JP2008109910A - Enzyme-compounded granule acting in intestine, and enzyme-compounded food using the enzyme-compounded granule - Google Patents

Enzyme-compounded granule acting in intestine, and enzyme-compounded food using the enzyme-compounded granule Download PDF

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JP2008109910A
JP2008109910A JP2006296290A JP2006296290A JP2008109910A JP 2008109910 A JP2008109910 A JP 2008109910A JP 2006296290 A JP2006296290 A JP 2006296290A JP 2006296290 A JP2006296290 A JP 2006296290A JP 2008109910 A JP2008109910 A JP 2008109910A
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enzyme
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intestine
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granule
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Toshihiro Nomura
俊博 野村
Hiroyuki Ijima
弘之 井島
Tomoaki Takeda
知晶 武田
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Abstract

<P>PROBLEM TO BE SOLVED: To make an enzyme and an enteric substance to arrive at an intestine without being exposed to a gastric juice. <P>SOLUTION: An oil liquid 2 containing CoQ<SB>10</SB>of enteric substance is encapsulated with a gelatin coating film 3 to form a seamless nucleus 1, and an enzyme-containing coating film 4 is disposed on the surface of the seamless nucleus 1 to form an enzyme-compounded granule 5. The enzyme-compounded granules 5 are charged and sealed in a hard capsule 6, and the whole surface of the capsule is coated with zein 7 to form an enzyme-compounded food 8. When the enzyme-compounded food 8 is drunk, the enzyme-compounded food 8 arrives at the intestine through a stomach without being dissolved in a gastric juice due to the existence of the coating layer of the zein 7. The coating layer of the zein 7, and the hard capsule 6 are sequentially collapsed in the intestine, and the enzyme compounded in the enzyme-containing coating films 4 of the enzyme-compounded granules 5 are released in the intestine. The gelatin coating films 3 of the seamless nuclei 1 exposed by the collapse of the coating films 4 are collapsed to release the oil liquid 2 containing the CoQ<SB>10</SB>in the intestine. <P>COPYRIGHT: (C)2008,JPO&INPIT

Description

本発明は、動物由来、植物由来、微生物由来等の酵素を腸内で機能させるようにすると同時に、所要の脂溶性有効成分を腸内に放出できる酵素配合顆粒、及び、該酵素配合顆粒を用いた酵素配合食品に関するものである。   The present invention uses an enzyme-containing granule capable of releasing a necessary fat-soluble active ingredient into the intestine while allowing enzymes derived from animals, plants, microorganisms, etc. to function in the intestine, and the enzyme-containing granule. It is related to the enzyme-mixed food.

人の肉体的、精神的活動を支えているエネルギーは、いくつかの酵素の複合体(複合酵素)により食べ物を消化し、体内で代謝することで生み出されている。したがって、各種の消化酵素や代謝酵素が非常に重要な働きを担っているが、これらの酵素のうち、消化酵素の働きによって、食べたものが良く消化されなければ、それらに含まれている栄養素を体内へ吸収することができず、したがって、体内での代謝にも利用することができなくなる。   The energy that supports human physical and mental activities is generated by digesting food with a complex of several enzymes (complex enzyme) and metabolizing it in the body. Therefore, various digestive enzymes and metabolic enzymes play a very important role, but among these enzymes, if the food you eat is not digested well due to the action of the digestive enzymes, the nutrients contained in them Cannot be absorbed into the body and therefore cannot be utilized for metabolism in the body.

ところで、個人差はあるが、一般に、老化や加齢に伴い、体内の酵素全体の量が次第に減少していくときには、体内での代謝に関わる代謝酵素に重点が置かれるため、消化酵素にまで対応することができなくなって、消化や吸収は衰える傾向にあり、そのために、蛋白質、脂肪、糖質がうまく分解できなくなることがある。たとえば、年々、歳とともに、嗜好する食材が、肉を中心としたものから魚や野菜を中心としたものに変わるのは、肉を消化するために使用される酵素の量が、加齢により減少することに伴うためと考えられる。そこで、各種の酵素を外部より食品として取ることで、体内の酵素を補うことが考えられる。   By the way, although there are individual differences, in general, when the amount of the whole enzyme in the body gradually decreases with aging and aging, the emphasis is placed on metabolic enzymes involved in metabolism in the body, so even digestive enzymes Digestion and absorption tend to decline due to the inability to respond, which may make it difficult to break down proteins, fats and sugars. For example, with the age of years, the preferred ingredients change from meat-centric to fish and vegetable-centric because the amount of enzymes used to digest meat decreases with age. This is thought to be due to this. Therefore, it is conceivable to supplement the enzymes in the body by taking various enzymes as food from the outside.

ところで、従来提案されている酵素食品としては、たとえば、麦胚芽、大豆胚芽、米胚芽、玄米胚芽を蒸して、麹菌、酵母、イースト菌等で発酵させるようにしたものを、粉末、顆粒、錠剤の形で経口摂取できるようにしたものがある(たとえば、特許文献1参照)。   By the way, as a conventionally proposed enzyme food, for example, wheat germ, soybean germ, rice germ, brown rice germ steamed and fermented with koji mold, yeast, yeast, etc., powder, granule, tablet There is one that can be taken orally in a form (for example, see Patent Document 1).

なお、栄養補助食品等の機能性を有する食品の形状(剤形)としては、錠剤、ハードカプセル、ソフトカプセル、顆粒が広く一般的に用いられている。   Note that tablets, hard capsules, soft capsules, and granules are widely used as shapes (dosage forms) of foods having functionality such as nutritional supplements.

又、食品を顆粒状に成形する場合において、粒度の揃った顆粒を製造するために、真球度が高く且つシャープな粒度分布を備えた砂糖の球形粒子を核として、その表面に所望する成分をコーティングする手法が従来知られている(たとえば、特許文献2参照)。   In addition, when a food product is formed into granules, in order to produce granules of uniform particle size, the desired components on the surface are formed with sugar spherical particles having a high sphericity and a sharp particle size distribution as the core. Conventionally, a technique for coating the film is known (see, for example, Patent Document 2).

更に、同軸二重ノズルを用いた滴下法により、所要の油液をゼラチン等のカプセル被膜の中に内包させて形成してなるシームレスカプセルは従来知られている(たとえば、特許文献3参照)。   Furthermore, a seamless capsule formed by encapsulating a required oil liquid in a capsule film such as gelatin by a dropping method using a coaxial double nozzle is conventionally known (see, for example, Patent Document 3).

又、経口摂取物を胃液に接触させないで腸内に到達させるための手法として、経口摂取物を内包させたハードカプセルを、とうもろこしから抽出、精製された難胃溶性で且つ腸溶性を備えたツェイン(ツェン、ゼイン)で腸溶性コーティングした腸溶性コーティング食品も従来提案されている(たとえば、特許文献4参照)。   In addition, as a method for reaching the intestine without bringing oral ingestion into contact with gastric juice, hard capsules containing oral ingestion are extracted from corn, purified zein that is difficult to dissolve in gastrointestinal and has enteric properties ( Enteric-coated foods that are enteric-coated with zen or zein have also been proposed (see, for example, Patent Document 4).

特開2001−120203号公報JP 2001-120203 A 特開平5−229961号公報Japanese Patent Laid-Open No. 5-229961 特開平7−196478号公報JP-A-7-196478 特開2001−309756号公報JP 2001-309756 A

ところが、特許文献1に記載された酵素食品は、麦胚芽、大豆胚芽、米胚芽、玄米胚芽に含まれる蛋白質、脂肪、糖分において体内でうまく分解できないものを、予め、麹菌、酵母、イースト菌等で発酵させることにより、消化、吸収され易い状態としてから粉末、顆粒、錠剤として経口摂取できるようにしたものに過ぎず、加齢と共に体内、特に腸内で不足しがちになる消化酵素を外部から補うことができるものとはなっていない。   However, the enzyme foods described in Patent Document 1 are proteins, fats, and sugars contained in wheat germ, soybean germ, rice germ, brown rice germ, which cannot be degraded well in the body, in advance with koji mold, yeast, yeast, etc. Fermentation makes it easy to digest and absorb, and then it can only be taken orally as powders, granules, or tablets, and supplements from the outside digestive enzymes that tend to be deficient in the body, especially in the intestines with age. It is not something that can be done.

したがって、腸内で不足する消化酵素を外部から補うことができるようにした酵素配合食品は、従来は特に提案されていないというのが実状である。   Therefore, the actual condition is that no enzyme-enriched food that can supplement the digestive enzyme deficient in the intestine from the outside has been proposed.

ところで栄養補助食品等の機能性を有する食品に広く用いられている各種剤形のうち、錠剤は、飲み込み易く、所望する成分をコンパクトにまとめることが可能であり、更に、糖衣錠としたり、フィルムコートすることにより、異味、異臭成分をマスキングすることも可能であるが、上記所望する成分を均一に混合するための賦形剤、及び、押し固めるための結合剤が必要とされることから、添加物が多量となって、主成分の配合率が低くなってしまうという問題がある。又、通常、錠剤に配合できるのは、水溶性物質のような粉末化、固形化が容易な成分に限られており、脂溶性物質は、一旦粉末化できるものであれば、配合することが可能であるが、液状のままでは配合することが困難である。   By the way, among various dosage forms widely used for functional foods such as nutritional supplements, tablets are easy to swallow and the desired ingredients can be gathered compactly. Although it is possible to mask off-flavor and off-flavor components, an excipient for uniformly mixing the desired components and a binder for compaction are required. There is a problem that the amount of the product becomes large and the mixing ratio of the main component becomes low. In addition, normally, tablets can only be blended with ingredients that are easily powdered and solidified, such as water-soluble substances, and fat-soluble substances can be blended if they can be powdered once. Although it is possible, it is difficult to mix in a liquid state.

ソフトカプセルは、脂溶性物質を油に溶かした状態で内包させることができるものであるため、カプセル内容物の空気酸化に対する安定度が高く、又、製造工程においては、40℃以上の加温、加熱工程や加圧工程がなく、内容成分が空気と接触する時間が少ないため、品質劣化要因や人的加工要因が少ないという利点があると共に、大きさや、内容成分の含有量のばらつきが少なく、内溶液の均一性を高めたり、異味、異臭成分をマスキングすることができ、更には、内容物は油脂であり、被膜の水分活性が低いため、微生物汚染され難く、しかも、嚥下し易いという利点はある。しかし、最小でも一粒当り200mg程度の大きさとしてあり、そのうちカプセル被膜は重量比で約30%となっているため、残部の約70%が内包させる油性の成分(油液)となっており、脂溶性有効成分のほかに、必要量以上の食用油が配合されている。すなわち、たとえば、コエンザイムQ10(CoQ10)を1カプセル当り30mg程度として配合したい場合であっても、そのほかに110mg程度の食用油を配合する必要が生じることから、過剰な油を摂取しなければならないという問題が懸念される。又、水溶性物質を配合するには、界面活性剤を使用して油脂に溶かす必要があるため、加工し難く、又、その配合量も制限されてしまう。更に、この配合量が少なく制限されてしまう水溶性物質である有効成分の摂取量を、一日摂取所望量に到達させるには、5〜6錠のソフトカプセルを飲むことが必要とされることがあり、このような場合は、油の摂取量が更に多くなってしまう。しかも、従来、ソフトカプセルのカプセル被膜は、通常、ゼラチン被膜としてあるため、長期保管していると、ソフトカプセル同士が癒着し易くなる虞も懸念される。 Since soft capsules can be encapsulated in a state in which a fat-soluble substance is dissolved in oil, the capsule contents have high stability against air oxidation, and in the manufacturing process, heating and heating at 40 ° C. or higher. Since there is no process or pressurization process and the content components are not in contact with air, there is an advantage that there are few quality degradation factors and human processing factors, and there is little variation in size and content of content components. It is possible to enhance the uniformity of the solution, mask off taste and odor components, and further, the contents are oils and fats, and the water activity of the film is low, so that it is difficult to be contaminated by microorganisms and easy to swallow. is there. However, the size is about 200 mg per grain at least, and the capsule coating is about 30% by weight, so the remaining 70% is an oily component (oil solution) to be included. In addition to the fat-soluble active ingredient, more than the required amount of edible oil is blended. That is, for example, even when coenzyme Q 10 (CoQ 10 ) is desired to be added at about 30 mg per capsule, it is necessary to add about 110 mg of edible oil in addition to that, so excessive oil must be consumed. We are concerned about the problem of not becoming. Moreover, in order to mix | blend a water-soluble substance, since it is necessary to melt | dissolve in fats and oils using surfactant, it is difficult to process and the compounding quantity will also be restrict | limited. Furthermore, it is necessary to drink 5 to 6 soft capsules in order to bring the intake amount of the active ingredient, which is a water-soluble substance whose amount is limited to a small amount, to the desired daily intake amount. Yes, in such a case, the amount of oil intake is further increased. Moreover, conventionally, since capsule capsules of soft capsules are usually gelatin films, there is a concern that soft capsules may easily adhere to each other when stored for a long time.

ハードカプセルは、内包物をマスキングでき、そのため、色素や染色性のある素材でも口内や歯、あるいは、容器を汚さないようにすることができ、又、製造工程においては、加温、加熱、加湿、乾燥、加圧工程がないため、錠剤に比して品質劣化の原因が極めて少ないという利点があると共に、添加物を少なくすることができて、主成分の配合率を高いものとすることが可能になるものであるが、配合できるのは、上記錠剤と同様に、水溶性物質のような粉末化や顆粒化等の固形化が容易な成分に限られており、脂溶性物質は、一旦粉末化する等、固形化する必要があり、液状のままでは配合が困難である。しかも、ハードカプセル自体は胃で溶けるため、内包物は胃で放出されてしまうこととなる。   Hard capsules can mask inclusions, so that even pigments and dyeable materials can keep the mouth, teeth, or containers clean, and in the manufacturing process, heating, heating, humidification, Since there is no drying or pressing process, there is an advantage that the cause of quality deterioration is extremely small compared to tablets, and it is possible to reduce the amount of additives and increase the main component content. However, as in the case of the above-mentioned tablets, it is limited to ingredients that can be easily solidified such as powdered or granulated, such as water-soluble substances. It is necessary to solidify such as to form, and it is difficult to mix in a liquid state. Moreover, since the hard capsule itself dissolves in the stomach, the inclusion is released in the stomach.

そこで、上記特許文献4に示されているように、ハードカプセルの内包物を胃液に接触させないで腸内に到達させることができるようにするために、ハードカプセルを、難胃溶性で且つ腸溶性を備えたツェインで腸溶性コーティングすることが従来考えられているが、この場合であっても、脂溶性物質の配合が困難であるという点を改善することができるものではない。   Therefore, as shown in Patent Document 4 above, in order to allow the inclusion of the hard capsule to reach the intestine without being in contact with the gastric juice, the hard capsule is hardly gastrolytic and enteric. However, even in this case, it is not possible to improve the point that it is difficult to blend a fat-soluble substance.

上記特許文献2に示された真球度が高く粒度分布の揃った砂糖の球形粒子を核として、その表面に所望成分をコーティングして製造する顆粒状の食品は、粉末より飲み易く、早い吸収を促すことができるほか、賦形剤や結合剤等の添加物の量を少なくすることができると共に、真球度の高い顆粒とすることができるため、外観を向上させることができるとされているが、顆粒の製造のためには砂糖製の核が必要とされるため、糖の摂取量が多くなる虞が懸念される。又、上記顆粒に脂溶性物質を配合することは困難である。   Granular foods produced by coating the desired ingredients on the surface of sugar spherical particles with a high sphericity and a uniform particle size distribution as shown in Patent Document 2 are easier to drink than powder and absorb quickly. In addition to being able to reduce the amount of additives such as excipients and binders, and to be able to make granules with high sphericity, it is said that the appearance can be improved However, since a sugar core is required for the production of granules, there is a concern that sugar intake may increase. Moreover, it is difficult to mix a fat-soluble substance with the granule.

因みに、特許文献3に示されたシームレスカプセルは水溶性のため、その内包物は油液に限られ、よって、上述したソフトカプセルと同様に、脂溶性物質は配合できるが、水溶性物質の配合は困難である。又、ゼラチン製のシームレスカプセルは、そのまま摂取すると、胃に達する時点で速やかに溶解されるため、内包物は胃で放出されてしまい、胃液に触れさせずに腸まで到達させることは困難である。   Incidentally, since the seamless capsule shown in Patent Document 3 is water-soluble, its inclusion is limited to an oily liquid. Therefore, as with the soft capsule described above, a fat-soluble substance can be blended, but a water-soluble substance is blended. Have difficulty. In addition, gelatin-free seamless capsules dissolve quickly when they reach the stomach, so that the inclusions are released in the stomach, making it difficult to reach the intestine without touching the gastric juice. .

又、上記各特許文献2、3、4には、腸内で不足する消化酵素を外部から補う考えはない。   In addition, the above Patent Documents 2, 3, and 4 have no idea of supplementing the digestive enzyme deficient in the intestine from outside.

そこで、本発明は、腸内で不足する消化酵素等の酵素を外部から腸内に到達させて補うことができるようにするために、動物由来、植物由来、微生物由来等の所要の酵素を腸内で放出させて機能させることができるようにすると同時に、所要の脂溶性有効成分をも一緒に腸内に放出させることができるようにする酵素配合顆粒、及び、該酵素配合顆粒を用いた酵素配合食品を提供しようとするものである。   In view of this, the present invention provides an enzyme such as an animal-derived, plant-derived, or microorganism-derived enzyme in the intestine so that an enzyme such as a digestive enzyme deficient in the intestine can reach the intestine from the outside to be supplemented. The enzyme-containing granule that allows the desired fat-soluble active ingredient to be released into the intestine at the same time, as well as the enzyme using the enzyme-containing granule It is intended to provide a combination food.

本発明は、上記課題を解決するために、請求項1に対応して、脂溶性有効成分を食用油に溶解してなる脂溶性有効成分含有油液を、ゼラチン被膜に内包させてシームレス核を形成し、該シームレス核の表面を、所要の酵素を含む酵素含有コーティング被膜で覆ってなる構成を有する腸で機能させる酵素配合顆粒とする。   In order to solve the above-mentioned problem, the present invention, corresponding to claim 1, comprises a fat-soluble active ingredient-containing oil solution obtained by dissolving a fat-soluble active ingredient in edible oil, and encapsulating it in a gelatin coating to form a seamless core. Formed into an enzyme-containing granule that functions in the intestine having a structure in which the surface of the seamless core is covered with an enzyme-containing coating film containing a required enzyme.

又、請求項2に対応して、脂溶性有効成分を食用油に溶解してなる脂溶性有効成分含有油液を、ゼラチン被膜に内包させてシームレス核を形成し、該シームレス核の表面を、所要の酵素を含む酵素含有コーティング被膜で覆って酵素配合顆粒を形成し、該酵素配合顆粒を、ハードカプセルに封入して、該ハードカプセルの表面を、胃難溶性で且つ腸溶性物質で全面に亘りコーティングしてなる構成を有する酵素配合食品とする。   According to claim 2, a fat-soluble active ingredient-containing oil solution obtained by dissolving a fat-soluble active ingredient in edible oil is encapsulated in a gelatin coating to form a seamless core, and the surface of the seamless core is An enzyme-containing granule is formed by covering with an enzyme-containing coating film containing the required enzyme, and the enzyme-containing granule is encapsulated in a hard capsule, and the surface of the hard capsule is coated over the entire surface with a gastric insoluble and enteric substance. It is set as the enzyme mixing | blending foodstuff which has the structure formed.

更に、上記酵素配合食品の構成における酵素配合顆粒のシームレス核を、脂溶性有効成分含有油液と、ゼラチン被膜形成用のゼラチン溶液を原料としてシームレスなカプセル状とし、且つ、上記シームレス核の表面に、所要の酵素と賦形剤を含んだ粉末原料を、所要のコーティング液を介し所要厚みで積層させて酵素含有コーティング被膜を形成して酵素配合顆粒とした構成とする。   Furthermore, the seamless core of the enzyme-blended granules in the above-mentioned enzyme-blended food composition is made into a seamless capsule using a fat-soluble active ingredient-containing oil solution and a gelatin solution for forming a gelatin coating as a raw material, and on the surface of the seamless nucleus The powder raw material containing the required enzyme and excipient is laminated with the required thickness via the required coating solution to form an enzyme-containing coating film to form an enzyme-containing granule.

更に又、上記酵素配合食品の各構成における酵素含有コーティング被膜に、微生物由来、植物由来、動物由来の酵素と、上記微生物由来、植物由来、動物由来の酵素ごとに異なる色の色素とを個別に配合してなる3種の酵素配合顆粒を形成して、該3種の酵素配合顆粒を、1種ごと又は複数種を混合してハードカプセルに封入するようにした構成とする。   Furthermore, the enzyme-containing coating film in each component of the enzyme-containing food is individually provided with microorganism-derived, plant-derived, and animal-derived enzymes, and pigments of different colors for the microorganism-derived, plant-derived, and animal-derived enzymes. Three types of enzyme-mixed granules formed by mixing are formed, and the three types of enzyme-containing granules are mixed one by one or a plurality of types and sealed in a hard capsule.

本発明によれば、以下の如き優れた効果を発揮する。
(1)脂溶性有効成分を食用油に溶解してなる脂溶性有効成分含有油液を、ゼラチン被膜に内包させてシームレス核を形成し、該シームレス核の表面を、所要の酵素を含む酵素含有コーティング被膜で覆ってなる構成を有する腸で機能させる酵素配合顆粒としてあるので、該酵素配合顆粒が腸内へ到達させて、酵素含有コーティング被膜を腸内で崩壊させると、該酵素含有コーティング被膜に含まれている酵素を腸内へ放出できて、該酵素の機能を腸内で発揮させることができるようになる。同時に、上記酵素含有コーティング被膜の崩壊に伴って露出されるシームレス核のゼラチン被膜が腸内で溶解することで、該ゼラチン被膜に内包されていた脂溶性有効成分含有油液に含まれる脂溶性有効成分をも、上記酵素と一緒に腸内へ放出することができるようになる。
(2)したがって、本来水溶性である酵素を乾燥状態で配合でき、しかも、一緒に脂溶性有効成分をも容易に配合可能な顆粒とすることができる。
(3)脂溶性有効成分を食用油に溶解してなる脂溶性有効成分含有油液を、ゼラチン被膜に内包させてシームレス核を形成し、該シームレス核の表面を、所要の酵素を含む酵素含有コーティング被膜で覆って酵素配合顆粒を形成し、該酵素配合顆粒を、ハードカプセルに封入して、該ハードカプセルの表面を、胃難溶性で且つ腸溶性物質で全面に亘りコーティングしてなる構成を有する酵素配合食品としてあるので、上記胃難溶性で且つ腸溶性物質の存在により、ハードカプセルの胃での崩壊を防止できて、該ハードカプセル内に封入されている酵素配合顆粒を、胃液との接触を防止した状態で確実に腸内へ到達させることができる。その後、上記酵素配合食品が腸内に達すると、上記胃難溶性で且つ腸溶性物質のコーティングが速やかに溶解されてハードカプセルが露出されることで、該ハードカプセルを崩壊させることができるため、該ハードカプセル内に封入されている酵素配合顆粒を腸内に放出させて、該酵素配合顆粒の酵素含有コーティング被膜を崩壊させることができる。これにより、上記酵素含有コーティング被膜に含まれていた酵素を、胃液との接触で失活する虞を未然に防止した状態で腸内に到達させて、腸内で該酵素の機能を腸内で発揮させるようにすることが可能となると共に、上記酵素含有コーティング被膜の崩壊に伴って露出されるシームレス核のゼラチン被膜が崩壊することにより、該ゼラチン被膜に内包されている脂溶性有効成分含有油液に含まれている脂溶性有効成分をも、胃液との接触を未然に防いだ状態で腸内に放出させることができるようになる。
(4)したがって、上記酵素配合食品は、所要の酵素と脂溶性有効成分を共に腸内に到達させる機能を有する食品とすることができる。
(5)酵素配合顆粒のシームレス核を、脂溶性有効成分含有油液と、ゼラチン被膜形成用のゼラチン溶液を原料としてシームレスなカプセル状とし、且つ、上記シームレス核の表面に、所要の酵素と賦形剤を含んだ粉末原料を、所要のコーティング液を介し所要厚みで積層させて酵素含有コーティング被膜を形成して酵素配合顆粒とした構成とすることにより、上記シームレス核を真球状で且つ粒径の揃った粒とすることができると共に、該シームレス核を中心核として形成する酵素配合顆粒を、真球状で且つ粒径の揃ったものとすることができる。これにより、該酵素配合顆粒を、その後、ハードカプセルに封入するための充填作業を行う際の充填量のコントロールが容易なものとすることができる。
(6)酵素含有コーティング被膜に、微生物由来、植物由来、動物由来の酵素と、上記微生物由来、植物由来、動物由来の酵素ごとに異なる色の色素とを個別に配合してなる3種の酵素配合顆粒を形成して、該3種の酵素配合顆粒を、1種ごと又は複数種を混合してハードカプセルに封入するようにした構成とすることにより、胃難溶性で且つ腸溶性物質で全面に亘りコーティングされているハードカプセルを通して観察される酵素配合顆粒の色から、本発明の酵素配合食品の1つのカプセルに配合されてる酵素が、微生物由来、植物由来、動物由来のいずれの酵素であるか、あるいは、微生物由来、植物由来、動物由来の酵素のうちの2種又は3種を含んでいるかを、容易に判断することが可能になるという外観上の訴求効果が期待できる。
According to the present invention, the following excellent effects are exhibited.
(1) A fat-soluble active ingredient-containing oil solution obtained by dissolving a fat-soluble active ingredient in edible oil is encapsulated in a gelatin coating to form a seamless nucleus, and the surface of the seamless nucleus contains an enzyme containing a required enzyme. Since it is an enzyme-containing granule that functions in the intestine and is covered with a coating film, when the enzyme-containing granule reaches the intestine and disintegrates the enzyme-containing coating film in the intestine, the enzyme-containing coating film The contained enzyme can be released into the intestine, and the function of the enzyme can be exerted in the intestine. At the same time, the gelatin coating of the seamless core that is exposed as the enzyme-containing coating film collapses dissolves in the intestine, so that the fat-soluble effective contained in the oil solution containing the fat-soluble active ingredient contained in the gelatin film. The components can also be released into the intestine together with the enzyme.
(2) Therefore, an enzyme that is inherently water-soluble can be blended in a dry state, and a fat-soluble active ingredient can be easily blended together into a granule.
(3) A fat-soluble active ingredient-containing oil solution obtained by dissolving a fat-soluble active ingredient in edible oil is encapsulated in a gelatin coating to form a seamless nucleus, and the surface of the seamless nucleus contains an enzyme containing a required enzyme. Enzyme-containing granule is formed by covering with a coating film, the enzyme-containing granule is enclosed in a hard capsule, and the surface of the hard capsule is coated with a gastric insoluble and enteric substance over the entire surface. Because it is a blended food, the presence of the above-mentioned poorly soluble and enteric substance in the stomach can prevent the hard capsule from collapsing in the stomach, and the enzyme-containing granule enclosed in the hard capsule can be prevented from coming into contact with the gastric juice. It is possible to reliably reach the intestines in a state. Thereafter, when the enzyme-containing food reaches the intestine, the hard capsule can be disintegrated by rapidly dissolving the gastric insoluble and enteric substance coating and exposing the hard capsule. The enzyme-containing granule encapsulated therein can be released into the intestine, and the enzyme-containing coating film of the enzyme-containing granule can be disrupted. As a result, the enzyme contained in the enzyme-containing coating film is allowed to reach the intestine in a state where the possibility of being deactivated by contact with gastric juice is prevented, and the function of the enzyme in the intestine An oil containing a fat-soluble active ingredient contained in the gelatin coating as a result of the collapse of the gelatin coating of the seamless core that is exposed as the enzyme-containing coating coating is collapsed. The fat-soluble active ingredient contained in the liquid can also be released into the intestine while preventing contact with the gastric juice.
(4) Therefore, the enzyme-containing food can be a food having a function of allowing both a required enzyme and a fat-soluble active ingredient to reach the intestine.
(5) The seamless core of the enzyme-blended granule is made into a seamless capsule using an oil solution containing a fat-soluble active ingredient and a gelatin solution for forming a gelatin coating, and the surface of the seamless core is coated with the required enzyme. The above-mentioned seamless core is made into a spherical shape and particle size by laminating the powder raw material containing the formant with the required thickness through the required coating liquid to form an enzyme-containing coating film to form an enzyme-containing granule. In addition, the enzyme-containing granule formed with the seamless core as a central core can be made into a spherical shape and a uniform particle size. Thereby, it is possible to easily control the filling amount when performing the filling operation for encapsulating the enzyme-containing granule in a hard capsule.
(6) Three types of enzymes obtained by individually blending an enzyme-containing coating film with microorganism-derived, plant-derived, and animal-derived enzymes, and pigments having different colors for the microorganism-derived, plant-derived, and animal-derived enzymes. By forming a blended granule and configuring the three kinds of enzyme blended granule to be sealed in a hard capsule by mixing one kind or plural kinds, it is difficult to dissolve in the stomach and enteric substances on the entire surface. From the color of the enzyme-containing granule observed through the hard capsule coated, whether the enzyme contained in one capsule of the enzyme-containing food of the present invention is a microorganism-derived, plant-derived or animal-derived enzyme, Or the appearance appeal effect that it becomes possible to judge easily whether it contains 2 or 3 types of enzymes derived from microorganisms, plants and animals is expected.

以下、本発明を実施するための最良の形態を図面を参照して説明する。   The best mode for carrying out the present invention will be described below with reference to the drawings.

図1(イ)(ロ)は本発明の酵素配合食品の実施の一形態を示すもので、以下のような構成としてある。   1 (a) and 1 (b) show an embodiment of the enzyme-containing food of the present invention, which has the following configuration.

すなわち、脂溶性有効成分として、たとえば、CoQ10を所要の食用油に所要濃度で溶解させて調整した脂溶性有効成分含有油液としてのCoQ10含有油液2を、膜厚が0.2〜0.4mmのゼラチン被膜3に内包させてなる直径0.7〜1.2mmのシームレスカプセル状のシームレス核1を形成し、該シームレス核1の表面を、酵素を含む酵素含有コーティング被膜4で覆って酵素配合顆粒5を製造する。更に、上記酵素配合顆粒5を、所要量ずつゼラチン製のハードカプセル6に封入すると共に、該ハードカプセル6の表面を、胃難溶性で且つ腸溶性物質としてのツェイン7で全面に亘りコーティングして本発明の酵素配合食品8とする。 That is, as a fat-soluble active ingredient, for example, CoQ 10- containing oil liquid 2 as a fat-soluble active ingredient-containing oil liquid prepared by dissolving CoQ 10 in a required concentration in a required edible oil has a film thickness of 0.2 to A seamless capsule-shaped seamless nucleus 1 having a diameter of 0.7 to 1.2 mm is formed by being encapsulated in a 0.4 mm gelatin coating 3, and the surface of the seamless nucleus 1 is covered with an enzyme-containing coating coating 4 containing an enzyme. Thus, the enzyme-containing granule 5 is produced. Further, the enzyme-containing granule 5 is encapsulated in a hard capsule 6 made of gelatin in a required amount, and the surface of the hard capsule 6 is coated over the entire surface with zein 7 as an enteric substance that is hardly soluble in the stomach. The enzyme-containing food 8

以下、上記酵素配合食品8の構成を、製造手順に沿って詳述する。   Hereinafter, the structure of the said enzyme compound food 8 is explained in full detail along a manufacture procedure.

上記酵素配合食品8を製造する場合は、先ず、脂溶性有効成分として、加齢に伴って減少し、且つ不足分を補うことで細胞の活性が活発になる効果が知られているCoQ10を、食用油として、たとえば、中鎖脂肪酸トリグリセリド(MCT)に混合して溶解させてCoQ10含有油液2を製造する。この際、該CoQ10含有油液2中における上記CoQ10の濃度は、たとえば、最終的に製造される酵素配合食品8の1カプセル当りに封入されるすべての酵素配合顆粒5に内包されているCoQ10含有液2の合計量中に含まれるCoQ10の量が、約30mgとなるように調整するようにしておく。 In the case of producing the enzyme-mixed food 8, first, CoQ 10 , which is known as a fat-soluble active ingredient, decreases with aging and is known to have an effect of activating cell activity by supplementing the deficiency. As an edible oil, for example, a CoQ 10- containing oil liquid 2 is produced by mixing and dissolving in medium chain fatty acid triglyceride (MCT). At this time, the concentration of the CoQ 10 in the CoQ 10- containing oil liquid 2 is included in, for example, all the enzyme-containing granules 5 sealed per capsule of the enzyme-containing food 8 to be finally produced. the amount of CoQ 10 contained in the total amount of CoQ 10 containing liquid 2 in advance so as to adjust to approximately 30 mg.

次に、上記CoQ10含有油液2と、ゼラチン被膜3形成用のゼラチン溶液とを用いて、製剤技術の1つとして広く知られている同軸二重ノズルを用いた滴下法により上記シームレス核1を形成する。具体的には、同心円状の二重ノズルの内側(中心側)の流路から、上記CoQ10含有油液2を、又、上記二重ノズルの外側(外周側)の流路から上記ゼラチン溶液を、それぞれ同時に吐出させることにより、表面張力(界面張力)を利用して上記CoQ10含有油液2を、上記ゼラチン溶液に内包させた後、このゼラチン溶液を固化させて上記所定膜厚のゼラチン被膜3を形成させる。これにより、中心部のCoQ10含有油液2を均一なゼラチン被膜3で被覆してなる構成を備えた上記所定直径の真球状のシームレス核1を製造する。 Next, using the CoQ 10- containing oil solution 2 and the gelatin solution for forming the gelatin coating 3, the seamless core 1 is formed by a dropping method using a coaxial double nozzle, which is widely known as one of pharmaceutical technologies. Form. Specifically, the CoQ 10- containing oil solution 2 is supplied from the inner (center side) flow path of the concentric double nozzle, and the gelatin solution is supplied from the outer (outer peripheral side) flow path of the double nozzle. Are simultaneously discharged, the CoQ 10- containing oil solution 2 is encapsulated in the gelatin solution by utilizing surface tension (interfacial tension), and then the gelatin solution is solidified to obtain the gelatin having the predetermined film thickness. A coating 3 is formed. As a result, the spherical seamless core 1 having the above-mentioned predetermined diameter having a configuration in which the CoQ 10- containing oil solution 2 in the center is coated with the uniform gelatin coating 3 is manufactured.

次いで、上記シームレス核1を、たとえば、図示しないローターで回転させることによる遠心力と、スリットエアーを用いて遊星運動させるよう撹拌させ、所要のコーティング液(結合液)を定量的にスプレーしながら、所要の酵素と、賦形剤と、その他配合を所望する所要の添加剤とを含んだ粉末原料を、定量的に散布することにより、上記粉末原料を、上記シームレス核1の表面に所要の厚みで積層させて酵素含有コーティング被膜4を形成させる。これにより、図1(ロ)に示す如き上記真球状のシームレス核1の表面を均一な酵素含有コーティング被膜4で被覆してなる真球状で且つ粒度の揃った酵素配合顆粒5を製造する。   Next, the seamless core 1 is agitated so as to make a planetary motion using, for example, a centrifugal force by rotating with a rotor (not shown) and slit air, while quantitatively spraying a required coating liquid (binding liquid), A powder raw material containing a required enzyme, an excipient, and other required additives to be blended is quantitatively dispersed, whereby the powder raw material is applied to the surface of the seamless core 1 with a required thickness. To form an enzyme-containing coating film 4. As a result, enzyme-containing granules 5 having a spherical shape and a uniform particle size are produced by coating the surface of the spherical seamless core 1 with a uniform enzyme-containing coating film 4 as shown in FIG.

上記酵素含有コーティング被膜4を形成する際に配合する酵素としては、微生物由来、植物由来、動物由来の各種酵素を適宜選定して用いるようにすればよい。具体的には、微生物由来の酵素としては、たとえば、腸内でセルロースを分解させて腹部の膨満感やガスを減らす効果が期待できる菌由来のセルラーゼを用いたり、乳酸菌由来の各種酵素を含んでいて栄養素を体内に効率よく取り入れるために腸内環境を整える効果が期待できる乳酸菌代謝物等を用いることができる。又、植物由来の酵素としては、たとえば、蛋白質分解酵素であって消化を助ける効果が期待できるパパインや、蛋白質分解酵素であるアクチニジンを含み、更に、天然のビタミンCやビタミンEを含むキウイ果汁末等を用いることができる。又、動物由来の酵素としては、たとえば、菌の溶解作用が期待できる卵白リゾチームや、酵素に加えてアミノ酸や蛋白質を含むプラセンタエキス末等を用いることができる。   As the enzyme to be blended when forming the enzyme-containing coating film 4, various enzymes derived from microorganisms, plants, and animals may be appropriately selected and used. Specifically, examples of microorganism-derived enzymes include cellulases derived from bacteria that can be expected to have the effect of reducing cellulose in the intestine to reduce abdominal bloating and reducing gas, and include various enzymes derived from lactic acid bacteria. In order to efficiently incorporate nutrients into the body, lactic acid bacteria metabolites and the like that can be expected to improve the intestinal environment can be used. Examples of plant-derived enzymes include papain, which is a proteolytic enzyme and can be expected to aid digestion, and actinidin, a proteolytic enzyme, and kiwi juice powder containing natural vitamin C and vitamin E. Etc. can be used. Moreover, as an enzyme derived from an animal, for example, egg white lysozyme which can be expected to have a lytic action of bacteria, placenta extract powder containing amino acids and proteins in addition to enzymes can be used.

又、上記酵素含有コーティング被膜4を形成させる際に配合する添加剤としては、たとえば、消費者に対する外観上の訴求効果を高めることを目的として、後工程でハードカプセル6に封入される酵素配合顆粒5を予め着色しておくための色素を含んだ添加剤を配合するようにしてもよい。この種の色素を含んだ添加剤としては、赤色の着色を目的とする場合には、たとえば、赤色の色素に加えて、コレステロールの低下効果が期待できるメビノリンを含んだ紅麹を用いるようにすればよい。又、緑色の着色を目的とする場合には、たとえば、緑色色素であって且つ鉄分不足を補う効果が期待できるクロロフィルを用いるようにすればよい。又、黄色の着色を目的とする場合には、たとえば、黄色物質であって且つ細胞の再生や生成を促進する効果が期待できるビタミンB等を用いるようにすればよい。 Moreover, as an additive mix | blended when forming the said enzyme-containing coating film 4, the enzyme mixing | blending granule 5 enclosed by the hard capsule 6 at a post process is aimed at improving the appeal effect on the external appearance with respect to a consumer, for example. You may make it mix | blend the additive containing the pigment | dye for coloring previously. As an additive containing this type of pigment, if red coloring is intended, for example, in addition to the red pigment, red yeast rice containing mevinolin that can be expected to lower cholesterol is used. That's fine. For the purpose of green coloring, for example, a chlorophyll that is a green pigment and can be expected to compensate for the lack of iron may be used. For the purpose of yellowing, for example, vitamin B 2 which is a yellow substance and can be expected to promote the regeneration and generation of cells may be used.

更に、上記酵素配合顆粒5を、配合されている酵素の種類別に着色するようにしてもよい。具体的には、たとえば、上述したような微生物由来の酵素を含む酵素含有コーティング被膜4には紅麹を配合しておくことにより、該微生物由来の酵素を含む酵素配合顆粒5を赤色に着色し、又、植物由来の酵素を含む酵素含有コーティング被膜4にはクロロフィルを配合しておくことにより、該植物由来の酵素を含む酵素配合顆粒5を緑色に着色し、又、上記動物由来の酵素を含む酵素含有コーティング被膜4にはビタミンB6を配合しておくことにより、該動物由来の酵素を含む酵素配合顆粒5は黄色に着色するようにすれば、各酵素配合顆粒5に配合されている酵素が、微生物由来、植物由来、又は、動物由来のいずれであるかを顆粒の色から容易に判別できるという外観上の訴求効果も期待できる。   Furthermore, you may make it color the said enzyme mixing granule 5 according to the kind of enzyme currently mix | blended. Specifically, for example, the enzyme-containing coating film 4 containing the microorganism-derived enzyme as described above is blended with red yeast so that the enzyme-containing granule 5 containing the microorganism-derived enzyme is colored red. In addition, by adding chlorophyll to the enzyme-containing coating film 4 containing a plant-derived enzyme, the enzyme-containing granule 5 containing the plant-derived enzyme is colored green, and the animal-derived enzyme is If the enzyme-containing granule 5 containing the animal-derived enzyme is colored yellow by blending vitamin B6 in the enzyme-containing coating film 4 to be contained, the enzyme contained in each enzyme-containing granule 5 However, it is also possible to expect an appealing effect on the appearance that it can be easily distinguished from the color of the granule whether it is derived from microorganisms, plants, or animals.

その後、上記製造された酵素配合顆粒5を、ハードカプセル6に所要量ずつ充填して封入させる。この充填、封入作業の際、上記酵素配合顆粒5は、真球状で且つ粒度が揃っているため、ハードカプセル6への充填量を正確に且つ容易にコントロールすることが可能になる。   Thereafter, the produced enzyme-containing granule 5 is filled into the hard capsule 6 in a required amount and sealed. During the filling and enclosing operation, the enzyme-containing granule 5 has a spherical shape and a uniform particle size, so that the filling amount into the hard capsule 6 can be controlled accurately and easily.

更に、上記ハードカプセル6に酵素配合顆粒5を充填、封入する際、たとえば、上記したような微生物由来、植物由来、動物由来のそれぞれの酵素を個別に含むと共に該酵素の種類ごとに赤色、緑色、黄色に色分けされた酵素配合顆粒5を、2種類又は3種類混合して上記ハードカプセル6に充填、封入させるようにしてもよく、この場合には、上記酵素配合顆粒5が、真球状で且つ粒度が揃ったものとしてあるために、上記種類の異なる酵素を個別に含む2種類又は3種類の酵素配合顆粒5を、所定の混合比、たとえば、等量ずつとなるように混合量を正確にコントロールしてハードカプセル6に充填、封入することが可能になる。   Furthermore, when filling and encapsulating the enzyme-containing granule 5 in the hard capsule 6, for example, the above-mentioned microorganism-derived, plant-derived, and animal-derived enzymes are individually included and red, green, Two or three kinds of enzyme-containing granules 5 color-coded in yellow may be mixed and filled into the hard capsule 6 so that the enzyme-containing granules 5 are spherical and have a particle size. Therefore, two or three types of enzyme-containing granules 5 that individually contain the above-mentioned different types of enzymes are precisely controlled so that the mixing amount becomes a predetermined mixing ratio, for example, equal amounts. Thus, the hard capsule 6 can be filled and sealed.

しかる後、上記酵素配合顆粒5を封入してなるハードカプセル6の表面の全面に、上記ツェイン7を、所要の厚み、具体的には、本発明の酵素配合食品8が胃を通過する間は該ツェイン7のコーティング層が胃液に曝されても溶解せず、且つ酵素配合食品8が腸に達した時点で上記ツェイン7のコーティング層が速やかに溶解するような所要の厚み寸法となるようにコーティングして、本発明の酵素配合食品8を形成するようにしてある。   Thereafter, the zein 7 is applied to the entire surface of the hard capsule 6 encapsulating the enzyme-containing granule 5 with the required thickness, specifically, while the enzyme-containing food 8 of the present invention passes through the stomach. Coating is performed so that the coating layer of zein 7 does not dissolve even when exposed to gastric juice, and has the required thickness dimension so that the coating layer of zein 7 dissolves quickly when the enzyme-mixed food 8 reaches the intestine. Thus, the enzyme-containing food 8 of the present invention is formed.

以上の構成としてある本発明の酵素配合食品8を飲み込むと、該酵素配合食品8は、最外層に形成してあるツェイン7のコーティング層の存在により、胃でのハードカプセルの崩壊が防止されることから、該ハードカプセル内に封入された酵素配合顆粒は、胃液との接触が防止された状態で胃を通過される。その後、腸内に達すると、上記ツェイン7のコーティング層が速やかに溶解するためハードカプセル6が露出され、次いで、該ハードカプセル6が崩壊して内部の酵素配合顆粒5が腸内に放出される。更に、上記酵素配合顆粒5の酵素含有コーティング被膜4が崩壊されることで、該酵素含有コーティング被膜4に配合されていた微生物由来、植物由来、動物由来等の酵素が腸内に放出されて、該酵素の機能が腸内で発揮されると共に、酵素含有コーティング被膜4に配合されていた酵素、添加剤等の水溶性の物質の腸での吸収が図られる。   When the enzyme-containing food 8 of the present invention having the above structure is swallowed, the enzyme-containing food 8 is prevented from disintegrating hard capsules in the stomach due to the presence of the coating layer of zein 7 formed in the outermost layer. Thus, the enzyme-containing granules encapsulated in the hard capsule are passed through the stomach in a state where contact with the gastric juice is prevented. Thereafter, when reaching the intestine, the hard capsule 6 is exposed because the coating layer of the zein 7 is rapidly dissolved, and then the hard capsule 6 is disintegrated and the internal enzyme-containing granules 5 are released into the intestine. Furthermore, by disintegrating the enzyme-containing coating film 4 of the enzyme-containing granule 5, enzymes derived from microorganisms, plants, animals, and the like mixed in the enzyme-containing coating film 4 are released into the intestine, The function of the enzyme is exhibited in the intestine, and absorption of water-soluble substances such as enzymes and additives mixed in the enzyme-containing coating film 4 in the intestine is achieved.

更に、上記酵素含有コーティング被膜4の崩壊に伴ってシームレス核1が露出されると、該シームレス核1における外層のゼラチン被膜3が崩壊することにより、該ゼラチン被膜3に内包されていたCoQ10含有油液2が腸内に放出されて、該油液2に配合されている脂溶性有効成分であるCoQ10の腸での吸収が図られるようになる。 Further, when the seamless nucleus 1 is exposed as the enzyme-containing coating film 4 is collapsed, the outer gelatin film 3 in the seamless nucleus 1 is collapsed, so that the CoQ 10 contained in the gelatin film 3 is contained. The oil liquid 2 is released into the intestine, and absorption of CoQ 10 which is a fat-soluble active ingredient blended in the oil liquid 2 into the intestine is achieved.

このように、本発明の酵素配合食品8によれば、配合されている酵素を、胃液による分解を受けることなく腸内に到達させて、該腸内で酵素の機能を発揮させることができて、腸内で不足する消化酵素等の酵素を補うことが可能になる。更に、上記酵素配合食品8には、本来水溶性である上記酵素を乾燥状態で配合できると共に、脂溶性の物質であるCoQ10をも一緒に且つ容易に配合することができるため、脂溶性有効成分としてのCoQ10も胃液に曝すことなく腸内に到達させて放出することができて、腸内での吸収に供することができる。 Thus, according to the enzyme-containing food 8 of the present invention, the compounded enzyme can reach the intestine without being decomposed by gastric juice, and the function of the enzyme can be exhibited in the intestine. It is possible to supplement enzymes such as digestive enzymes that are deficient in the intestines. Furthermore, the enzyme-mixed food 8 can be blended with the enzyme that is inherently water-soluble in a dry state, and can also be blended with CoQ 10 that is a fat-soluble substance together easily. CoQ 10 as a component can also be released by reaching the intestine without being exposed to gastric juice, and can be used for absorption in the intestine.

又、上記真球度が高く且つ粒度の揃った酵素配合顆粒5は、CoQ10含有油液2をゼラチン被膜3に封入してなるシームレスカプセル状のシームレス核1を中心核として、その周りを酵素含有コーティング被膜4で被覆して形成させるようにしてあるため、従来、真球度の高い顆粒を製造するために特許文献2に記載された手法で用いられていたような砂糖の球形粒子を核とする必要がないことから、糖の摂取量を削減することが可能になる。 The enzyme-containing granule 5 having a high sphericity and a uniform particle size has a seamless capsule-like seamless core 1 in which a CoQ 10- containing oil solution 2 is enclosed in a gelatin coating 3 as a central core, and the surroundings of the enzyme-containing granule 5. Since the coating film 4 is formed by coating, the sugar spherical particles as conventionally used in the technique described in Patent Document 2 to produce granules having a high sphericity are cores. Therefore, it is possible to reduce sugar intake.

更に、上記脂溶性物質であるCoQ10を配合するための油は、各シームレス核1にてゼラチン被膜3に内包されているCoQ10含有油液2のみであるため、従来、脂溶性物質を配合するための剤形として用いられているソフトカプセルに比して、油の使用量を低減させることができて、油の摂取量を削減することも可能になる。 Furthermore, since the oil for blending CoQ 10 which is the above fat-soluble substance is only CoQ 10- containing oil liquid 2 included in the gelatin coating 3 in each seamless core 1, conventionally, a fat-soluble substance is blended. The amount of oil used can be reduced and the amount of oil intake can be reduced as compared with the soft capsule used as a dosage form.

上記酵素配合顆粒5は、滴下法で製造することで真球度が高く且つ粒度が揃ったシームレスカプセル状のシームレス核1を中心核として、その周りを酵素含有コーティング被膜4で被覆することで、それ自体を、真球度が高く且つ粒度が揃った顆粒とすることができる。そのため、ハードカプセル6への充填する際の充填量を正確に且つ容易にコントロールすることができ、又、微生物由来、植物由来、動物由来のそれぞれの酵素を個別に含む酵素配合顆粒5を、2種類又は3種類混合して上記ハードカプセル6に充填、封入させる場合であっても、上記種類の異なる酵素を個別に含む2種類又は3種類の酵素配合顆粒5を、所定の混合比となるように混合量を正確にコントロールすることができる。   The enzyme-containing granule 5 is produced by a dropping method, with the seamless capsule-shaped seamless core 1 having a high sphericity and a uniform particle size as the central core, and the periphery thereof is coated with the enzyme-containing coating film 4. As such, it can be a granule having a high sphericity and a uniform particle size. Therefore, the filling amount when filling the hard capsule 6 can be controlled accurately and easily, and two types of enzyme-containing granules 5 each containing each of the enzymes derived from microorganisms, plants and animals are separately provided. Or, even when three types of the above-mentioned hard capsules 6 are mixed and filled, the two or three types of enzyme-containing granules 5 individually containing the different types of enzymes are mixed at a predetermined mixing ratio. The amount can be accurately controlled.

更に又、上記微生物由来、植物由来、動物由来のそれぞれの酵素を個別に含む酵素配合顆粒5を、赤色、緑色、黄色に色分けするようにしておけば、ハードカプセル6を通して観察される上記酵素配合顆粒5の色から、消費者が、本発明の酵素配合食品8に配合されてる酵素が、微生物由来、植物由来、動物由来のいずれであるかを、容易に判断することが可能になる。   Furthermore, the enzyme-containing granule 5 that is observed through the hard capsule 6 if the enzyme-containing granule 5 that individually contains the microorganism-derived, plant-derived, and animal-derived enzymes is color-coded into red, green, and yellow. From the color of 5, the consumer can easily determine whether the enzyme blended in the enzyme blended food 8 of the present invention is derived from microorganisms, plants, or animals.

なお、本発明は上記実施の形態のみに限定されるものではなく、酵素含有コーティング被膜4に配合する酵素は、食品に配合が可能で且つ腸内に到達させることが望まれる酵素であれば、上記実施の形態で例示した以外のいかなる酵素を用いるようにしてもよい。   The present invention is not limited only to the above embodiment, and the enzyme to be blended in the enzyme-containing coating film 4 is an enzyme that can be blended in food and desired to reach the intestines. Any enzyme other than those exemplified in the above embodiment may be used.

酵素配合顆粒を着色する場合の色は、上記実施の形態で例示した以外のいかなる色に設定してもよく、該着色に用いるための色素を含んだ添加物としては、食品に配合が可能であって且つ該酵素配合顆粒5に配合される酵素等の他の成分や、シームレス核1のゼラチン被膜3と反応する虞のないものであれば、いかなる色素を含んだ添加物を用いるようにしてもよい。   The color in the case of coloring the enzyme-containing granule may be set to any color other than those exemplified in the above embodiment, and as an additive containing a pigment for use in the coloring, it can be added to food. As long as there is no risk of reacting with the gelatin coating 3 of the seamless core 1 or other components such as the enzyme blended in the enzyme blending granule 5, an additive containing any pigment should be used. Also good.

脂溶性有効成分含有油液に配合する脂溶性有効成分としては、食品に配合可能で且つ摂取が望まれる脂溶性有効成分であれば、CoQ10以外のいかなる脂溶性有効成分を用いるようにしてもよい。又、CoQ10含有油液2を製造するためにCoQ10を溶解させる食用油としては、MCT以外のいかなる食用油を使用するようにしてもよい。 As the fat-soluble active ingredient to be blended in the oil solution containing the fat-soluble active ingredient, any fat-soluble active ingredient other than CoQ 10 may be used as long as it is a fat-soluble active ingredient that can be blended in food and desired to be ingested. Good. Further, any edible oil other than MCT may be used as the edible oil for dissolving CoQ 10 in order to produce the CoQ 10- containing oil liquid 2.

シームレス核1の製造は、CoQ10含有油液2を均一なゼラチン被膜3に内包させることができれば、上記実施の形態で説明した以外の手法を採用してもよい。又、酵素配合顆粒5の製造は、上記シームレス核1の表面に、所要の厚みで酵素含有コーティング被膜4を形成させることができれば、上記実施の形態で説明した以外の手法を採用してもよい。その他本発明の要旨を逸脱しない範囲内において種々変更を加え得ることは勿論である。 The seamless core 1 may be manufactured by a method other than that described in the above embodiment as long as the CoQ 10- containing oil solution 2 can be included in the uniform gelatin coating 3. In addition, if the enzyme-containing granule 5 can be formed on the surface of the seamless core 1 with a required thickness, a method other than that described in the above embodiment may be adopted. . Of course, various changes can be made without departing from the scope of the present invention.

本発明の酵素配合食品の実施の一形態を示すもので、(イ)はハードカプセルの中心軸に沿って切断した状態を示す概略図、(ロ)は酵素配合顆粒の一粒を拡大して示す断面図である。BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 shows an embodiment of an enzyme-containing food according to the present invention, in which (A) is a schematic diagram showing a state cut along the central axis of a hard capsule, and (B) shows an enlarged granule of enzyme-containing granules. It is sectional drawing.

符号の説明Explanation of symbols

1 シームレス核
2 CoQ10含有油液(脂溶性物質配合油液)
3 ゼラチン被膜
4 酵素含有コーティング被膜
5 酵素配合顆粒
6 ハードカプセル
7 ツェイン(胃難溶性で且つ腸溶性物質)
8 酵素配合食品
1 Seamless core 2 CoQ 10 containing oil solution (oil solution containing fat-soluble substance)
3 Gelatin coating 4 Enzyme-containing coating coating 5 Enzyme-containing granule 6 Hard capsule 7 Zein (stomach-soluble and enteric substance)
8 Enzyme-containing food

Claims (4)

脂溶性有効成分を食用油に溶解してなる脂溶性有効成分含有油液を、ゼラチン被膜に内包させてシームレス核を形成し、該シームレス核の表面を、所要の酵素を含む酵素含有コーティング被膜で覆ってなる構成を有することを特徴とする腸で機能させる酵素配合顆粒。   A fat-soluble active ingredient-containing oil solution obtained by dissolving a fat-soluble active ingredient in edible oil is encapsulated in a gelatin coating to form a seamless nucleus, and the surface of the seamless nucleus is coated with an enzyme-containing coating film containing a required enzyme. An enzyme-containing granule that functions in the intestine, characterized by having a covering structure. 脂溶性有効成分を食用油に溶解してなる脂溶性有効成分含有油液を、ゼラチン被膜に内包させてシームレス核を形成し、該シームレス核の表面を、所要の酵素を含む酵素含有コーティング被膜で覆って酵素配合顆粒を形成し、該酵素配合顆粒を、ハードカプセルに封入して、該ハードカプセルの表面を、胃難溶性で且つ腸溶性物質で全面に亘りコーティングしてなる構成を有することを特徴とする酵素配合食品。   A fat-soluble active ingredient-containing oil solution obtained by dissolving a fat-soluble active ingredient in edible oil is encapsulated in a gelatin coating to form a seamless nucleus, and the surface of the seamless nucleus is coated with an enzyme-containing coating film containing a required enzyme. Covering to form enzyme-containing granules, encapsulating the enzyme-containing granules in a hard capsule, and coating the entire surface of the hard capsule with a gastric insoluble substance and an enteric substance. Enzyme combination food. 酵素配合顆粒のシームレス核を、脂溶性有効成分含有油液と、ゼラチン被膜形成用のゼラチン溶液を原料としてシームレスなカプセル状とし、且つ、上記シームレス核の表面に、所要の酵素と賦形剤を含んだ粉末原料を、所要のコーティング液を介し所要厚みで積層させて酵素含有コーティング被膜を形成して酵素配合顆粒とした請求項2記載の酵素配合食品。   The seamless core of the enzyme-blended granule is made into a seamless capsule using the oil solution containing the fat-soluble active ingredient and the gelatin solution for forming the gelatin film, and the required enzymes and excipients are placed on the surface of the seamless core. The enzyme blended food according to claim 2, wherein the powder raw material contained is laminated with a required thickness through a required coating solution to form an enzyme-containing coating film to form enzyme-mixed granules. 酵素含有コーティング被膜に、微生物由来、植物由来、動物由来の酵素と、上記微生物由来、植物由来、動物由来の酵素ごとに異なる色の色素とを個別に配合してなる3種の酵素配合顆粒を形成して、該3種の酵素配合顆粒を、1種ごと又は複数種を混合してハードカプセルに封入するようにした請求項2又は3記載の酵素配合食品。   Three types of enzyme-containing granules composed of an enzyme-containing coating film, each of which contains a microorganism-derived, plant-derived, or animal-derived enzyme and a pigment of a different color for each of the microorganism-derived, plant-derived, or animal-derived enzymes. The enzyme-containing food according to claim 2 or 3, wherein the three kinds of enzyme-containing granules are formed and mixed in one or more kinds and encapsulated in a hard capsule.
JP2006296290A 2006-10-31 2006-10-31 Enzyme-compounded granule acting in intestine, and enzyme-compounded food using the enzyme-compounded granule Pending JP2008109910A (en)

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JP2013231017A (en) * 2012-05-02 2013-11-14 Nisshin Pharma Inc Large intestinal delivery preparation of seamless capsule and method for producing the same
JP2016074615A (en) * 2014-10-03 2016-05-12 富士カプセル株式会社 Trilaminar structure seamless capsule
JP2019034974A (en) * 2018-12-05 2019-03-07 富士カプセル株式会社 Trilaminar structure seamless capsule

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JPH11302158A (en) * 1998-04-16 1999-11-02 Oruto Corporation:Kk Health food having intestinal function controlling action and produced by using enteric seam capsule
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JP2005220025A (en) * 2004-02-03 2005-08-18 Kenko Tsusho Kk Oral ingestion composition

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JPS6415A (en) * 1988-03-17 1989-01-05 Freunt Ind Co Ltd Absorption-improving drug preparation
JPH11302158A (en) * 1998-04-16 1999-11-02 Oruto Corporation:Kk Health food having intestinal function controlling action and produced by using enteric seam capsule
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JP2005220025A (en) * 2004-02-03 2005-08-18 Kenko Tsusho Kk Oral ingestion composition

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2013231017A (en) * 2012-05-02 2013-11-14 Nisshin Pharma Inc Large intestinal delivery preparation of seamless capsule and method for producing the same
JP2016074615A (en) * 2014-10-03 2016-05-12 富士カプセル株式会社 Trilaminar structure seamless capsule
JP2019034974A (en) * 2018-12-05 2019-03-07 富士カプセル株式会社 Trilaminar structure seamless capsule

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