JP2002188095A - Vegetable oil and fat powder and food composition containing the powder - Google Patents

Vegetable oil and fat powder and food composition containing the powder

Info

Publication number
JP2002188095A
JP2002188095A JP2000388036A JP2000388036A JP2002188095A JP 2002188095 A JP2002188095 A JP 2002188095A JP 2000388036 A JP2000388036 A JP 2000388036A JP 2000388036 A JP2000388036 A JP 2000388036A JP 2002188095 A JP2002188095 A JP 2002188095A
Authority
JP
Japan
Prior art keywords
powder
fat
vegetable oil
oil
mass
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.)
Pending
Application number
JP2000388036A
Other languages
Japanese (ja)
Inventor
Yoshimitsu Takai
良充 高井
Kentarou Ohari
健太郎 小治
Mitsuo Kise
光男 喜瀬
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
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 Fancl Corp filed Critical Fancl Corp
Priority to JP2000388036A priority Critical patent/JP2002188095A/en
Publication of JP2002188095A publication Critical patent/JP2002188095A/en
Pending legal-status Critical Current

Links

Abstract

PROBLEM TO BE SOLVED: To obtain powder useful as a lubricant or a fluidity promoter and a food composition containing the same. SOLUTION: This vegetable oil and fat powder comprises vegetable oils and fats, a glucide and a protein or a lipophilic modified starch. This food composition contains the vegetable oil and fat powder. The vegetable oil and fat powder is useful as a lubricant which has excellent lubricating effect, not only has no influence on hardness, disintegration time,, flavor, etc., of tablet or tablet candy, but also has no rough feeling in the oral cavity, provides a smooth touch and has excellent preservation stability. This fluidity promoter has excellent fluidity promotion effect, not only does not provide dispersion of filled amount of powder or granule but also does not cause mutual agglomeration of content powder or content granules in a capsule after filling and has excellent stability.

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】本発明は滑沢剤または流動促
進剤として有用な植物性油脂粉末、およびそれを含む食
品組成物に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a vegetable oil or fat powder useful as a lubricant or a glidant, and a food composition containing the same.

【0002】[0002]

【従来の技術】錠剤または錠菓の製造において、粉末や
顆粒状の原料を打錠する必要がある。打錠においては、
脱型の際に錠剤の上杵側が帽子状に薄く剥がれるキャッ
ピング、打錠中に粉が杵に付着して杵離れが悪く、錠剤
表面に傷が付くスティッキング、錠剤と臼の摩擦が大き
く、打錠後の錠剤の排出性が悪くなるバインディングを
生じることがあり、このような打錠障害がひどくなると
スムーズに打錠できなくなる。
2. Description of the Related Art In the production of tablets or confectionery, it is necessary to compress powdery or granular raw materials. In tableting,
Capping in which the upper punch side of the tablet peels off thinly in the shape of a hat during demolding, powder adheres to the punch during tableting, sticking away from the punch, sticking to the tablet surface, sticking, and large friction between the tablet and the die. In some cases, binding that makes the ejection property of the tablet after tableting worse may occur. If such a tableting trouble becomes severe, tableting cannot be performed smoothly.

【0003】そこで、打錠においては、滑沢剤を使用す
ることにより、原料粉体の流動性を向上させ、打錠機の
臼に一定量が充填されるようにすると同時に、キャッピ
ング、スティッキングおよびバインディング等の打錠障
害を防止し、錠剤の表面に光沢を与える。そのためには
従来からショ糖脂肪酸エステル、ポリグリセリン脂肪酸
エステル、植物極度硬化油、精製タルク、ステアリン酸
マグネシウム等の滑沢剤が使用されてきた。
Therefore, in tableting, a lubricant is used to improve the fluidity of the raw material powder so that a certain amount is filled in a die of a tableting machine, and at the same time, capping, sticking, and the like are performed. Prevents tableting troubles such as binding and gives the tablet surface a gloss. For that purpose, lubricants such as sucrose fatty acid ester, polyglycerin fatty acid ester, extremely hardened vegetable oil, purified talc, magnesium stearate and the like have been used.

【0004】しかしながら、これらの滑沢剤は一般に撥
水性があるため、添加濃度が高くなると錠剤が容易に水
分を吸収しなくなり、崩壊時間が遅延する。また、錠剤
の硬度は内部の粒子間接触面積に関係するため、滑沢剤
の添加濃度が高くなることによって粒子間の結合力が減
少し、その結果、硬度の低下をきたすこともある。
[0004] However, since these lubricants generally have water repellency, when the added concentration is high, the tablet does not easily absorb water, and the disintegration time is delayed. Further, since the hardness of the tablet is related to the internal contact area between the particles, the bonding strength between the particles is reduced by increasing the concentration of the lubricant, and as a result, the hardness may be reduced.

【0005】例えばショ糖脂肪酸エステルは、多くが一
度塊状にしたものを粉砕して得られるために形状が球形
ではなく、近年の錠剤形状の複雑化に伴って添加量が増
加するため、崩壊時間遅延および不均一化、硬度低下の
他、充填率のバラツキによる製品重量の不均一化、コス
ト等に問題が生じていた。ポリグリセリン脂肪酸エステ
ルはその滑沢効果が低いために、充分な効果を発揮させ
るには多量添加をしなければならず、それによって崩壊
時間の遅延や硬度の低下のみならず、風味が悪くなる等
の問題もあった。また植物極度硬化油も滑沢剤としての
効果が低く、且つ夏場での倉庫等の保管においてブロッ
キングを起こしやすいといった問題がある。さらに、近
年欧米諸国において、トランス脂肪酸の摂取と血清コレ
ステロール濃度の上昇、または癌との関係が取りざたさ
れてもいることから、製剤中への添加は好ましくない。
精製タルクもまた滑沢剤としての効果が低い上に、食品
への使用量に制限があるため、あまり用いられない。一
方、ステアリン酸マグネシウムの場合は、少量の添加で
滑沢効果を引き出すことができるが、食品添加物として
許容されていないといった不都合があり、その用途は医
薬品に限定されてしまうため、汎用性に乏しい。
For example, most of sucrose fatty acid esters are obtained by pulverizing a lump that has been once formed into a lump, and thus are not spherical in shape. In addition to delay and non-uniformity and a decrease in hardness, there have been problems in non-uniformity in product weight due to uneven filling rate, cost, and the like. Polyglycerol fatty acid esters have a low lubricating effect, so they must be added in large amounts to exhibit a sufficient effect, thereby delaying disintegration time and lowering hardness, as well as deteriorating flavor. There was also a problem. In addition, extremely hardened vegetable oil has a low effect as a lubricant, and has a problem that blocking easily occurs during storage in a warehouse or the like in summer. Furthermore, in recent years, trans-fatty acid intake and an increase in serum cholesterol level or a relationship with cancer have been attempted in Western countries, and therefore, addition to a preparation is not preferred.
Purified talc is also rarely used because of its low effect as a lubricant and its limited use in foods. On the other hand, in the case of magnesium stearate, a lubricating effect can be brought out with a small amount of addition, but there is a disadvantage that it is not allowed as a food additive, and its use is limited to pharmaceuticals, so versatility. poor.

【0006】ところで、口腔は刺激や異物感等の感触や
風味等に非常に敏感な部位である。傷や炎症等の障害が
口腔内にある場合には、その感触はさらに敏感になる。
そのため、錠剤または錠菓には、滑らかさやざらつき等
の口あたり、ならびに風味等が非常に重要視される。
[0006] The oral cavity is a part that is extremely sensitive to the feel and the flavor, such as irritation and foreign body sensation. If there is an injury, such as a wound or inflammation, in the mouth, the feel becomes more sensitive.
For this reason, the mouthfeel such as smoothness and roughness, as well as the flavor and the like are very important for tablets or confectionery.

【0007】口腔内における感触の良好な錠剤を製造す
るための先行技術としては、特開平8−333243号
公報があるが、油脂類を3〜15重量%と高含有する顆
粒と油脂類を含有しない顆粒の2種類の顆粒を調製する
煩雑さがあり、またステアリン酸マグネシウム等の滑沢
剤の添加が要求される。同様の先行技術として、特開平
9−71523号公報や、特開平11−12161号公
報、特開平11−35451号公報があるが、いずれに
おいてもステアリン酸マグネシウムやステアリン酸カル
シウム、ヒドロキシプロピルセルロース、クロスポビド
ン、クロスカルメロースナトリウム等の食品添加物とし
て許容されていない添加剤が必須となるため、その用途
は医薬品に限定されてしまう。
As a prior art for producing a tablet having a good feel in the oral cavity, there is JP-A-8-333243. However, granules containing fats and oils as high as 3 to 15% by weight and fats and oils are contained. There is the complexity of preparing two types of granules, and the addition of a lubricant such as magnesium stearate is required. As similar prior arts, there are JP-A-9-71523, JP-A-11-12161, and JP-A-11-35451. In each case, magnesium stearate, calcium stearate, hydroxypropylcellulose, crospovidone are used. Additives that are not allowed as food additives, such as croscarmellose sodium, are essential, and their use is limited to pharmaceuticals.

【0008】即ち、広い用途に使用でき、ざらつき感を
与えずに滑らかな口あたりを有し、キャッピングやステ
ィッキング、バインディング等の打錠障害を防止でき、
かつ硬度の低下および崩壊時間の遅延を引き起こさない
等のすべての条件を満たす滑沢剤は、従来知られていな
い。
That is, it can be used for a wide range of uses, has a smooth mouth without giving a rough feeling, and can prevent tableting troubles such as capping, sticking, binding and the like,
Lubricants satisfying all conditions such as not causing a decrease in hardness and a delay in disintegration time have not been known.

【0009】次に、ハードカプセルの製造においては、
粉末や顆粒状の原料を充填する必要がある。カプセル充
填に関しては、内容粉末あるいは内容顆粒の流動性、吸
湿性、みかけ比重、充填性等に加え、充填方式や充填速
度等がカプセル剤の充填量、崩壊性、溶出性に大きく影
響を与える。特に、流動性を向上させる必要があり、流
動性が不良の場合には、充填量のばらつきが発生すると
いう問題が生じる。さらに、吸湿性が高い場合には、ハ
ードカプセル内で内容粉末あるいは内容顆粒同士の凝集
が起こり、保存安定性が劣るといった問題もあった。
Next, in the production of hard capsules,
It is necessary to fill powdered or granular raw materials. As for the filling of capsules, the filling method, filling rate, etc., in addition to the fluidity, hygroscopicity, apparent specific gravity, filling properties, etc. of the content powder or granules, greatly affect the filling amount, disintegration, and dissolution of the capsules. In particular, it is necessary to improve the fluidity, and when the fluidity is poor, there arises a problem that the filling amount varies. Furthermore, when the hygroscopicity is high, there is a problem that the content powder or the content granules agglomerate in the hard capsule and storage stability is deteriorated.

【0010】そこで、ハードカプセルの充填において
は、流動促進剤を添加することにより、内容粉末あるい
は内容顆粒の流動性を向上させ、ハードカプセル内へ一
定量が充填されるようにする必要がある。そのために
は、従来からショ糖脂肪酸エステル、植物極度硬化油、
精製タルク、ステアリン酸マグネシウム、コーンスター
チ等が使用されてきた(林 信一「粉体工学研究会誌」V
ol.6、No.4、第286〜291ページ、三輪 茂雄著
「粉粒体工学」(朝倉書店)第272〜283ペー
ジ)。
Therefore, in filling the hard capsule, it is necessary to improve the fluidity of the content powder or the granule by adding a glidant so that the hard capsule is filled in a fixed amount. For that purpose, sucrose fatty acid ester, vegetable hardened oil,
Purified talc, magnesium stearate, corn starch, etc. have been used (Shinichi Hayashi, Journal of the Society of Powder Engineering, V
ol. 6, No. 4, pp. 286-291, Shigeo Miwa, "Powder and Particle Engineering" (Asakura Shoten), pp. 272-283).

【0011】しかしながら、一般にこれらの流動促進剤
は流動促進効果が低いか、吸水性あるいは膨潤性を有し
ているため、充填量のばらつき、あるいは保存安定性が
劣るといった問題が生じていた。
However, in general, these flow promoters have a low flow promoting effect, or have water absorption or swelling properties, so that there has been a problem that the filling amount varies or the storage stability is poor.

【0012】前述のように、例えばショ糖脂肪酸エステ
ルは、形状が球形ではないため、流動促進剤としての効
果が低く、充填率のバラツキによる製品重量の不均一化
が問題となっていた。また、植物極度硬化油も流動促進
剤としての効果が低く、且つ前述のように、夏場での保
管、トランス脂肪酸の摂取と血清コレステロール濃度の
上昇、癌との関係等の問題があり、製剤中への添加は好
ましくない。精製タルクもまた流動促進剤としての効果
が低い上に、食品への使用量に制限がある。ステアリン
酸マグネシウムの場合は、少量の添加で流動促進効果を
引き出すことができるが、食品添加物として許容されて
いないといった不都合がある。一方、コーンスターチの
場合は、食品での利用も盛んに行われており、流動促進
効果も充分認められているが、内容粉末あるいは内容顆
粒の吸湿性が高い場合には、コーンスターチの有する吸
水性のために、ハードカプセル内において凝集が起こる
ため、ハードカプセル品としての長期保存が困難とな
る。
As described above, for example, sucrose fatty acid esters are not spherical in shape, and therefore have a low effect as a glidant, and there has been a problem of non-uniform product weight due to variations in the filling rate. Also, extremely hardened vegetable oil has a low effect as a glidant, and as described above, there are problems such as storage in summer, intake of trans fatty acids and increase in serum cholesterol concentration, and the relationship with cancer. Is not preferred. Purified talc is also less effective as a glidant and has a limited amount of use in foods. In the case of magnesium stearate, a flow-promoting effect can be obtained by adding a small amount, but there is a disadvantage that it is not allowed as a food additive. On the other hand, in the case of corn starch, the use in foods is also actively carried out, and the effect of promoting fluidity has been sufficiently recognized.However, when the content powder or granule has high hygroscopicity, the water absorption of corn starch is high. Therefore, coagulation occurs in the hard capsule, so that long-term storage as a hard capsule product becomes difficult.

【0013】即ち、広い用途に使用でき、粉末あるいは
顆粒の充填量にばらつきを与えず、内容粉末あるいは内
容顆粒同士の凝集を防止する等のすべての条件を満たす
ものは、流動促進剤には従来知られていない。
In other words, those which can be used for a wide range of applications, do not cause variation in the filling amount of powder or granules, and satisfy all conditions such as prevention of agglomeration of content powders or content granules are conventionally used as flow promoters. unknown.

【0014】[0014]

【発明が解決しようとする課題】本発明は、滑沢剤また
は流動促進剤として有用な粉末を提供すること、さら
に、これを含む食品組成物を提供することをその課題と
する。
SUMMARY OF THE INVENTION An object of the present invention is to provide a powder useful as a lubricant or a glidant, and to provide a food composition containing the same.

【0015】[0015]

【課題を解決するための手段】本発明者は、植物性油
脂、糖質および蛋白質もしくは親油性加工澱粉を含む植
物性油脂粉末が、上記課題を解決し得ることを見出し、
本発明に至った。即ち、本発明は、 1.植物性油脂、糖質および蛋白質もしくは親油性加工
澱粉を含む植物性油脂粉末、 2.植物性油脂100質量部に対して、糖質を30〜4
0質量部および蛋白質8〜12質量部含むか、または糖
質を70〜90質量部および親油性加工澱粉10〜30
質量部含む前記1記載の植物性油脂粉末、 3.植物性油脂の固体脂指数が20℃で40以上であ
り、かつ40℃で70以下である前記1または2記載の
植物性油脂粉末、 4.植物性油脂に糖質および蛋白質もしくは親油性加工
澱粉を配合して乳化させ、噴霧乾燥することを特徴とす
る前記1、2または3に記載の植物性油脂粉末の製造方
法、 5.前記1、2または3記載の植物性油脂粉末を含有す
る食品組成物、 6.前記1、2または3記載の植物性油脂粉末を含む、
滑沢剤または流動促進剤、 7.前記6記載の滑沢剤または流動促進剤を0.1〜1
0質量%含有する食品組成物、 8.固体の形態である前記7記載の食品組成物、であ
る。
Means for Solving the Problems The present inventor has found that vegetable oil and fat powder containing vegetable oil and fat, saccharide and protein or lipophilic modified starch can solve the above problems,
The present invention has been reached. That is, the present invention provides: 1. vegetable oils and fats, including vegetable oils, sugars and protein or lipophilic modified starch; 30 to 4 sugars per 100 parts by mass of vegetable fats and oils
0 parts by weight and 8 to 12 parts by weight of protein, or 70 to 90 parts by weight of saccharide and 10 to 30 parts of lipophilic modified starch
2. The vegetable fat / oil powder according to the above 1, which contains parts by mass. 3. The vegetable fat or oil powder according to 1 or 2, wherein the solid fat index of the vegetable fat is 20 or more at 40C and 70 or less at 40C. 4. The method for producing a vegetable oil or fat powder according to the above item 1, 2 or 3, wherein the sugar and protein or lipophilic modified starch is blended with the vegetable oil and emulsified, followed by spray drying. 5. A food composition containing the vegetable oil powder according to the above 1, 2, or 3, Including the vegetable oil powder according to the above 1, 2, or 3,
6. a lubricant or glidant; 7. The lubricant or glidant of the above item 6 in an amount of 0.1 to 1
7. a food composition containing 0% by mass; 8. The food composition according to the above 7, which is in a solid form.

【0016】本発明の植物性油脂粉末は、滑沢効果に優
れ、錠剤または錠菓の硬度や崩壊時間および風味等に影
響がないということだけに留まらず、口腔内においてざ
らつき感がなく、滑らかな感触を与える保存安定性に優
れた滑沢剤として有用である。さらに、本発明の植物性
油脂粉末は、流動促進効果に優れ、粉末あるいは顆粒の
充填量にばらつきを与えないということだけに留まら
ず、充填後にカプセル内において内容粉末あるいは内容
顆粒同士の凝集が起こらない、安定性に優れた流動促進
剤として有用である。
The vegetable oil powder of the present invention has an excellent lubricating effect, not only that it has no effect on the hardness, disintegration time, flavor and the like of tablets or confectionery. It is useful as a lubricant with excellent storage stability that gives a pleasant feel. Furthermore, the vegetable oil powder of the present invention is excellent not only in that it has an excellent fluidity promoting effect and does not cause variation in the filling amount of the powder or granules, but also causes agglomeration of the contents powder or the contents granules in the capsule after the filling. It is useful as a glidant with excellent stability.

【0017】[0017]

【発明の実施の形態】以下に本発明を詳細に説明する。
本発明における植物性油脂は、アブラヤシの果肉部およ
び果実の核から採油されるパーム油およびパーム核油、
カカオの種子から採油されるカカオ脂等の常温で半固形
状の油脂が適するが、これらのみに限定されるものでは
ない。
DESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention will be described below in detail.
Vegetable oils and fats in the present invention are palm oil and palm kernel oil extracted from the pulp and fruit core of oil palm,
Suitable are semi-solid fats and oils at room temperature, such as cocoa butter, which is oiled from cocoa seeds, but is not limited thereto.

【0018】本発明において使用する植物性油脂は、固
体脂指数(SFI)が、20℃で40以上であり、かつ4
0℃で70以下のものが好ましい。より詳細には、20
℃で50以上であり、40℃で65以下であるものが好
ましく、20℃で60以上であり、40℃で60以下で
あるものが特に好ましい。更に、この条件に加えて、2
5℃で35以上であり、35℃で80以下であることが
一層好ましく、25℃で40以上であり、35℃で78
以下であるものがより一層好ましく、25℃で50以上
であり、35℃で76以下であるものが特に一層好まし
い。
The vegetable fat used in the present invention has a solid fat index (SFI) of 40 or more at 20 ° C.
Those at 70 ° C. or less at 0 ° C. are preferred. More specifically, 20
It is preferably at least 50 at 40 ° C. and at most 65 at 40 ° C., particularly preferably at least 60 at 20 ° C. and at most 60 at 40 ° C. Furthermore, in addition to this condition, 2
It is more preferably 35 or more at 5 ° C and 80 or less at 35 ° C, more preferably 40 or more at 25 ° C and 78 or more at 35 ° C.
The following are still more preferred, those at 50 ° C. or more at 25 ° C., and those at 76 or less at 35 ° C. are particularly preferred.

【0019】ここで、本発明における植物性油脂の固体
脂指数(SFI)とは、各温度での油脂中の固体脂の割合
を百分率で表したもので、膨張計によって測定された値
のことである(「基準油脂分析法 日本油化学協会編」
2.4.19.2−18)。固体脂指数がこれらの範囲
外である場合には、口腔内においてざらつき感が生じて
滑らかな感触が失われたり、保存安定性低下、硬度低
下、あるいは崩壊時間延長等が起こる傾向が生じること
がある。
Here, the solid fat index (SFI) of the vegetable fat in the present invention is the percentage of the solid fat in the fat at each temperature, which is a value measured by a dilatometer. (“Standard Oil and Fat Analysis Method, Japan Oil Chemistry Association”)
2.4.19.2.2-18). If the solid fat index is outside of these ranges, a rough feel occurs in the oral cavity and a smooth feel is lost, storage stability decreases, hardness decreases, or a tendency to cause disintegration time extension or the like may occur. is there.

【0020】本発明において使用する糖質としては、乳
糖、デキストリン、澱粉、アラビアガム、キサンタンガ
ム、トラガントガム、プルラン、ブドウ糖、果糖、麦芽
糖、ソルビトール、マンノース、フラクトース、キシロ
ースを挙げることができる。これらは一種で使用するこ
とも、二種以上組合わせて使用することもできる。な
お、ここでいう糖質には、親油性加工澱粉は含まれな
い。
Examples of the saccharide used in the present invention include lactose, dextrin, starch, gum arabic, xanthan gum, tragacanth, pullulan, glucose, fructose, maltose, sorbitol, mannose, fructose and xylose. These can be used alone or in combination of two or more. In addition, the saccharides here do not include lipophilic modified starch.

【0021】本発明における蛋白質としてはカゼインナ
トリウム、ゼラチン、アルブミン、大豆蛋白質、小麦グ
ルテンを挙げることができる。
The protein in the present invention includes sodium caseinate, gelatin, albumin, soy protein, and wheat gluten.

【0022】本発明における親油性加工澱粉とは、澱粉
の一部水酸基がオクテニルコハク酸エステル化、酢酸エ
ステル化、アジピン酸エステル化、もしくはリン酸エス
テル化等エステル化処理が施され、親水性および親油性
の両者を兼ね備えた全ての澱粉のことである。一例を挙
げると、ワキシーコーンスターチの一部水酸基をオクテ
ニルコハク酸エステル化し、加水分解、加熱乾燥した
後、粉砕することによって得られる。ただしこれは一例
であって、この製法によって親油性加工澱粉が限定され
るものではない。
The lipophilic modified starch in the present invention is a starch whose partial hydroxyl group is subjected to an esterification treatment such as octenylsuccinate esterification, acetate esterification, adipate esterification, or phosphate esterification to give hydrophilicity and hydrophilicity. It refers to all starches that have both oiliness. As an example, it is obtained by converting a part of hydroxyl group of waxy corn starch into octenyl succinate, hydrolyzing, heating and drying, and then pulverizing. However, this is only an example, and the lipophilic modified starch is not limited by this production method.

【0023】本発明の植物性油脂粉末は植物性油脂を主
成分とするものであり、植物性油脂の特徴、利点を損な
わない範囲で崩壊剤や賦形剤、吸収剤等の添加剤を配合
して使用することができる。このようなものとして、例
えばリン酸カルシウム、炭酸カルシウム等が挙げられ
る。また、ステアリン酸マグネシウム、精製タルク、シ
ョ糖脂肪酸エステル、ポリグリセリン脂肪酸エステル、
脂肪酸アルカリ金属塩、ラウリル硫酸アルカリ金属塩、
脂肪族アミノ酸、芳香族アミノ酸、複素環式アミノ酸、
ホウ酸、アジピン酸、フマル酸、コハク酸、安息香酸ア
ルカリ金属塩、硫酸ナトリウム、ポリエチレングリコー
ル、植物硬化油といった従来の滑沢剤を併用することも
できる。
The vegetable fat / oil powder of the present invention contains vegetable fat / oil as a main component, and contains additives such as disintegrants, excipients, and absorbents within a range that does not impair the characteristics and advantages of the vegetable fat / oil. Can be used. Examples of such a material include calcium phosphate and calcium carbonate. Also, magnesium stearate, purified talc, sucrose fatty acid ester, polyglycerin fatty acid ester,
Fatty acid alkali metal salts, lauryl sulfate alkali metal salts,
Aliphatic amino acids, aromatic amino acids, heterocyclic amino acids,
Conventional lubricants such as boric acid, adipic acid, fumaric acid, succinic acid, alkali metal benzoate, sodium sulfate, polyethylene glycol, and hardened vegetable oil can also be used in combination.

【0024】本発明の植物性油脂粉末は、植物性油脂に
蛋白質および糖質、あるいは親油性加工澱粉および糖質
を添加して粉末化したものである。好ましくは、植物性
油脂を45質量%以上含む。その平均粒子径は、好まし
くは850μm以下、さらに好ましくは50〜500μ
m、特に好ましくは、50〜250μmであり、これら
の中でも80〜150μm、さらには、100〜150
μmの微粉末が好ましい。滑沢効果は滑沢化しようとす
る粉末または顆粒に比べ、その粒子径が小さいほど粉体
粒子の被覆力が強いため、滑沢剤の粒子径はその性能に
大きく影響を与える。平均粒子径が850μmを超える
と、打錠後の錠剤表面に植物性油脂粉末がしみのように
浮き出て、美しさに欠けることがある。ここでいう平均
粒子径とは、二種以上の粒径を持つ粒子群の代表径のこ
とをいい、比表面積測定法による中央累積値として求め
たものである。
The vegetable oil / fat powder of the present invention is obtained by adding protein and carbohydrate or lipophilic modified starch and carbohydrate to vegetable oil / fat and pulverizing it. Preferably, it contains 45% by mass or more of vegetable fats and oils. The average particle size is preferably 850 μm or less, more preferably 50 to 500 μm.
m, particularly preferably 50 to 250 μm, among which 80 to 150 μm, further preferably 100 to 150 μm.
A fine powder of μm is preferred. As for the lubricating effect, the smaller the particle size of the powder or granules to be lubricated, the stronger the covering power of the powder particles. Therefore, the particle size of the lubricant greatly affects its performance. If the average particle size exceeds 850 μm, the vegetable oil or fat powder may appear on the surface of the tablet after tableting like a stain, and may lack beauty. Here, the average particle diameter refers to a representative diameter of a group of particles having two or more kinds of particle diameters, and is obtained as a central cumulative value by a specific surface area measurement method.

【0025】本発明の植物性油脂粉末は、植物性油脂に
蛋白質および糖質、あるいは親油性加工澱粉および糖質
を配合して乳化させ、噴霧乾燥することによって製造す
ることができる。具体的には、例えば、適量の水に植物
性油脂と蛋白質、糖質を配合して乳化させ、噴霧乾燥に
よって粉末化することができる。あるいは、適量の水に
植物性油脂と親油性加工澱粉、糖質を配合して乳化さ
せ、噴霧乾燥によって粉末化することができる。ただし
これは一例であって、この製法により本発明における植
物性油脂粉末が限定されるものではない。必要に応じ
て、ポリグリセリン脂肪酸エステルやリン酸塩、ビタミ
ンEといった食品添加物を加えて製造してもかまわな
い。
The vegetable oil / fat powder of the present invention can be produced by blending a vegetable oil / fat with a protein and a saccharide or a lipophilic modified starch and a saccharide to emulsify and spray-dry. Specifically, for example, vegetable oils and fats, proteins and carbohydrates are blended in an appropriate amount of water, emulsified, and powdered by spray drying. Alternatively, a vegetable oil and fat, a lipophilic modified starch, and a saccharide are blended in an appropriate amount of water to emulsify the mixture, and the mixture can be powderized by spray drying. However, this is only an example, and the vegetable oil powder in the present invention is not limited by this production method. If necessary, food additives such as polyglycerin fatty acid esters, phosphates, and vitamin E may be added for production.

【0026】植物性油脂粉末中の蛋白質、糖質および親
油性加工澱粉の含有量としては、植物性油脂100質量
部に対して蛋白質8〜12質量部、糖質30〜40質量
部、あるいは、植物性油脂100質量部に対して親油性
加工澱粉10〜30質量部、糖質70〜90質量部であ
ることが好ましい。さらに好ましくは、植物性油脂10
0質量部に対して蛋白質8〜10質量部、糖質30〜3
6質量部、あるいは、植物性油脂100質量部に対して
親油性加工澱粉15〜30質量部、糖質70〜85質量
部であり、特に好ましくは、植物性油脂100質量部に
対して蛋白質8〜9質量部、糖質32〜35質量部、あ
るいは、植物性油脂100質量部に対して親油性加工澱
粉20〜28質量部、糖質70〜78質量部である。蛋
白質、糖質および親油性加工澱粉の含有量がこれらの範
囲を逸脱すると、油滴の浮上または油滴同士の凝集が発
生して安定な乳化を行うことができないため、平均粒子
径をコントロールすることができないことがある。よっ
て、蛋白質および糖質、あるいは親油性加工澱粉および
糖質の含有量は、上記範囲内であることが望ましい。
The content of protein, sugar and lipophilic modified starch in the vegetable oil / fat powder is 8 to 12 parts by mass of protein, 30 to 40 parts by mass of saccharide, or It is preferable that the lipophilic modified starch is 10 to 30 parts by mass and the saccharide is 70 to 90 parts by mass with respect to 100 parts by mass of the vegetable oil and fat. More preferably, vegetable oil 10
8 to 10 parts by mass of protein and 30 to 3 saccharides per 0 parts by mass
6 parts by mass, or 15 to 30 parts by mass of lipophilic modified starch and 70 to 85 parts by mass of carbohydrate with respect to 100 parts by mass of vegetable oil and fat, particularly preferably protein 8 with respect to 100 parts by mass of vegetable oil and fat. 20 to 28 parts by mass of lipophilic modified starch and 70 to 78 parts by mass of saccharide with respect to 100 parts by mass of vegetable fats and oils. If the contents of protein, carbohydrate and lipophilic modified starch deviate from these ranges, floating of oil droplets or aggregation of oil droplets occur and stable emulsification cannot be performed, so the average particle diameter is controlled. You may not be able to do it. Therefore, it is desirable that the contents of protein and saccharide, or lipophilic modified starch and saccharide are within the above range.

【0027】本発明は、植物性油脂粉末を含む食品組成
物を含む。食品組成物は固体の形態であることができ、
例えば、錠剤、錠菓、ハードカプセル剤である。これら
は一般的な製造方法に準じて製造される。
The present invention includes a food composition containing a vegetable oil powder. The food composition can be in a solid form;
For example, tablets, tablets and hard capsules. These are manufactured according to a general manufacturing method.

【0028】例えば、錠剤、錠菓の場合は、医薬品また
は食品をそのまま、または賦形剤、結合剤、崩壊剤もし
くはその他の適当な添加剤を均等に混和したものを、適
当な方法で顆粒状とした後、本発明の植物性油脂粉末を
滑沢剤として加え、その他の適当な添加剤を加えて圧縮
成型する。あるいは、医薬品または食品に本発明の植物
性粉末を加え、そのまま、または賦形剤、結合剤、崩壊
剤もしくはその他の適当な添加剤を均等に混和したもの
を、直接圧縮成型して製造するか、またはあらかじめ製
造した顆粒に医薬品または食品、および本発明の植物性
油脂粉末を加えてそのまま、もしくは適当な添加剤を加
えて均等に混合した後、圧縮成型する。
For example, in the case of tablets and tablet confections, a drug or food as it is, or a mixture of excipients, binders, disintegrants or other suitable additives is mixed in an appropriate manner into granules. Then, the vegetable oil powder of the present invention is added as a lubricant, and other appropriate additives are added, followed by compression molding. Alternatively, it is prepared by adding the vegetable powder of the present invention to a drug or food, and directly compress-molding the mixture as it is or evenly mixing excipients, binders, disintegrants or other suitable additives. Alternatively, the medicament or food and the vegetable oil or fat powder of the present invention are added to the granules prepared in advance, and the mixture is compressed as it is, or after an appropriate additive is added and uniformly mixed, followed by compression molding.

【0029】錠剤または錠菓の製造過程は、圧縮成型す
るための粉末または顆粒を製造する造粒プロセスと、圧
縮成型する打錠プロセスに分けられるが、本発明の植物
性油脂粉末を添加するタイミングはいずれの過程におい
てもその効果が発揮される。つまり、本発明の植物性油
脂粉末は親水性が強いために、造粒プロセスにおいて添
加しても粒子間の結合を妨げることはない。
The production process of tablets or confections is divided into a granulation process for producing powders or granules for compression molding and a tableting process for compression molding. The timing of adding the vegetable oil powder of the present invention is Exerts its effect in any process. That is, since the vegetable oil powder of the present invention has a strong hydrophilicity, even if added in the granulation process, it does not hinder the bonding between the particles.

【0030】打錠する際の粉体中に占める植物性油脂粉
末の添加量は、0.1〜10質量%が適当であるが、特
に好ましくは0.2〜5質量%である。要求される機能
によって添加量はその限りではないが、添加量がこれら
の範囲を逸脱すると、崩壊時間の遅延や硬度低下、キャ
ッピング、スティッキングおよびバインディング等の打
錠障害が起こる傾向にあるため、上記範囲内であること
が望ましい。また本発明に用いられる滑沢剤である植物
性油脂粉末は、直接錠剤製造法、湿式錠剤製造法のどち
らにも用いることができる。
The amount of the vegetable oil and fat powder occupied in the powder at the time of tableting is suitably from 0.1 to 10% by mass, and particularly preferably from 0.2 to 5% by mass. The addition amount is not limited depending on the required function, but if the addition amount deviates from these ranges, tableting failure such as delay in disintegration time, decrease in hardness, capping, sticking and binding tends to occur. It is desirable to be within the range. In addition, the vegetable oil-fat powder which is a lubricant used in the present invention can be used in both a direct tablet production method and a wet tablet production method.

【0031】本発明における食品組成物に含まれる錠剤
または錠菓は、前記のようにして製造した素錠、コーテ
ィング錠、糖衣錠、多層錠、有核錠、発泡錠、チュアブ
ル錠、バッカル錠、舌下錠、付着錠、トローチ錠、溶解
錠、試薬錠等すべての錠剤または錠菓を含み、その形状
および重量に左右されることはない。
The tablets or tablet confections contained in the food composition of the present invention include the uncoated tablets, coated tablets, sugar-coated tablets, multilayer tablets, dry-coated tablets, effervescent tablets, chewable tablets, buccal tablets, and tongues produced as described above. It includes all tablets or tablets such as lower tablets, adhesive tablets, troches, dissolving tablets, reagent tablets, etc., and is not affected by the shape and weight.

【0032】また、ハードカプセルの場合は、例えば、
医薬品または食品をそのまま、または賦形剤、結合剤、
崩壊剤もしくはその他の適当な添加剤を均等に混和した
ものを、適当な方法で顆粒状とした後、本発明の植物性
油脂粉末を流動促進剤として、その他の適当な添加剤を
加えてカプセル充填する。あるいは、医薬品または食品
に本発明の植物性油脂粉末を加え、そのまま、または賦
形剤、結合剤、崩壊剤もしくはその他の適当な添加剤を
均等に混和したものを、直接カプセル充填して製造する
か、またはあらかじめ製造した顆粒に医薬品または食
品、および本発明の流動促進剤である植物性油脂粉末を
加えてそのまま、もしくは適当な添加剤を加えて均等に
混合した後、カプセル充填する。
In the case of a hard capsule, for example,
Drugs or foods as is, or excipients, binders,
After uniformly disintegrating a disintegrating agent or other appropriate additives, granulate by an appropriate method, the vegetable oil powder of the present invention is used as a glidant, and other appropriate additives are added to the capsule. Fill. Alternatively, it is produced by adding the vegetable oil powder of the present invention to a medicine or food, and directly mixing the excipient, a binder, a disintegrant or other appropriate additives with capsules, and directly filling the capsule. Alternatively, a medicament or food and a vegetable oil powder as a glidant of the present invention are added to the granules prepared in advance, and the mixture is added as it is, or the mixture is uniformly mixed with an appropriate additive, and then filled into capsules.

【0033】ハードカプセルの製造過程も錠剤または錠
菓の製造と同様に、充填するための粉末または顆粒を製
造する造粒プロセスと、直接充填するプロセスに分けら
れるが、本発明の植物性油脂粉末(流動促進剤)を添加
するタイミングは、前記ハードカプセル製造のいずれの
過程においてもその効果が発揮される。つまり、本発明
による植物性油脂粉末は親水性が強いために、造粒プロ
セスにおいて添加しても粒子間の結合を妨げることはな
い。
The process for producing hard capsules is also divided into a granulation process for producing a powder or granules for filling and a process for directly filling, as in the production of tablets or tablet confections. Regarding the timing of adding the (flow promoter), the effect is exhibited in any process of the production of the hard capsule. That is, since the vegetable oil powder according to the present invention has a strong hydrophilicity, even if added in the granulation process, it does not hinder the bonding between particles.

【0034】カプセル充填する際の粉体中に占める植物
性油脂粉末の添加量は、0.1〜10質量%が適当であ
るが、特に好ましくは0.2〜5質量%である。要求さ
れる機能によって添加量はその限りではないが、添加量
がこれらの範囲を逸脱すると、粉末あるいは顆粒の充填
ばらつき、粉末あるいは顆粒の所定量充填不足が起こる
傾向にあるため、上記範囲内であることが望ましい。充
填量にばらつきがあるハードカプセル剤とは、第十二改
正日本薬局方に基づいて重量偏差試験を行った結果が不
適となったもののことである。本発明における食品組成
物は、前記のようにして製造したすべてのカプセル剤の
ことで、その形状、サイズおよび材質に左右されること
はない。
The amount of the vegetable oil and fat powder occupying in the powder when filling the capsule is suitably 0.1 to 10% by mass, particularly preferably 0.2 to 5% by mass. The addition amount is not limited by the required function, but if the addition amount deviates from these ranges, there is a tendency that the filling of the powder or granules will be uneven, and the filling of the predetermined amount of the powder or granules tends to occur. Desirably. Hard capsules having a variation in the filling amount are those in which the result of the weight deviation test based on the 12th Revised Japanese Pharmacopoeia becomes inappropriate. The food composition according to the present invention refers to all capsules produced as described above, and is not affected by the shape, size and material.

【0035】[0035]

【実施例】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 Examples of the present invention will be shown below, but the present invention is not limited only to these.

【0036】[植物性油脂粉末] 実施例 1 70℃の温水125質量部に、澱粉の6-位の水酸基がオ
クテニルコハク酸エステル化された親油性加工澱粉25
質量部、デキストリン37.5質量部、乳糖37.5質
量部を添加して約20分間攪拌した。次に、100質量
部の食用パーム油を75℃に加熱溶解し、上記水溶液に
徐々に添加して乳化した。得られたエマルジョンを噴霧
乾燥して油脂粉末を作製した。この油脂粉末の平均粒子
径は約150μmであった。使用した食用パーム油のS
FI値を、表1に示す。
Example 1 Vegetable oil and fat powder Example 1 A lipophilic modified starch 25 in which the hydroxyl group at the 6-position of the starch was octenylsuccinic esterified to 125 parts by mass of 70 ° C. hot water.
Parts by mass, dextrin 37.5 parts by mass, and lactose 37.5 parts by mass were added and stirred for about 20 minutes. Next, 100 parts by mass of edible palm oil was heated and dissolved at 75 ° C., and gradually added to the above aqueous solution and emulsified. The obtained emulsion was spray-dried to prepare a fat and oil powder. The average particle size of this fat powder was about 150 μm. S of edible palm oil used
The FI values are shown in Table 1.

【0037】実施例2 食用パーム油に代えてカカオ脂を使用した以外は実施例
1と同様にして油脂粉末を作製した。この油脂粉末の平
均粒子径は約180μmであった。使用したカカオ脂の
SFI値を、表1に示す。
Example 2 A fat and oil powder was prepared in the same manner as in Example 1 except that cocoa butter was used instead of edible palm oil. The average particle size of this fat powder was about 180 μm. Table 1 shows the SFI values of the cocoa butter used.

【0038】実施例3 60℃の温水57質量部に、カゼインソーダ8.6質量
部、デキストリン17.1質量部、乳糖17.1質量部
を添加して約10分間攪拌した。次に、100質量部の
食用パーム油(実施例1で使用したものと同じもの)を
65℃に加熱溶解し、上記水溶液に徐々に添加して乳化
した。得られたエマルジョンを噴霧乾燥して油脂粉末を
作製した。この油脂粉末の平均粒子径は約230μmで
あった。
Example 3 8.6 parts by mass of casein soda, 17.1 parts by mass of dextrin and 17.1 parts by mass of lactose were added to 57 parts by mass of hot water at 60 ° C., and the mixture was stirred for about 10 minutes. Next, 100 parts by mass of edible palm oil (the same as used in Example 1) was heated and dissolved at 65 ° C., and gradually added to the aqueous solution to emulsify. The obtained emulsion was spray-dried to prepare a fat and oil powder. The average particle size of this fat powder was about 230 μm.

【0039】実施例4 食用パーム油に代えて食用ヤシ油を使用した以外は実施
例3と同様にして粉末油脂を作製した。この粉末油脂の
平均粒子径は約230μmであった。使用した食用ヤシ
油のSFI値を、表1に示す。
Example 4 A powdered fat was prepared in the same manner as in Example 3 except that edible palm oil was used instead of edible palm oil. The average particle size of the powdered fat was about 230 μm. Table 1 shows the SFI values of the edible coconut oil used.

【0040】[0040]

【表1】 [Table 1]

【0041】[錠剤] 実施例A−1 無水結晶ブドウ糖85質量部、デキストリン15質量部
を混合して顆粒状に造粒した後、滑沢剤として上記実施
例1で得た油脂粉末を全体に対して3質量部になるよう
に加え、5分間V型混合機で混合し、この混合物を打錠
径=5mm、打錠圧=1200kgfで打錠し、錠剤を
得た。この評価結果を表2に示す。
[Tablets] Example A-1 85 parts by weight of anhydrous crystalline glucose and 15 parts by weight of dextrin were mixed and granulated, and then the fat and oil powder obtained in Example 1 was used as a lubricant. The mixture was added so that the amount became 3 parts by mass, and the mixture was mixed with a V-type mixer for 5 minutes. The mixture was tableted with a tableting diameter of 5 mm and a tableting pressure of 1200 kgf to obtain tablets. Table 2 shows the evaluation results.

【0042】実施例A−2 実施例1の油脂粉末に代えて実施例2の油脂粉末を使用
した以外は実施例A−1と同様にして、錠剤を得た。こ
の評価結果を表2に示す。 実施例A−3 実施例1の油脂粉末に代えて実施例4の油脂粉末を使用
した以外は実施例A−1と同様にして、錠剤を得た。こ
の評価結果を表2に示す。 比較例A−1〜比較例A−4 実施例1の油脂粉末に代えて表2に示した滑沢剤を使用
した以外は実施例A−1と同様にして、錠剤を得た。こ
の評価結果を表2に示す。
Example A-2 A tablet was obtained in the same manner as in Example A-1, except that the oil and fat powder of Example 2 was used instead of the oil and fat powder of Example 1. Table 2 shows the evaluation results. Example A-3 A tablet was obtained in the same manner as in Example A-1, except that the oil and fat powder of Example 4 was used instead of the oil and fat powder of Example 1. Table 2 shows the evaluation results. Comparative Examples A-1 to A-4 Tablets were obtained in the same manner as in Example A-1, except that the lubricants shown in Table 2 were used instead of the fat and oil powder of Example 1. Table 2 shows the evaluation results.

【0043】なお、錠剤は以下の方法により試験した。 試験方法 1.食感(口腔内における感触) 錠剤を口に含んだ時の滑らかさの官能検査を10名の被
験者に対して行った。評価は次のとおりである。口腔内
でざらつきを感じて服用しづらいと答えたのが2名以下
であるもの:○口腔内でざらつきを感じて服用しづらい
と答えたのが3名以上であるもの:×
The tablets were tested by the following methods. Test method Texture (feel in the oral cavity) A sensory test of smoothness when the tablet was contained in the mouth was performed on 10 subjects. The evaluation is as follows. No more than two people answered that they felt rough in the oral cavity and it was difficult to take them: ○ Three or more people answered that they felt rough and difficult to take the oral cavity: ×

【0044】2.保存安定性試験 上記のようにして製造した錠剤を40℃、相対湿度75
%の雰囲気中に30日間保存し、外観の変化を観察し
た。評価は次の通りである。 外観に全く変化のなかったもの:◎ 外観に若干の変化が起こったもの:○ 錠剤表面が劣化して外観に明らかなる変化が起こったも
の:×
2. Storage stability test Tablets prepared as described above were subjected to storage at 40 ° C and a relative humidity of 75.
% For 30 days and observed for changes in appearance. The evaluation is as follows. No change in appearance: ◎ A slight change in appearance: ○ A tablet surface deteriorated and a change was apparent in appearance: ×

【0045】3.硬度(木屋式デジタル硬度計) 試料20錠の硬度を硬度測定器(岡田精工社製TS-50N)
を用いて測定した。20錠を用いて試験した結果、その
平均値を表に示した。
3. Hardness (Kiya type digital hardness tester) Hardness tester for hardness of 20 tablets (TS-50N manufactured by Okada Seiko Co., Ltd.)
It measured using. As a result of a test using 20 tablets, the average value is shown in the table.

【0046】4.崩壊性試験 試験液に水を用い、日本薬局方に基づいて試験を行っ
た。崩壊時間を表に示した。
4. Disintegration test Water was used as a test solution, and a test was performed based on the Japanese Pharmacopoeia. The disintegration time is shown in the table.

【0047】5.外観検査 キャッピング、スティッキング、バインディング等の打
錠障害の有無、および錠剤表面に浮き出るしみの有無を
目視検査した。評価は、次のとおりである。 打錠障害またはしみの発生が全くなかったもの:◎ 打錠障害またはしみの発生のどちらか一方でも起こって
いたもの:○ 打錠障害およびしみの発生のどちらとも起こっていたも
の:×
5. Visual Inspection Visual inspection was performed to determine whether there were any tableting troubles such as capping, sticking, binding, etc., and whether there was any blot on the tablet surface. The evaluation is as follows. No tableting failure or no spots: ◎ One of tableting failures or spots: ○ Both tableting failure and spots: ×

【0048】[0048]

【表2】 [Table 2]

【0049】実施例A−1およびA−2の錠剤では、食
感、保存安定性、硬度および崩壊時間に対する影響、滑
沢性、外観等の性能がすべて優れており、実施例A−3
の錠剤も硬度以外はほぼ優れていた。一方、比較例 A
−1〜A−4では、いずれにおいても口腔内においてざ
らつきを感じて服用しづらく、比較例A−1および比較
例A−2においては崩壊時間の遅延がみられ、比較例A
−3およびA−4においてはキャッピング現象、スティ
ッキング現象、およびバインディング現象がみられた。
The tablets of Examples A-1 and A-2 were all excellent in texture, storage stability, effects on hardness and disintegration time, lubricity, appearance, and the like.
Tablets were almost excellent except for hardness. On the other hand, Comparative Example A
-1 to A-4, all of them felt rough in the oral cavity and were hard to take. In Comparative Examples A-1 and A-2, the disintegration time was delayed, and Comparative Example A
In -3 and A-4, a capping phenomenon, a sticking phenomenon, and a binding phenomenon were observed.

【0050】[カプセル剤]実施例B−1ローヤルゼリ
ーの凍結乾燥粉末を75質量部、乳糖を12質量部、結
晶セルロースを10質量部、上記実施例1の油脂粉末を
3質量部加え、5分間V型混合機で混合した。カプセル
充填機ZANASI−Z60を使用し、この混合物を所定充填量
として220mgになるように55個/分の速度で2号
サイズのハードカプセル(ワーナー・ランバート製)に
充填し、カプセル剤を得た。この評価結果を表3に示
す。
[Capsule] Example B-1 75 parts by mass of lyophilized powder of royal jelly, 12 parts by mass of lactose, 10 parts by mass of crystalline cellulose, and 3 parts by mass of the oil and fat powder of Example 1 are added for 5 minutes. The mixture was mixed with a V-type mixer. Using a capsule filling machine ZANASI-Z60, this mixture was filled into a No. 2 size hard capsule (manufactured by Warner Lambert) at a rate of 55 pieces / min so as to obtain a predetermined filling amount of 220 mg, to obtain a capsule. Table 3 shows the evaluation results.

【0051】実施例B−2 実施例1の油脂粉末に代えて、実施例2の油脂粉末を使
用した以外は実施例B−1と同様にしてカプセル剤を得
た。この評価結果を表3に示す。 実施例B−3 実施例1の油脂粉末に代えて、実施例4の油脂粉末を使
用した以外は実施例B−1と同様にしてカプセル剤を得
た。この評価結果を表3に示す。 比較例B−1〜比較例B−3 実施例1の油脂粉末に代えて、表5に示した流動促進剤
を使用した以外は実施例B−1と同様にしてカプセル剤
を得た。この評価結果を表3に示す。
Example B-2 A capsule was obtained in the same manner as in Example B-1, except that the fat and oil powder of Example 2 was used instead of the fat and oil powder of Example 1. Table 3 shows the evaluation results. Example B-3 A capsule was obtained in the same manner as in Example B-1, except that the fat and oil powder of Example 4 was used instead of the fat and oil powder of Example 1. Table 3 shows the evaluation results. Comparative Example B-1 to Comparative Example B-3 Capsules were obtained in the same manner as in Example B-1 except that the fluid promoter shown in Table 5 was used instead of the fat and oil powder of Example 1. Table 3 shows the evaluation results.

【0052】なお、カプセル剤は以下の方法により試験
した。 試験方法 1.充填ばらつき 第十二改正日本薬局方に基づいて、重量偏差試験を行っ
た。充填後のハードカプセル剤を20個とり、その重量
を精密に量り、平均重量を計算した。評価は次のとおり
である。 この平均値と個々の重量との偏差(%)が10%以下の
もの:○ 偏差が10%を超えた場合、さらにハードカプセル剤を
20個とり、個々の内容物についての重量を精密に量
り、平均値を計算した。 この平均値と個々の重量との偏差(%)が10%を超え
るものが3個以上か、若しくは25%を超えるものが1
個でもあったもの:×
The capsules were tested by the following methods. Test method Filling Variation A weight deviation test was performed based on the 12th revised Japanese Pharmacopoeia. Twenty hard capsules after filling were taken, weighed precisely, and the average weight was calculated. The evaluation is as follows. When the deviation (%) between the average value and the individual weight is 10% or less: ○ If the deviation exceeds 10%, take another 20 hard capsules, precisely measure the weight of each content, The average was calculated. The deviation (%) between the average value and the individual weight exceeds 10%, 3 or more, or 1% exceeds 25%.
What was also: ×

【0053】2.保存安定性試験 ハードカプセル剤を40℃、相対湿度75%の雰囲気中
に30日間保存し、内容物の変化を観察した。評価は次
のとおりである。 内容物に全く変化の認められなかったもの:◎ 内容物に少し変化のあったもの:○ 内容物が完全に凝集を起こし、外観に明らかなる変化が
起こったもの:×
2. Storage stability test Hard capsules were stored in an atmosphere at 40 ° C. and a relative humidity of 75% for 30 days, and changes in the contents were observed. The evaluation is as follows. No change was observed in the content: ◎ A slight change was observed in the content: ○ A content was completely agglomerated and a change was apparent in the appearance: ×

【0054】3.外観検査 ハードカプセル内に浮き出るしみの有無を目視検査し
た。評価は次のとおりである。 しみの発生が全く認められなかったもの:◎ しみの発生が少しあったもの:○ しみの発生が顕著に見られたもの:×
3. Appearance inspection The presence or absence of stains emerging in the hard capsule was visually inspected. The evaluation is as follows. No occurrence of spots was observed: ◎ Some occurrence of spots: ○ One where remarkable occurrence of spots was observed: ×

【0055】[0055]

【表3】 [Table 3]

【0056】実施例B−1、実施例B−2、実施例B−
3では、ハードカプセル充填性、保存安定性および外観
等の性能がすべて優れていた。一方比較例B−1、比較
例B−2および比較例B−3では、保存安定性試験にお
いて、いずれもハードカプセル内で内容粉末に内容粉末
の凝集が認められ、比較例B−1および2では、充填ば
らつきが見られた。また比較例B−3では、充填ばらつ
きはなかったものの、内容粉末のローヤルゼリー凍結乾
燥粉末の吸湿性が高いために、コーンスターチの有する
吸水性によって、ハードカプセル内において凝集が起こ
っていた。
Example B-1, Example B-2, Example B-
In No. 3, the properties such as hard capsule filling property, storage stability and appearance were all excellent. On the other hand, in Comparative Example B-1, Comparative Example B-2 and Comparative Example B-3, in the storage stability test, aggregation of the content powder was observed in the content powder in the hard capsule, and in Comparative Examples B-1 and 2, , Filling variation was observed. In Comparative Example B-3, although there was no variation in filling, the royal jelly freeze-dried powder of the content powder had a high hygroscopicity, so that the corn starch caused agglomeration in the hard capsule due to the water absorption.

【0057】[0057]

【発明の効果】上述のように、本発明の植物性油脂粉末
によれば、従来の滑沢剤を使用するよりも口腔内におけ
る感触が良好で、かつ保存安定性に優れ、キャッピン
グ、スティッキング、バインディング等の打錠障害およ
びしみの発生が起こらず、硬度および崩壊時間に影響の
ない錠剤または錠菓を得ることができる。また、本発明
によれば、従来の流動促進剤を使用するよりもハードカ
プセル充填性が良好で、かつ保存安定性に優れ、外観に
影響の出ないハードカプセル剤を得ることができる。さ
らに、本発明によって得られる滑沢剤を使用した錠剤、
錠菓、ハードカプセル剤は、医薬品に限らず造形剤等の
診断用薬品、健康食品や機能性食品等、本製剤の特性を
活かした様々な用途に応用することができる。
As described above, according to the vegetable oil powder of the present invention, the feeling in the oral cavity is better than that of using a conventional lubricant, and the storage stability is excellent, and capping, sticking, Tablets or tablet confections which do not suffer from tableting troubles such as binding and occurrence of stains and which do not affect hardness and disintegration time can be obtained. Further, according to the present invention, it is possible to obtain a hard capsule agent which has a better filling property of the hard capsule than the conventional glidant is used, has excellent storage stability, and does not affect the appearance. Furthermore, tablets using the lubricant obtained by the present invention,
Tablets and hard capsules can be applied not only to pharmaceuticals but also to various uses utilizing the characteristics of the present preparation, such as diagnostic drugs such as modeling agents, health foods and functional foods.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) A61K 9/20 A61K 47/26 47/26 47/42 47/42 47/44 47/44 A23G 3/00 // A23G 3/00 A23D 9/00 518 (72)発明者 喜瀬 光男 神奈川県横浜市戸塚区上品濃12番13号 株 式会社ファンケル中央研究所内 Fターム(参考) 4B014 GB08 GE01 GG14 GK07 GL08 GL11 GP23 GQ07 4B026 DG01 DG02 DG03 DL03 DL04 DP01 DP10 DX08 4B035 LC03 LC05 LE05 LE12 LG12 LG15 LG19 LG20 LG21 LK09 LP21 LP24 LP31 LP34 LP55 4C076 AA36 BB01 CC40 DD67 EE38 EE41 EE53 FF09 4H059 BA17 BB15 BB22 BB44 BB45 BB51 BC13 BC43 BC45 BC46 DA03 DA16 ──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 7 Identification symbol FI Theme coat ゛ (Reference) A61K 9/20 A61K 47/26 47/26 47/42 47/42 47/44 47/44 A23G 3/00 // A23G 3/00 A23D 9/00 518 (72) Inventor Mitsuo Kise 12-13, Kaminoshino, Totsuka-ku, Yokohama-shi, Kanagawa Prefecture F-term in FANCL Central Research Laboratories F term (reference) 4B014 GB08 GE01 GG14 GK07 GL08 GL11 GP23 GQ07 4B026 DG01 DG02 DG03 DL03 DL04 DP01 DP10 DX08 4B035 LC03 LC05 LE05 LE12 LG12 LG15 LG19 LG20 LG21 LK09 LP21 LP24 LP31 LP34 LP55 4C076 AA36 BB01 CC40 DD67 EE38 EE41 EE53 FF09 4H059 BA17 BB15 BB15 BB15 BB15 BB15 BB15 BB15 BB15 BC15 BC

Claims (8)

【特許請求の範囲】[Claims] 【請求項1】 植物性油脂、糖質および蛋白質もしくは
親油性加工澱粉を含む植物性油脂粉末。
1. A vegetable oil powder comprising vegetable oil, sugar and protein or modified lipophilic starch.
【請求項2】 植物性油脂100質量部に対して、糖質
を30〜40質量部および蛋白質8〜12質量部含む
か、または糖質を70〜90質量部および親油性加工澱
粉10〜30質量部含む請求項1記載の植物性油脂粉
末。
2. 100 parts by mass of vegetable oils and fats, containing 30 to 40 parts by mass of saccharide and 8 to 12 parts by mass of protein, or 70 to 90 parts by mass of saccharide and 10 to 30 parts of lipophilic modified starch. The vegetable fat / oil powder according to claim 1, which contains parts by mass.
【請求項3】 植物性油脂の固体脂指数が20℃で40
以上であり、かつ40℃で70以下である請求項1また
は2記載の植物性油脂粉末。
3. The solid fat index of a vegetable fat or oil at 20 ° C. is 40.
The vegetable oil or fat powder according to claim 1 or 2, which is 70 or less at 40 ° C.
【請求項4】 植物性油脂に糖質および蛋白質もしくは
親油性加工澱粉を配合して乳化させ、噴霧乾燥すること
を特徴とする請求項1〜3のいずれか1項記載の植物性
油脂粉末の製造方法。
4. The vegetable oil / fat powder according to any one of claims 1 to 3, wherein the vegetable oil / fat is blended with a carbohydrate and a protein or a lipophilic modified starch, and the mixture is emulsified and spray-dried. Production method.
【請求項5】 請求項1〜3のいずれか1項記載の植物
性油脂粉末を含有する食品組成物。
5. A food composition containing the vegetable fat or oil powder according to claim 1.
【請求項6】 請求項1〜3のいずれか1項記載の植物
性油脂粉末を含む滑沢剤または流動促進剤。
6. A lubricant or a glidant comprising the vegetable fat or oil powder according to claim 1. Description:
【請求項7】 請求項6記載の滑沢剤または流動促進剤
を0.1〜10質量%含有する食品組成物。
7. A food composition containing 0.1 to 10% by mass of the lubricant or glidant according to claim 6.
【請求項8】 固体の形態である請求項7記載の食品組
成物。
8. The food composition according to claim 7, which is in a solid form.
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