JP2000093125A - Drink or food comprising edible fibers - Google Patents

Drink or food comprising edible fibers

Info

Publication number
JP2000093125A
JP2000093125A JP10284785A JP28478598A JP2000093125A JP 2000093125 A JP2000093125 A JP 2000093125A JP 10284785 A JP10284785 A JP 10284785A JP 28478598 A JP28478598 A JP 28478598A JP 2000093125 A JP2000093125 A JP 2000093125A
Authority
JP
Japan
Prior art keywords
food
drink
dietary fiber
viscosity
acidic
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
JP10284785A
Other languages
Japanese (ja)
Inventor
Yoshiaki Oshida
喜昭 押田
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to JP10284785A priority Critical patent/JP2000093125A/en
Publication of JP2000093125A publication Critical patent/JP2000093125A/en
Pending legal-status Critical Current

Links

Landscapes

  • Coloring Foods And Improving Nutritive Qualities (AREA)
  • Non-Alcoholic Beverages (AREA)

Abstract

PROBLEM TO BE SOLVED: To provide a drink or food which comprises edible fibers, can easily be drunk and can be expected to act in bodies. SOLUTION: This drink or food comprising edible fibers uses an acidic polysaccharide which can be cross-linked with polyvalent metal ions. Therein, the acidic polysaccharide is used in a state substantially not cross-linked, and has a viscosity of 2-10 mm2/s in a 0.5% aqueous solution.

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】本発明は食物繊維からなる飲
食品に関する。
[0001] The present invention relates to a food or drink comprising dietary fiber.

【0002】[0002]

【従来の技術】食物繊維を用いた飲食品が、栄養補助食
品として公知である。食物繊維は、ヒトの消化酵素で消
化されない食品中の難消化性成分の総体と定義され、そ
の性質から、水溶性食物繊維と不溶性食物繊維に分類さ
れている。食物繊維は従来不要なものとされていたが、
近年、便秘を予防したり、食物中の有害物質を吸着して
体外に排泄する作用等により、糖尿病や大腸がんの予防
効果などが認められている。
2. Description of the Related Art Food and drink products using dietary fiber are known as dietary supplements. Dietary fiber is defined as the total of indigestible components in food that cannot be digested by human digestive enzymes, and is classified into water-soluble dietary fiber and insoluble dietary fiber based on its properties. Dietary fiber was previously considered unnecessary,
In recent years, the effects of preventing constipation, adsorbing harmful substances in food and excreting the same outside the body, and the like, have been observed to prevent diabetes and colorectal cancer.

【0003】食物繊維の具体的な生理作用として、主に
消化管機能に対して、消化管内容物の増加と消化管通過
時間の変化、栄養成分や有害物質の消化吸収などの影
響、さらに脂質などの代謝、腸内細菌叢への影響など多
くの作用が報告されている。これらの生理作用から、肥
満、糖尿病、高脂血症、動脈硬化、大腸疾患、便秘、胆
石、胆嚢炎など、非常に多種類の疾病に対する応用が期
待されている。
[0003] Specific physiological actions of dietary fiber mainly include an increase in gastrointestinal contents and a change in gastrointestinal transit time, effects on digestive absorption of nutrients and harmful substances, mainly on gastrointestinal functions, and lipids. Many effects have been reported, such as metabolism and the effect on intestinal flora. Due to these physiological effects, application to a wide variety of diseases such as obesity, diabetes, hyperlipidemia, arteriosclerosis, colorectal disease, constipation, gallstones, and cholecystitis is expected.

【0004】[0004]

【発明が解決しようとする課題】食物繊維の生理作用の
多くは、より高分子で、高い粘性を有する水溶性食物繊
維に認められる。しかしながら、水溶性食物繊維の分子
量が大きく、水溶液の粘性が高いことは、飲食品として
利用する場合に、非常に利用しにくいという欠点となっ
てしまい、水溶性食物繊維の応用が困難となっているの
が現状である。
Many of the physiological effects of dietary fiber are found in water soluble dietary fiber which is higher in molecular weight and has higher viscosity. However, the high molecular weight of the water-soluble dietary fiber and the high viscosity of the aqueous solution, when used as a food or drink, have the disadvantage of being very difficult to use, making the application of the water-soluble dietary fiber difficult. That is the current situation.

【0005】例えば水溶性食物繊維を粉体の状態で飲用
する場合は、口の中で高粘度の塊となってしまい、上記
の体内での作用が期待できない。また、水溶液として飲
料する場合は、粘性が高いため非常に飲用しにくく、ま
た、実用的な粘性の範囲の水溶液では濃度を高くするこ
とができない為、食物繊維の持つ効果が期待できなくな
ってしまう。
For example, when drinking water-soluble dietary fiber in the form of a powder, it becomes a highly viscous mass in the mouth, and the above-mentioned effects in the body cannot be expected. In addition, when drinking as an aqueous solution, it is very difficult to drink due to high viscosity, and since the concentration cannot be increased in an aqueous solution within a practical viscosity range, the effect of dietary fiber cannot be expected. .

【0006】また、現在、栄養補助食品として市販され
ている水溶性食物繊維は、水に対する溶解性は良好であ
るが、50%エタノール水にも溶解する。このような物
質は高分子ではなく、粘性も低いことから上記のような
生理作用は期待できない。
[0006] In addition, water-soluble dietary fiber currently marketed as a dietary supplement has good solubility in water, but is also soluble in 50% ethanol water. Since such a substance is not a polymer and has a low viscosity, the above physiological action cannot be expected.

【0007】本発明は上記従来技術の欠点を解決するた
めになされたものであり、飲食がし易く、かつ、体内で
の作用が充分期待できる食物繊維からなる飲食品を提供
することを目的とする。
SUMMARY OF THE INVENTION The present invention has been made to solve the above-mentioned drawbacks of the prior art, and has as its object to provide a food or drink made of dietary fiber which is easy to eat and drink and can be expected to have a sufficient effect in the body. I do.

【0008】[0008]

【課題を解決するための手段】本発明は、(1)多価金
属イオンにより架橋可能な酸性多糖類を用いたことを特
徴とする食物繊維からなる飲食品、(2)酸性多糖類が
実質的に未架橋の状態である上記(1)記載の飲食品、
(3)酸性多糖類の0.5%水溶液の粘度が2〜10m
2 /sである上記(2)記載の食物繊維からなる飲食
品、を要旨とするものである。
The present invention provides (1) a food or drink comprising dietary fiber, characterized by using an acidic polysaccharide which can be cross-linked by a polyvalent metal ion; The food or drink according to the above (1), which is in an uncrosslinked state,
(3) The viscosity of a 0.5% aqueous solution of an acidic polysaccharide is 2 to 10 m.
A food or drink comprising the dietary fiber according to the above (2), which has a m 2 / s.

【0009】[0009]

【発明の実施の形態】本発明において酸性多糖類とは硫
酸基やカルボキシル基等の酸性基を含む多糖類をいう。
酸性多糖類は構造、分子量等は特に限定されず、植物又
は動物より抽出されたもの及びその分解物等の天然物、
あるいは合成物のいずれでもよい。
BEST MODE FOR CARRYING OUT THE INVENTION In the present invention, an acidic polysaccharide refers to a polysaccharide containing an acidic group such as a sulfate group and a carboxyl group.
Acidic polysaccharides are not particularly limited in structure, molecular weight, etc., and natural products such as those extracted from plants or animals and their decomposed products,
Alternatively, any of synthetic compounds may be used.

【0010】酸性多糖類として具体的には、カルボキシ
ル基を含むものとしてアルギン酸、ペクチン酸等、硫酸
基を含むものとして、カラゲナン、コロイダン等、ヘキ
ソサミンとウロン酸からなるヒアルロン酸、コンドロイ
チン硫酸や、合成の硫酸化多糖類としてデキストラン硫
酸やセルロース硫酸、キトサン等が挙げられる。上記の
なかでも、安価であることからアルギン酸又はペクチン
酸が好ましい。アルギン酸は、D−マンヌロン酸及びL
−グルロン酸とで構成される直鎖型ポリマーである。
Specific examples of acidic polysaccharides include those containing carboxyl groups, such as alginic acid and pectic acid; those containing sulfate groups, such as carrageenan and colloidan; hyaluronic acid consisting of hexosamine and uronic acid; chondroitin sulfate; Sulfated polysaccharides include dextran sulfate, cellulose sulfate, chitosan and the like. Of the above, alginic acid or pectic acid is preferred because of its low cost. Alginic acid is D-mannuronic acid and L
-A linear polymer composed of guluronic acid.

【0011】酸性多糖類の溶解性、粘性、ゲル化性、凝
固性等は、その構成糖や結合様式,、分子量、酸性基の
置換の程度により様々であるが、一般的には、その水溶
液の粘度は高い。上記の酸性多糖類はいずれも高分子化
合物であり、粘度が高いので、飲用の際に飲みやすさを
考慮した場合、粘性の低い水溶液となるように、上記酸
性多糖類を原料として構造を変化させて用いるのが好ま
しい。とくに酸性多糖類は、0.5%水溶液の粘度(2
5℃、オストワルド粘度計で測定)が、2〜10mm2
/sであることが、更に飲食品としての利用が容易にな
り好ましい。
The solubility, viscosity, gelling properties, coagulation properties, etc. of acidic polysaccharides vary depending on their constituent sugars, bonding modes, molecular weight, and the degree of substitution of acidic groups. Has a high viscosity. Since the above acidic polysaccharides are all high molecular compounds and have high viscosities, the structure is changed using the above acidic polysaccharides as a raw material so as to be a low-viscosity aqueous solution in consideration of ease of drinking when drinking. It is preferable to use them. Particularly, acidic polysaccharides have a viscosity of 0.5% aqueous solution (2
5 ° C., measured with an Ostwald viscometer) 2-10 mm 2
/ S is preferred because it can be more easily used as food and drink.

【0012】酸性多糖類は、加水分解を行うことで低分
子化し、粘性の低い水溶液が得られる。加水分解は、
酸、アルカリ、酵素、分解剤等を用いた分解、その他の
分解に必要な操作を利用できる。分解条件の具体例を以
下の実験例で示す。
The acidic polysaccharide is reduced in molecular weight by hydrolysis, and an aqueous solution having low viscosity is obtained. The hydrolysis is
Decomposition using an acid, an alkali, an enzyme, a decomposing agent, and the like, and other operations required for decomposition can be used. Specific examples of the decomposition conditions are shown in the following experimental examples.

【0013】実験例1 〔ペクチンのアルカリ加水分解〕ペクチン30gを0.
1mol/リットルの水酸化ナトリウムに溶解し、80
℃で4時間加熱した。冷却後、等量のエタノールを加
え、生じた沈澱物をロ別した。沈澱物はエタノールで洗
浄後、乾燥させ、低分子化ペクチン21.3gを得た。
Experimental Example 1 [Alkaline hydrolysis of pectin]
Dissolve in 1 mol / L sodium hydroxide, 80
Heated at 0 ° C for 4 hours. After cooling, an equal volume of ethanol was added and the resulting precipitate was filtered off. The precipitate was washed with ethanol and dried to obtain 21.3 g of low molecular weight pectin.

【0014】実験例2 〔アルギン酸のアルカリ加水分解〕アルギン酸30gを
0.1mol/リットルの水酸化ナトリウムに溶解し、
80℃で4時間加熱した。冷却後、等量のエタノールを
加え、生じた沈澱物をロ別した。沈澱物はエタノールで
洗浄後、乾燥させ、低分子化アルギン酸25.1gを得
た。
Experimental Example 2 [Alkaline hydrolysis of alginic acid] Alginic acid (30 g) was dissolved in 0.1 mol / L sodium hydroxide,
Heated at 80 ° C. for 4 hours. After cooling, an equal volume of ethanol was added and the resulting precipitate was filtered off. The precipitate was washed with ethanol and dried to obtain 25.1 g of low molecular weight alginic acid.

【0015】〔粘度及びゲル形成量の測定〕実験例1及
び実験例2で用いたペクチン及びアルギン酸、ならびに
実験例1及び実験例2で得られた低分子化ペクチン及び
低分子化アルギン酸を試料として、動粘度及びゲル形成
量を測定した測定結果を表1に示す。粘度の測定方法
は、試料0.5%水溶液の粘度をオストワルドの粘度計
を用いて25℃で測定した。またゲル形成量は、試料各
々500mgを精製水100mlに溶解し、等量の塩化
カルシウムを加えゲルを形成させ、ろ紙上で自然ろ過
し、ろ液量を測定し、下記の〔数1〕式からゲル形成量
を求めた。
[Measurement of Viscosity and Gel Forming Amount] The pectin and alginic acid used in Experimental Examples 1 and 2, and the low-molecular-weight pectin and low-molecular-weight alginic acid obtained in Experimental Examples 1 and 2 were used as samples. Table 1 shows the measurement results obtained by measuring the kinematic viscosity and the gel formation amount. The viscosity was measured by measuring the viscosity of a 0.5% aqueous solution of the sample at 25 ° C. using an Ostwald viscometer. The amount of gel formed was determined by dissolving 500 mg of each sample in 100 ml of purified water, adding an equal amount of calcium chloride to form a gel, performing natural filtration on filter paper, measuring the amount of filtrate, and calculating the following [Equation 1]. The amount of gel formed was determined from.

【数1】 ゲル形成量(ml)=100−ろ液量(ml)## EQU00001 ## Gel formation amount (ml) = 100-filtrate amount (ml)

【0016】[0016]

【表1】 [Table 1]

【0017】表1に示すように、加水分解を行うことで
アルギン酸は動粘度が大きく低下した。またペクチンは
加水分解後も、ほとんど動粘度に変化は認められなかっ
たが、溶解性は良好となった。
As shown in Table 1, the kinematic viscosity of alginic acid was significantly reduced by the hydrolysis. Pectin showed almost no change in kinematic viscosity after hydrolysis, but showed good solubility.

【0018】酸性多糖類は、分子中の酸性基によって、
多価金属イオンの存在により容易にゲル化する。これは
多価金属イオンが酸性基と結合して酸性多糖類の分子ど
うしを架橋するからである。酸性多糖類は、飲食した
後、胃内において多価金属イオンの作用でゲル化させる
ことができる。ゲルの形成は、用いる酸性多糖類が高分
子であっても、低分子であってもほぼ同様に行われるの
で、上記の低分子化した物質を用いても高分子化合物と
同様の生理作用が期待できる。
The acidic polysaccharide is formed by an acidic group in the molecule.
Gels easily due to the presence of polyvalent metal ions. This is because the polyvalent metal ion bonds to the acidic group and crosslinks the molecules of the acidic polysaccharide. After eating and drinking, the acidic polysaccharide can be gelled in the stomach by the action of polyvalent metal ions. Gel formation is carried out in substantially the same manner whether the acidic polysaccharide used is a polymer or a small molecule, so that the same physiological action as that of a polymer compound can be obtained using the above-mentioned reduced-molecular substance. Can be expected.

【0019】本発明の食物繊維を用いた飲食品は、酸性
多糖類が多価金属イオンを含まない未架橋の状態として
おくのが好ましい。このように、酸性多糖類が多価金属
イオンにより架橋しない状態であれば、飲食の際には粘
性の低い状態あるいはゲル状にならず利用し易い状態で
ある。そして酸性多糖類といっしょに多価金属イオンを
摂取すれば、消化管内で酸性多糖類が多価金属イオンと
反応して架橋し増粘ゲル化するから、食物繊維の持つ作
用を充分に発揮することができる。
The food or drink using the dietary fiber of the present invention is preferably in an uncrosslinked state in which the acidic polysaccharide does not contain a polyvalent metal ion. As described above, when the acidic polysaccharide is not crosslinked by the polyvalent metal ion, it is in a state of low viscosity or in a state of being easy to use without being gelled during eating and drinking. Ingestion of polyvalent metal ions together with acidic polysaccharides causes the acidic polysaccharides to react with polyvalent metal ions in the digestive tract and cross-link to form a thickened gel. be able to.

【0020】上記多価金属イオンとして、上記目的には
2価の金属イオンが適当であるが、人体に有害な金属塩
は使用できないので、特にカルシウムイオンやマグネシ
ウムイオン等のアルカリ金属塩が適している。またアル
カリ金属塩を直接飲用するだけではなく、アルカリ金属
塩を多量に含む食品を同時に摂取することでも、胃等の
内部で酸性多糖類をゲル化させることができる。
As the above polyvalent metal ion, a divalent metal ion is suitable for the above purpose, but a metal salt harmful to the human body cannot be used. Therefore, an alkali metal salt such as a calcium ion or a magnesium ion is particularly suitable. I have. Further, not only by directly drinking the alkali metal salt but also by simultaneously ingesting a food containing a large amount of the alkali metal salt, the acidic polysaccharide can be gelled inside the stomach or the like.

【0021】上記目的の為のアルカリ金属塩含む食品
は、カルシウムイオンやマグネシウムイオン等を多く多
量に含有し、液状の飲料物が好ましく、具体的には牛
乳、スキムミルク、ヨーグルト(乳精)等の乳製品が挙
げられる。牛乳やスキムミルクなどでは、粘度の上昇が
見られるがゲル化しないので、好ましくはアルカリ金属
塩を添加する。また、ヨーグルトの乳精を用いた場合に
は、充分なゲルが形成された。
The food containing the alkali metal salt for the above purpose contains a large amount of calcium ions, magnesium ions and the like, and is preferably a liquid beverage, and specifically, milk, skim milk, yogurt (milk semen) and the like. Dairy products. In cow's milk and skim milk, etc., an increase in viscosity is observed but it does not gel, so that an alkali metal salt is preferably added. When yogurt milk was used, a sufficient gel was formed.

【0022】本発明において酸性多糖類が多価金属イオ
ンを含まない未架橋の状態とは、酸性多糖類が多価金属
イオンにより実質的に架橋していないということであっ
て、微量の多価金属イオンの存在をも否定するものでは
ない。例えば水溶液の飲料物として提供する場合に、一
般に使用する水の中には微量のカルシウムイオンやマグ
ネシウムイオン等の多価金属イオンが含まれるが、これ
らの多価金属イオンが存在していても、その程度であれ
ば、飲料物の粘性に大きく影響を与えることは無いため
特に問題はない。
In the present invention, the non-crosslinked state in which the acidic polysaccharide does not contain a polyvalent metal ion means that the acidic polysaccharide is not substantially crosslinked by the polyvalent metal ion, and a trace amount of the polyvalent metal ion. It does not deny the existence of metal ions. For example, when provided as an aqueous beverage, generally used water contains a trace amount of polyvalent metal ions such as calcium ions and magnesium ions, even if these polyvalent metal ions are present, At that level, there is no particular problem because the viscosity of the beverage is not significantly affected.

【0023】本発明の飲食品は、少なくとも酸性多糖類
からなる食物繊維を含むものであれば、その形態は特に
限定されない。具体的には、水溶液状にした飲料水の形
態、或いは固体状の食品等の形成のいずれでもよい。ま
た、飲食品には、その他の添加剤などを添加してもよ
い。
The form of the food or drink of the present invention is not particularly limited as long as it contains dietary fiber comprising at least an acidic polysaccharide. Specifically, it may be in the form of drinking water in the form of an aqueous solution or in the form of a solid food or the like. Further, other additives may be added to the food or drink.

【0024】[0024]

【発明の効果】本発明の食物繊維からなる飲食品は、多
価金属イオンにより架橋可能な酸性多糖類を用いたこと
により、飲食がし易く、かつ、体内での作用が充分期待
できるものである。
The food and drink comprising the dietary fiber of the present invention is easy to eat and drink and can be expected to have a sufficient action in the body by using an acidic polysaccharide which can be crosslinked by polyvalent metal ions. is there.

【0025】食物繊維からなる飲食品は糖尿病の治療に
利用できる。糖尿病は、インスリンの不足によりグルコ
ースの利用が障害されて血糖濃度が上昇し、尿糖として
排出される疾患であり、糖代謝をはじめとする広範な代
謝異常ならびに種々の合併症を引き起こす。糖尿病の治
療法として、食事療法、運動療法、経口剤療法、インス
リン療法が行われている。特に食事療法は非常に重要で
あり、基本的な原理は摂取カロリーを必要最小限に制限
することで、体内のインスリンの作用の不足を軽減する
ことである。酸性多糖類からなる水溶性繊維は、胃で膨
潤することで胃内食物の体積を増加させ、粘性を上昇さ
せる為、食物の胃内滞留時間を延長することで血糖上昇
抑制効果がある。その結果インスリンを効率良く働かせ
ることが可能であることが、以前から知られている。
Foods and drinks made of dietary fiber can be used for treating diabetes. Diabetes mellitus is a disease in which glucose utilization is impaired due to a lack of insulin, blood glucose levels increase, and urinary glucose is excreted, causing a wide range of metabolic abnormalities including glucose metabolism and various complications. Diet therapy, exercise therapy, oral drug therapy, and insulin therapy have been used as treatments for diabetes. In particular, diet is very important, and the basic principle is to limit the caloric intake to the minimum necessary, thereby reducing the lack of action of insulin in the body. The water-soluble fiber composed of an acidic polysaccharide increases the volume of food in the stomach by swelling in the stomach and increases the viscosity, and thus has an effect of suppressing an increase in blood glucose by extending the residence time of the food in the stomach. It has long been known that insulin can work efficiently as a result.

【0026】本発明の食物繊維からなる飲食品につい
て、グルコース負荷試験を行って血糖上昇抑制効果を試
験した結果を表2に示す。表2から明らかなように、飲
食した場合に明らかな血糖抑制効果が見られた。なお試
験方法は、オトコ、43歳を被験者とした、75gグル
コース負荷試験において、実験例2で得た低分子化アル
ギン酸1.5g及び硫酸カルシウム1.0gを直前に経
口投与した場合と、両者を未投与の場合について、血糖
値の値を測定して比較した。
Table 2 shows the results of a glucose tolerance test performed on the food or drink comprising the dietary fiber of the present invention to test the effect of suppressing an increase in blood glucose. As is evident from Table 2, a clear blood sugar suppressing effect was observed when eating and drinking. The test method was as follows. In a 75 g glucose tolerance test using a male, 43 years old as a subject, 1.5 g of the low-molecular-weight alginic acid and 1.0 g of calcium sulfate obtained in Experimental Example 2 were orally administered immediately before. In the case of no administration, the blood glucose level was measured and compared.

【0027】[0027]

【表2】 [Table 2]

【0028】次に上記のグルコース負荷試験において空
腹時と負荷30分経過後のインスリン量を比較した結果
を表3に示す。
Next, Table 3 shows the results of comparing the amount of insulin at the time of fasting and 30 minutes after the load in the glucose tolerance test.

【0029】[0029]

【表3】 [Table 3]

【0030】また、食物繊維は胆汁酸の排泄を促し、コ
レステロール値を低下させることから、高脂血症の予防
効果が期待できる。また、食物繊維は食品中の重金属類
などの有害物質を吸着し体内での吸収速度を低下させる
ことから、その毒性の発現を低下させる為、ダイオキシ
ン等で汚染された食品に対する防御、アトピー性皮膚炎
などのアレルギー疾患に対する改善作用があると言われ
る。その為、本発明の食物繊維を用いた飲食品も同様の
効果が得られる。
Further, dietary fiber promotes excretion of bile acids and lowers cholesterol level, so that the effect of preventing hyperlipidemia can be expected. In addition, dietary fiber adsorbs harmful substances such as heavy metals in foods and reduces the rate of absorption in the body. Therefore, in order to reduce the manifestation of its toxicity, it protects foods contaminated with dioxins, etc., and has atopic skin. It is said to have an improving effect on allergic diseases such as inflammation. Therefore, the same effects can be obtained with food and drink using the dietary fiber of the present invention.

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】 多価金属イオンにより架橋可能な酸性多
糖類を用いたことを特徴とする食物繊維からなる飲食
品。
1. A food or drink comprising dietary fiber, wherein an acidic polysaccharide crosslinkable by a polyvalent metal ion is used.
【請求項2】 酸性多糖類が実質的に未架橋の状態であ
る請求項1記載の食物繊維からなる飲食品。
2. The food or drink comprising dietary fiber according to claim 1, wherein the acidic polysaccharide is in a substantially uncrosslinked state.
【請求項3】 酸性多糖類の0.5%水溶液の粘度が2
〜10mm2 /sである請求項2記載の食物繊維からな
る飲食品。
3. A 0.5% aqueous solution of an acidic polysaccharide has a viscosity of 2%.
3. A food or drink comprising the dietary fiber according to claim 2, wherein the food and drink is from 10 to 10 mm 2 / s.
JP10284785A 1998-09-21 1998-09-21 Drink or food comprising edible fibers Pending JP2000093125A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10284785A JP2000093125A (en) 1998-09-21 1998-09-21 Drink or food comprising edible fibers

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10284785A JP2000093125A (en) 1998-09-21 1998-09-21 Drink or food comprising edible fibers

Publications (1)

Publication Number Publication Date
JP2000093125A true JP2000093125A (en) 2000-04-04

Family

ID=17682996

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10284785A Pending JP2000093125A (en) 1998-09-21 1998-09-21 Drink or food comprising edible fibers

Country Status (1)

Country Link
JP (1) JP2000093125A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004065191A (en) * 2002-08-09 2004-03-04 Tsi:Kk Functional supplementary drink product

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004065191A (en) * 2002-08-09 2004-03-04 Tsi:Kk Functional supplementary drink product

Similar Documents

Publication Publication Date Title
AU2015354845B2 (en) A dietary fibre composition
EP0493265A1 (en) Algin-containing food and beverage
US20100247582A1 (en) Method of preparing fibre-containing pectin product and pectin products hereof
CA2676058C (en) Diet product comprising alginate
JPH0326169B2 (en)
JP5079713B2 (en) Gastric raft composition comprising preferably processed starch for inducing satiety
JP2000093125A (en) Drink or food comprising edible fibers
JP2983716B2 (en) Food composition comprising a water-soluble dietary fiber complex
JP4001443B2 (en) Phosphorus absorption inhibitor and therapeutic agent containing the same
CN113575956A (en) Application of chitosan and chitosan oligosaccharide in inhibiting protein absorption
WO2021067076A1 (en) Methods for treating or preventing obesity and body weight management
KR100473445B1 (en) cholesterol reducer and health food containing chitosan and ε-polylysine
JP2004051615A (en) Bile acids adsorbent using chitosan-orotic acid salt
EP1043022B1 (en) Sodium ion absorption inhibitors and sodium ion excretion accelerators as preventive and therapeutic agents for diseases resulting from excessive intake of common salt
US20240122965A1 (en) pH-RESPONSIVE HYDROGEL AND MANUFACTURING METHOD THEREOF
JPH1067804A (en) Chitosan derivative, its production and its use
KR100539662B1 (en) Rice coated with a composition comprising alginic acid and porphyran
JPH0256433A (en) Relieving of constipation caused by administration of barium
JP2005112838A (en) Hyperkalemia-improving agent by using calcium chitin chitosan
JPH03127953A (en) Apple fiber-containing konjak
JPH09241169A (en) Gel state composition having compound releasing and adsorbing property
WO2005067719A1 (en) Chitosan-psyllium complexes and methods for making and using same
KR20030014007A (en) Health assistant foodstuffs comprising of functional chitosan-lactic salts and preparing method thereof