JP2008072915A - Film-like food - Google Patents

Film-like food Download PDF

Info

Publication number
JP2008072915A
JP2008072915A JP2006253264A JP2006253264A JP2008072915A JP 2008072915 A JP2008072915 A JP 2008072915A JP 2006253264 A JP2006253264 A JP 2006253264A JP 2006253264 A JP2006253264 A JP 2006253264A JP 2008072915 A JP2008072915 A JP 2008072915A
Authority
JP
Japan
Prior art keywords
film
supplement
food
component
supplement component
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
JP2006253264A
Other languages
Japanese (ja)
Inventor
Tadao Tsukioka
忠夫 月岡
Misao Nishimura
美佐夫 西村
Katsuhisa Yamada
勝久 山田
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.)
Tsukioka KK
DHC Corp
Original Assignee
Tsukioka KK
DHC 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 Tsukioka KK, DHC Corp filed Critical Tsukioka KK
Priority to JP2006253264A priority Critical patent/JP2008072915A/en
Publication of JP2008072915A publication Critical patent/JP2008072915A/en
Pending legal-status Critical Current

Links

Landscapes

  • General Preparation And Processing Of Foods (AREA)
  • Jellies, Jams, And Syrups (AREA)
  • Medicinal Preparation (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Coloring Foods And Improving Nutritive Qualities (AREA)
  • Grain Derivatives (AREA)

Abstract

<P>PROBLEM TO BE SOLVED: To provide a film-like food from which unstable supplement components are stabilized so as to be efficiently taken with a rapid and easy means. <P>SOLUTION: The film-like food is obtained by including supplement components, such as ubiquinone, alpha-lipoic acid, catechin, carnitine, theanine, citric acid, B-complex vitamins, vitamin E, an oil-soluble vitamin C derivative, minerals and retinoids with cyclodextrin that make the film hold the supplement components which comprises a film-forming materia, such as starch. <P>COPYRIGHT: (C)2008,JPO&INPIT

Description

本発明はサプリメント成分を含むフィルム状食品及びその製造方法に関するものである。   The present invention relates to a film-like food containing a supplement component and a method for producing the same.

フィルム状食品としては、従来より種々のものが開発されており、古くはオブラートの名称で知られる澱粉からなるフィルムがある。澱粉からなるものの他に、ゼラチンやプルラン,アルギン酸ナトリウムを主成分とするものなども知られている。近年、種々の食品の包装や、また、フィルム自体にサプリメントや香味料等を保持させた可食性フィルムが提案されている(特許文献1および2)。
特開2004−222663号公報 特開2004−248665号公報
Various foods have been developed as film-like foods, and there is a film made of starch known by the name of oblate in the old days. In addition to starch, those containing gelatin, pullulan and sodium alginate as main components are also known. In recent years, various food packagings and edible films in which supplements, flavors and the like are held on the film itself have been proposed (Patent Documents 1 and 2).
JP 2004-222663 A JP 2004-248665 A

これまで不安定なユビキノン、α−リポ酸、カテキン、油溶性ビタミンC誘導体、レチノイド類は安定に食品として供する手段として、ゼラチンなどで成形したハードカプセルやソフトカプセルに封入して製剤化していた。これらの製剤化されたもは、ピルケースなどの容器に入れて持ち運ばなくてはならず、摂取するには水を必要とするなどの問題点があった。
一方、薄いフィルムとすることで口の中で容易に溶けて水を必要とせずに摂取できることから可食性フィルムに種々の成分を担持させることが考えられている。可食性フィルムとして、甘味料や香料などを保持させたものは実用化されたものもあるが、サプリメント成分には湿度や温度に対して不安定なものもあることから、より安定に成分を保持できるようにしたフィルム状食品が求められている。
本発明は、上記サプリメント成分を安定して保持させることができ、かつ摂取し易いフィルム状食品を提供せんとするものである。
Up to now, unstable ubiquinone, α-lipoic acid, catechin, oil-soluble vitamin C derivatives, and retinoids have been formulated as hard capsules or soft capsules molded with gelatin or the like as means for providing them as food stably. These preparations had to be carried in containers such as pill cases and had problems such as requiring water for consumption.
On the other hand, since a thin film can be easily dissolved in the mouth and ingested without the need for water, it is considered that various components are supported on the edible film. Some edible films that have sweeteners, flavors, etc., have been put to practical use, but some supplement ingredients are unstable with respect to humidity and temperature, so the ingredients are more stable. There is a need for film foods that can be made.
The present invention is intended to provide a film-like food that can stably retain the supplement component and is easy to ingest.

本発明のフィルム状食品は、目的とするサプリメント成分をシクロデキストリン(CD)に包接(包摂)させ、得られたCD包接体をフィルム形成材料に混入して所望の厚さのフィルムに成形するか、またはフィルム形成材料からなる可食性フィルムにCD包接体を塗布してしてなることを特徴とするものである。
本発明において、サプリメント成分としては、ユビキノン(コエンザイムQ10)、α−リポ酸、カテキン、カルニチン、テアニン、クエン酸、ビタミンB群、ビタミンE、油溶性ビタミンC誘導体、ミネラル類およびレチノイド類などが挙げられる。
In the film-like food of the present invention, the target supplement component is included (included) in cyclodextrin (CD), and the resulting CD inclusion is mixed into the film-forming material and formed into a film of a desired thickness. Or a CD inclusion body is applied to an edible film made of a film forming material.
In the present invention, examples of supplement components include ubiquinone (coenzyme Q10), α-lipoic acid, catechin, carnitine, theanine, citric acid, vitamin B group, vitamin E, oil-soluble vitamin C derivatives, minerals, and retinoids. It is done.

本発明のフィルム状食品は、サプリメント成分をシクロデキストリンで包接することによって、種々のフィルム形成成分との親和性が向上し、フィルム中に確実に保持されるとともに、任意の厚さの薄い安定なフィルム状とすることができ、種々の成分を含む層の積層フィルムとすることもできる。それによって、携帯が容易で,摂取にあたり水等が不用であるなどの利点を有し、種々の成分を積層することによって種々の成分を一度に摂取できる。   The film-like food of the present invention improves the affinity with various film-forming components by enclosing the supplement component with cyclodextrin, and is securely held in the film, and is stable and thin in any thickness. It can be made into a film and can also be a laminated film of layers containing various components. Thereby, it is easy to carry and has the advantage that water or the like is not required for ingestion, and various components can be ingested at once by stacking various components.

サプリメント成分の多くは、フィルム形成材料に対して溶解性、分散性、混和性等が悪
く、フィルム形成が困難である。本発明のサプリメント成分であるユビキノン(コエンザイムQ10)、α−リポ酸、カテキンなどは疎水性の粉末であり、油溶性ビタミンC誘導体、レチノイド類は疎水性の液体であり、そのままではフィルム形成成分との混和性等に問題があるが、シクロデキストリン(CD)に包接させることによって水になじみ易い粉体とすることができる。
シクロデキストリンによる包接効果は、シクロデキストリン自体の物性によるものもあるが、上記サプリメント成分の多くは種々の成分からなる天然物由来のものや、また、合成品であっても副生物を含むものと推測されるが、シクロデキストリンの包接によって包接される成分とされない成分とに分離され、フィルム形成性等を阻害する成分が除かれる等の効果もあるものと思われる。これらのことから、シクロデキストリンの選択効果を利用することによって、サプリメント成分は上記のものに限定されることなく,本発明に使用できる。
Many of the supplement components have poor solubility, dispersibility, miscibility, and the like with respect to the film-forming material, and film formation is difficult. Ubiquinone (coenzyme Q10), α-lipoic acid, catechin and the like, which are supplement components of the present invention, are hydrophobic powders, and oil-soluble vitamin C derivatives and retinoids are hydrophobic liquids. Although there is a problem in the miscibility, etc., it can be made into a powder that is easily compatible with water by inclusion in cyclodextrin (CD).
The inclusion effect by cyclodextrin may be due to the physical properties of cyclodextrin itself, but many of the above-mentioned supplement components are derived from natural products consisting of various components, and even synthetic products contain by-products. However, it is considered that there are effects such as separation of components that are not included by inclusion of cyclodextrin and components that are not included, and removal of components that inhibit film formation and the like. From these facts, the supplement component can be used in the present invention without being limited to the above by utilizing the selective effect of cyclodextrin.

シクロデキストリンは、サプリメント成分に応じてα−CD、β−CD、γ−CDのなかから選択して使用することができるが、好ましくはβ−CDまたはγ−CDである。
このほかフィルム形成成分との親和性、混和性等で選択してもよく、水溶性の点でα−CDを選択するなどとしてもよい。
シクロデキストリンは、上記のものを併せて使用してもよい。包接は一つのサプリメント成分ごとに通常行うが2成分以上を併せて行ってもよい。
The cyclodextrin can be selected from α-CD, β-CD, and γ-CD depending on the supplement component, and is preferably β-CD or γ-CD.
In addition, it may be selected based on affinity with the film-forming component, miscibility, or the like, or α-CD may be selected from the viewpoint of water solubility.
Cyclodextrins may be used in combination with the above. Inclusion is usually performed for each supplement component, but two or more components may be combined.

フィルム形成成分としては、デンプン、プルラン、アラビノキシラン、グアーガム分解物、アルギン酸ナトリウム、カラギーナン、寒天、ペクチン、セルロース等の多糖類、およびゼラチン、シルク分解物、カゼイン分解物等のペプチド系物質など、従来の可食性フィルムに使用されているものが使用できる。これらは、1種または2種以上を併せて使用することができる。
本発明において、好ましくは、デンプン、アルギン酸ナトリウム、カラギーナン、ペクチン、セルロース等の多糖類、ゼラチン、シルク分解物、カゼイン分解物等が挙げられる。
フィルム形成成分は、フィルムとしての特性を生かすために、薄く成形できること、食したときに口腔内に付着しないこと、適度の速さで溶解すること、目的とするサプリメント成分を充分に保持させることができること、更には、適度の強度を有していること等の種々の要件を満足することを考慮して選択使用される。
Examples of film-forming components include starch, pullulan, arabinoxylan, guar gum degradation products, sodium alginate, carrageenan, agar, pectin, polysaccharides such as cellulose, and peptide substances such as gelatin, silk degradation products, and casein degradation products. What is used for an edible film can be used. These can be used alone or in combination of two or more.
In the present invention, preferably, starch, sodium alginate, carrageenan, pectin, cellulose and other polysaccharides, gelatin, silk degradation product, casein degradation product and the like can be mentioned.
The film-forming component can be molded thinly to take advantage of the properties as a film, does not adhere to the oral cavity when eaten, dissolves at an appropriate speed, and sufficiently retains the desired supplement component In addition, it is selected and used in consideration of satisfying various requirements such as being able to be performed and having appropriate strength.

上記のほかにフィルム形成成分として、通常この種の分野で使用される成分を用いることができる。例えば、アルギン酸ナトリウムに対するカルシウムイオン、フィルムの可塑剤としてのラクチトール,マルチトール,エリスリトール,マンニトール等、フィルム強化剤としての多糖類、フレーバーおよび甘味料等を含ませてもよい。このほか、CD包接体としなくても安定なサプリメント成分を含ませてもよい。
フィルム形成材料は、上記各成分を含む水溶液または水性分散液として調製される。フィルム形成材料は、食品として使用可能なアルコール、グリセロール、界面活性剤等を用いることができる。
In addition to the above, components usually used in this type of field can be used as film forming components. For example, calcium ions for sodium alginate, lactitol, maltitol, erythritol, mannitol, etc. as a film plasticizer, polysaccharides, flavors, sweeteners, etc. as film strengthening agents may be included. In addition, a stable supplement component may be included even if it is not a CD inclusion body.
The film-forming material is prepared as an aqueous solution or aqueous dispersion containing the above components. As the film-forming material, alcohol, glycerol, surfactants and the like that can be used as food can be used.

本発明のフィルム状食品は、サプリメント成分を含む1枚の可食性フィルムでもよく、またこのようなフィルムを多層に積層したものでもよく、更にはサプリメント成分を含まない可食性フィルムとの積層体であってもよい。
フィルム状食品の成形にあたっては、通常、一つのサプリメント成分包接体を有するフィルムを作るが、2以上のサプリメント成分包接体を含む一つのフィルムとしてもよい。
フィルム状食品は、原理的には、デンプン等からなるフィルム形成材料を適当な濃度の水溶液として、ガラス板等の平滑な基板や平滑なプラスチックフィルム面に薄く塗布し、乾燥してフィルムとし、剥離することによって作成される。工業的には、例えば、平滑面
を有する回転ドラムの表面にフィルム成形材料を塗布し、乾燥して巻き取るなどの連続的な製法によって作られる。
サプリメント成分CD包接体(以下、場合により単に、CD包接体という)は水性分散液として、フィルム形成材料に添加する。
フィルムの積層は、一旦フィルムとして巻き取った後に他のフィルムと積層してもよく、また、巻き取り時に他のフィルムと一体的に巻き取る方法によってもよい。
The film-like food of the present invention may be a single edible film containing a supplement component, a laminate of such films, or a laminate with an edible film not containing a supplement component. There may be.
In forming a film-like food, a film having one supplement component inclusion is usually produced, but one film including two or more supplement component inclusions may be used.
In principle, a film-like food is made by applying a film-forming material made of starch or the like as an aqueous solution of appropriate concentration, thinly onto a smooth substrate such as a glass plate or a smooth plastic film, and drying to form a film. Created by. Industrially, for example, it is produced by a continuous production method such as applying a film molding material to the surface of a rotating drum having a smooth surface, drying it and winding it.
The supplement component CD inclusion body (hereinafter, simply referred to as “CD inclusion body” in some cases) is added to the film forming material as an aqueous dispersion.
Lamination of the film may be carried out as a film and then laminated with another film, or may be carried out by a method of winding up with another film at the time of winding.

成形されるフィルムの厚さは特に限定されないが、30〜300μm程度とするとよい。
フィルムの厚さは、主としてフィルムの強度と溶解性で選択される。積層フィルムの場合には、表面層のフィルムをサプリメント成分の含まないものとし、強度のあるものを選択することによってフィルム状食品を薄くすることができる。
サプリメント成分を含まないフィルムは、強度のほかに、積層した時の上下のサプり成分含有フィルムの間にあってバリヤーの役割をするとか、また,最表面に設けて水分、空気等を遮断する役割をさせてもよい。例えば、油溶性ビタミンCはシクロデキストリンで包接しても鉄イオンとの反応性は残っているので、褐変現象が生じるがバリヤーフィルムを設けることでこの現象を阻止できる。
Although the thickness of the film shape | molded is not specifically limited, It is good to set it as about 30-300 micrometers.
The thickness of the film is selected mainly by the strength and solubility of the film. In the case of a laminated film, a film-like food can be made thin by selecting a film having a surface layer that does not contain a supplement component and having strength.
In addition to strength, the film that does not contain a supplement component acts as a barrier between the upper and lower supplement component-containing films when laminated, and also has a role of blocking moisture, air, etc. by providing it on the outermost surface. You may let them. For example, since oil-soluble vitamin C remains reactive with iron ions even if it is included in cyclodextrin, a browning phenomenon occurs, but this phenomenon can be prevented by providing a barrier film.

形成されたフィルムへ後からCD包接体を保持させる方法は、例えば、フィルム形成時にCD包接体の分散液を噴霧する等の方法によって行うことができる。分散液にはデンプン等の結合剤、グリセロール等の付着剤を含ませてもよく、また、単なる水溶液として半乾燥時のフィルム自体の接着力で付着させてもよい。CD包接体を付着させたフィルムは,バリヤーフィルム等と積層するとよい。   A method of holding the CD inclusion body on the formed film later can be performed by, for example, a method of spraying a dispersion liquid of the CD inclusion body at the time of film formation. The dispersion may contain a binder such as starch and an adhesive such as glycerol, or may be attached as a simple aqueous solution with the adhesive strength of the film itself during semi-drying. The film to which the CD inclusion body is attached may be laminated with a barrier film or the like.

以下、本発明の製造例および実施例を示すが、本発明はこれに限定されるものではない。
製造例1 サプリメント成分を含まない可食性フィルムの作成(バリヤーフィルム)
適量のイオン交換水に、攪拌しながら、フィルム形成成分として、デンプン、グリセリン、セルロースを添加し、添加終了後、攪拌を停止する。得られた混合液を加温して糊化して適当な濃度と粘度のデンプン溶液とし、この溶液に甘味料溶液、香料を加え均一な塗布液とし、この塗布液を表面平滑な回転ドラムに適当な厚さに塗布し、乾燥し、乾燥したフィルムを剥離してサプリメント成分を含まない可食性フィルムを得る。
Hereinafter, although the manufacture example and Example of this invention are shown, this invention is not limited to this.
Production Example 1 Preparation of an edible film containing no supplement components (barrier film)
While stirring, an appropriate amount of ion-exchanged water is added with starch, glycerin, and cellulose as film-forming components. The resulting mixed solution is heated to gelatinize to obtain a starch solution having an appropriate concentration and viscosity, and a sweetener solution and a fragrance are added to this solution to form a uniform coating solution. This coating solution is applied to a surface-smooth rotating drum. The edible film which does not contain a supplement component is obtained by peeling and drying the dried film.

製造例2 サプリメントCD包接体を含む可食性フィルムの作成
70℃程度に加温した熱水に、攪拌しながら、フィルム形成成分として、ゼラチン、グリセリン、セルロース、耐熱性サプリメント素材などを添加し、添加終了後、攪拌を停止する。得られた混合液を加温して糊化し、適当な濃度と粘度の溶液とするとともに脱泡する。この脱泡したゼラチン溶液を温度50℃程度の保温釜に移し、再度攪拌しながら、甘味料、色素溶解液、熱に弱いサプリメント素材、乳化済み香料、水又は湯に分散させたサプリメントCD包接体、酸味料溶液を順次加えて均一な塗布液とする。酸味料溶液添加後の塗布液はpH4以上であることが好ましい。このように調製した塗布液を表面平滑な回転ドラムに適当な厚さに塗布し、乾燥し、乾燥したフィルムを回転ドラムから剥離してサプリメント成分を含むフィルム状食品を得る。
Production Example 2 Preparation of edible film containing supplement CD inclusion body Add gelatin, glycerin, cellulose, heat-resistant supplement material, etc. as film forming ingredients while stirring to hot water heated to about 70 ° C., Stirring is stopped after the addition is complete. The obtained mixed solution is heated and gelatinized to obtain a solution having an appropriate concentration and viscosity, and defoamed. The defoamed gelatin solution is transferred to a heat-retaining kettle at a temperature of about 50 ° C., and while being stirred again, the supplement CD is dispersed in a sweetener, a dye solution, a heat-sensitive supplement material, an emulsified flavor, water or hot water. The body and the acidulant solution are sequentially added to obtain a uniform coating solution. The coating solution after addition of the acidulant solution is preferably pH 4 or higher. The coating solution thus prepared is applied to a rotating drum having a smooth surface, dried, and the dried film is peeled off from the rotating drum to obtain a film-like food containing a supplement component.

製造例2のフィルムの作成において、CD包接体としてのサプリメント成分を変えることによって、ユビキノン、α−リポ酸、カテキン、油溶性ビタミンC誘導体、レチノイド類等のそれぞれを含むフィルム状食品が得られる。また、製造例1で得られた可食性フィルムの上面に製造例2の塗布液を塗布し、乾燥して積層したフィルム状食品を得ることができる。
製造例2の製法は、フィルム形成材料にCD包接体を混入する方法であるが、製造例1で形成されたフィルムの表面に、水または湯に分散させたサプリメントCD包接体液を噴霧または塗布してサプリメント成分を保持したフィルム状食品を作成することができる。得られたフィルム状食品のCD包接体保持面にバリヤーフィルを積層して積層フィルム状食品としても良い。
上記製造例において塗布液を回転ドラムに塗布するのではなく、ポリエチレンテレフタレート(PET)フィルムなどのプラスチックフィルムの表面に塗布して、乾燥用の回転ドラムや乾燥炉を通して乾燥してプラスチックフィルムと可食性フィルム(フィルム状食品)を分離する方法などによって製造される。
In the production of the film of Production Example 2, a film-like food containing each of ubiquinone, α-lipoic acid, catechin, oil-soluble vitamin C derivative, retinoids and the like can be obtained by changing the supplement component as a CD inclusion. . Moreover, the film-form foodstuff which apply | coated the coating liquid of the manufacture example 2 on the upper surface of the edible film obtained by the manufacture example 1 and dried and can laminate | stack can be obtained.
The production method of Production Example 2 is a method in which the CD inclusion body is mixed into the film forming material, but the supplement CD inclusion body liquid dispersed in water or hot water is sprayed on the surface of the film formed in Production Example 1 or It is possible to prepare a film-like food that is applied and retains a supplement component. A laminated film-like food may be obtained by laminating a barrier fill on the CD clathrate holding surface of the obtained film-like food.
In the above production example, the coating solution is not applied to the rotating drum, but applied to the surface of a plastic film such as a polyethylene terephthalate (PET) film, and then dried through a rotating drum for drying or a drying furnace to be edible. It is manufactured by a method of separating a film (film-like food).

以下に実施例を示す。
表1に示す各成分を各配合ごとに水溶液に調製し、各配合をあわせてフィルム形成用混合液とする。得られた混合液を表面平滑なプラスチックシート面に塗布し、乾燥後剥離してカテキンCD包接体を含む可食性フィルム(厚さ100μm)を得た。
フィルム形成成分が、実施例1はカゼインナトリウム、実施例2はトウモロコシ加工デンプン、実施例3はプルラン、実施例4はアルギン酸ナトリウムを用いた例である。

Figure 2008072915
Examples are shown below.
Each component shown in Table 1 is prepared in an aqueous solution for each formulation, and each formulation is combined to form a mixed liquid for film formation. The obtained mixture was applied to a smooth plastic sheet surface, dried and peeled to obtain an edible film (thickness: 100 μm) containing a catechin CD inclusion body.
Examples of the film-forming components are sodium caseinate in Example 1, modified corn starch in Example 2, pullulan in Example 3, and sodium alginate in Example 4.
Figure 2008072915

実施例1〜4で得られたフィルムは、成形性、強度、溶解性が良好で、CD包接体はいずれのフィルム形成成分でも良好な可食性フィルムが得られることを示している。
サプリメント成分をカテキンに代えてユビキノン、α−リポ酸を用いて行って、上記と同様な結果を得た。
The films obtained in Examples 1 to 4 have good moldability, strength, and solubility, and the CD inclusions indicate that any film-forming component can provide a good edible film.
The supplement component was replaced with catechin, and ubiquinone and α-lipoic acid were used to obtain the same results as above.

次に、CD包接したサプリメント成分と非包接サプリメント成分を含む可食性フィルムについて比較した例を示す。
表2に示す各材料を各配合ごとにそれぞれ溶解して溶液または分散液とし、これらを合
わせて適当な粘度の塗工液に調製した。この塗工液をOPP(配向ポリプロピレン)フィルム面に塗布し、水分含量7%まで乾燥してフィルム(厚さ100μm)を作成した。

Figure 2008072915
Next, the example which compared the edible film containing the supplement component which carried out CD inclusion and the non-inclusion supplement component is shown.
Each material shown in Table 2 was dissolved for each formulation to obtain a solution or dispersion, and these were combined to prepare a coating solution with an appropriate viscosity. This coating solution was applied to an OPP (oriented polypropylene) film surface and dried to a moisture content of 7% to prepare a film (thickness: 100 μm).
Figure 2008072915

得られたフィルムについて、成形性、耐湿性、耐乾燥性について調査した。
調査は下記の方法によった。
成形性: 上記の製法でOPPフィルム上に形成した可食性フィルムがフィルムとして剥離できるか否かで判定した。
耐湿性: 22×33mmのフィルム24枚をプラスチックケースに入れ、恒温恒湿槽(40℃、R.H.70%)で2日間処理した後のフィルム同士の付着度合いを確認した。プラスチックケースはケース内寸法が22×33×2.5mmで、側端に取り出しスリットを有する非密閉容器である(以下同じ)。
耐乾燥性: 22×33mmのフィルム24枚をプラスチックケースに入れ、恒温恒湿槽(30℃、R.H.32%)で2日間処理した後の脆さを確認した。
結果を表3に示す。

Figure 2008072915
表3に示すとおり、CDで包接したα−リポ酸を含むフィルムの方がCDで包接しないα−リポ酸を含むフィルムに比して、耐湿性、耐乾燥性に優れており、折り曲げ強度も優れていることがわかる。 About the obtained film, it investigated about the moldability, moisture resistance, and drying resistance.
The survey was conducted according to the following method.
Formability: Judgment was made based on whether or not the edible film formed on the OPP film by the above production method could be peeled off as a film.
Moisture resistance: 24 films of 22 × 33 mm were placed in a plastic case, and the degree of adhesion between the films after being treated in a constant temperature and humidity chamber (40 ° C., RH 70%) for 2 days was confirmed. The plastic case is a non-sealed container having a case inner dimension of 22 × 33 × 2.5 mm and having a take-out slit at the side end (the same applies hereinafter).
Drying resistance: 24 sheets of 22 × 33 mm films were put in a plastic case, and the brittleness after being treated in a constant temperature and humidity chamber (30 ° C., RH 32%) for 2 days was confirmed.
The results are shown in Table 3.
Figure 2008072915
As shown in Table 3, the film containing α-lipoic acid clathrated with CD is superior in moisture resistance and drying resistance compared to the film containing α-lipoic acid not clad with CD. It can be seen that the strength is also excellent.

試験例:フィルムサプリの効果
CD包接体としたサプリメント成分とCD包接しないサプリメント成分を含むフィルム(フィルムサプリ)の美容等に及ぼす効果について比較した。
I.試験試料
実施例A1:
前記実施例1の処方で作成した、美容系サプリメント成分としてα−リポ酸、カテキン、コエンザイムQ10、真珠粉、ビタミンCの各CD包接体を含むフィルムサプリ(フィルム形成成分:カゼインナトリウム)。
比較例B1:
実施例A1と同じ処方で、サプリメント成分としてCD包接しない実施例A1に記載の成分を含むフィルムサプリ。
実施例A2:
前記実施例2の処方で作成した、健康系サプリメント成分としてα−リポ酸、カテキン、コエンザイムQ10、クエン酸、ビタミンB1、ビタミンB6の各CD包接体を含むフィルムサプリ(フィルム形成成分:トウモロコシデンプン)。
比較例B2:
実施例A2と同じ処方で、サプリメント成分としてCD包接しない実施例A2に記載の成分を含むフィルムサプリ。

II.フィルムサプリの仕様は、22×33×0.1mm(横×縦×厚さ)

III.判定基準
A 顕著に改善した
B 改善した
C わずかに改善
D 変化認めず
E 増悪
Test Example: Effect of Film Supplement The effects on the beauty and the like of a film containing a supplement component as a CD inclusion body and a supplement component that does not include a CD (film supplement) were compared.
I. Test sample Example A1:
A film supplement (film forming component: sodium caseinate) containing CD inclusion bodies of α-lipoic acid, catechin, coenzyme Q10, pearl powder, and vitamin C as a cosmetic supplement component prepared by the formulation of Example 1.
Comparative Example B1:
A film supplement containing the components described in Example A1, which is the same formulation as Example A1 and does not include CD as a supplement component.
Example A2:
A film supplement containing α-lipoic acid, catechin, coenzyme Q10, citric acid, vitamin B1 and vitamin B6 CD inclusions (film-forming component: corn starch) prepared as a health supplement component prepared in the formulation of Example 2 ).
Comparative Example B2:
A film supplement containing the components described in Example A2 which is the same formulation as Example A2 and does not include CD as a supplement component.

II. The film supplement specification is 22 x 33 x 0.1 mm (width x length x thickness)

III. Judgment criteria A Significantly improved B Improved C Slightly improved D No change E Exacerbated

〔モニターテスト〕
(1)肌状態改善効果
肌に衰えを訴えた30〜40歳台の女性ボランティアを1群10名で2群募り、1群には実施例A1(フィルムサプリ;美容系)をもう1群には比較例B1を1日5枚ずつ2週間連続摂取させた。その後前記の判定基準に基づいて使用前後の肌状態を、肌のうるおい感、肌のつや、肌のハリ、血色の4項目についてモニター試験を行った。なお、本試験期間を通して身体に異常を訴えた者はなかった。
実施例A1には比較例B1に比べて、明瞭な肌質改善作用が認められた。結果を表4〜7に示す。
[Monitor test]
(1) Skin condition improvement effect Two groups of female volunteers in the 30 to 40-year-old age group who complained of skin deterioration were recruited in 10 groups per group, and Example A1 (film supplement; beauty system) was assigned to the other group. Took Comparative Example B1 5 times a day for 2 weeks. After that, based on the above criteria, the skin condition before and after use was subjected to a monitor test with respect to four items of moisture feeling, skin gloss, skin firmness, and blood color. None of the patients complained of physical abnormalities throughout the study period.
In Example A1, a clear skin quality improving action was recognized as compared with Comparative Example B1. The results are shown in Tables 4-7.

Figure 2008072915
Figure 2008072915
Figure 2008072915
Figure 2008072915

(2)心身改善効果
心身に衰えを訴えた40〜50歳台の女性ボランティアを1群10名で2群募り、1群には実施例A2(フィルムサプリ;元気系)をもう1群には比較例B2を1日5枚ずつ2週間連続摂取させた。その後前記の判定基準に基づいて使用前後の心身の状態を、寝起き、就労中の倦怠感、就労後の疲労感の3項目についてモニター試験を行った。なお、本試験期間を通して身体に異常を訴えた者はなかった。
(2) Mental and physical improvement effects Two groups of 10 to 40-year-old female volunteers who complained of mental and physical decline were recruited in one group, and one group was given Example A2 (Film Supplement; Genki). Comparative Example B2 was ingested for 5 consecutive days for 2 weeks. Thereafter, based on the above criteria, a monitor test was conducted on the mental and physical conditions before and after use for three items: waking up, feeling tired during working, and feeling tired after working. None of the patients complained of physical abnormalities throughout the study period.

Figure 2008072915
Figure 2008072915

上記表4〜10に示すとおり、CD包接体を含むフィルムサプリは、美容および健康の面で非包接成分を含むフィルムサプリに比べて良好な結果を示した。また、CD包接体を含むフィルムサプリは、フィルム同士が付着したり、摂取時にフィルムが欠けたりすることも無く、口腔内での良好であるとのパネラーからの報告も得られた。   As shown in Tables 4 to 10 above, the film supplement containing the CD inclusion body showed better results than the film supplement containing the non-inclusion component in terms of beauty and health. Moreover, the film supplement containing CD inclusion body did not adhere to each other film, or the film was not chipped when ingested, and a report from the panel that it was good in the oral cavity was also obtained.

空気中で不安定であるとか、非水溶性であるため水に分散または溶解し難い物質や、また、カテキンのように天然物由来の物質であるため多数の化合物の混合体であるため従来の可食性フィルムの製法では包含させることができなかったものも、本発明によるシクロデキストリンの使用方法によって、選択的に包接させた包接体を用いることによって、安定化した充分にサプリメント成分を含むフィルム状食品を得ることができる。   Substances that are unstable in the air, are insoluble in water and are difficult to disperse or dissolve in water, and are natural substances such as catechins. Even those that could not be included in the process of making an edible film include a sufficiently supplemented component that has been stabilized by using the inclusion body selectively included by the method of using cyclodextrin according to the present invention. A film-like food can be obtained.

Claims (5)

シクロデキストリンに包接させたサプリメント成分を澱粉等からなる可食性フィルムに保持させたことを特徴とするフィルム状食品。   A film-like food characterized in that a supplement component encapsulated in cyclodextrin is held in an edible film made of starch or the like. サプリメント成分が、ユビキノン、α−リポ酸、カテキン、カルニチン、テアニン、クエン酸、ビタミンB群、ビタミンE、油溶性ビタミンC誘導体、ミネラル類およびレチノイド類からなる群から選ばれる1種または2種の物質であることを特徴とする請求項1に記載のフィルム状食品。   The supplement component is one or two selected from the group consisting of ubiquinone, α-lipoic acid, catechin, carnitine, theanine, citric acid, vitamin B group, vitamin E, oil-soluble vitamin C derivative, minerals and retinoids The film-like food according to claim 1, which is a substance. 可食性フィルムが、デンプン、プルラン、アラビノキシラン、グアーガム分解物、アルギン酸ナトリウム、カラギーナン、寒天、ペクチン、セルロース等の多糖類、およびゼラチン、シルク分解物、カゼイン分解物等のペプチド系物質から選ばれるフィルム形成成分よりなることを特徴とする請求項1に記載のフィルム状食品。   Film formation in which the edible film is selected from starch, pullulan, arabinoxylan, guar gum degradation product, polysaccharides such as sodium alginate, carrageenan, agar, pectin, cellulose, and peptide substances such as gelatin, silk degradation product, and casein degradation product The film-like food according to claim 1, comprising an ingredient. サプリメント成分を保持させた可食性フィルムを2以上に積層するか、またはサプリメント成分を保持させた可食性フィルムと成分非保持可食性フィルムを多層に積層してなる請求項1に記載のフィルム状食品。   The film-like food according to claim 1, wherein the edible film holding the supplement component is laminated in two or more, or the edible film holding the supplement component and the non-component edible film are laminated in multiple layers. . サプリメント成分をシクロデキストリンに包接させ、得られたCD包接体をフィルム形成材料に混入して所要の粘度の溶液とし、該溶液を所望の厚さのフィルムに成形することからなるフィルム状食品の製造方法。   A film-shaped food product comprising inclusion of a supplement component in cyclodextrin, mixing the obtained CD inclusion body into a film-forming material to form a solution having a required viscosity, and forming the solution into a film having a desired thickness Manufacturing method.
JP2006253264A 2006-09-19 2006-09-19 Film-like food Pending JP2008072915A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2006253264A JP2008072915A (en) 2006-09-19 2006-09-19 Film-like food

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2006253264A JP2008072915A (en) 2006-09-19 2006-09-19 Film-like food

Publications (1)

Publication Number Publication Date
JP2008072915A true JP2008072915A (en) 2008-04-03

Family

ID=39345643

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2006253264A Pending JP2008072915A (en) 2006-09-19 2006-09-19 Film-like food

Country Status (1)

Country Link
JP (1) JP2008072915A (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011125091A1 (en) * 2010-04-02 2011-10-13 株式会社 ツキオカ Edible film
JP2013241394A (en) * 2012-04-25 2013-12-05 Kobayashi Pharmaceutical Co Ltd Agent for increasing water content of skin
CN104151628A (en) * 2014-08-18 2014-11-19 苏州市盛百威包装设备有限公司 Food packaging material and preparation method thereof
CN104693811A (en) * 2015-03-27 2015-06-10 四川大学 Functional gelatin food packaging film and preparation method thereof
JP2016506381A (en) * 2012-11-30 2016-03-03 株式会社アモーレパシフィックAmorepacific Corporation Catechin bioavailability enhancer containing cyclodextrin
CN105561329A (en) * 2016-01-22 2016-05-11 辽宁万嘉医药科技有限公司 Cyclodextrin triad-supramolecular inclusion compound compounded by water-soluble coenzymes Q10 and alpha-lipoic acid and preparing method
JP2021072850A (en) * 2010-03-13 2021-05-13 イーストポンド・ラボラトリーズ・リミテッド Fat binding composition
JP2021083826A (en) * 2019-11-29 2021-06-03 Nissha株式会社 Production method for edible film, film preparation, and edible film
US11446255B2 (en) 2019-03-20 2022-09-20 Ricoh Company, Ltd. Sheet, sheet laminate, pharmaceutical drug, sheet producing method, sheet producing apparatus, sheet laminate producing method, and sheet laminate producing apparatus

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63218663A (en) * 1987-03-09 1988-09-12 Bayer Yakuhin Kk Dihydropyridine-hydroxypropylcyclodextrin inclusion complex
JP2003064103A (en) * 2001-08-27 2003-03-05 Kanagawa Prefecture Method for producing insoluble cyclodextrin polymer
JP2004222663A (en) * 2003-01-27 2004-08-12 Ni Corportion Co Ltd Edible film
WO2004091528A2 (en) * 2003-04-14 2004-10-28 Fmc Corporation Delivery systems of homogeneous thermoreversible alginate films
JP2004305116A (en) * 2003-04-08 2004-11-04 Nippon Shokuhin Kako Co Ltd Food or beverage and method for producing the same
JP2005034083A (en) * 2003-07-17 2005-02-10 Japan Tobacco Inc Coating material for microwave cooking deep-fried food, deep-fried food for microwave cooking, coating material for deep-fried food, and deep-fried food
WO2005041945A1 (en) * 2003-10-31 2005-05-12 Kaneka Corporation Composition containing reduced coenzyme q
JP2007277112A (en) * 2006-04-03 2007-10-25 Soft99 Corporation Edible film for preventing sleepiness

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63218663A (en) * 1987-03-09 1988-09-12 Bayer Yakuhin Kk Dihydropyridine-hydroxypropylcyclodextrin inclusion complex
JP2003064103A (en) * 2001-08-27 2003-03-05 Kanagawa Prefecture Method for producing insoluble cyclodextrin polymer
JP2004222663A (en) * 2003-01-27 2004-08-12 Ni Corportion Co Ltd Edible film
JP2004305116A (en) * 2003-04-08 2004-11-04 Nippon Shokuhin Kako Co Ltd Food or beverage and method for producing the same
WO2004091528A2 (en) * 2003-04-14 2004-10-28 Fmc Corporation Delivery systems of homogeneous thermoreversible alginate films
JP2005034083A (en) * 2003-07-17 2005-02-10 Japan Tobacco Inc Coating material for microwave cooking deep-fried food, deep-fried food for microwave cooking, coating material for deep-fried food, and deep-fried food
WO2005041945A1 (en) * 2003-10-31 2005-05-12 Kaneka Corporation Composition containing reduced coenzyme q
JP2007277112A (en) * 2006-04-03 2007-10-25 Soft99 Corporation Edible film for preventing sleepiness

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2021072850A (en) * 2010-03-13 2021-05-13 イーストポンド・ラボラトリーズ・リミテッド Fat binding composition
WO2011125091A1 (en) * 2010-04-02 2011-10-13 株式会社 ツキオカ Edible film
JP2013241394A (en) * 2012-04-25 2013-12-05 Kobayashi Pharmaceutical Co Ltd Agent for increasing water content of skin
JP2016506381A (en) * 2012-11-30 2016-03-03 株式会社アモーレパシフィックAmorepacific Corporation Catechin bioavailability enhancer containing cyclodextrin
CN104151628A (en) * 2014-08-18 2014-11-19 苏州市盛百威包装设备有限公司 Food packaging material and preparation method thereof
CN104693811A (en) * 2015-03-27 2015-06-10 四川大学 Functional gelatin food packaging film and preparation method thereof
CN105561329A (en) * 2016-01-22 2016-05-11 辽宁万嘉医药科技有限公司 Cyclodextrin triad-supramolecular inclusion compound compounded by water-soluble coenzymes Q10 and alpha-lipoic acid and preparing method
US11446255B2 (en) 2019-03-20 2022-09-20 Ricoh Company, Ltd. Sheet, sheet laminate, pharmaceutical drug, sheet producing method, sheet producing apparatus, sheet laminate producing method, and sheet laminate producing apparatus
JP2021083826A (en) * 2019-11-29 2021-06-03 Nissha株式会社 Production method for edible film, film preparation, and edible film
US12059019B2 (en) 2019-11-29 2024-08-13 Nissha Co., Ltd. Method of producing edible film, film formulation, and edible film

Similar Documents

Publication Publication Date Title
JP2008072915A (en) Film-like food
KR101388955B1 (en) Sealed, edible film strip packets and methods of making and using them
EP2318191B1 (en) Method for producing films directly in blister trays
JPS63501794A (en) Methods for providing pharmaceutically active substances, reagents, and other active substances or for producing dosage forms
CN101316579A (en) Uniform films for rapid-dissolve dosage form incorporating anti-tacking compositions
MXPA05005500A (en) Flavor coated drinking straw or other article and coating methods therefor.
TWI304424B (en)
WO2007040021A1 (en) Soluble film
WO2014188079A1 (en) Printed dosage forms
JP2004222663A (en) Edible film
WO2015052597A1 (en) Ultrathin metal coated referred herein as metalized edible film and hygienic process for preparation thereof
WO2016005930A1 (en) Ultrathin water resistant metalized edible film and hygienic process for preparation thereof
CN103283919A (en) Preparation method of candies
US20190269625A1 (en) Printed Delivery Device Having Supplements
US20220331263A1 (en) Printed Delivery Device Having Supplements
US11439162B2 (en) Dissolvable composition having indicia
US20230312204A1 (en) Packaged food concentrate with barrier properties provided by an edible packaging
US20220080050A1 (en) Printed Delivery Device Having Supplements
Chaudhary et al. Edible Packaging: A Vehicle for Functional Bioactive Compounds
US20130345305A1 (en) Powder emulsifier
JP2023527201A (en) Drinking straw with inner coating
GB2588299A (en) A dosage in film package form, an film composition and a process for preparation thereof
WO2023097074A1 (en) Printed delivery device having supplements
BR102020022369A2 (en) Nutraceutical edible coating containing spirulina platensis for post-harvest fruit conservation
BR102022003079A2 (en) EDIBLE NUTRACEUTICAL COATING CONTAINING CHLORELLA SP. FOR POST-HARVEST STORAGE OF FRUITS

Legal Events

Date Code Title Description
A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20090908

A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20101118

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20110119

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20110322

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20110413

A02 Decision of refusal

Free format text: JAPANESE INTERMEDIATE CODE: A02

Effective date: 20111019