JP2009072124A - Granular food composition and method for producing the same - Google Patents

Granular food composition and method for producing the same Download PDF

Info

Publication number
JP2009072124A
JP2009072124A JP2007244432A JP2007244432A JP2009072124A JP 2009072124 A JP2009072124 A JP 2009072124A JP 2007244432 A JP2007244432 A JP 2007244432A JP 2007244432 A JP2007244432 A JP 2007244432A JP 2009072124 A JP2009072124 A JP 2009072124A
Authority
JP
Japan
Prior art keywords
food composition
granular food
extract
dried
mixed
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
JP2007244432A
Other languages
Japanese (ja)
Inventor
Noriyuki Takegawa
昇志 竹川
Toshifumi Taketsuru
敏文 竹鶴
Yoichi Yasuda
陽一 安田
Hiroko Kikuchi
宏子 菊池
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.)
Noevir Co Ltd
Original Assignee
Noevir Co Ltd
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 Noevir Co Ltd filed Critical Noevir Co Ltd
Priority to JP2007244432A priority Critical patent/JP2009072124A/en
Publication of JP2009072124A publication Critical patent/JP2009072124A/en
Pending legal-status Critical Current

Links

Images

Landscapes

  • Coloring Foods And Improving Nutritive Qualities (AREA)

Abstract

<P>PROBLEM TO BE SOLVED: To provide a granular food composition which is soft and pleasant to the tongue, is free of sensation of surface roughness and collapses quickly in oral cavities, does not leave sensation of surface roughness, and moreover, has more markedly promoted absorbability, after being administered, than conventional granular food compositions. <P>SOLUTION: Dry Cordyceps sinensis Sacc. and water are mixed with each other at a rate of 1 kg and 9 liter, respectively, and then refluxed at 95 to 100°C for 5 hours to obtain a hot water extract. The extraction residue is dried, crushed, and then mixed with 15 MPa carbon dioxide at a flow rate of 700 liter/hour at 40°C, to obtain a supercritical fluid extract. The prepared hot water extract is mixed with dextrin as a vehicle, processed into a proper aqueous solution, and then spray-dried to obtain fine grains. The fine grains are transferred to a stirring granulator, mixed with this supercritical fluid extract, kneaded and then stirred and mixed uniformly. The mixture is transferred to an extrusion granulator, extruded into granules, dried and then graded to obtain the granular food composition. <P>COPYRIGHT: (C)2009,JPO&INPIT

Description

本発明は、顆粒状食品組成物及びその製造方法に関する。さらに詳しくは、本製造方法を用いることによって、舌触りが滑らかで、ざらつき感がなく、口腔内で速やかに崩壊して、ざらつき感が残らない顆粒状食品組成物が得られるというもの。またさらには、本製造方法を用いることによって、服用後の吸収率が、従来品に比べて顕著に促進された顆粒状食品組成物に関するものである。   The present invention relates to a granular food composition and a method for producing the same. More specifically, by using this production method, a granular food composition is obtained that has a smooth texture, does not feel rough, disintegrates rapidly in the oral cavity, and does not leave a rough feeling. Furthermore, the present invention relates to a granular food composition in which the absorption rate after taking is significantly promoted as compared with conventional products.

食品組成物や医薬製剤において、製剤形態としては、顆粒もしくは錠剤、カプセル剤が採用される。錠剤は徐放性とか持続性を調節できることや、老人にも服用しやすいことから最も多く使われている。顆粒剤は本来散剤を飲みやすくした形態であるが、やはり錠剤に比べると服用しづらく、徐放性等の調整が困難などの欠点がある。しかしながら、有効成分をなるべく高濃度で製剤化でき、粘膜への吸収が速く良い点で顆粒は汎用されている。   In food compositions and pharmaceutical preparations, granules, tablets or capsules are employed as the form of preparation. Tablets are most often used because of their ability to control sustained release and sustainability, and because they are easy to take for the elderly. Granules are originally in a form that makes it easy to take powders, but they are also difficult to take compared to tablets, and there are drawbacks such as difficulty in adjusting sustained release. However, granules are widely used in that the active ingredient can be formulated in as high a concentration as possible and can be absorbed quickly into the mucous membrane.

顆粒形態を形成するためには、造粒工程が必要であるが、製剤中に含まれる凝集力の高い成分や、糖などの賦形剤や結合剤が、この過程で起こる凝集、乾燥という形態変化によって、どうしてもざらつきを生じてしまうのは避けようがない現象である。   In order to form a granule form, a granulation process is required. However, a highly cohesive component contained in the preparation, an excipient such as sugar, and a binder are aggregated and dried in this process. It is an unavoidable phenomenon that roughness is inevitably caused by change.

冬虫夏草、アガリクス、メシマコブ、チャーガ、ハナビラタケ、マツタケ、マイタケ、ヤマブシタケ、霊芝等の担子菌類は、健康食品に多く用いられており、様々な形態の食品組成物が上市されている。これらは、健康食品においては原体のまま用いられることは少なく、抽出物の形で利用されることが一般的である。   Basidiomycetes such as Cordyceps, Agaricus, Meshimakobu, Chaga, Hanabiratake, Matsutake, Maitake, Yamabushitake, Ganoderma are widely used for health foods, and various forms of food compositions are marketed. These are rarely used as such in health foods and are generally used in the form of extracts.

これらを顆粒剤として製剤化する場合、これら抽出物に含まれる多糖体がさらに造粒時の凝集性に影響し、ざらつきが強くなる現象がみられる。   When these are formulated as granules, there is a phenomenon in which the polysaccharides contained in these extracts further affect the cohesiveness during granulation and become rough.

本発明は、このような顆粒剤の欠点に着目し、担子菌類から抽出された有効成分を全て凝縮した顆粒剤の製造方法について検討した結果、舌触りが滑らかで、ざらつき感がなく、さらに口腔内で速やかに崩壊して、ざらつき感が残らない顆粒状食品組成物が得られたというものである。またさらには、本発明の製造方法を用いることにより、従来品に比べて、服用後の吸収率が顕著に促進された顆粒状食品組成物を提供するものである。   The present invention pays attention to the disadvantages of such a granule, and as a result of examining a method for producing a granule in which all the active ingredients extracted from basidiomycetes are condensed, the tongue feel is smooth, there is no roughness, and the oral cavity It is said that a granular food composition that disintegrated quickly and did not leave a rough feeling was obtained. Furthermore, by using the production method of the present invention, a granular food composition in which the absorption rate after taking is significantly accelerated as compared with conventional products is provided.

これら担子菌類の食品組成物の製造方法に関する文献として、アガリクスエキスおよび/またはアガリクス乾燥粉末にでんぷん分解物と結晶セルロースを所定量添加し、アルコール水溶液を添加して段階的な造粒処理を施すこと特徴とする顆粒の製造方法(特許文献1参照)が開示されている。この方法は、顆粒が水に溶けにくい、口中で喉に詰まってむせる、口中でアガリクス特有のまずい味が直接的に感じられてしまう等の問題点を解決するものである。また、ハナビラタケ乾燥体および/またはハナビラタケ抽出エキスに、還元麦芽糖水飴や結晶セルロースなどの賦形剤を所定量添加し、造粒処理を施すこと特徴とするハナビラタケ含有顆粒の製造方法およびその製造方法により得られるハナビラタケ含有顆粒(特許文献2参照)の開示がある。これは、口中で喉に詰まってむせる、フィルムスティックなどの容器からの開封時に粉体がスムーズに出にくい、開封時に粉体が舞う、などの問題点が解決されたハナビラタケ含有顆粒に関するものである。これらは、いずれも担子菌類を含む食品組成物の味や飲用しやすさを改善する顆粒剤の製造方法に関する発明であり、造粒工程で生じるざらつき感に着目したものではない。   As literature on the method for producing food compositions of these basidiomycetes, a predetermined amount of starch degradation product and crystalline cellulose are added to Agaricus extract and / or Agaricus dry powder, and an aqueous alcohol solution is added to perform stepwise granulation treatment. A characteristic granule production method (see Patent Document 1) is disclosed. This method solves the problems that the granules are difficult to dissolve in water, clogged in the throat in the mouth, and the bad taste peculiar to Agaricus is directly felt in the mouth. According to a method for producing a granule containing Hanabira bamboo, characterized by adding a predetermined amount of an excipient such as reduced maltose starch syrup or crystalline cellulose to dried dried bamboo shoots and / or an extract of Hanabira bamboo, and subjecting to granulation treatment There is a disclosure of the resulting Hanabira bamboo-containing granules (see Patent Document 2). This is related to the granule containing Hanabiratake, which has solved the problems such as clogging in the throat in the mouth, difficulty in smoothly releasing powder when opened from a container such as a film stick, and powder flying when opened. . These are all inventions relating to a method for producing granules that improve the taste and ease of drinking of food compositions containing basidiomycetes, and do not focus on the rough feeling that occurs in the granulation process.

食品組成物を製造する際の造粒時のざらつきの解消に関する文献として、次のような文献が挙げられる。顆粒及び圧縮成型した錠剤形態のクレアチンを含有する食品または医薬品を製造することにおいて、予め、クレアチンを微粉砕した後、原料の混合、造粒、打錠という工程で製造を行うに当たり、クレアチンの粒子径を5μm〜200μmにそろえることにより砂的なザラツキの発生を防止すると共に顆粒及び錠剤がかんだ際に歯につくことを防止した錠剤を得るというものである(特許文献3参照)。これは、溶解性の低い、結晶性の薬剤の欠点を、粒子径をコントロールすることで解消した例である。   The following literature is mentioned as literature regarding the cancellation of the roughness at the time of granulation at the time of manufacturing a food composition. In producing a food or pharmaceutical containing creatine in the form of granules and compressed tablets, after pulverizing creatine in advance, the production of creatine particles in the process of mixing raw materials, granulation and tableting By adjusting the diameter to 5 μm to 200 μm, it is possible to obtain a tablet which prevents the occurrence of sandy roughness and prevents the granules and tablets from sticking to the teeth when biting (see Patent Document 3). This is an example in which the defect of a crystalline drug having low solubility is solved by controlling the particle diameter.

特開2001−112429公報JP 2001-112429 A 特開2004−290158公報JP 2004-290158 A 特開2000−245396公報JP 2000-245396 A

しかしながら、担子菌類から抽出された有効成分を含む顆粒状組成物のざらつき感に着目した報告はない。特に、ざらつきの解消のために、新たなざらつき防止成分を用いて、これら課題を解決する有効な手段についての報告はない。また、製造方法によって、服用後の吸収率が顕著に促進されたという報告例もない。   However, there is no report which paid attention to the rough feeling of the granular composition containing the active ingredient extracted from basidiomycetes. In particular, there is no report on an effective means for solving these problems by using a new texture-preventing component for eliminating the texture. Moreover, there is no report example that the absorption rate after taking was significantly promoted by the production method.

本発明は、担子菌類から抽出された有効成分を全て凝縮した顆粒剤の製造方法ならびにその組成物に関する発明であって、舌触りが滑らかで、ざらつき感がなく、さらに口腔内においても速やかに崩壊して、ざらつき感が残らない、さらには、従来品に比べ服用後の吸収率が顕著に促進された顆粒状食品組成物を得る方法について鋭意検討した。   The present invention relates to a method for producing a granule in which all the active ingredients extracted from basidiomycetes are condensed, and a composition thereof, which is smooth to the touch, has no roughness, and rapidly disintegrates in the oral cavity. Thus, the present inventors have intensively studied a method for obtaining a granular food composition that does not leave a rough feeling and that has a significantly enhanced absorption rate after taking compared to conventional products.

本発明者は、前記課題を解決するために研究を行った結果、造粒工程において、担子菌類から超臨界流体又は亜臨界流体により抽出して得られる抽出物を用いて顆粒剤を製造することよって、これらの課題を全て解消できることを見いだし、本発明を完成するに至ったものである。   As a result of conducting research to solve the above problems, the present inventor produces granules by using an extract obtained by extraction from basidiomycetes with a supercritical fluid or subcritical fluid in a granulation step. Therefore, it has been found that all of these problems can be solved, and the present invention has been completed.

本発明により、舌触りが滑らかで、ざらつき感がなく、さらに口腔内においても速やかに崩壊して、ざらつき感が残らない、さらには、従来品に比べ服用後の吸収率が顕著に促進された担子菌類の抽出物を全て凝縮した純度の高い顆粒状食品組成物が得られる。   According to the present invention, the texture of the tongue is smooth, does not feel rough, disintegrates rapidly in the oral cavity, does not leave a rough feeling, and has a significantly enhanced absorption rate after taking compared to conventional products. A granular food composition with high purity is obtained by condensing all the fungal extracts.

本発明の実施の形態を説明する。   An embodiment of the present invention will be described.

本発明に用いる担子菌類としては、冬虫夏草、アガリクス、メシマコブ、チャーガ、ハナビラタケ、マツタケ、マイタケ、ヤマブシタケ、霊芝等を用いることができる。   As basidiomycetes used in the present invention, cordyceps, Agaricus, Meshimakobu, Chaga, Hanabiratake, Matsutake, Maitake, Yamabushitake, Reishi, etc. can be used.

これらの抽出物が含まれる顆粒状食品組成物を製造する場合、最初にこれら担子菌類の乾燥物を粉砕し、熱水抽出を行い、抽出物を得る。これにとうもろこし澱粉、結晶セルロース、デキストリン、乳糖などの賦形剤を加え、スプレードライ等を行って乾燥・篩過し、細粒を得る。この細粒を造粒することで顆粒状に調製するものである。   When producing a granular food composition containing these extracts, first, the dried product of these basidiomycetes is pulverized and subjected to hot water extraction to obtain an extract. To this, an excipient such as corn starch, crystalline cellulose, dextrin, lactose, etc. is added, followed by spray drying and the like, followed by drying and sieving to obtain fine granules. This fine granule is granulated to prepare it.

顆粒剤を製造する際の造粒方法としては、乾式造粒法と湿式造粒法がある。乾式造粒法は、原料粉末と結合剤を混合した後、強圧をかけてスラッグ(小さな塊)を作り、粉砕、分級を行って一定の粒度物を得る製法で、収率が悪いのが欠点としてある。これに対し、湿式造粒法は、原料粉末を一旦濡れ状態にした後、粒子を大きくしたり、一定粒度物を調整する方法で、押し出し造粒法、転動造粒法、噴霧法などがあり、顆粒剤の製造方法としては、湿式造粒法が一般に行われる。   As granulation methods for producing granules, there are dry granulation methods and wet granulation methods. The dry granulation method is a production method in which raw powder and binder are mixed, and then a strong pressure is applied to make slugs (small lumps), which are pulverized and classified to obtain a certain particle size. It is as. On the other hand, the wet granulation method is a method in which the raw material powder is once wetted, and then the particle size is increased or a constant particle size is adjusted, such as extrusion granulation method, rolling granulation method, spraying method, etc. In addition, as a method for producing granules, wet granulation is generally performed.

押し出し造粒法は、原料粉末に結合剤溶液を加えて練合し、スクリーンから押出す製造方法である。転動造粒法は、濡れ状態にした原料粉末に回転や振動を与えることで、粉末どうしを凝集させて、一定の粒子とする製造方法である。噴霧法は、スラリー状に調製した原料を特殊な造粒機を用いて、微小液滴状態にして噴霧し、熱風を吹き付けて乾燥し造粒するものである。   The extrusion granulation method is a production method in which a binder solution is added to a raw material powder, kneaded, and extruded from a screen. The rolling granulation method is a production method in which powders are agglomerated by giving rotation or vibration to the raw material powder in a wet state to obtain constant particles. In the spraying method, a raw material prepared in a slurry state is sprayed in a fine droplet state using a special granulator, and dried by hot air and dried for granulation.

本発明に用いる製造方法は、このうち湿式造粒法である押し出し造粒法を用いると均一な顆粒が得られやすいので好ましいが、特に限定するものではない。   Of these, the production method used in the present invention is not particularly limited, although the extrusion granulation method, which is a wet granulation method, is preferable because uniform granules are easily obtained.

本発明では、担子菌類の熱水抽出物に賦形剤を加えて調製した細粒に、湿式造粒法を用いて造粒処理を行い、顆粒剤を得る。まず細粒を攪拌造粒機に投入し、別に調製した、担子菌類の子実体及び/又は菌糸体から超臨界流体又は亜臨界流体により抽出して得られる抽出物を加え、練合を開始する。   In the present invention, granules prepared by adding excipients to a basidiomycete hot water extract are subjected to granulation treatment using a wet granulation method to obtain granules. First, the fine granules are put into a stirring granulator, and an extract obtained by supercritical fluid or subcritical fluid extraction from a basidiomycete fruit body and / or mycelium prepared separately is added, and kneading is started. .

担子菌類を超臨界流体又は亜臨界流体により抽出して得られる抽出物を得るには、超臨界抽出装置を用いた超臨界流体抽出法又は亜臨界流体抽出法を用いる。超臨界流体抽出法又は亜臨界流体抽出法で用いる抽出剤には特に制限はなく、例えば、水、二酸化炭素、エチレン、プロピレン、エタン、プロパン、一酸化二窒素、クロロジフルオロメタン、クロロトリフルオロメタン、キセノン、アンモニア、メタノール、エタノールなどを使用することができるが、最終製品が食品であることから、安全性、製品への混入による毒性などを考慮すると、二酸化炭素を使用することが好ましい。抽出圧力は、使用する抽出剤の臨界圧力に応じて適宜選定することができるが、通常は3〜70MPaであることが好ましく、特に二酸化炭素を使用するときは4〜60MPaが好ましく、最も好ましくは5〜40MPaである。   In order to obtain an extract obtained by extracting basidiomycetes with a supercritical fluid or a subcritical fluid, a supercritical fluid extraction method or a subcritical fluid extraction method using a supercritical extraction device is used. There is no particular limitation on the extraction agent used in the supercritical fluid extraction method or the subcritical fluid extraction method, for example, water, carbon dioxide, ethylene, propylene, ethane, propane, dinitrogen monoxide, chlorodifluoromethane, chlorotrifluoromethane, Xenon, ammonia, methanol, ethanol, and the like can be used. However, since the final product is a food, it is preferable to use carbon dioxide in view of safety, toxicity due to mixing into the product, and the like. The extraction pressure can be appropriately selected according to the critical pressure of the extractant to be used, but it is usually preferably 3 to 70 MPa, particularly 4 to 60 MPa, most preferably when carbon dioxide is used. 5-40 MPa.

練合に際しての攪拌造粒機としては、ハイスピードミキサー(フロイント産業製)やバーチカルグラニュレーター(深江パウテック製)などを用いることができる。この時、適度な濡れ状態にするために、エチルアルコールや水を加えてもよいが、可能な限り最小限に抑えるほうが、ざらつきのない顆粒剤を得られやすい。次にこれを、押し出し造粒機に移し、造粒を開始する。押し出し造粒機としては、ドームグラン(不二パウダル製)などを用いることができる。ドームグランは押し出し部が、ドーム型であることから、均一な顆粒を調製することができる。これを乾燥・整粒することで顆粒剤が製造される。乾燥に際しては、流動乾燥法や棚乾燥(静置乾燥)などがあるが、特に限定されない。混合・造粒・乾燥がひとつの機械で行えるフローコーター(フロイント産業製)やグラット流動造粒・乾燥機(株式会社パウレック製)などを用いることもできる。   As the agitation granulator at the time of kneading, a high speed mixer (manufactured by Freund Corporation), a vertical granulator (manufactured by Fukae Powtech) or the like can be used. At this time, ethyl alcohol or water may be added in order to obtain an appropriate wet state, but it is easier to obtain a rough granule if it is minimized as much as possible. Next, this is transferred to an extrusion granulator and granulation is started. As an extruding granulator, a dome gran (made by Fuji Powder) or the like can be used. Since the extruded portion of the dome granule has a dome shape, uniform granules can be prepared. Granules are produced by drying and sizing this. The drying includes a fluidized drying method and shelf drying (stationary drying), but is not particularly limited. A flow coater (manufactured by Freund Sangyo) that can be mixed, granulated, and dried by a single machine, or a glat fluidized granulator / dryer (manufactured by POWREC Co., Ltd.) can also be used.

次に、以下に本発明の実施例を挙げてさらに具体的に説明する。本発明の技術的範囲はこれらによりなんら限定されるものでではない。   Next, the present invention will be described more specifically with reference to examples. The technical scope of the present invention is not limited by these.

[実施例1]冬虫夏草を用いた顆粒状食品組成物の製造方法
冬虫夏草(Cordyceps sinensis)乾燥物に水を加え(冬虫夏草乾燥物1Kgあたり9リットルの水)、95〜100℃にて5時間還流して抽出した後、抽出液をろ過して回収し、溶媒を除去し冬虫夏草の熱水抽出物を得た。次に、超臨界抽出装置を用いて冬虫夏草の超臨界流体抽出物を調製する。先に抽出処理を行った冬虫夏草の抽出残試料をさらに乾燥粉砕する。エントレーナとして0.003%のエタノールを加えた後、40℃において15MPaの二酸化炭素を分離槽出口での大気圧下での二酸化炭素の流量が700リットル/時間となるように調節しながら超臨界状態の二酸化炭素を供給した。その後、抽出槽の圧力を減圧し抽出物を取り出し、冬虫夏草の超臨界流体抽出物を得た。先に調製した冬虫夏草の熱水抽出物に賦形剤としてデキストリンを加え、適度な水溶液に調製し、スプレードライにより細粒を得た。これを攪拌造粒機(ハイスピードミキサー)に移し、先に調製した冬虫夏草の超臨界流体抽出物を加え、練合処理を行い、混合均一攪拌する。次に押し出し造粒機に移し、顆粒状に押し出された後、乾燥・整粒し、顆粒状食品組成物を得た。
[Example 1] Method for producing granular food composition using Cordyceps sinensis Water is added to dried Cordyceps sinensis (9 liters of water per kg of Cordyceps sinensis ) and refluxed at 95-100 ° C for 5 hours. After extraction, the extract was collected by filtration, the solvent was removed, and a hot water extract of Cordyceps was obtained. Next, a supercritical fluid extract of Cordyceps sinensis is prepared using a supercritical extraction apparatus. The extract residue sample of Cordyceps sinensis previously extracted is further dried and ground. After adding 0.003% ethanol as an entrainer, supercritical state while adjusting the flow rate of carbon dioxide of 15 MPa at 40 ° C. under atmospheric pressure at the outlet of the separation tank to 700 liter / hour Of carbon dioxide. Thereafter, the pressure in the extraction tank was reduced, the extract was taken out, and a supercritical fluid extract of Cordyceps was obtained. Dextrin was added as an excipient to the hot water extract of Cordyceps prepared earlier to prepare an appropriate aqueous solution, and fine particles were obtained by spray drying. This is transferred to a stirring granulator (high speed mixer), and the supercritical fluid extract of Cordyceps prepared above is added, kneaded, and mixed and stirred uniformly. Next, the mixture was transferred to an extrusion granulator, extruded into granules, dried and sized, and a granular food composition was obtained.

[比較例1]冬虫夏草の熱水抽出物及び超臨界流体抽出物を含む顆粒状食品組成物において、造粒工程で超臨界流体抽出物を用いない製造方法
冬虫夏草(Cordyceps sinensis)乾燥物に水を(実施例1と同様の割合)加え、95〜100℃にて5時間還流して抽出した後、抽出液をろ過して回収し、溶媒を除去し冬虫夏草の熱水抽出物を得た。この抽出残試料をさらに乾燥粉砕し、超臨界抽出装置を用いて冬虫夏草の超臨界流体抽出物を調製する。エントレーナとして0.003%のエタノールを加えた後、40℃において15MPaの二酸化炭素を分離槽出口での大気圧下での二酸化炭素の流量が700リットル/時間となるように調節しながら超臨界状態の二酸化炭素を供給した。その後、抽出槽の圧力を減圧し抽出物を取り出し、冬虫夏草の超臨界流体抽出物を得た。この超臨界流体抽出物と、先に調製した冬虫夏草の熱水抽出物とを混合し、賦形剤としてデキストリンを加え、適度な水溶液に調製し、スプレードライにより細粒を得た。次にこれを攪拌造粒機に移し、結合剤及び湿気を与える目的で、乳糖水溶液を加え、練合処理を行い、混合均一攪拌する。次に押し出し造粒機に移し、顆粒状に押し出された後、乾燥・整粒し、顆粒状食品組成物を得た。
[Comparative Example 1] In a granular food composition containing a hot water extract of Cordyceps sinensis and a supercritical fluid extract, a manufacturing method that does not use the supercritical fluid extract in the granulation process. Water is added to the dried Cordyceps sinensis dry product. (The same ratio as in Example 1) In addition, after extraction by refluxing at 95-100 ° C for 5 hours, the extract was collected by filtration, the solvent was removed, and a hot water extract of Cordyceps was obtained. This extraction residue sample is further dried and ground, and a supercritical fluid extract of Cordyceps is prepared using a supercritical extraction device. After adding 0.003% ethanol as an entrainer, supercritical state while adjusting the flow rate of carbon dioxide of 15 MPa at 40 ° C. under atmospheric pressure at the outlet of the separation tank to 700 liter / hour Of carbon dioxide. Thereafter, the pressure in the extraction tank was reduced, the extract was taken out, and a supercritical fluid extract of Cordyceps was obtained. This supercritical fluid extract and the hot water extract of Cordyceps sinensis prepared above were mixed, dextrin was added as an excipient to prepare an appropriate aqueous solution, and fine granules were obtained by spray drying. Next, this is transferred to an agitation granulator, and for the purpose of imparting a binder and moisture, an aqueous lactose solution is added, kneaded, and mixed and stirred uniformly. Next, the mixture was transferred to an extrusion granulator, extruded into granules, dried and sized, and a granular food composition was obtained.

[官能評価]
(a)試験方法
実施例1及び比較例1の顆粒状食品組成物について、10名の専用パネラーにより官能評価を行った。評価は、舌触りの滑らかさ(ざらつき感)、口腔内での崩壊性、崩壊後のざらつき感の3項目について実施した。評価基準は以下に示すとおりである。
(b)試験結果
試験結果を表1に示す。数値は10名専用パネラーのスコアの平均値を示す。
[評価基準]
(1)舌触りの滑らかさ
1:ざらつきがなく滑らか
2:わずかにざらつきを感じる
3:ざらつきを感じる
(2)崩壊性
1:すぐに溶けて気にならない
2:少し気になる
3:溶けにくく残り感が気になる
(3)崩壊後のざらつき感
1:ざらつきがなく滑らか
2:わずかにざらつきを感じる
3:ざらつきを感じる
[sensory evaluation]
(A) Test Method The granular food compositions of Example 1 and Comparative Example 1 were subjected to sensory evaluation by 10 dedicated panelists. The evaluation was carried out for three items of smooth touch (feeling of roughness), disintegration property in the oral cavity, and feeling of roughness after disintegration. The evaluation criteria are as shown below.
(B) Test results Table 1 shows the test results. A numerical value shows the average value of the score of 10 panelists.
[Evaluation criteria]
(1) Smoothness of tongue touch 1: Smooth without roughness 2: Feeling slightly rough 3: Feeling rough (2) Disintegration 1: Immediately melted and not bothered 2: Slightly worried 3: Remains difficult to melt (3) Roughness after collapse 1: Smooth without any roughness 2: Slightly feels rough 3: Feels rough

Figure 2009072124
Figure 2009072124

表1の結果より、本発明の製造方法である実施例1の顆粒剤の方が、比較例1に比べて、3項目共スコアが低く、本発明の顆粒状食品組成物は、明らかに舌触りが滑らかで、ざらつき感がなく、口腔内での崩壊性にも優れ、その後もざらつき感が残らないことが確認された。   From the results in Table 1, the granule of Example 1, which is the production method of the present invention, has a lower score for all three items than Comparative Example 1, and the granular food composition of the present invention is clearly It was confirmed that was smooth and free of roughness, excellent disintegration in the oral cavity, and no roughness after that.

[透過性試験]
(a)試験方法
実施例1及び比較例1の顆粒状食品組成物について、市販の評価キット(日本ベクトン・ディッキンソン株式会社製、BD GentestプレコートPAMPAプレートシステム)を用いて透過性試験を行った。本システムは、予めPAMPA膜がコートされたフィルタープレートと、レシーバープレートから成る96ウェルインサートシステムで、下層にサンプルを添加し、上層に緩衝液を添加し、室温放置後、上層と下層のサンプル濃度を測定することで、浸透速度を計算する。サンプル濃度は、冬虫夏草中のアデノシンの濃度を指標とした。
(b)試験結果
サンプル中のアデノシン定量試験結果を表2に示す。実施例1及び比較例1には、同濃度のアデノシンが含まれることが確認された。次に、
上層/(上層+下層)×100
により、上層へのアデノシン移行率(%)を求めた。2.5時間後、5時間後、7.5時間後のアデノシン移行率(2回の平均値)に関して試験を行い、結果を図1に示す。
[Permeability test]
(A) Test method The granular food compositions of Example 1 and Comparative Example 1 were subjected to a permeability test using a commercially available evaluation kit (manufactured by Nippon Becton Dickinson Co., Ltd., BD Genest pre-coated PAMPA plate system). This system is a 96-well insert system consisting of a filter plate pre-coated with a PAMPA membrane and a receiver plate. A sample is added to the lower layer, a buffer solution is added to the upper layer, and after standing at room temperature, the sample concentrations in the upper and lower layers The permeation rate is calculated by measuring The sample concentration was based on the concentration of adenosine in cordyceps.
(B) Test results Table 2 shows the results of the adenosine quantitative test in the samples. It was confirmed that Example 1 and Comparative Example 1 contain the same concentration of adenosine. next,
Upper layer / (upper layer + lower layer) × 100
Thus, the adenosine transfer rate (%) to the upper layer was determined. A test was conducted with respect to the adenosine transfer rate (average value of 2 times) after 2.5 hours, after 5 hours, and after 7.5 hours, and the results are shown in FIG.

Figure 2009072124
Figure 2009072124

図1の結果より、本発明の製造方法を用いた実施例1の顆粒剤の方が、比較例1に比べて、移行率が高く、2.5時間後の値では、4.3倍、7.5時間後の値では、4.6倍の移行率を示した。本試験(BD GentestプレコートPAMPAプレートシステム)は、in vivoにおける薬物透過性の予測ツールとして有用で、ヒトにおける吸収と高い相関性をもつ試験法である。よって、本発明の製造方法を用いた顆粒状食品組成物は、服用後の吸収率が、比較品に比べて顕著に促進されることが確認された。   From the results of FIG. 1, the granule of Example 1 using the production method of the present invention has a higher migration rate than Comparative Example 1, and the value after 2.5 hours is 4.3 times. The value after 7.5 hours showed a 4.6-fold transfer rate. This test (BD Gentest precoated PAMPA plate system) is useful as a tool for predicting drug permeability in vivo and is a test method having a high correlation with absorption in humans. Therefore, it was confirmed that the granular food composition using the production method of the present invention has a significantly accelerated absorption rate after taking compared to the comparative product.

次に本発明の顆粒状食品組成物の製造方法およびその製造方法を用いた顆粒状食品組成物を実施例により説明する。   Next, the manufacturing method of the granular food composition of this invention and the granular food composition using the manufacturing method are demonstrated by an Example.

[実施例2]アガリクス子実体を用いた顆粒状食品組成物の製造方法
アガリクス・ブラゼイ(Agaricus blazei)の子実体の乾燥物に水を加え(アガリクス子実体乾燥物1Kgあたり10リットルの水)、95〜100℃にて5時間還流して抽出した後、抽出液をろ過して回収し、溶媒を除去しアガリクス子実体の熱水抽出物を得た。次に、超臨界抽出装置を用いて、超臨界炭酸ガスによりアガリクス子実体の超臨界流体抽出物を調製する。先に抽出処理を行ったアガリクス子実体の抽出残試料をさらに乾燥粉砕する。抽出条件は、温度40℃、圧力14MPa〜15MPa、時間5時間とした。次にアガリクス子実体の熱水抽出物に賦形剤としてトウモロコシデンプン及び乳糖を加え、適度な水溶液に調製し、スプレードライにより細粒を得た。これを攪拌造粒機に移し、先に調製したアガリクス子実体の超臨界流体抽出物を加え、練合処理を行い、混合均一攪拌する。次に押し出し造粒機に移し、顆粒状に押し出された後、乾燥・整粒し、顆粒状食品組成物を得た。
[Example 2] Method for producing granular food composition using Agaricus fruit body Water is added to the dried fruit body of Agaricus blazei (10 liters of water per 1 kg of dried Agaricus fruit body), After extraction by refluxing at 95 to 100 ° C. for 5 hours, the extract was collected by filtration, and the solvent was removed to obtain a hot water extract of Agaricus fruiting body. Next, a supercritical fluid extract of Agaricus fruiting bodies is prepared with supercritical carbon dioxide using a supercritical extraction apparatus. The extraction residual sample of Agaricus fruiting body that has been subjected to the extraction process is further dried and pulverized. The extraction conditions were a temperature of 40 ° C., a pressure of 14 MPa to 15 MPa, and a time of 5 hours. Next, corn starch and lactose were added to the hot water extract of Agaricus fruit bodies as excipients to prepare an appropriate aqueous solution, and fine granules were obtained by spray drying. This is transferred to a stirring granulator, and the supercritical fluid extract of Agaricus fruit body prepared earlier is added, kneaded, and mixed and stirred uniformly. Next, the mixture was transferred to an extrusion granulator, extruded into granules, dried and sized, and a granular food composition was obtained.

[実施例3]赤霊芝を用いた顆粒状食品組成物の製造方法
赤霊芝の乾燥物の粉砕物に水を加え(赤霊芝1Kgあたり9リットルの水)、95〜100℃にて5時間還流して抽出した後、抽出液をろ過して回収し、溶媒を除去し赤霊芝の熱水抽出物を得た。この抽出残試料をさらに乾燥粉砕し、これに超臨界炭酸ガスを用いて超臨界流体抽出物を調製する。条件は、温度60℃、圧力25MPa、時間5時間供給する。炭酸ガスと抽出物を分離し、抽出物を約10g得た。次に、先に調製した赤霊芝の熱水抽出物に賦形剤として結晶セルロース及び乳糖を加え、適度な水溶液に調製し、スプレードライにより細粒を得た。これを攪拌造粒機に移し、先に調製した赤霊芝の超臨界流体抽出物を加え、練合処理を行い、混合均一攪拌する。次に押し出し造粒機に移し、顆粒状に押し出された後、乾燥・整粒し、顆粒状食品組成物を得た。
[Example 3] Production method of granular food composition using red ganoderma turf The dried red ganoderma pulverized product was added with water (9 liters of water per 1 kg of red ganoderma lucidum) at 95-100 ° C. After extraction by refluxing for 5 hours, the extract was collected by filtration, the solvent was removed, and a hot water extract of red ganoderma was obtained. The extraction residue sample is further dried and pulverized, and a supercritical fluid extract is prepared using supercritical carbon dioxide gas. The conditions are a temperature of 60 ° C., a pressure of 25 MPa, and a time of 5 hours. Carbon dioxide and the extract were separated to obtain about 10 g of the extract. Next, crystalline cellulose and lactose were added as excipients to the hot water extract of red ganoderma prepared previously to prepare an appropriate aqueous solution, and fine granules were obtained by spray drying. This is transferred to a stirring granulator, and the supercritical fluid extract of red ganoderma prepared previously is added, kneaded, and mixed and stirred uniformly. Next, the mixture was transferred to an extrusion granulator, extruded into granules, dried and sized, and a granular food composition was obtained.

以上のようにして得られた本発明による顆粒状食品組成物は、舌触りが滑らかでざらつき感がなく、口腔内での崩壊性にも優れ、その後もざらつき感が残らないことが確認された。また、透過性試験においても、高い移行率を示した。   It was confirmed that the granular food composition according to the present invention obtained as described above has a smooth texture and no rough feeling, is excellent in disintegration in the oral cavity, and does not remain rough thereafter. Also in the permeability test, a high migration rate was shown.

実施例1と比較例1のアデノシン移行率を比較する画像である。It is an image which compares the adenosine transfer rate of Example 1 and Comparative Example 1.

Claims (3)

担子菌類の子実体及び/又は菌糸体の熱水抽出物を含有する食品組成物において、該熱水抽出物を賦形剤と共に乾燥細粒化した後、前記担子菌類の子実体及び/又は菌糸体から超臨界流体又は亜臨界流体により抽出して得られる抽出物を用いて造粒することを特徴とする顆粒状食品組成物の製造方法。 In a food composition containing a basidiomycetous fruit body and / or a mycelium hot water extract, the hot water extract is dried and granulated together with an excipient, and then the basidiomycet fruit body and / or mycelium A method for producing a granular food composition, comprising granulating using an extract obtained by extraction from a body with a supercritical fluid or a subcritical fluid. 担子菌類が冬虫夏草、アガリクス、メシマコブ、チャーガ、ハナビラタケ、マツタケ、マイタケ、ヤマブシタケ及び霊芝からなる群から選択される1種又は2種以上である、請求項1記載の顆粒状食品組成物の製造方法。 The method for producing a granular food composition according to claim 1, wherein the basidiomycetes are one or more selected from the group consisting of Cordyceps sinensis, Agaricus, Meshimakobu, Chaga, Hanabiratake, Matsutake, Maitake, Yamabushitake and Reishi. . 請求項1または2記載の製造方法を用いた顆粒状食品組成物。 The granular food composition using the manufacturing method of Claim 1 or 2.
JP2007244432A 2007-09-20 2007-09-20 Granular food composition and method for producing the same Pending JP2009072124A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2007244432A JP2009072124A (en) 2007-09-20 2007-09-20 Granular food composition and method for producing the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2007244432A JP2009072124A (en) 2007-09-20 2007-09-20 Granular food composition and method for producing the same

Publications (1)

Publication Number Publication Date
JP2009072124A true JP2009072124A (en) 2009-04-09

Family

ID=40607782

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2007244432A Pending JP2009072124A (en) 2007-09-20 2007-09-20 Granular food composition and method for producing the same

Country Status (1)

Country Link
JP (1) JP2009072124A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2012077004A (en) * 2010-09-30 2012-04-19 Tokyo Institute Of Technology Insulin secretion promoter, agent for preventing/ameliorating diabetes, comprising the same as main component or containing the same and food for preventing/ameliorating diabetes
JP2013216642A (en) * 2012-04-12 2013-10-24 Ominedo Yakuhin Kogyo Kk Composition for lipase activity inhibition containing mushroom extract by supercritical carbon dioxide extraction
CN103637187A (en) * 2013-11-21 2014-03-19 威海五谷怡健食品有限公司 Human body immunity improvement antifatigue health food and preparation method thereof
CN105212127A (en) * 2014-06-16 2016-01-06 唐梦瑜 A kind of preparation method of queen bee tire particle
CN105264059A (en) * 2013-05-29 2016-01-20 福瑞托-雷北美有限公司 Supercritical fluid extruded food product
KR20170050310A (en) * 2015-10-30 2017-05-11 심영보 Method for extraction of Paecilomyces sp. and the extracts

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2012077004A (en) * 2010-09-30 2012-04-19 Tokyo Institute Of Technology Insulin secretion promoter, agent for preventing/ameliorating diabetes, comprising the same as main component or containing the same and food for preventing/ameliorating diabetes
JP2013216642A (en) * 2012-04-12 2013-10-24 Ominedo Yakuhin Kogyo Kk Composition for lipase activity inhibition containing mushroom extract by supercritical carbon dioxide extraction
CN105264059A (en) * 2013-05-29 2016-01-20 福瑞托-雷北美有限公司 Supercritical fluid extruded food product
CN103637187A (en) * 2013-11-21 2014-03-19 威海五谷怡健食品有限公司 Human body immunity improvement antifatigue health food and preparation method thereof
CN105212127A (en) * 2014-06-16 2016-01-06 唐梦瑜 A kind of preparation method of queen bee tire particle
KR20170050310A (en) * 2015-10-30 2017-05-11 심영보 Method for extraction of Paecilomyces sp. and the extracts
KR101963640B1 (en) 2015-10-30 2019-07-31 심영보 Method for extraction of Paecilomyces sp. and the extracts

Similar Documents

Publication Publication Date Title
EP1873196B1 (en) Porous cellulose aggregate and molding composition thereof
EP1712583B1 (en) Porous cellulose aggregate and formed product composition comprising the same
JP5718231B2 (en) Erythritol tableting
EP1634908B1 (en) Cellulose powder
JP2974719B2 (en) Direct compression cholestyramine tablets and solventless coatings thereof
JP5209492B2 (en) Pharmaceutical formulations for the production of fast-disintegrating tablets
US8951636B2 (en) Composite particles which contain both cellulose and inorganic compound
JP6086798B2 (en) Tablet manufacturing method
JP2009072124A (en) Granular food composition and method for producing the same
TWI617326B (en) Composite particles containing cellulose, inorganic compounds and hydroxypropyl cellulose
JP6133445B2 (en) Oral rapidly disintegrating composition for solid preparation
TWI729476B (en) Cellulose powder, its use and lozenges
JP6809675B2 (en) Method for Producing Immediate Oral Granules Containing Plant Extract
KR101827609B1 (en) Making Method of Red Ginseng Tablet
TWI724534B (en) Cellulose powder, lozenges and methods for manufacturing lozenges
Christensen et al. Moisture-activated dry granulation in a high shear mixer
JPWO2020071475A1 (en) A method for producing plant extract-containing granules, a method for suppressing the generation of fine powder from the plant extract-containing granules, and a method for suppressing the unpleasant taste of the plant extract-containing granules.
JP2010154769A (en) Polyphenol-containing granule or polyphenol-containing chewable tablet, and method for producing the tablet or the granule
JP3872369B2 (en) Processed honoki leaves and method for producing the same
TW201927340A (en) Cellulose powder
CN109316459A (en) A kind of preparation method of curcumin effervescent tablet
JP3515954B2 (en) Propolis processed food
JP6700083B2 (en) Orally fast disintegrating tablets
JP2005255616A (en) Solid pharmaceutical preparation composition comprising liquid or semi-solid active ingredient and porous cellulose aggregate particle
RU2191571C1 (en) Method of chloropyramine-base tablets preparing