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JP2013039079A - Method for dissolving stevia extract - Google Patents

Method for dissolving stevia extract Download PDF

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JP2013039079A
JP2013039079A JP2011178350A JP2011178350A JP2013039079A JP 2013039079 A JP2013039079 A JP 2013039079A JP 2011178350 A JP2011178350 A JP 2011178350A JP 2011178350 A JP2011178350 A JP 2011178350A JP 2013039079 A JP2013039079 A JP 2013039079A
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stevia extract
stevia
rebaudioside
water
solution
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Manabu Matsuda
松田  学
Makoto Machida
誠 町田
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Nippon Paper Industries Co Ltd
Jujo Paper Co Ltd
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Nippon Paper Industries Co Ltd
Jujo Paper Co Ltd
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Abstract

PROBLEM TO BE SOLVED: To provide a method for ameliorating dissolubility of a stevia extract having high content ratio of slightly soluble rebaudioside-A and improving stability of a solution when dissolving the stevia extract in an aqueous solvent such as water to prepare the solution.SOLUTION: The method for dissolving a stevia extract containing 90 wt.% or more of rebaudioside-A having 5.0 g/100 g or less of solubility to water includes mixing a soluble polysaccharide to the stevia extract so that a dry weight ratio of the stevia extract to the soluble polysaccharide is 100:5-0.4:99.6, and dissolving the obtained mixture to dissolve in the aqueous solvent.

Description

本発明は、難溶解性のRebaudioside−Aを90重量%以上含有するステビア抽出物の溶解方法に関する。   The present invention relates to a method for dissolving a stevia extract containing 90% by weight or more of hardly soluble Rebaudioside-A.

ステビア抽出物は、ステビア(キク科の植物。学名:ステビア レバウディアナ ベルトニー(Stevia rebaudiana BERTONI)の植物体の抽出物であり、通常はステビアの葉部の抽出物である。ステビア抽出物は甘味成分を含むので、ステビア甘味料とも呼ばれる。
ステビア抽出物の甘味成分としては、主成分であるSteviosideをはじめ、Rebaudioside−A、Rubusoside、Dulcoside−A、Steviobioside、Rebaudioside−C、Rebaudioside−B、Rebaudioside−D、Rebaudioside−F等のステビオール配糖体が知られている。
ステビア抽出物の甘味度は、ショ糖の200〜300倍である。よって、ショ糖と同じ甘味を得るために使用されるステビア抽出物の量はショ糖と比較して非常に少量でよいことから、実質的にノンカロリー甘味料として使用されている。また、ステビア抽出物は天然甘味料であることから、食品工業界でも多く使用されており、食経験も多い(特許文献1)。
ステビア抽出物としては、Steviosideの含有比率の高いステビア抽出物(通常抽出品)、及びRebaudioside−Aの含有比率の高いステビア抽出物(調整品)が知られている。Steviosideの含有比率の高いステビア抽出物の甘味は比較的砂糖に似ているが、苦み等の異味が後味に残るという欠点がある。一方、Rebaudioside−Aの含有比率の高いステビア抽出物は、異味が少ない良質な甘味を呈する。つまり、Rebaudioside−Aの含有比率の高いステビア抽出物甘味成分が高純度化されることになる。
Stevia extract is an extract of Stevia (Asteraceae plant. Scientific name: Stevia rebaudiana BERTONI), usually an extract of Stevia leaves. Because it contains, it is also called a stevia sweetener.
As a sweetening component of stevia extract, including Stevioside, which is a main component, Rebaudioside-A, Rubusoside, Dulcoside-A, Stevioside, Rebaudioside-C, Rebaudioside-B, Rebaudioside-D, Rebaudioside-D, Rebaudioside-D, Steboside-D It has been known.
The sweetness of stevia extract is 200 to 300 times that of sucrose. Thus, the amount of stevia extract used to obtain the same sweetness as sucrose may be very small compared to sucrose, so it is used substantially as a non-caloric sweetener. Stevia extract is a natural sweetener, so it is also used in the food industry and has a lot of food experience (Patent Document 1).
As stevia extract, stevia extract having a high content ratio of stevioside (normal extract) and stevia extract having a high content ratio of Rebaudioside-A (adjusted product) are known. The sweetness of stevia extract with a high content ratio of stevioside is relatively similar to sugar, but has the disadvantage that off-flavors such as bitterness remain in the aftertaste. On the other hand, a stevia extract with a high content ratio of Rebaudioside-A exhibits a good quality sweetness with less off-taste. That is, the stevia extract sweetness component with a high content ratio of Rebaudioside-A is highly purified.

一般的にはRebaudioside−Aを90重量%以上含有するステビア抽出物は、植物体からの抽出、精製、乾燥、再溶解、再結晶化、乾燥の手順で製造されるが、Rebaudioside−Aの含有比率の高いステビア抽出物は、水系溶媒への溶解性が低いため、製造過程で大量の水分を蒸発することが必要となり、生産効率が大幅に低下するとともに、溶液からの異物除去のための濾過における作業が大幅に増加する。このため、Rebaudioside−Aを90重量%以上含有するステビア抽出物を高濃度に溶解する方法が求められていた。また、別の問題として、飲食品等の甘味料は、一定の濃度で保持した甘味料であることが一般的であるが、Rebaudioside−Aの含有比率の高いステビア抽出物は、溶解性の高い低いにかかわらず、再結晶化しやすいため、飲食品中において、一定濃度で保持されることが困難であるといった問題がある。
これらの問題に対して、Rebaudioside−Aを含有するステビア抽出物のシクロデキストリン錯体とすることで溶解性を改善する方法が開示されている(特許文献2)。
In general, stevia extract containing 90% by weight or more of Rebaudioside-A is produced by extraction, purification, drying, re-dissolution, recrystallization, and drying procedures from plant bodies, but it contains Rebaudioside-A. Stevia extract, which has a high ratio, has low solubility in aqueous solvents, so it is necessary to evaporate a large amount of water during the manufacturing process, greatly reducing production efficiency and filtering to remove foreign substances from the solution. Work in is greatly increased. For this reason, the method of melt | dissolving the stevia extract containing 90 weight% or more of Rebaudioside-A in high concentration was calculated | required. As another problem, sweeteners such as foods and drinks are generally sweeteners maintained at a constant concentration, but stevia extract with a high content ratio of Rebaudioside-A is highly soluble. Although it is low, it is easy to recrystallize, and thus there is a problem that it is difficult to maintain a constant concentration in food and drink.
In order to solve these problems, a method for improving the solubility by using a cyclodextrin complex of stevia extract containing Rebaudioside-A has been disclosed (Patent Document 2).

特開2000−236842号公報JP 2000-236842 A 特表2010−527609号公報Special table 2010-527609

しかしながら、特許文献2に開示された方法では、多くの工程が必要となるため、作業性が低下する問題があった。
そこで、本発明の目的は、難溶性であるRebaudioside−Aの含有比率の高いステビア抽出物の溶解性を改善し、該ステビア抽出物を水等の水性溶媒に溶解して溶液とした際に、該溶液の安定性を向上させるための手段を提供することを目的とする。
However, the method disclosed in Patent Document 2 has a problem that workability is lowered because many steps are required.
Therefore, the object of the present invention is to improve the solubility of stevia extract having a high content ratio of Rebaudioside-A, which is hardly soluble, and when the stevia extract is dissolved in an aqueous solvent such as water to form a solution, An object is to provide means for improving the stability of the solution.

本発明は、以下の〔1〕〜〔2〕を提供する。
〔1〕水に対する溶解度が5.0g/100g以下であるRebaudioside−Aを90重量%以上含有するステビア抽出物の溶解方法であって、該ステビア抽出物に対して水溶性多糖を、乾燥重量比が該ステビア抽出物:該水溶性多糖=100:5〜0.4:99.6となるように混合し、得られる混合物を水性溶媒に溶解することを特徴とするステビア抽出物の溶解方法。
〔2〕請求項1で得られる水溶液を、乾燥させることにより得られる溶解性を改善した固形物。
The present invention provides the following [1] to [2].
[1] A method for dissolving a stevia extract containing 90% by weight or more of Rebaudioside-A having a solubility in water of 5.0 g / 100 g or less, wherein the water-soluble polysaccharide is added to the stevia extract in a dry weight ratio. Is mixed with Stevia extract: water-soluble polysaccharide = 100: 5 to 0.4: 99.6, and the resulting mixture is dissolved in an aqueous solvent.
[2] A solid matter with improved solubility obtained by drying the aqueous solution obtained in claim 1.

本発明によれば、難溶性であるRebaudioside−Aを90重量%以上含有するステビア抽出物の溶解性を改善し、該ステビア抽出物を水等の水性溶媒に溶解して溶液とした際に、該溶液の安定性を向上させることができる。   According to the present invention, when improving the solubility of a stevia extract containing 90% by weight or more of Rebaudioside-A, which is hardly soluble, and dissolving the stevia extract in an aqueous solvent such as water, The stability of the solution can be improved.

本発明は、水に対する溶解度が5.0g/100g以下であるRebaudioside−Aを90重量%以上含有するステビア抽出物(以下、難溶性ステビア抽出物ということがある。)の溶解方法であって、該ステビア抽出物に対して水溶性多糖を、乾燥重量比が該ステビア抽出物:該水溶性多糖=100:5〜0.4:99.6となるように混合し、得られる混合物を水性溶媒に溶解することを特徴とするステビア抽出物の溶解方法に関する。   The present invention is a method for dissolving a stevia extract containing 90% by weight or more of Rebaudioside-A having a solubility in water of 5.0 g / 100 g or less (hereinafter sometimes referred to as a hardly soluble stevia extract), The water-soluble polysaccharide is mixed with the stevia extract so that the dry weight ratio of the stevia extract: the water-soluble polysaccharide = 100: 5 to 0.4: 99.6, and the resulting mixture is mixed with an aqueous solvent. The present invention relates to a method for dissolving a stevia extract characterized by being dissolved in

本発明において、ステビア抽出物とは、ステビアの植物体の抽出物を意味する。第73回JECFA(FAO/WHO合同食品添加物専門委員会)におけるステビア抽出物の規格は、Stevioside、Rubusoside、Dulcoside−A、Steviobioside、Rebaudioside−C、Rebaudioside−B、Rebaudioside−D、Rebaudioside−F、及びRebaudioside−Aを、これらの合計含量で95重量%以上含むものである。なお、この規格は、第73回JECFA(FAO/WHO合同食品添加物専門委員会)において、国際的に認知されたものである。本発明においても、上記JECFAの規格に適合したステビア抽出物が好ましく用いられるが、Rebaudioside−Aを90重量%以上含有するステビア抽出物であれば上記JECFAの規格に適合したステビア抽出物以外のものを用いてもよい。また、Rebaudioside−Aを90重量%以上含有するステビア抽出物に代えて、これと同様の組成を持つ化学合成品を用いてもよい。   In the present invention, the stevia extract means an extract of a stevia plant. The standard of stevia extract in the 73rd JECFA (FAO / WHO Joint Food Additives Expert Committee) is: And Rebaudioside-A in a total content of 95% by weight or more. This standard was internationally recognized by the 73rd JECFA (FAO / WHO Joint Food Additives Expert Committee). In the present invention, a stevia extract that conforms to the JECFA standard is preferably used. However, any stevia extract that contains 90% by weight or more of Rebaudioside-A is not a stevia extract that conforms to the JECFA standard. May be used. Further, instead of a stevia extract containing 90% by weight or more of Rebaudioside-A, a chemically synthesized product having the same composition as this may be used.

Rebaudioside−Aを90重量%以上含有するステビア抽出物は、キク科植物であるステビアの植物体の全体又は一部、通常は葉部から、抽出されればよく、抽出条件に制限はない。製造方法の一例を挙げると以下の通りである。ステビアの葉部、例えば乾燥葉から、抽出溶媒(例えば、水、または含水有機溶媒(含水アルコール(メタノール、エタノール、多価アルコールなど)、含水アセトン等))にて抽出する。抽出液はそのまま、或いは濃縮して得られる濃縮液を、必要に応じて、陽イオン交換樹脂、陰イオン交換樹脂、活性炭等の吸着剤を用いて上記抽出液或いはその濃縮液中のイオン性不純物を除去し、吸着剤に甘味成分を吸着させる。甘味成分を親水性溶媒で吸着剤から溶離して溶離液を濃縮して得られる濃縮液を得る。さらに該濃縮液を乾燥して乾燥物を得る。この乾燥物をステビア抽出物としている。   The stevia extract containing 90% by weight or more of Rebaudioside-A may be extracted from the whole or a part of Stevia plant, which is a asteraceae plant, usually from a leaf portion, and the extraction conditions are not limited. An example of the manufacturing method is as follows. Extract from Stevia leaves, for example, dried leaves, with an extraction solvent (for example, water or a water-containing organic solvent (water-containing alcohol (such as methanol, ethanol, polyhydric alcohol), water-containing acetone)). The extract is used as it is or after being concentrated, if necessary, using an adsorbent such as cation exchange resin, anion exchange resin, activated carbon, etc. And the sweetening component is adsorbed on the adsorbent. The sweetened component is eluted from the adsorbent with a hydrophilic solvent to obtain a concentrated solution obtained by concentrating the eluent. Further, the concentrated solution is dried to obtain a dried product. This dried product is used as a stevia extract.

このようにして得られるステビア抽出物が、Rebaudioside−Aを90重量%以上含んでいる場合には、本発明においてそのまま利用できる。一方、得られるステビア抽出物におけるRebaudioside−Aの含有量を90重量%以上に調整するために、さらに膜分離、アルコール抽出(例:メタノールを用いる抽出)、結晶化等の慣用手段を、適宜施してもよい。これらの操作は、必要に応じて撹拌や加温(例えば30〜70℃程度)と組み合わせてもよい。結晶化にあたっては、結晶溶媒として、有機溶媒(エタノール、メタノール等)、上記有機溶媒に水を添加したもの、を適宣使用することができる。   When the stevia extract obtained in this way contains 90% by weight or more of Rebaudioside-A, it can be used as it is in the present invention. On the other hand, in order to adjust the content of Rebaudioside-A in the obtained stevia extract to 90% by weight or more, conventional means such as membrane separation, alcohol extraction (eg, extraction using methanol), crystallization and the like are appropriately applied. May be. These operations may be combined with stirring and heating (for example, about 30 to 70 ° C.) as necessary. In crystallization, an organic solvent (ethanol, methanol, etc.) or a solution obtained by adding water to the organic solvent can be appropriately used as a crystallization solvent.

本発明において、Rebaudioside−Aを90重量%以上含むステビア抽出物は、1種類であってもよいし2種類以上の組み合わせであってもよい。2種類以上の組み合わせの例としては、抽出条件、Rebaudioside−Aの含有量、Rebaudioside−A以外の甘味成分の含有量等、が異なる2種類以上のステビア抽出物の組み合わせが挙げられる。   In the present invention, the stevia extract containing 90% by weight or more of Rebaudioside-A may be one kind or a combination of two or more kinds. Examples of combinations of two or more types include combinations of two or more types of stevia extracts that differ in extraction conditions, content of Rebaudioside-A, content of sweetening components other than Rebaudioside-A, and the like.

一般的にはRebaudioside−Aを90重量%以上含有するステビア抽出物は、植物体からの抽出、精製、乾燥、再溶解、再結晶化、乾燥の手順で製造されるが、Rebaudioside−Aの含有量が高くなるにつれて水への溶解性が低下する。このため、Rebaudioside−Aを90重量%以上含有するステビア抽出物の製造にあたっては大量の水分を蒸発することが必要となり、生産効率が大幅に低下するとともに、溶液からの異物除去のための濾過における作業が大幅に増加する。   In general, stevia extract containing 90% by weight or more of Rebaudioside-A is produced by extraction, purification, drying, re-dissolution, recrystallization, and drying procedures from plant bodies, but it contains Rebaudioside-A. As the amount increases, the solubility in water decreases. For this reason, in producing a stevia extract containing 90% by weight or more of Rebaudioside-A, it is necessary to evaporate a large amount of water, greatly reducing the production efficiency, and in filtration for removing foreign substances from the solution. Work is greatly increased.

また、Rebaudioside−Aを90重量%以上含有するステビア抽出物の水への溶解度は、その粒子径、形状、結晶性などにより異なり、抽出、精製、乾燥、再溶解などの製造工程では、水への溶解度が高いRebaudioside−Aを90重量%以上含有するステビア抽出物が選択的に抽出される。この結果、水への溶解度の低いRebaudioside−Aを90重量%以上含有するステビア抽出物は、Rebaudioside−Aの含有比率が少ないステビア抽出物と混合して使用されることが一般的である。このようなことから、市販されているRebaudioside−Aを90重量%以上含有するステビア抽出物は水への溶解度が高いものとなっている。なお、溶解性の低いRebaudioside−Aを90重量%以上含有するステビア抽出物の水への溶解度は1〜5g/100g程度である。   In addition, the solubility in water of stevia extract containing 90% by weight or more of Rebaudioside-A varies depending on the particle size, shape, crystallinity, etc., and in the manufacturing process such as extraction, purification, drying, re-dissolution, etc. Stevia extract containing 90% by weight or more of Rebaudioside-A having a high solubility of is selectively extracted. As a result, a stevia extract containing 90% by weight or more of Rebaudioside-A having low solubility in water is generally used by mixing with a stevia extract having a low content of Rebaudioside-A. For this reason, a stevia extract containing 90% by weight or more of Rebaudioside-A that is commercially available has a high solubility in water. In addition, the solubility in water of the stevia extract containing 90 weight% or more of Rebaudioside-A with low solubility is about 1 to 5 g / 100 g.

本発明において、水溶性多糖とは、水溶性の多糖(多数(例えば10個以上)の単糖が結合してなる糖)を意味する。水溶性多糖は、天然物および合成物のいずれであってもよい。水溶性多糖は1種類でもよいし、2種類以上の組み合わせであってもよい。   In the present invention, the water-soluble polysaccharide means a water-soluble polysaccharide (a sugar formed by binding a large number (for example, 10 or more) monosaccharides). The water-soluble polysaccharide may be a natural product or a synthetic product. One type of water-soluble polysaccharide may be sufficient and the combination of two or more types may be sufficient.

水溶性多糖としては、通常は食品または食品添加物として利用できる水溶性多糖が好ましい。水溶性多糖としては、例えば、ペクチン、グアーガム、アラビアガム、メチルセルロース、カルボキシメチルセルロース、プルラン、デキストラン、デンプン、アミロース、アミロペクチン、デキストリン、シクロデキストリン等が挙げられる。このうち、単糖としてのグルコースが結合してなる水溶性多糖を含むことが好ましい。具体的には、デンプン、アミロース、アミロペクチン及びデキストリンからなる群から選ばれる1種以上が含まれることにより、Rebaudioside−Aを90重量%以上含有するステビア抽出物の溶解性をより顕著に向上させることができるので、好ましい。水溶性多糖としては、デキストリンが含まれることがより好ましい。これにより、ステビア組成物は異味が少なくより良好な甘味を呈するものとなる。   The water-soluble polysaccharide is preferably a water-soluble polysaccharide that can be used as a food or food additive. Examples of the water-soluble polysaccharide include pectin, guar gum, gum arabic, methyl cellulose, carboxymethyl cellulose, pullulan, dextran, starch, amylose, amylopectin, dextrin, cyclodextrin and the like. Among these, it is preferable to include a water-soluble polysaccharide formed by binding glucose as a monosaccharide. Specifically, by including at least one selected from the group consisting of starch, amylose, amylopectin and dextrin, the solubility of stevia extract containing 90% by weight or more of Rebaudioside-A is more remarkably improved. Is preferable. More preferably, the water-soluble polysaccharide contains dextrin. As a result, the stevia composition exhibits less sweetness and better sweetness.

本発明において、難溶性ステビア抽出物と水溶性多糖の混合物における、乾燥重量比は、難溶性ステビア抽出物:水溶性多糖=100:5〜0.4:99.6であることが必要であり、好ましくは難燃性ステビア抽出物:水溶性多糖=100:10〜100:30である。これにより、難溶性ステビア抽出物の溶解性を改善することができる。   In the present invention, the dry weight ratio in the mixture of the hardly soluble stevia extract and the water-soluble polysaccharide needs to be hardly soluble stevia extract: water-soluble polysaccharide = 100: 5 to 0.4: 99.6. The flame retardant stevia extract: water-soluble polysaccharide is preferably 100: 10 to 100: 30. Thereby, the solubility of a hardly soluble stevia extract can be improved.

本発明の難燃性ステビア抽出物と水溶性発多糖の混合物(以下、「ステビア混合物」ということがある。)は、本発明の目的に反しない範囲で、さらに他の成分を含んでいてもよい。係る成分としては、公知の添加剤が例示される。公知の添加剤としては例えば、本発明のステビア組成物以外の甘味料(例:糖アルコール、アセスルファムカリウム、スクラロース、アスパルテームなど)が挙げられる。   The flame retardant stevia extract and water-soluble polysaccharide mixture (hereinafter sometimes referred to as “stevia mixture”) of the present invention may further contain other components within the scope of the object of the present invention. Good. Examples of such components include known additives. Examples of known additives include sweeteners (eg, sugar alcohol, acesulfame potassium, sucralose, aspartame, etc.) other than the stevia composition of the present invention.

本発明において、難燃性ステビア抽出物と水溶性多糖の混合物の溶解方法としては、乾燥重量比が、難燃性ステビア抽出物:水溶性多糖=100:5〜0.4:99.6となるように混合すればよく、それ以外の条件は特には限定されない。混合の際には、該難燃性ステビア抽出物と該水溶性多糖とをそのまま混合してもよいが、該難燃性ステビア抽出物の溶液(水性溶媒への溶液、通常は、水溶液)及び水溶性多糖の溶液(水性溶媒への溶液、通常は、水溶液)を混合してもよい。混合の際には、必要に応じて撹拌を加えてもよい。   In the present invention, as a method for dissolving the mixture of the flame retardant stevia extract and the water-soluble polysaccharide, the dry weight ratio is flame retardant stevia extract: water-soluble polysaccharide = 100: 5 to 0.4: 99.6. What is necessary is just to mix so that it may become, and other conditions are not specifically limited. In mixing, the flame retardant stevia extract and the water-soluble polysaccharide may be mixed as they are, but the flame retardant stevia extract solution (solution in an aqueous solvent, usually an aqueous solution) and A solution of a water-soluble polysaccharide (solution in an aqueous solvent, usually an aqueous solution) may be mixed. In mixing, stirring may be added as necessary.

本発明のステビア混合物は、優れた溶解性を有し、溶解安定性に優れる。また、ステビア混合物の水溶液を、乾燥させることにより得られる溶解性を改善した固形物も優れた溶解性を有し、溶解安定性に優れる。さらに、ステビア混合物の水溶液、その水溶液を乾燥した固形物は良質な甘味を呈するので、甘味料等の飲食品の一成分として利用することができ、飲食品添加物として利用することができる。飲食品の種類には特に制限はないが、水分を含む飲食品(例えば、ジュース、炭酸飲料、コーヒー飲料、茶飲料、乳飲料、アルコール飲料)であると、本発明の効果が発揮されるので、好ましい。飲食品添加物の種類には特に制限はないが、例えば、甘味料が挙げられる。   The stevia mixture of the present invention has excellent solubility and excellent dissolution stability. Moreover, the solid substance which improved the solubility obtained by drying the aqueous solution of a stevia mixture also has the outstanding solubility, and is excellent in dissolution stability. Furthermore, since the aqueous solution of a stevia mixture and the solid substance which dried the aqueous solution exhibit good quality sweetness, it can be utilized as one component of food / beverage products, such as a sweetener, and can be utilized as a food / beverage product additive. Although there is no restriction | limiting in particular in the kind of food / beverage products, since the effect of this invention is exhibited if it is food / beverage products containing water (for example, juice, carbonated drinks, coffee drinks, tea drinks, milk drinks, alcoholic drinks). ,preferable. Although there is no restriction | limiting in particular in the kind of food-drinks additive, For example, a sweetener is mentioned.

本発明により、ステビア残渣の水性溶媒への溶解性の向上、再結晶化の防止が実現できる。言い換えれば、水系溶媒に対して難溶性であるRebaudioside−Aを90重量%以上含有するステビア抽出物を、単独では溶解不可能な濃度において、水性溶媒に対し安定的に溶解させることができる。   According to the present invention, it is possible to improve the solubility of stevia residue in an aqueous solvent and prevent recrystallization. In other words, a stevia extract containing 90% by weight or more of Rebaudioside-A that is hardly soluble in an aqueous solvent can be stably dissolved in an aqueous solvent at a concentration that cannot be dissolved alone.

以下に具体的な実施例を示すが、本発明はこれに限定されるものではない。
以下の実施例において、食品添加物公定書法第8版に従って行われたステビアの定性試験とは、下記の試験を意味する。
Specific examples are shown below, but the present invention is not limited thereto.
In the following examples, the qualitative test of stevia conducted in accordance with the Food Additives Official Law 8th edition means the following test.

試料0.06〜0.12gを精密に量り、アセトニトリル/水混液(4:1)に溶かして正確に100mlとし、検液とする。別に定量用Steviosideを乾燥し、その約0.05gを精密に量り、アセトニトリル/水混液(4:1)に溶かして正確に100mlとし、標準液とする。検液及び標準液をそれぞれ10μlずつ量り、以下の操作条件で液体クロマトグラフィーを行う。検液のSteviosideのピーク面積Aa、Dulcoside−Aのピーク面積Ab、Rebaudioside−Cのピーク面積Ad、Rebaudioside−Aのピーク面積Ac、及び標準液のSteviosideのピーク面積Asをそれぞれ測定する。次式により各ステビオール配糖体の含量を求める。
(ステビオール配糖体の含量
Steviosideの含量(重量%)=(定量用Steviosideの採取量(mg)/乾燥物換算した試料採取量(mg))×(Aa/As)×100
Dulcoside−Aの含量(重量%)=(定量用Steviosideの採取量(mg)/乾燥物換算した試料採取量(mg))×(Ab×0.98/As)×100
Rebaudioside−Aの含量(重量%)=(定量用Steviosideの採取量(mg)/乾燥物換算した試料採取量(mg))×(Ac×1.20/As)×100
Rebaudioside−Cの含量(重量%)=(定量用Steviosideの採取量(mg)/乾燥物換算した試料採取量(mg))×(Ad×1.18/As)×100
ステビオール配糖体の合計含量(重量%)=Steviosideの含量(重量%)+Dulcoside−Aの含量(重量%)+Rebaudioside−Aの含量(重量%)+Rebaudioside−Cの含量(重量%)
(操作条件)
検出器 紫外吸光光度計(測定波長 210nm)
カラム充てん剤 5μmの液体クロマトグラフィー用アミノ基結合型シリカゲル
カラム管 内径4.6mm、長さ15cmのステンレス管
カラム温度 40℃
移動相 アセトニトリル/水混液(4:1)
Weigh 0.06 to 0.12 g of the sample accurately, dissolve in acetonitrile / water mixture (4: 1) to make exactly 100 ml, and use this as the test solution. Separately, Stevioside for quantification is dried, and about 0.05 g thereof is accurately weighed and dissolved in an acetonitrile / water mixture (4: 1) to make exactly 100 ml, which is used as a standard solution. Measure 10 μl each of the test solution and standard solution, and perform liquid chromatography under the following operating conditions. Stevioside peak area A a of the test solution, Dulcoside-A of the peak area A b, Rebaudioside-C of the peak area A d, Rebaudioside-A of the peak area A c, and respectively measure the peak area A s of Stevioside the standard solution To do. The content of each steviol glycoside is determined by the following formula.
(Steviol glycoside content Stevioside content (% by weight) = (Stevioside sample for quantification (mg) / Dry sampled sample (mg)) × (A a / A s ) × 100
Dulcoside-A content (% by weight) = (collection amount of stevioside for determination (mg) / sample collection amount in terms of dry matter (mg)) × (A b × 0.98 / A s ) × 100
Rebaudioside-A content (% by weight) = (collection amount of stevioside for quantification (mg) / sample collection amount in terms of dry matter (mg)) × (A c × 1.20 / A s ) × 100
Rebaudioside-C content (% by weight) = (collection amount of stevioside for quantification (mg) / sample collection amount in terms of dry matter (mg)) × (A d × 1.88 / A s ) × 100
Total content of steviol glycosides (% by weight) = Stevioside content (% by weight) + Dulcoside-A content (% by weight) + Rebaudioside-A content (% by weight) + Rebaudioside-C content (% by weight)
(Operating conditions)
Detector Ultraviolet absorptiometer (measurement wavelength 210nm)
Column packing 5 μm amino group-bonded silica gel for liquid chromatography Column tube Stainless steel tube with inner diameter of 4.6 mm and length of 15 cm Column temperature 40 ° C.
Mobile phase Acetonitrile / water mixture (4: 1)

[実験1]
Rebaudioside−A含量が91重量%であり、ステビア4成分(Stevioside、Dulcoside−A、Rebaudioside−C、Rebaudioside−A)の総含量が95重量%であるステビア抽出物(以下、ステビア甘味料1という。)の溶解性を調査した。なお、ステビア甘味料1は以下のようにして調整した。
[Experiment 1]
A Stevia extract (hereinafter referred to as Stevia sweetener 1) having a Rebaudioside-A content of 91% by weight and a total content of 4 components of Stevia (Stevioside, Dulcoside-A, Rebaudioside-C, Rebaudioside-A) of 95% by weight. ) Was investigated. Stevia sweetener 1 was prepared as follows.

<ステビア甘味料1>
Rebaudioside−A、B及びCを豊富に含有する市販のステビア抽出物(守田化学工業、レバウディオP9)1部に対してメタノール9部を添加して攪拌懸濁させた。攪拌を続けながら室温から55℃に加温した後、攪拌放冷にて室温まで冷却した。その後12時間以上攪拌を続け、懸濁液を得た。この懸濁液をろ過・乾燥し、得られた結晶を粉砕してステビア甘味料1の粉末を得た。なお、ステビア甘味料1の水への溶解度は4g/100gであった。
<Stevia sweetener 1>
9 parts of methanol was added to 1 part of a commercially available stevia extract (Morita Chemical Industry, Rebaudio P9) containing abundant Rebaudioside-A, B and C, and suspended by stirring. The mixture was heated from room temperature to 55 ° C. while continuing to stir, and then cooled to room temperature by stirring and cooling. Thereafter, stirring was continued for 12 hours or more to obtain a suspension. The suspension was filtered and dried, and the obtained crystals were pulverized to obtain Stevia sweetener 1 powder. The solubility of Stevia sweetener 1 in water was 4 g / 100 g.

[実施例1]
ステビア甘味料1 4.5gを25℃の水50mlに混和後、デキストリン0.5gを溶解した50ml溶液を加え、攪拌した結果、30分以下で溶解した。また、得られたステビア甘味料1の溶液を4℃で12時間放置した結果、未溶解物は発生しなかった。
[Example 1]
After mixing 4.5 g of Stevia sweetener 1 in 50 ml of water at 25 ° C., a 50 ml solution in which 0.5 g of dextrin was dissolved was added and stirred. As a result, it was dissolved in 30 minutes or less. Moreover, as a result of leaving the solution of the obtained stevia sweetener 1 at 4 degreeC for 12 hours, the undissolved substance did not generate | occur | produce.

[実施例2]
ステビア甘味料1 32gを25℃
の水50mlに混和後、デキストリン8gを溶解した50ml溶液を加え、攪拌した結果、1時間で溶解した。また、得られたステビア甘味料1の溶液を4℃で12時間放置した結果、未溶解物は発生しなかった。
[Example 2]
Stevia sweetener 1 32g at 25 ° C
After mixing in 50 ml of water, a 50 ml solution in which 8 g of dextrin was dissolved was added and stirred, and dissolved in 1 hour. Moreover, as a result of leaving the solution of the obtained stevia sweetener 1 at 4 degreeC for 12 hours, the undissolved substance did not generate | occur | produce.

[実験2]
Rebaudioside−A含量97%のステビア甘味料2の溶解性を調査した。ステビア甘味料2中のステビア4成分(Stevioside、Dulcoside−A、Rebaudioside−C、Rebaudioside−A)の総含量は、98重量%であった。ステビア甘味料2の調製は以下のようにして行った。
[Experiment 2]
The solubility of Stevia sweetener 2 with Rebaudioside-A content 97% was investigated. The total content of Stevia 4 components (Stevioside, Dulcoside-A, Rebaudioside-C, Rebaudioside-A) in Stevia sweetener 2 was 98% by weight. Stevia sweetener 2 was prepared as follows.

<ステビア甘味料2>
Rebaudioside−A、B及びCを豊富に含有する市販のステビア抽出物(守田化学工業、レバウディオP9)1部に対してメタノール9部を添加して攪拌懸濁させた。攪拌を続けながら室温から55℃に加温した後、攪拌放冷にて室温まで冷却した。その後12時間以上攪拌を続け、懸濁液を得た。この懸濁液をろ過・乾燥し、得られた結晶を粉砕してステビア甘味料2の粉末を得た。
なお、ステビア甘味料2の水への溶解度は4g/100gであった。
<Stevia sweetener 2>
9 parts of methanol was added to 1 part of a commercially available stevia extract (Morita Chemical Industry, Rebaudio P9) containing abundant Rebaudioside-A, B and C, and suspended by stirring. The mixture was heated from room temperature to 55 ° C. while continuing to stir, and then cooled to room temperature by stirring and cooling. Thereafter, stirring was continued for 12 hours or more to obtain a suspension. This suspension was filtered and dried, and the obtained crystals were pulverized to obtain Stevia sweetener 2 powder.
The solubility of Stevia sweetener 2 in water was 4 g / 100 g.

[実施例3]
ステビア甘味料2 4.5gを25℃の水50mlに混和後、デキストリン0.5gを溶解した50ml溶液を加え、攪拌した結果、30分以下で溶解した。また、得られたステビア甘味料2の溶液を4℃で12時間放置した結果、未溶解物は発生しなかった。
[Example 3]
After mixing 4.5 g of Stevia sweetener 2 in 50 ml of water at 25 ° C., a 50 ml solution in which 0.5 g of dextrin was dissolved was added and stirred. As a result, it was dissolved in 30 minutes or less. Moreover, as a result of leaving the solution of the obtained stevia sweetener 2 at 4 degreeC for 12 hours, the undissolved substance did not generate | occur | produce.

[実施例4]
ステビア甘味料2 32gを25℃の水50mlに混和後、デキストリン8gを溶解した50ml溶液を加え、攪拌した結果、1時間で溶解した。また、得られたステビア残渣1の溶液を4℃で12時間放置した結果、未溶解物は発生しなかった。
[Example 4]
After mixing 32 g of Stevia sweetener 2 in 50 ml of water at 25 ° C., a 50 ml solution in which 8 g of dextrin was dissolved was added and stirred, and dissolved in 1 hour. Moreover, as a result of leaving the solution of the obtained stevia residue 1 at 4 degreeC for 12 hours, the undissolved substance did not generate | occur | produce.

[実施例5]
ステビア甘味料2 4.5gを25℃の水50mlに混和後、アミロース0.5gを溶解した50ml溶液を加え、攪拌した結果、30分以下で溶解した。また、得られたステビア甘味料2の溶液を4℃で12時間放置した結果、未溶解物は発生しなかった。
[Example 5]
After mixing 4.5 g of Stevia sweetener 2 in 50 ml of water at 25 ° C., a 50 ml solution in which 0.5 g of amylose was dissolved was added and stirred. As a result, it was dissolved in 30 minutes or less. Moreover, as a result of leaving the solution of the obtained stevia sweetener 2 at 4 degreeC for 12 hours, the undissolved substance did not generate | occur | produce.

[実施例6]
ステビア甘味料2 32gを25℃の水50mlに混和後、アミロース8gを溶解した50ml溶液を加え、攪拌した結果、1時間で溶解した。また、得られたステビア残渣1の溶液を4℃で12時間放置した結果、未溶解物は発生しなかった。
[Example 6]
After mixing 32 g of Stevia sweetener 2 in 50 ml of water at 25 ° C., a 50 ml solution in which 8 g of amylose was dissolved was added and stirred, and dissolved in 1 hour. Moreover, as a result of leaving the solution of the obtained stevia residue 1 at 4 degreeC for 12 hours, the undissolved substance did not generate | occur | produce.

Claims (2)

水に対する溶解度が5.0g/100g以下であるRebaudioside−Aを90重量%以上含有するステビア抽出物の溶解方法であって、該ステビア抽出物に対して水溶性多糖を、乾燥重量比が該ステビア抽出物:該水溶性多糖=100:5〜0.4:99.6となるように混合し、得られる混合物を水性溶媒に溶解することを特徴とするステビア抽出物の溶解方法。   A method for dissolving a stevia extract containing 90% by weight or more of Rebaudioside-A having a solubility in water of 5.0 g / 100 g or less, wherein the water-soluble polysaccharide is added to the stevia extract in a dry weight ratio of the stevia extract. Extract: A method for dissolving a stevia extract, wherein the water-soluble polysaccharide is mixed so as to be 100: 5 to 0.4: 99.6, and the resulting mixture is dissolved in an aqueous solvent. 請求項1で得られる水溶液を、乾燥させることにより得られる溶解性を改善した固形物。   The solid substance which improved the solubility obtained by drying the aqueous solution obtained in Claim 1.
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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR3002446A1 (en) * 2013-02-28 2014-08-29 Oreal Cosmetic composition, useful for stimulating, restoring or regulating the metabolism of melanocyte in the skin, skin cells or semi-mucous membranes, comprises rebaudioside A and at least one cellulose substitute in a medium
WO2015014958A1 (en) * 2013-07-31 2015-02-05 Dsm Ip Assets B.V. Stable sweetener compositions
JP2015100274A (en) * 2013-11-21 2015-06-04 池田食研株式会社 Packed composition
EP3082461A4 (en) * 2013-12-16 2017-06-28 Cargill, Incorporated Stabilized steviol glycoside in concentrated syrup
JP2022537386A (en) * 2019-06-19 2022-08-25 テイト アンド ライル ソリューションズ ユー・エス・エー エル・エル・シー stable liquid concentrate composition

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR3002446A1 (en) * 2013-02-28 2014-08-29 Oreal Cosmetic composition, useful for stimulating, restoring or regulating the metabolism of melanocyte in the skin, skin cells or semi-mucous membranes, comprises rebaudioside A and at least one cellulose substitute in a medium
WO2015014958A1 (en) * 2013-07-31 2015-02-05 Dsm Ip Assets B.V. Stable sweetener compositions
CN105407739A (en) * 2013-07-31 2016-03-16 帝斯曼知识产权资产管理有限公司 Stable sweetener compositions
JP2015100274A (en) * 2013-11-21 2015-06-04 池田食研株式会社 Packed composition
EP3082461A4 (en) * 2013-12-16 2017-06-28 Cargill, Incorporated Stabilized steviol glycoside in concentrated syrup
JP2022537386A (en) * 2019-06-19 2022-08-25 テイト アンド ライル ソリューションズ ユー・エス・エー エル・エル・シー stable liquid concentrate composition
JP7742312B2 (en) 2019-06-19 2025-09-19 テイト アンド ライル ソリューションズ ユー・エス・エー エル・エル・シー Stable liquid concentrate composition

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