JP3345312B2 - Granular raffinose - Google Patents

Granular raffinose

Info

Publication number
JP3345312B2
JP3345312B2 JP23186797A JP23186797A JP3345312B2 JP 3345312 B2 JP3345312 B2 JP 3345312B2 JP 23186797 A JP23186797 A JP 23186797A JP 23186797 A JP23186797 A JP 23186797A JP 3345312 B2 JP3345312 B2 JP 3345312B2
Authority
JP
Japan
Prior art keywords
raffinose
granular
sweetness
crystals
mouth
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
JP23186797A
Other languages
Japanese (ja)
Other versions
JPH1156292A (en
Inventor
泰三 名倉
勉 有塚
要 鳥山
司 恵本
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.)
Nippon Beet Sugar Manufacturing Co Ltd
Original Assignee
Nippon Beet Sugar Manufacturing Co Ltd
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Filing date
Publication date
Application filed by Nippon Beet Sugar Manufacturing Co Ltd filed Critical Nippon Beet Sugar Manufacturing Co Ltd
Priority to JP23186797A priority Critical patent/JP3345312B2/en
Publication of JPH1156292A publication Critical patent/JPH1156292A/en
Application granted granted Critical
Publication of JP3345312B2 publication Critical patent/JP3345312B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、顆粒状ラフィノー
スの製造及びその利用に関するものである。
The present invention relates to the production of granular raffinose and its use.

【0002】[0002]

【従来の技術】ラフィノースは、ビフィズス因子や肝機
能改善作用等のすぐれた生理活性作用を有する機能性オ
リゴ糖であって、最近になって工業的製造が開始される
ようになった。しかしながら、結晶ラフィノースは、溶
解度が低く、針状結晶であるため、これを経口摂取する
際、口中で結晶が残留して、口溶け、食感が悪く、乳幼
児や高齢者、病弱者はもとより、成人にあっても摂取し
にくいものであり、この欠点は、ラフィノース単独の場
合はもちろんのこと、他の食品と混合した場合にも認め
られ、当業界においては、その改善が強く希求されてい
る。
2. Description of the Related Art Raffinose is a functional oligosaccharide having an excellent physiological activity such as a bifidobacterium and liver function-improving activity, and its industrial production has recently started. However, since crystalline raffinose has low solubility and is a needle-shaped crystal, when it is taken orally, the crystal remains in the mouth, dissolves in the mouth, has a poor texture, and is suitable for adults as well as infants, the elderly, and the sick. However, this disadvantage is recognized not only when raffinose is used alone, but also when it is mixed with other foods, and the improvement is strongly demanded in the art.

【0003】[0003]

【発明が解決しようとする課題】ラフィノースは機能性
オリゴ糖として非常に有用な天然物であるにもかかわら
ず、上記したような欠点を有し、可食性の面で問題があ
る点に鑑み、本発明者らは、ラフィノースの経口摂取を
容易ならしめる必要性をはじめて認識し、経口摂取しや
すいラフィノース製品を開発することとした。
In view of the fact that raffinose is a natural product that is very useful as a functional oligosaccharide, it has the disadvantages described above and has a problem in terms of edibility. The present inventors have recognized for the first time the need to facilitate oral ingestion of raffinose and have decided to develop a raffinose product that is easy to ingest.

【0004】[0004]

【課題を解決するための手段】本発明は、上記した性質
を有するラフィノース製品を新たに開発する目的でなさ
れたものであって、代表的な糖であるスクロースについ
て、結晶スクロースと顆粒スクロースとでは単位時間当
りの溶解量(以下、溶解量と記す)に格別の相違がない
ことが当然に予想され、そして後記するところからも明
らかなように(図1参照)、実際の溶解量測定の結果、
予想どおり結晶と顆粒とでは溶解量に格別の相違が認め
られない。
DISCLOSURE OF THE INVENTION The present invention has been made for the purpose of newly developing a raffinose product having the above-mentioned properties. A typical sugar, sucrose, is composed of crystalline sucrose and granular sucrose. It is naturally expected that there is no significant difference in the amount of dissolution per unit time (hereinafter referred to as the amount of dissolution), and as will be apparent from the following description (see FIG. 1), the results of the actual measurement of the amount of dissolution ,
As expected, there is no particular difference in the amount of dissolution between the crystals and the granules.

【0005】したがって、ラフィノースについても、結
晶と顆粒との間で溶解量に格別の相違がないものと予想
されるところ、本発明者らは、あえてこのような予想に
対して、結晶ラフィノースと顆粒ラフィノースの溶解量
を測定したところ、全く予期せざることに、予想とは全
く逆に結晶と顆粒とでは溶解量に大きな相違があり、し
かも結晶に比して顆粒の方が著しく溶解量が高いという
きわめて有用な新知見を得た。
Therefore, it is expected that there is no particular difference in the amount of raffinose dissolved between the crystal and the granules. When the amount of raffinose dissolved was measured, there was a large difference in the amount of dissolution between crystals and granules, which was quite unexpectedly unexpected, and the amount of dissolution was significantly higher in granules than in crystals. That is a very useful new finding.

【0006】そこで本発明者らは、顆粒状ラフィノース
にはじめて着目し、各方面からその性質を検討した結
果、結晶ラフィノースに比して、口溶け、甘味の切れが
向上して食感が著しく改善され、また甘味度も増強され
るという、特に経口摂取する際に有用な諸性質が得られ
ることも実際に併せ確認し、遂に本発明を完成するに至
った。
Accordingly, the present inventors have paid attention to granular raffinose for the first time, and examined the properties of the raffinose from various directions. As a result, compared with crystalline raffinose, the mouth melting and sweetness were improved and the texture was significantly improved. In addition, the inventors have also confirmed that various properties useful especially when taken orally can be obtained, that is, the sweetness is also enhanced, and finally completed the present invention.

【0007】すなわち本発明は顆粒状ラフィノースの創
製にはじめて成功したものであって、可食性にすぐれ、
特に経口摂取するのに好適なラフィノース、及び、それ
を用いた錠剤等の製剤をはじめて提供するものであっ
て、ラフィノースが有する生理活性を多くの人々が利用
できることを可能にしたものである。以下、本発明につ
いて詳述する。
That is, the present invention has been successful for the first time in the production of granular raffinose, and is excellent in edibility.
In particular, the present invention provides, for the first time, raffinose suitable for oral ingestion and a preparation such as a tablet using the same, which enables many people to utilize the physiological activity of raffinose. Hereinafter, the present invention will be described in detail.

【0008】本発明を実施するには、ラフィノースを顆
粒化処理する必要があるが、顆粒化処理としては、湿式
造粒法と乾式造粒法のいずれもが使用可能である。
In order to carry out the present invention, it is necessary to subject raffinose to a granulation treatment. As the granulation treatment, any of a wet granulation method and a dry granulation method can be used.

【0009】湿式造粒法は、ラフィノースの結晶(無水
結晶でもよいし、一水塩〜五水塩等の含水結晶のいずれ
でもよいが、五水塩が最も安定しており、工業的には五
水塩を使用するのが有利である。)を粉末化し、粉末粒
子を湿潤させて個々の粒子を相互に凝集させ、形状を大
きくする方法であって、例えば、次のような方法が例示
されるが、これらの内、工業的には押出し造粒法が好適
である。
In the wet granulation method, raffinose crystals (anhydrous crystals or hydrated crystals such as monohydrate to pentahydrate may be used, but pentahydrate is the most stable, and industrially, It is advantageous to use a pentahydrate salt), to wet the powder particles, to aggregate the individual particles with each other, and to enlarge the shape, for example, the following method is exemplified. Of these, the extrusion granulation method is industrially preferred.

【0010】・転動造粒法:傾斜ドラムまたは傾斜皿型
容器を回転し、その中に原料粉体と水とを連続的に供給
する造粒方法。 ・押出し造粒法:原材料に加水、加熱、捏和らの前工程
をおこなうことにより造粒に適した物性を与え、適当な
押出し機構によってスクリーン、ダイスの孔より材料を
押出し成形する方法。 ・破砕造粒状:原料粉体にやや多めの水分を添加して大
きい凝集体をつくらせ、これを高速回転羽根でせん断し
て球形または不規則状の顆粒にする方法。 ・攪拌造粒法:加湿した粉体に混合作用を与えて造粒す
る方法。
Rolling granulation method: A granulation method in which an inclined drum or an inclined dish type container is rotated, and raw material powder and water are continuously supplied therein. -Extrusion granulation method: A method in which physical properties suitable for granulation are given to raw materials by performing pre-processes such as water addition, heating, and kneading, and the material is extruded from a screen or a die hole by an appropriate extrusion mechanism. -Crushed granulation: A method in which a relatively large amount of water is added to the raw material powder to form large agglomerates, which are sheared by high-speed rotating blades into spherical or irregular granules. Agitation granulation method: A method of granulating a humidified powder by giving a mixing action.

【0011】また、ラフィノース結晶を溶液となし、こ
れを顆粒状にしてもよく、例えば、次のような方法が例
示されるが、これらの内、工業的には噴霧造粒法が好適
である。 ・流動乾燥型:結晶を熱風によって流動状態におき、同
じ物質の水溶液を流動層内に噴霧して結晶表面を被覆す
るとともに、水分を蒸発させて結晶の粒度を増大させる
方法。 ・噴霧造粒法:向流または並流気流中に液状材料を噴霧
して、液滴と気流との間の熱と物質の移動によって球状
の粒子を得る方法。なおこの場合、ラフィノース溶液と
しては、各種濃度の水溶液が適宜利用可能であるが、可
能な限り濃厚な液を使用するのがよく、工業的には飽和
溶液を使用するのが好適である。
The raffinose crystals may be formed into a solution and formed into granules. For example, the following methods are exemplified. Among them, the spray granulation method is industrially preferable. . Fluid drying type: A method in which crystals are placed in a fluidized state by hot air, an aqueous solution of the same substance is sprayed into a fluidized bed to coat the crystal surface, and water is evaporated to increase the crystal grain size. -Spray granulation method: A method in which a liquid material is sprayed in a countercurrent or cocurrent stream to obtain spherical particles by transferring heat and substances between the droplets and the stream. In this case, as the raffinose solution, aqueous solutions having various concentrations can be appropriately used. However, it is preferable to use a solution as thick as possible, and it is preferable to use a saturated solution industrially.

【0012】また、上記した湿式造粒法のほか、乾式造
粒法も使用可能であって、例えばラフィノースを高圧ロ
ーラーで圧延して成型した後、粗砕して整粒する方法
や、ラフィノースを粉末化しこれを型に入れて打錠した
りする方法が適宜使用可能である。
In addition to the above-mentioned wet granulation method, a dry granulation method can also be used. For example, a method of rolling and molding raffinose with a high-pressure roller and then coarsely crushing and sizing the raffinose, A method of pulverizing the powder, putting it in a mold, and tableting can be used as appropriate.

【0013】このようにして製造した顆粒状ラフィノー
スは、口溶け、食感、甘味度、甘味の切れが結晶ラフィ
ノースよりは大幅に向上しており、これを口中に入れて
もザラザラした食感がなく、しかも甘味度は上昇し、そ
れでいて後味はサッパリしており、経口摂取するのにき
わめて適している。
[0013] The granular raffinose produced in this way has much improved melting, mouthfeel, sweetness, and sweetness crispness than crystalline raffinose, and it does not have a rough texture even when it is put in the mouth. Moreover, the sweetness is increased and the aftertaste is refreshing, making it very suitable for oral consumption.

【0014】したがって、顆粒状ラフィノースは、それ
自体で機能性オリゴ糖として、直接あるいは他の飲食品
に添加して、乳幼児、高齢者、病中や病後の患者、はも
とより、健常者においても保健用に適宜経口摂取するこ
とができる。
[0014] Therefore, granular raffinose can be used as a functional oligosaccharide by itself or directly added to other foods and drinks to be used in healthy children as well as infants, the elderly, sick and post-sick patients. It can be taken orally as needed.

【0015】また更に、本発明に係る顆粒状ラフィノー
スは、必要な添加料を加え、打錠して錠剤の形態に製剤
することも可能である。あるいは、必要な添加料を加え
て混合し、カプセル等の容器に充填して製剤することも
可能である。
Further, the granular raffinose according to the present invention can be formulated into tablets by adding necessary additives and tableting. Alternatively, it is also possible to add a necessary additive, mix and fill the mixture into a container such as a capsule to prepare a preparation.

【0016】製剤化に当っては、主薬である顆粒状ラフ
ィノースに必要あれば添加料を加えた後、賦形剤、結合
剤、崩壊剤、滑沢剤、矯味矯臭剤、溶解補助剤、懸濁
剤、コーティング剤などの錠剤やカプセル剤の製剤技術
分野において通常使用される既知の補助剤を用いて製剤
化すればよい。
In the preparation of pharmaceutical preparations, after adding additives as needed to granular raffinose as the main drug, excipients, binders, disintegrants, lubricants, flavoring agents, solubilizing agents, suspensions The preparation may be carried out using known auxiliaries usually used in the technical field of tablet or capsule preparation such as turbidity agents and coating agents.

【0017】打錠に加工するには、湿式顆粒圧縮法、乾
式顆粒圧縮法、直接粉末圧縮法等一般の打錠技術が適宜
使用可能であるが、ラフィノースについては本発明によ
ってはじめてその顆粒化技術が確立されたため、前二者
の打錠技術の利用が可能となった。その内、特に湿式顆
粒圧縮法によるタブレットは、その強度がすぐれてい
る。
For processing into tablets, general tableting techniques such as wet granulation, dry granulation, and direct powder compression can be used as appropriate. For raffinose, the granulation technique for the first time according to the present invention is used. As a result, the use of the former two tableting technologies became possible. Among them, the tablet obtained by the wet granule compression method is particularly excellent in strength.

【0018】添加料としては、ビタミンC等のビタミン
類;カルシウム等のミネラル類;グルコース、ラクトー
ス、マルトース、シュークロース、ステビア等の甘味
料;マルチトール等の糖アルコール;クエン酸等の酸味
料;各種オリゴ糖;乳製品;その他の食品添加物が適宜
使用される。
As additives, vitamins such as vitamin C; minerals such as calcium; sweeteners such as glucose, lactose, maltose, sucrose, stevia; sugar alcohols such as maltitol; acidulants such as citric acid; Various oligosaccharides; dairy products; and other food additives are appropriately used.

【0019】ラフィノース錠剤やカプセル剤の製造にお
いて、顆粒状ラフィノースの含有量については、その使
用目的や使用者の年齢等によって左右され、厳密に規定
されるものではないが、顆粒状ラフィノース50%以
上、添加料50%未満1%以上とするのが好適である。
以下、本発明の実施例について述べる。
In the production of raffinose tablets and capsules, the content of granular raffinose depends on the purpose of use, age of the user, etc. and is not strictly specified, but is not limited to 50% or more of granular raffinose. It is preferable that the additive be less than 50% and 1% or more.
Hereinafter, examples of the present invention will be described.

【0020】[0020]

【実施例1】ラフィノース結晶を乳鉢で微粉砕した後、
ラフィノース100に対して水10を加え、均一に混合
した。これを押出し造粒機(不二パウダル(株)製、FI
NERYUZER 型式EXR-60、処理能力40-150kg/hr)にて粒
造し、70℃の送風定温恒温機(ヤマト科学(株)型式
DN910)で3時間乾燥し、顆粒状ラフィノースを製造し
た。
Example 1 After raffinose crystals were pulverized in a mortar,
Water 10 was added to raffinose 100 and mixed uniformly. This was extruded by a granulator (Fuji Paudal Co., Ltd., FI
NERYUZER Model EXR-60, processing capacity 40-150kg / hr), granulated, 70 ° C blast constant temperature thermostat (Yamato Scientific Co., Ltd. model)
DN910) for 3 hours to produce granular raffinose.

【0021】結晶ラフィノースと微粉砕ラフィノース、
顆粒状ラフィノースの官能試験を実施した。得られた結
果を下記表1に示した。表1に示すように、微粉砕ラフ
ィノースは結晶ラフィノースより甘味が強くなり、口溶
けや甘味の切れが向上し、総合的に好ましいという結果
が得られた。さらに顆粒状ラフィノースでは微粉砕ラフ
ィノースに対して甘味の強さは変わらないものの、口溶
けや甘味の切れが向上し、総合評価も高かった。
Crystalline raffinose and finely ground raffinose,
A sensory test of granular raffinose was performed. The results obtained are shown in Table 1 below. As shown in Table 1, the sweetness of the finely ground raffinose was stronger than that of the crystalline raffinose, the melting in the mouth and the cut of sweetness were improved, and the overall favorable results were obtained. Further, the granular raffinose did not change the sweetness intensity compared to the finely ground raffinose, but improved melting in the mouth and sweetness, and the overall evaluation was also high.

【0022】[0022]

【表1】 [Table 1]

【0023】以上のことから、口溶け感や甘味のきれな
ど、食味や食感において敬遠される面があった針状結晶
ラフィノースは、微粉砕後、更に顆粒化することで、こ
れらの点を改善することができた。
From the above, needle-like crystalline raffinose, which had a surface that was avoided in terms of taste and texture, such as a feeling of melting in the mouth and a lack of sweetness, was improved by pulverization and further granulation to improve these points. We were able to.

【0024】[0024]

【実施例2】結晶および顆粒状に加工したラフィノース
とスクロースの経時的な溶解量を比較した。37℃に調
整された振とう恒温槽に100gの脱塩水を入れた50
0ml容三角フラスコをセットし、37℃に馴化させた
後、糖50gを加え、150rpmで振とうした。経時
的に上清を採取し、直ちに0.45μmのメンブランフ
ィルターでろ過し、糖濃度を測定した。図1に示したよ
うに、スクロースは短時間でほぼ完全に溶解したが、結
晶ラフィノースは緩慢な溶解を示した。一方、顆粒状ラ
フィノースは、短時間で高い溶解量を示し、120秒後
にはほぼ飽和濃度に達していた。
Example 2 The amounts of raffinose and sucrose dissolved into crystals and granules processed over time were compared. 100 g of demineralized water was placed in a shaking thermostat adjusted to 37 ° C. 50
A 0 ml Erlenmeyer flask was set, and after acclimation to 37 ° C., 50 g of sugar was added, and the mixture was shaken at 150 rpm. The supernatant was collected over time, immediately filtered through a 0.45 μm membrane filter, and the sugar concentration was measured. As shown in FIG. 1, sucrose dissolved almost completely in a short time, but crystalline raffinose showed slow dissolution. On the other hand, granular raffinose showed a high amount of dissolution in a short time, and reached almost saturated concentration after 120 seconds.

【0025】[0025]

【実施例3】図2に示すフローチャートにしたがって、
ラフィノース錠剤を製造した。顆粒状ラフィノース70
重量部及びビタミンC30重量部を秤量し、充分に混合
した。バインダーとして0.3%グアーガム溶液を20
%(w/w)噴霧して、流動層造粒(商品名:フローコ
ーター FLO−120型使用)により造粒した。な
お、バインダーには1.5% β−カロチン末を溶解せ
しめておいた。
Embodiment 3 In accordance with the flowchart shown in FIG.
Raffinose tablets were produced. Granular raffinose 70
Parts by weight and 30 parts by weight of vitamin C were weighed and mixed well. 20% 0.3% guar gum solution as binder
% (W / w), and granulated by fluidized bed granulation (trade name: Flow Coater FLO-120 type). In addition, 1.5% β-carotene powder was dissolved in the binder.

【0026】これを水分6%以下にまで乾燥した後、円
型シフターでふるい分けした(16メッシュで篩過)。
次いで、コニカル型混合機を用い、香料、滑沢剤(ステ
アリン酸マグネシウム)を添加して二次混合を行った。
After this was dried to a water content of 6% or less, it was sieved with a circular shifter (sieved with 16 mesh).
Next, using a conical mixer, a fragrance and a lubricant (magnesium stearate) were added to perform secondary mixing.

【0027】打錠処理は、打錠機FY30(富士薬品機
械株式会社商品名)を用い(剤型18φ;充填量150
0mg;錠厚5.0±0.3mm;硬度7kg±3;水
分8%以下)、ラフィノース含有錠剤を製造した。
The tableting process was performed using a tableting machine FY30 (trade name of Fuji Pharmaceutical Machinery Co., Ltd.) (formulation 18φ; filling amount 150).
0 mg; tablet thickness 5.0 ± 0.3 mm; hardness 7 kg ± 3; moisture 8% or less), and a raffinose-containing tablet was produced.

【0028】[0028]

【実施例4】顆粒状ラフィノース400重量部、結晶グ
ルコース10重量部、クエン酸7重量部、Na-Caseinate
7重量部、アスコルビン酸5重量部、硬化油3重量部を
用い、常法にしたがってラフィノース含有錠菓を製造し
た。
Example 4 400 parts by weight of granular raffinose, 10 parts by weight of crystalline glucose, 7 parts by weight of citric acid, Na-Caseinate
Using 7 parts by weight, 5 parts by weight of ascorbic acid, and 3 parts by weight of hardened oil, raffinose-containing tablet confections were produced according to a conventional method.

【0029】[0029]

【実施例5】顆粒状ラフィノース125重量部、精製炭
酸カルシウム20重量部、ラクトース103重量部、ス
テアリン酸マグネシウム2重量部を用い、これらの混合
物を250mgずつ1号カプセルに充填し、1カプセル
内に125mgのラフィノースを含有するカプセル剤を
製造した。
Example 5 125 parts by weight of granular raffinose, 20 parts by weight of purified calcium carbonate, 103 parts by weight of lactose, and 2 parts by weight of magnesium stearate were used. A capsule containing 125 mg of raffinose was produced.

【0030】[0030]

【発明の効果】本発明によって顆粒状ラフィノースの製
造がはじめて可能となった。顆粒状ラフィノースは、結
晶ラフィノースに比して、甘味度が高いだけでなく、口
中においてザラつくこともなくなめらかで口溶けがよ
く、食感もすぐれ、さわやかな後口があって非常に摂取
しやすくなっている。
According to the present invention, the production of granular raffinose has become possible for the first time. Granular raffinose is not only sweeter than crystalline raffinose, it also has a smooth mouth-melt without roughening in the mouth, has a good texture, and has a refreshing back mouth, making it very easy to take Has become.

【0031】したがって、従来摂取しにくかったラフィ
ノースを、乳幼児、高齢者、病中や病後の人でも容易に
摂取することができ、本来ラフィノースが有している各
種の生理活性を充分に利用することができる。
Therefore, raffinose, which was conventionally difficult to ingest, can be easily ingested by infants, the elderly, sick or post-sick, and fully utilize the various physiological activities inherent in raffinose. Can be.

【図面の簡単な説明】[Brief description of the drawings]

【図1】糖の経時的な溶解量の比較を示す。FIG. 1 shows a comparison of the amount of sugar dissolved over time.

【図2】ラフィノース錠剤の製造工程のフローチャート
である。
FIG. 2 is a flowchart of a raffinose tablet manufacturing process.

フロントページの続き (72)発明者 恵本 司 東京都中央区京橋2丁目3番13号 日本 甜菜製糖株式会社内 (56)参考文献 特開 昭62−126951(JP,A) 特開 平9−199(JP,A) 特開 昭61−9266(JP,A) 特開 平5−211900(JP,A) 特開 平9−224665(JP,A) 特開 昭54−49345(JP,A) (58)調査した分野(Int.Cl.7,DB名) A23L 1/236 A23L 1/22 C07H 3/06 Continuation of front page (72) Inventor Tsukasa Emoto 2-3-13 Kyobashi, Chuo-ku, Tokyo Inside of Sugar Beet Sugar Co., Ltd. (56) References JP-A-62-126951 (JP, A) JP-A-9-92 199 (JP, A) JP-A-61-9266 (JP, A) JP-A-5-211900 (JP, A) JP-A-9-224665 (JP, A) JP-A-54-49345 (JP, A) (58) Field surveyed (Int.Cl. 7 , DB name) A23L 1/236 A23L 1/22 C07H 3/06

Claims (6)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 ラフィノース結晶を粉末化し、粉末粒子
を湿潤させて個々の粒子を相互に凝集させ、形状を大き
くすること、を特徴とする顆粒状ラフィノースの製造方
法。
1. A method for producing granular raffinose, comprising the steps of: pulverizing raffinose crystals; wetting the powder particles to cause the individual particles to aggregate with each other;
【請求項2】 押出し造粒法によること、を特徴とする
請求項1に記載の顆粒状ラフィノースの製造方法。
2. The process for producing granular raffinose according to claim 1, wherein the process is performed by an extrusion granulation method.
【請求項3】 加水することによりラフィノース結晶の
粉末粒子を湿潤させること、を特徴とする請求項1又は
2に記載の顆粒状ラフィノースの製造方法。
3. The method for producing granular raffinose according to claim 1, wherein the raffinose crystal powder particles are wetted by adding water.
【請求項4】 ラフィノース結晶を粉砕し、ラフィノー
ス100に対して水10を加え、混合した後に押出し造
粒機にて造粒すること、を特徴とする請求項1〜3のい
ずれか1項に記載の顆粒状ラフィノースの製造方法。
4. The method according to claim 1, wherein the raffinose crystals are pulverized, water 10 is added to raffinose 100, the mixture is mixed, and the mixture is extruded and granulated by an extruder. A method for producing the granular raffinose as described above.
【請求項5】 請求項1〜4のいずれか1項に記載の方
法で製造してなる顆粒状ラフィノース。
5. A granular raffinose produced by the method according to any one of claims 1 to 4.
【請求項6】 120秒後にはほぼ飽和濃度に達すると
いう高い溶解度を示し、且つ、口溶け、甘味度、甘味の
切れ、の少なくともひとつが向上したものであること、
を特徴とする請求項5に記載の顆粒状ラフィノース。
6. It shows a high solubility of reaching a substantially saturated concentration after 120 seconds, and at least one of melting in the mouth, sweetness and sweetness is improved.
The granular raffinose according to claim 5, characterized in that:
JP23186797A 1997-08-14 1997-08-14 Granular raffinose Expired - Fee Related JP3345312B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP23186797A JP3345312B2 (en) 1997-08-14 1997-08-14 Granular raffinose

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP23186797A JP3345312B2 (en) 1997-08-14 1997-08-14 Granular raffinose

Publications (2)

Publication Number Publication Date
JPH1156292A JPH1156292A (en) 1999-03-02
JP3345312B2 true JP3345312B2 (en) 2002-11-18

Family

ID=16930270

Family Applications (1)

Application Number Title Priority Date Filing Date
JP23186797A Expired - Fee Related JP3345312B2 (en) 1997-08-14 1997-08-14 Granular raffinose

Country Status (1)

Country Link
JP (1) JP3345312B2 (en)

Also Published As

Publication number Publication date
JPH1156292A (en) 1999-03-02

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