killed.In the present invention, an anhydrous ethanol solution of shellac is used. Therefore, there is no fear of killing the bacteria.

顆粒中に含有される細菌の濃度は、例えばビヒダス細
菌の場合、顆粒1g中に5×109個以上、好ましくは1010
個/g以上である。
The concentration of bacteria contained in the granules is, for example, 5 × 10 9 or more, preferably 10 10
Pcs / g or more.

造粒法としては、圧力や熱を過大に加えない方式を採
用する必要があり、具体的には、多孔円筒による押出造
粒法、転動造粒法あるいは流動造粒法などが好適であ
る。
As the granulation method, it is necessary to adopt a method that does not excessively apply pressure or heat, and specifically, an extrusion granulation method using a porous cylinder, a rolling granulation method, a fluidized granulation method, or the like is preferable. .

このようにして得られた腸内有用細菌含有顆粒は、造
粒時に殆ど圧力、熱および水分が加わらないため、高濃
度の生菌が含有され、しかも、シェラックを結合剤とす
ることにより、生菌の保存安定性が極めて良好となる。
The granules containing useful intestinal bacteria obtained in this way are hardly subjected to pressure, heat and moisture during granulation, so that they contain a high concentration of viable bacteria and, furthermore, use shellac as a binder to produce granules. The storage stability of the bacteria becomes extremely good.

また、顆粒中の細菌濃度が約1010個/g以下とならない
範囲で他の栄養剤、呈味料、香料、細菌の繁殖に有用な
成分などを添加してもよく、これにより、日常、気軽に
食することのできる健康食品として有用な腸内有用細菌
含有顆粒が得られる。
In addition, other nutrients, flavors, flavors, components useful for the propagation of bacteria and the like may be added as long as the bacterial concentration in the granules does not fall below about 10 10 cells / g. A useful intestinal bacteria-containing granule useful as a health food that can be easily eaten is obtained.

さらに、本発明の腸内有用細菌含有顆粒は、整腸剤あ
るいは下痢の治療などの医薬品としての利用も可能であ
り、例えば、上記製法によって得られた顆粒を流動コー
ティング装置に仕込み、セルロースアセテートフタレー
ト、ヒドロキシプロピルメチルセルロースフタレート、
カルボキシメチルエチルセルロースなどの腸溶性被膜を
顆粒の表面に被着して胃酸による生菌の死滅の防止を図
ることによって、腸内で有効に薬効を発揮する医薬品を
得ることができる。
Furthermore, the intestinal useful bacteria-containing granules of the present invention can also be used as pharmaceuticals such as intestinal medicine or diarrhea treatment.For example, the granules obtained by the above-mentioned production method are charged into a fluid coating apparatus, and cellulose acetate phthalate, hydroxy Propyl methylcellulose phthalate,
By applying an enteric coating such as carboxymethylethylcellulose on the surface of the granules to prevent the killing of viable bacteria by stomach acid, it is possible to obtain a drug that effectively exerts its medicinal effect in the intestine.

〔発明の効果〕〔The invention's effect〕

無水エタノールに溶解したシェラックを用いて造粒し
た本発明の腸内有用細菌含有顆粒中には、高濃度の生菌
が含有され、しかも、シェラックを結合剤とすることに
よって、生菌の保存安定性が極めて良好になっている。
The intestinal useful bacteria-containing granules of the present invention granulated using shellac dissolved in absolute ethanol contain a high concentration of viable bacteria, and furthermore, by using shellac as a binder, the storage stability of viable bacteria is improved. The properties are extremely good.

また、顆粒状に成形されていることから、気軽に服用
することができる。
In addition, since it is formed into granules, it can be easily taken.

従って、本発明の腸内有用細菌含有顆粒は、健康食品
あるいは医薬品として極めて有用であり、ビヒダス菌や
乳酸菌などの腸内有用細菌を腸内に増殖させて健康の維
持を図るという目的を遺憾なく発揮させることができ
る。
Therefore, the intestinal useful bacteria-containing granules of the present invention are extremely useful as health foods or pharmaceuticals, and the purpose of maintaining healthy by growing intestinal useful bacteria such as bihidobacteria and lactic acid bacteria in the intestine is unfortunately regrettable. Can be demonstrated.

以下、実施例により本発明を詳述するが、本発明は、
下記の実施例に限定されるものではない。
Hereinafter, the present invention will be described in detail with reference to examples,
The present invention is not limited to the following embodiment.

〔実施例1〕 市販のビヒダス菌末「ミルフリーズ」(商品名:日本
凍結乾燥研究所株式会社製)を用いた。また、シェラッ
クとして「A−30」(商品名:株式会社岐阜セラック製
造所製)を用い、シェラック濃度8%の無水エタノール
溶液を調整した。
[Example 1] Commercially available Vihidas powder "Mill Freeze" (trade name: manufactured by Japan Freeze Drying Laboratory Co., Ltd.) was used. Moreover, "A-30" (trade name: manufactured by Gifu Shellac Mfg. Co., Ltd.) was used as shellac, and an anhydrous ethanol solution having a shellac concentration of 8% was prepared.

上記「ミルフリーズ」100gにシェラックの無水エタノ
ール溶液10mlを加え、円筒型押出造粒機(孔径24メッシ
ュ)を用いて造粒し、次いで直ちに流動層乾燥機「FL−
MINI」(商品名:フロイント産業株式会社製)により、
常温で20分間乾燥して良好な顆粒を得た。
10 ml of an anhydrous ethanol solution of shellac was added to 100 g of the above “Mill Freeze” and granulated using a cylindrical extrusion granulator (pore size: 24 mesh).
MINI "(trade name: manufactured by Freund Corporation)
Drying was performed at room temperature for 20 minutes to obtain good granules.

上記配合比から計算した顆粒1g中の生菌数と造粒直後
の顆粒を分析して実測した生菌数とを下記の表−1に示
す。また、得られた顆粒を2gずつ密封状態に分包して35
℃の室内に放置したときの生菌数(実測値)の経時変化
を併せて表−1に示す。
The number of viable bacteria in 1 g of granules calculated from the above mixing ratio and the number of viable bacteria actually measured by analyzing the granules immediately after granulation are shown in Table 1 below. In addition, the obtained granules are packaged in a sealed state by 2 g each, and
Table 1 also shows the time-dependent changes in the number of viable bacteria (actually measured values) when left in a room at ℃.

〔実施例2〕 シェラック濃度8%の無水エタノール溶液に代えてシ
ェラック濃度8%の80%エタノール溶液を用いた他は、
前記実施例1と同様の方法で造粒して顆粒を得た。
[Example 2] An 80% ethanol solution having a shellac concentration of 8% was used instead of the anhydrous ethanol solution having a shellac concentration of 8%.
Granulation was performed in the same manner as in Example 1 to obtain granules.

上記配合比から計算した顆粒1g中の生菌数と造粒直後
の顆粒を分析して実測した生菌数とを下記の表−1に示
す。また、得られた顆粒を2gずつ密封状態に分包して35
℃の室内に放置したときの生菌数(実測値)の経時変化
を併せて表−1に示す。
The number of viable bacteria in 1 g of granules calculated from the above mixing ratio and the number of viable bacteria actually measured by analyzing the granules immediately after granulation are shown in Table 1 below. In addition, the obtained granules are packaged in a sealed state by 2 g each, and
Table 1 also shows the time-dependent changes in the number of viable bacteria (actually measured values) when left in a room at ℃.

〔比較例〕 結合剤および溶媒を代えた以外は、前記実施例1と同
様の方法で造粒して得た顆粒1g中の生菌数と、造粒直後
の顆粒を分析して実測した生菌数とを下記の表−2に示
す。また、得られた顆粒を2gずつ密封状態に分包して35
℃の室内に放置したときの生菌数(実測値)の経時変化
を併せて表−2に示す。
[Comparative Example] The viable cell count in 1 g of granules obtained by granulating in the same manner as in Example 1 except that the binder and the solvent were changed, and the granules obtained by analyzing the granules immediately after granulation were measured. The number of bacteria is shown in Table 2 below. In addition, the obtained granules are packaged in a sealed state by 2 g each, and
Table 2 also shows the time-dependent changes in the number of viable bacteria (actually measured values) when left in a room at ℃.

〔実施例3〕 前記ビヒダス菌末「ミルフリーズ」9重量部に対し、
スキムミルク1重量部/ワックス・コーテッドL−アス
コルビン酸0.2重量部/ショ糖末2重量部/シテビア0.0
2重量部からなる呈味料1重量部を混合した分末を用い
た他は、前記実施例1と同様の方法で造粒して良好な顆
粒を得た。
[Example 3] With respect to 9 parts by weight of the Bididas bacterial powder "Mill Freeze",
Skim milk 1 part by weight / Wax coated L-ascorbic acid 0.2 part by weight / Sucrose powder 2 parts by weight / Sitevia 0.0
Good granules were obtained by granulating in the same manner as in Example 1 except that a powder obtained by mixing 1 part by weight of a flavorant consisting of 2 parts by weight was used.

上記配合比から計算した顆粒1g中の生菌数と造粒直後
の顆粒を分析して実測した生菌数とを下記の表−3に示
す。また、得られた顆粒を2gずつ密封状態に分包して25
℃および35℃の室内に放置したときの生菌数(実測値)
の経時変化を併せて表−3に示す。
Table 3 below shows the viable cell count in 1 g of the granules calculated from the above mixing ratio and the viable cell count actually measured by analyzing the granules immediately after granulation. In addition, the obtained granules are divided into 2 g each in a sealed state,
Viable cell count when left indoors at ℃ and 35 ℃ (actual measurement)
Table 3 also shows the change with time.

〔実施例4〕 市販の乳酸菌末(L.bulgaricus)20gにシェラック
(「A−30」)濃度8%の無水エタノール溶液2mlを加
え、前記円筒型押出造粒機(孔径24メッシュ)を用いて
造粒し、直ちに常温で16時間減圧乾燥して良好な顆粒を
得た。
Example 4 To 20 g of commercially available lactic acid bacterium powder (L. bulgaricus), 2 ml of an anhydrous ethanol solution having a shellac (“A-30”) concentration of 8% was added, and the above-mentioned cylindrical extrusion granulator (pore size: 24 mesh) was used. It was granulated and immediately dried under reduced pressure at room temperature for 16 hours to obtain good granules.

上記配合比から計算した顆粒1g中の生菌数と造粒直後
の顆粒を分析して実測した生菌数とを下記の表−4に示
す。また、得られた顆粒を2gずつ密封状態に分包して25
℃および35℃の室内に放置したときの生菌数(実測値)
の経時変化を併せて表−4に示す。
The number of viable bacteria in 1 g of granules calculated from the above mixing ratio and the number of viable bacteria measured by analyzing the granules immediately after granulation are shown in Table 4 below. In addition, the obtained granules are divided into 2 g each in a sealed state,
Viable cell count when left indoors at ℃ and 35 ℃ (actual measurement)
Table 4 also shows the time-dependent changes of.

〔実施例5〕 前記実施例1で用いたビヒダス菌末「ミルフリーズ」
150gを流動層造粒装置「FL−MINI」(商品名:フロイン
ト産業株式会社製)に仕込み、常温で流動させながらシ
ェラック(「A−30」)濃度15%の無水エタノール溶液
56mlを噴霧させつつ、造粒・乾燥して良好な顆粒を得
た。
Example 5 Bifidobacterium powder "Mill Freeze" used in Example 1
150 g of the fluidized-bed granulator “FL-MINI” (trade name: manufactured by Freund Corporation) is charged with an anhydrous ethanol solution having a shellac (“A-30”) concentration of 15% while flowing at room temperature.
While spraying 56 ml, the mixture was granulated and dried to obtain good granules.

上記配合比から計算した顆粒1g中の生菌数と造粒直後
の顆粒を分析して実測した生菌数とを下記の表−5に示
す。また、得られた顆粒を2gずつ密封状態に分包して25
℃および35℃の室内に配置したときの生菌数(実測値)
の経時変化を併せて表−5に示す。
The number of viable bacteria in 1 g of granules calculated from the above mixing ratio and the number of viable bacteria actually measured by analyzing the granules immediately after granulation are shown in Table 5 below. In addition, the obtained granules are divided into 2 g each in a sealed state,
Viable cell count when placed in a room at ℃ and 35 ℃ (actual measurement)
Table 5 also shows the time-dependent changes of.

以上のように、各実施例1〜5の腸内有用細菌含有顆
粒は、高濃度の生菌が含有され、しかも、生菌の保存安
定性が極めて良好であることが判明した。
As described above, it was found that the intestinal useful bacteria-containing granules of Examples 1 to 5 contained a high concentration of viable bacteria, and also had extremely good storage stability of viable bacteria.

Claims (5)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】腸内有用細菌または前記腸内有用細菌を担
持せしめた粉末をシェラックを結合剤として造粒してな
る腸内有用細菌含有顆粒。
1. Granules containing useful enteric bacteria, which are obtained by granulating useful enteric bacteria or a powder carrying said useful enteric bacteria using shellac as a binder.
【請求項2】腸内有用細菌がビヒダス菌であることを特
徴とする特許請求の範囲第1項記載の腸内有用細菌含有
顆粒。
2. The granule containing useful enteric bacteria according to claim 1, wherein the useful enteric bacteria is a bihidobacterium.
【請求項3】顆粒1g中にほぼ1×1010個のビヒダス菌を
含有せしめたことを特徴とする特許請求の範囲第2項記
載の腸内有用細菌含有顆粒。
3. The granule containing useful enteric bacteria according to claim 2, wherein 1 g of the granule contains approximately 1 × 10 10 viridus bacteria.
【請求項4】腸内有用細菌または前記腸内有用細菌を担
持せしめた粉末を造粒して顆粒を得るに際し、シェラッ
クの無水エタノール溶液を用いて造粒することを特徴と
する腸内有用細菌含有顆粒の製造方法。
4. An intestinal useful bacterium characterized in that granules are obtained by using an anhydrous ethanol solution of shellac when granulating the useful enteric bacteria or the powder carrying the useful enteric bacteria to obtain granules. Production method of contained granules.
【請求項5】押出造粒法、転動造粒法または流動造粒法
によって造粒することを特徴とする特許請求の範囲第4
項記載の腸内有用細菌含有顆粒の製造方法。
5. The method according to claim 4, wherein the granulation is performed by an extrusion granulation method, a tumbling granulation method or a fluidized granulation method.
The method for producing intestinal useful bacteria-containing granules according to the above item.
JP62221756A 1987-09-04 1987-09-04 Granules containing useful intestinal bacteria and method for producing the same Expired - Lifetime JP2612001B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP62221756A JP2612001B2 (en) 1987-09-04 1987-09-04 Granules containing useful intestinal bacteria and method for producing the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP62221756A JP2612001B2 (en) 1987-09-04 1987-09-04 Granules containing useful intestinal bacteria and method for producing the same

Publications (2)

Publication Number Publication Date
JPS6466124A JPS6466124A (en) 1989-03-13
JP2612001B2 true JP2612001B2 (en) 1997-05-21

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ID=16771713

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Application Number Title Priority Date Filing Date
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Country Link
JP (1) JP2612001B2 (en)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SE465206B (en) * 1989-12-22 1991-08-12 Eva Grahn PHARMACEUTICAL PREPARATION FOR COMBATING PATHOGENIC BACKGROUND
IT1254210B (en) * 1992-02-10 1995-09-14 Simone Claudio De DIETARY AND / OR PHARMACEUTICAL COMPOSITIONS BASED ON LYOPHILIZED LACTIC BACTERIA, THEIR PREPARATION AND USE
AT405235B (en) * 1995-11-02 1999-06-25 Helmut Dr Viernstein PROBIOTALLY EFFECTIVE FORMULATION
DE19826928A1 (en) * 1998-06-17 1999-12-23 Novartis Consumer Health Gmbh Medicines containing viable anaerobic bacteria that inhibit sulfate reduction by sulfate-reducing bacteria
EP1344458A1 (en) * 2002-03-12 2003-09-17 Société des Produits Nestlé S.A. Probiotic delivery system
WO2008035332A1 (en) * 2006-09-19 2008-03-27 Technion Research And Development Foundation Ltd. Probiotic compositions and methods of making same
CN112839527A (en) * 2018-10-05 2021-05-25 好侍健康食品株式会社 Method for producing plant extract-containing particles, method for suppressing generation of fine powder from plant extract-containing particles, and method for suppressing unpleasant taste of plant extract-containing particles

Also Published As

Publication number Publication date
JPS6466124A (en) 1989-03-13

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