JP2022162982A - Vitamin b2-containing oral liquid composition - Google Patents
Vitamin b2-containing oral liquid composition Download PDFInfo
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- JP2022162982A JP2022162982A JP2022050967A JP2022050967A JP2022162982A JP 2022162982 A JP2022162982 A JP 2022162982A JP 2022050967 A JP2022050967 A JP 2022050967A JP 2022050967 A JP2022050967 A JP 2022050967A JP 2022162982 A JP2022162982 A JP 2022162982A
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- liquid composition
- oral liquid
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- galangal
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- 239000000203 mixture Substances 0.000 title claims abstract description 72
- 239000007788 liquid Substances 0.000 title claims abstract description 71
- AUNGANRZJHBGPY-SCRDCRAPSA-N Riboflavin Chemical compound OC[C@@H](O)[C@@H](O)[C@@H](O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-SCRDCRAPSA-N 0.000 title claims abstract description 29
- 244000062241 Kaempferia galanga Species 0.000 claims abstract description 67
- 235000013421 Kaempferia galanga Nutrition 0.000 claims abstract description 67
- 239000000284 extract Substances 0.000 claims abstract description 59
- RYYVLZVUVIJVGH-UHFFFAOYSA-N caffeine Chemical compound CN1C(=O)N(C)C(=O)C2=C1N=CN2C RYYVLZVUVIJVGH-UHFFFAOYSA-N 0.000 claims abstract description 54
- ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Natural products OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 claims abstract description 30
- 235000019164 vitamin B2 Nutrition 0.000 claims abstract description 29
- 239000011716 vitamin B2 Substances 0.000 claims abstract description 29
- AUNGANRZJHBGPY-UHFFFAOYSA-N D-Lyxoflavin Natural products OCC(O)C(O)C(O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-UHFFFAOYSA-N 0.000 claims abstract description 27
- 229960002477 riboflavin Drugs 0.000 claims abstract description 27
- 239000004475 Arginine Substances 0.000 claims abstract description 26
- LPHGQDQBBGAPDZ-UHFFFAOYSA-N Isocaffeine Natural products CN1C(=O)N(C)C(=O)C2=C1N(C)C=N2 LPHGQDQBBGAPDZ-UHFFFAOYSA-N 0.000 claims abstract description 26
- 229930003471 Vitamin B2 Natural products 0.000 claims abstract description 26
- 229960001948 caffeine Drugs 0.000 claims abstract description 26
- VJEONQKOZGKCAK-UHFFFAOYSA-N caffeine Natural products CN1C(=O)N(C)C(=O)C2=C1C=CN2C VJEONQKOZGKCAK-UHFFFAOYSA-N 0.000 claims abstract description 26
- 235000019154 vitamin C Nutrition 0.000 claims abstract 2
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- 239000007787 solid Substances 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 12
- 229940088594 vitamin Drugs 0.000 claims description 11
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- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 abstract description 4
- ZZZCUOFIHGPKAK-UHFFFAOYSA-N D-erythro-ascorbic acid Natural products OCC1OC(=O)C(O)=C1O ZZZCUOFIHGPKAK-UHFFFAOYSA-N 0.000 abstract 1
- 229930003268 Vitamin C Natural products 0.000 abstract 1
- 235000009697 arginine Nutrition 0.000 description 22
- 229960003121 arginine Drugs 0.000 description 22
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- 150000003839 salts Chemical class 0.000 description 15
- OHSHFZJLPYLRIP-BMZHGHOISA-M Riboflavin sodium phosphate Chemical compound [Na+].OP(=O)([O-])OC[C@@H](O)[C@@H](O)[C@@H](O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O OHSHFZJLPYLRIP-BMZHGHOISA-M 0.000 description 10
- 238000000605 extraction Methods 0.000 description 10
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- 230000000052 comparative effect Effects 0.000 description 7
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- 240000002768 Alpinia galanga Species 0.000 description 5
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- 241000411851 herbal medicine Species 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
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- HRXKRNGNAMMEHJ-UHFFFAOYSA-K trisodium citrate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O HRXKRNGNAMMEHJ-UHFFFAOYSA-K 0.000 description 2
- 229940038773 trisodium citrate Drugs 0.000 description 2
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
- 235000003392 Curcuma domestica Nutrition 0.000 description 1
- ODKSFYDXXFIFQN-SCSAIBSYSA-N D-arginine Chemical compound OC(=O)[C@H](N)CCCNC(N)=N ODKSFYDXXFIFQN-SCSAIBSYSA-N 0.000 description 1
- 229930028154 D-arginine Natural products 0.000 description 1
- RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 description 1
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- MJNIWUJSIGSWKK-BBANNHEPSA-N Riboflavin butyrate Chemical compound CCCC(=O)OC[C@@H](OC(=O)CCC)[C@@H](OC(=O)CCC)[C@@H](OC(=O)CCC)CN1C2=CC(C)=C(C)C=C2N=C2C1=NC(=O)NC2=O MJNIWUJSIGSWKK-BBANNHEPSA-N 0.000 description 1
- 241000533293 Sesbania emerus Species 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
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- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 229930003451 Vitamin B1 Natural products 0.000 description 1
- 229930003779 Vitamin B12 Natural products 0.000 description 1
- 244000273928 Zingiber officinale Species 0.000 description 1
- 235000006886 Zingiber officinale Nutrition 0.000 description 1
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- 239000001361 adipic acid Substances 0.000 description 1
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- 229930013930 alkaloid Natural products 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- 229940024606 amino acid Drugs 0.000 description 1
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- Seasonings (AREA)
- Non-Alcoholic Beverages (AREA)
Abstract
Description
本発明は、ガランガル抽出物を配合した経口液体組成物に関する。より詳細には、ガランガル抽出物及びビタミンB2類を含有した組成物における特有の不快臭が抑制された経口液体組成物に関する。 The present invention relates to oral liquid compositions incorporating galangal extracts. More particularly, it relates to an oral liquid composition in which the unpleasant odor peculiar to a composition containing a galangal extract and vitamin B2s is suppressed.
近年、気分の高揚やリフレッシュを目的としたエナジードリンクの需要が高まっている。このようなエナジードリンクには、ビタミンB1、ビタミンB2、ビタミンB12、アスコルビン酸等のビタミン類が含まれることが多い。また、通常、中枢神経を興奮させることで覚醒作用を示すカフェインが含まれており、一般生活者の中には、より強力な覚醒感を求め、カフェイン配合量の多いエナジードリンクを選択することがある。 In recent years, there has been an increasing demand for energy drinks for the purpose of uplifting and refreshing the mood. Such energy drinks often contain vitamins such as vitamin B1, vitamin B2, vitamin B12, and ascorbic acid. In addition, it usually contains caffeine, which shows an awakening effect by stimulating the central nervous system, and some general consumers want a stronger sense of awakening and choose energy drinks with a large amount of caffeine. Sometimes.
また、カフェインと同様に覚醒作用等を有する食品素材の開発がなされており、その素材の1つとして、ショウガ科ハナミョウガ属植物であるガランガル(Alpinia galanga L.)の地下茎に、注意力や覚醒水準を高める効果が認められ、注目を集めている(非特許文献1)。
しかしながら、ガランガルを配合した飲料として、例えば、Organics by RedBullシンプリーコーラ(レッドブル・ジャパン社)や、XSエナジーコーヒー(日本アムウェイ社)等存在するが、その数は少ない。
In addition, food materials having stimulating effects similar to caffeine have been developed. As one of the materials, the rhizome of Alpinia galanga L., a plant belonging to the genus Zingiberaceae, has been shown to enhance alertness and alertness. The effect of raising the standard is recognized, and it is attracting attention (Non-Patent Document 1).
However, although there are, for example, Organics by RedBull Simply Cola (Red Bull Japan) and XS Energy Coffee (Amway Japan) as beverages containing galangal, they are few in number.
上記背景のもと、発明者らは、ビタミンB2若しくはその誘導体又はそれらの塩(以下、「ビタミンB2類」とも言う)をガランガルとともに配合することにより特有の不快臭を生じることを新たに見出した。
したがって、本発明は、ガランガル抽出物及びビタミンB2類を含有した経口液体組成物において、特有の不快臭が軽減された組成物を提供することである。
Based on the above background, the inventors have newly found that a unique unpleasant odor is produced by blending vitamin B2 or its derivatives or salts thereof (hereinafter also referred to as "vitamin B2s") with galangal. .
Accordingly, the present invention is to provide an oral liquid composition containing a galangal extract and vitamins B2, in which the characteristic unpleasant odor is reduced.
本発明者らは、上記課題を解決すべく鋭意検討を重ねた結果、ショウガ科ハナミョウガ属植物であるガランガル(Alpinia galanga L.)地下茎の抽出物及びビタミンB2類を含有した組成物において、カフェイン及び/又はアルギニンを配合することでガランガル抽出物及びビタミンB2類を含有させた時に生じる特有の不快臭を軽減できることを見出した。 The present inventors have made intensive studies to solve the above problems, and as a result, in a composition containing an extract of the rhizome of Alpinia galanga L., a plant belonging to the genus Zingiberaceae, and vitamin B2s, caffeine And/or it was found that the addition of arginine can reduce the peculiar unpleasant odor that occurs when the galangal extract and vitamin B2 are contained.
すなわち、本発明は、次のとおりである。
(1)A)ガランガル抽出物、B)ビタミンB2類、及びC)カフェイン及び/又はアルギニンを含有することを特徴とする経口液体組成物、
(2)A)ガランガル抽出物の濃度が乾燥固形分換算量として0.001~10質量%である(1)に記載の経口液体組成物、
(3)B)ビタミンB2類の濃度が0.0001~0.1質量%である(1)又は(2)に記載の経口液体組成物、
(4)C)カフェインの濃度が0.001~1質量%である(1)~(3)のいずれかに記載の経口液体組成物、
(5)C)アルギニン濃度が0.01~20質量%である(1)~(4)のいずれかに記載の経口液体組成物、
(6)pHが2.0~7.0である(1)~(5)のいずれかに記載の経口液体組成物、
(7)経口液体組成物が液体飲料である(1)~(6)のいずれかに記載の経口液体組成物、
(8)ガランガル抽出物及びビタミンB2類を含有する液体組成物における不快臭をカフェイン及び/又はアルギニンを含有させることで抑制する方法。
That is, the present invention is as follows.
(1) an oral liquid composition comprising A) a galangal extract, B) vitamin B2s, and C) caffeine and/or arginine;
(2) A) the oral liquid composition according to (1), wherein the concentration of the galangal extract is 0.001 to 10% by mass as a dry solid content;
(3) B) The oral liquid composition according to (1) or (2), wherein the concentration of vitamin B2 is 0.0001 to 0.1% by mass,
(4) C) The oral liquid composition according to any one of (1) to (3), wherein the caffeine concentration is 0.001 to 1% by mass.
(5) C) The oral liquid composition according to any one of (1) to (4), wherein the arginine concentration is 0.01 to 20% by mass.
(6) The oral liquid composition according to any one of (1) to (5), which has a pH of 2.0 to 7.0,
(7) the oral liquid composition according to any one of (1) to (6), wherein the oral liquid composition is a liquid drink;
(8) A method of suppressing an unpleasant odor in a liquid composition containing a galangal extract and vitamin B2s by adding caffeine and/or arginine.
本発明により、ガランガル抽出物及びビタミンB2類を含有させた経口液体組成物において特有の不快臭が軽減された経口液体組成物を提供することが可能となった。 INDUSTRIAL APPLICABILITY According to the present invention, it has become possible to provide an oral liquid composition containing a galangal extract and vitamins B2, in which the unpleasant odor peculiar to the oral liquid composition is reduced.
本発明におけるガランガル抽出物とは、ショウガ科ハナミョウガ属植物であるガランガル(Alpinia galanga L.)(別名として、ガランガ、ナンキョウ等と呼ばれることもある)の地下茎をそのまま、あるいは必要に応じて、乾燥、破砕、粉砕処理等を行った後に抽出することにより得られる。すなわち、本発明におけるガランガル抽出物とは、ガランガル地下茎の抽出物である。なお、ガランガルは、ショウガ科バンウコン属植物である黒ショウガやショウガ科クルクマ属植物であるウコンとは異なる。 The galangal extract in the present invention refers to the rhizome of Alpinia galanga L. (Alpinia galanga L.), which is a plant belonging to the genus Zingiberaceae (Alpinia galanga L.) (also known as galanga, nankyo, etc.). It can be obtained by extraction after crushing, pulverizing, or the like. That is, the galangal extract in the present invention is an extract of galangal rhizomes. Galangal is different from black ginger, which is a plant belonging to the genus Curcuma of the family Zingiberaceae, and turmeric, which is a plant of the genus Curcuma of the family Zingiberaceae.
抽出処理方法は、特に限定されず、例えば、エタノール等の有機溶媒や水またはそれらの混合物を用いた撹拌・振盪・浸漬抽出法や、減圧水蒸気蒸留抽出法等公知の抽出方法にて行えばよく、必要に応じて遠心処理、酵素処理(麹菌や黒麹菌などを基原とした酵素剤による処理)、カラム又はろ過(ストレーナーメッシュやメンブレンフィルターなどによるろ過)等により不溶物を除去してもよい。本発明におけるガランガル抽出物は、抽出溶媒として水及び/又はアルコールが用いられることが好ましく、アルコールとしてはエタノールがより好ましく、水単独で用いられることが特に好ましい。上記のように抽出されて得られた抽出液は、液体の状態で用いても良く、乾燥させて粉末の状態としたものを用いてもよく、粉末の状態で販売されている市販品(Enovate Biolife製のenXtraTM等)を用いてもよい。 The extraction treatment method is not particularly limited, and for example, a known extraction method such as a stirring/shaking/immersion extraction method using an organic solvent such as ethanol, water, or a mixture thereof, or a vacuum steam distillation extraction method may be used. If necessary, centrifugation, enzymatic treatment (treatment with an enzymatic agent based on koji mold or black koji mold), column or filtration (filtration with a strainer mesh, membrane filter, etc.) may be used to remove insoluble matter. . The galangal extract in the present invention preferably uses water and/or alcohol as an extraction solvent, more preferably ethanol as the alcohol, and particularly preferably water alone. The extract obtained by extraction as described above may be used in a liquid state, or may be dried and used in a powder state. Biolife's enXtra ™ , etc.) may also be used.
本発明におけるガランガル抽出物の含有量は、ガランガル抽出物の乾燥固形分換算量として、本発明の経口液体組成物中、0.001~10質量%が好ましく、0.01~5質量%がより好ましく、0.02~1質量%がさらに好ましく、0.05~0.5質量%がよりさらに好ましく、0.06~0.3質量%が特に好ましい。
ここで、「乾燥固形分換算量」とは水分を除いた部分の量に換算した量をいう。水分は、従来公知の加熱乾燥法やカール・フィッシャー法等を用いて測定することができる。
The content of the galangal extract in the present invention is preferably 0.001 to 10% by mass, more preferably 0.01 to 5% by mass, in terms of the dry solid content of the galangal extract in the oral liquid composition of the present invention. Preferably, 0.02 to 1% by mass is more preferable, 0.05 to 0.5% by mass is even more preferable, and 0.06 to 0.3% by mass is particularly preferable.
Here, the term "dry solid content conversion amount" refers to the amount converted to the amount of the portion excluding water. Moisture content can be measured using a conventionally known heat drying method, Karl Fischer method, or the like.
また、本発明におけるガランガル抽出物の含有量は、ガランガル地下茎の換算量として、本発明の経口液体組成物中、0.01~100質量%が好ましく、0.1~50質量%がより好ましく、0.2~10質量%がさらに好ましく、0.5~5質量%がよりさらに好ましく、0.6~3質量%が特に好ましい。 In addition, the content of the galangal extract in the present invention is preferably 0.01 to 100% by mass, more preferably 0.1 to 50% by mass, in terms of galangal rhizome, in the oral liquid composition of the present invention. 0.2 to 10% by mass is more preferable, 0.5 to 5% by mass is even more preferable, and 0.6 to 3% by mass is particularly preferable.
本発明におけるガランガル抽出物の1回当たりの経口摂取量は、ガランガル抽出物の乾燥固形分換算量として、本発明の経口液体組成物中、10~1000mgが好ましく、50~500mgがより好ましく、100~400mgがさらに好ましく、150~300mgがよりさらに好ましい。ここでの「1回当たりの経口摂取量」とは、本発明の経口液体組成物が一度に摂取される量、より詳細には、例えば30分以内程度の短い時間において断続的にまたは連続的に摂取される量を示し、例えば50mL~500mLである。 The oral intake of the galangal extract in the present invention is preferably 10 to 1000 mg, more preferably 50 to 500 mg, more preferably 100 mg, in terms of the dry solid content of the galangal extract in the oral liquid composition of the present invention. ~400 mg is more preferred, and 150-300 mg is even more preferred. The term "per oral intake" as used herein refers to the amount of the oral liquid composition of the present invention that is ingested at one time, more It indicates the amount to be ingested for a period of time, and is, for example, 50 mL to 500 mL.
本発明において、ビタミンB2類とは、ビタミンB2若しくはその誘導体又はそれら塩であり、通常可食性のものを指し、例えば、リボフラビン、リン酸リボフラビン、酪酸リボフラビン、フラビンアデニンジヌクレオチド及びそれら塩などを挙げることができる。本発明に使用する塩とは、ナトリウム塩が好ましく、本発明においては、リボフラビン5’-リン酸エステルナトリウムが特に好ましい。本発明で用いるビタミンB2類は、公知の方法により製造できるほか、市販品(DSM製のリボフラビン5’-リン酸エステルナトリウム、岩城製薬製のリボフラビン5’-リン酸エステルナトリウム等)を用いることもできる。 In the present invention, vitamin B2 refers to vitamin B2 or derivatives thereof or salts thereof, which are usually edible, and examples thereof include riboflavin, riboflavin phosphate, riboflavin butyrate, flavin adenine dinucleotide and salts thereof. be able to. The salt used in the present invention is preferably a sodium salt, and in the present invention, sodium riboflavin 5'-phosphate is particularly preferred. The vitamin B2s used in the present invention can be produced by known methods, and commercially available products (such as riboflavin 5'-phosphate sodium manufactured by DSM and riboflavin 5'-phosphate sodium manufactured by Iwaki Seiyaku Co., Ltd.) can also be used. can.
本発明におけるビタミンB2類の含有量は、本発明の経口液体組成物中、0.0001~0.1質量%が好ましく、0.0005~0.02質量%がより好ましく、0.001~0.01質量%がさらに好ましい。 The content of vitamin B2 in the present invention is preferably 0.0001 to 0.1% by mass, more preferably 0.0005 to 0.02% by mass, more preferably 0.001 to 0.001% by mass, in the oral liquid composition of the present invention. 0.01% by weight is more preferred.
本発明の経口液体組成物における、ガランガル抽出物の乾燥固形分換算量とビタミンB2類の質量比、すなわち、ガランガル抽出物の乾燥固形分換算量1質量部に対するビタミンB2類の含有量は、0.0002~100質量部が好ましく、0.0002~10質量部がより好ましく、0.03~10質量部がさらに好ましく、0.003~0.25質量部がよりさらに好ましく、0.006~0.25質量部が特に好ましい。 In the oral liquid composition of the present invention, the mass ratio of the dry solid content of the galangal extract and vitamin B2, that is, the content of vitamin B2 relative to 1 part by mass of the dry solid content of the galangal extract is 0 .0002 to 100 parts by mass is preferable, 0.0002 to 10 parts by mass is more preferable, 0.03 to 10 parts by mass is more preferable, 0.003 to 0.25 parts by mass is even more preferable, and 0.006 to 0 0.25 parts by weight is particularly preferred.
本発明の経口液体組成物における、ガランガル抽出物のガランガル地下茎換算量とビタミンB2類の質量比、すなわち、ガランガル抽出物のガランガル地下茎換算量1質量部に対するビタミンB2類の含有量は、0.00002~10質量部が好ましく、0.00002~1質量部がより好ましく、0.003~1質量部がさらに好ましく、0.0003~0.025質量部がよりさらに好ましく、0.0006~0.025質量部が特に好ましい。 In the oral liquid composition of the present invention, the mass ratio of the galangal rhizome-equivalent amount of the galangal extract and the vitamin B2s, that is, the content of the vitamin B2s relative to 1 part by mass of the galangal extract-equivalent galangal rhizome is 0.00002. ~10 parts by mass is preferable, 0.00002 to 1 part by mass is more preferable, 0.003 to 1 part by mass is more preferable, 0.0003 to 0.025 parts by mass is even more preferable, and 0.0006 to 0.025 Parts by weight are particularly preferred.
本発明において、カフェインとは、化学名としては1,3,7-トリメチルキサンチン
として示されるアルカロイドの1種であり、本発明には、特に制限されないが、公知の方法により製造できる化学合成品や、カフェインを含有する植物(コーヒー豆や、茶葉、コーラの実等)の抽出物及びそれらの濃縮精製物などを用いることができ、市販品(白鳥製薬製のカフェイン抽出物等)を用いることもできる。
In the present invention, caffeine is one of alkaloids whose chemical name is 1,3,7-trimethylxanthine, and is not particularly limited in the present invention, but is a chemically synthesized product that can be produced by a known method. Alternatively, extracts of caffeine-containing plants (coffee beans, tea leaves, cola seeds, etc.) and concentrated purified products thereof can be used. can also be used.
本発明におけるカフェインの含有量は、ガランガル抽出物由来の不快臭を十分に改善するという観点から、本発明の経口液体組成物中、0.001~1質量%が好ましく、0.01~0.5質量%がより好ましく、0.01~0.2質量%がさらに好ましく、0.02~0.2質量%がよりさらに、0.05~0.2質量%の順に好ましい。 The content of caffeine in the present invention is preferably 0.001 to 1 mass%, preferably 0.01 to 0, in the oral liquid composition of the present invention from the viewpoint of sufficiently improving the unpleasant odor derived from the galangal extract. 0.5% by weight is more preferred, 0.01 to 0.2% by weight is more preferred, 0.02 to 0.2% by weight is even more preferred, and 0.05 to 0.2% by weight is even more preferred.
本発明の経口液体組成物における、ガランガル抽出物の乾燥固形分換算量とカフェインの質量比、すなわち、ガランガル抽出物の乾燥固形分換算量1質量部に対するカフェインの含有量は、0.0001~200質量部が好ましく、0.0001~10質量部がより好ましく、0.005~2.5質量部がさらに好ましい。 In the oral liquid composition of the present invention, the mass ratio of the dry solid content of the galangal extract and caffeine, that is, the content of caffeine relative to 1 part by mass of the dry solid content of the galangal extract is 0.0001. Up to 200 parts by mass is preferable, 0.0001 to 10 parts by mass is more preferable, and 0.005 to 2.5 parts by mass is even more preferable.
本発明の経口液体組成物における、ガランガル抽出物のガランガル地下茎換算量とカフェインの質量比、すなわち、ガランガル抽出物のガランガル地下茎換算量1質量部に対するカフェインの含有量は、0.00001~20質量部が好ましく、0.00001~1質量部がより好ましく、0.0005~0.25質量部がさらに好ましい。 In the oral liquid composition of the present invention, the mass ratio of the amount of galangal extract converted to galangal rhizome and caffeine, that is, the content of caffeine relative to 1 part by mass of galangal extract converted to galangal rhizome is 0.00001 to 20. Parts by mass are preferable, 0.00001 to 1 part by mass is more preferable, and 0.0005 to 0.25 parts by mass is even more preferable.
本発明の経口液体組成物における、ビタミンB2類とカフェインの質量比、すなわち、ビタミンB2類1質量部に対するカフェインの含有量は、質量比で0.001~100質量部が好ましく、0.001~50質量部がより好ましく、0.001~10質量部がさらに好ましく、0.001~5質量部がよりさらに好ましく、0.05~2.5質量部が特に好ましい。 The mass ratio of vitamin B2 and caffeine in the oral liquid composition of the present invention, that is, the content of caffeine relative to 1 part by mass of vitamin B2, is preferably 0.001 to 100 parts by mass, and 0.001 to 100 parts by mass. 001 to 50 parts by mass, more preferably 0.001 to 10 parts by mass, even more preferably 0.001 to 5 parts by mass, and particularly preferably 0.05 to 2.5 parts by mass.
本発明におけるアルギニン又はその塩は、化学名としては2-アミノ-5-グアニジノペンタン酸又はその塩をいう。L-アルギニン、D-アルギニン、ラセミ体であるDL-アルギニンのいずれを用いてもよい。本発明には、遊離アルギニンを用いてもよいし、塩の形態のアルギニンを用いてもよい。塩の形態のアルギニンとしては、飲食用として許容される塩であれば特に限定されないが、たとえば塩酸塩、硝酸塩、硫酸塩、クエン酸塩、酢酸塩、グルタミン酸塩等が挙げられる。本発明で用いるアルギニン又はアルギニンの塩は、公知の方法により製造できるほか、市販品(中原製のL-アルギニン、 協和発酵バイオ製のアルギニン、味の素ヘルシーサプライ製のL-アルギニン等)を用いることもできる。 Arginine or a salt thereof in the present invention refers to 2-amino-5-guanidinopentanoic acid or a salt thereof as a chemical name. Any of L-arginine, D-arginine, and racemic DL-arginine may be used. Free arginine may be used in the present invention, or arginine in the form of a salt may be used. The salt form of arginine is not particularly limited as long as it is a salt that is acceptable for eating and drinking, and examples thereof include hydrochloride, nitrate, sulfate, citrate, acetate and glutamate. The arginine or arginine salt used in the present invention can be produced by a known method, or commercially available products (L-arginine manufactured by Nakahara, arginine manufactured by Kyowa Hakko Bio, L-arginine manufactured by Ajinomoto Healthy Supply, etc.). can.
本発明におけるアルギニン又はその塩の含有量は、ガランガル抽出物由来の不快臭を十分に改善するという観点から、本発明の経口液体組成物中、0.001~10質量%が好ましく、0.01~5質量%がより好ましく、0.05~1.5質量%が特に好ましい。 The content of arginine or a salt thereof in the present invention is preferably 0.001 to 10% by mass in the oral liquid composition of the present invention from the viewpoint of sufficiently improving the unpleasant odor derived from the galangal extract, and 0.01 ~5% by mass is more preferred, and 0.05 to 1.5% by mass is particularly preferred.
本発明の経口液体組成物における、ガランガル抽出物の乾燥固形分換算量とアルギニン又はその塩の質量比、すなわち、ガランガル抽出物の乾燥固形分換算量1質量部に対するアルギニン又はその塩の含有量は、0.001~100質量部が好ましく、0.01~50質量部がより好ましく、0.3~15質量部がさらに好ましい。 In the oral liquid composition of the present invention, the mass ratio of the dry solid content of the galangal extract and arginine or its salt, that is, the content of arginine or its salt relative to 1 part by mass of the dry solid content of the galangal extract , preferably 0.001 to 100 parts by mass, more preferably 0.01 to 50 parts by mass, and even more preferably 0.3 to 15 parts by mass.
本発明の経口液体組成物における、ガランガル抽出物のガランガル地下茎換算量とアルギニンの質量比、すなわち、ガランガル抽出物のガランガル地下茎換算量1質量部に対するアルギニンの含有量は、0.0001~10質量部が好ましく、0.001~5質量部がより好ましく、0.03~1.5質量部がさらに好ましい。 In the oral liquid composition of the present invention, the mass ratio of the galangal rhizome equivalent amount of the galangal extract and arginine, that is, the content of arginine relative to 1 part by mass of the galangal extract equivalent galangal rhizome amount is 0.0001 to 10 parts by mass. is preferred, 0.001 to 5 parts by weight is more preferred, and 0.03 to 1.5 parts by weight is even more preferred.
本発明の経口液体組成物における、ビタミンB2類とアルギニンの質量比、すなわち、ビタミンB2類1質量部に対するアルギニンの含有量は、0.1~200000質量部が好ましく、10~15000質量部がより好ましく、10~1000質量部がさらに好ましく、10~300質量部が特に好ましい。 The mass ratio of vitamin B2 and arginine in the oral liquid composition of the present invention, that is, the content of arginine per 1 part by mass of vitamin B2 is preferably 0.1 to 200000 parts by mass, more preferably 10 to 15000 parts by mass. It is preferably 10 to 1000 parts by mass, particularly preferably 10 to 300 parts by mass.
本発明の経口液体組成物のpHは、特に限定されないが、飲用に適するという観点で下限値として2.0~7.0が好ましく、2.5~4.5がより好ましく、3.0~4.0がさらに好ましい。本発明の経口液体組成物のpH調整は、通常使用されるpH調整剤を使用することができる。具体的なpH調整剤としては、クエン酸、リンゴ酸、酒石酸、コハク酸、乳酸、酢酸、マレイン酸、グルコン酸、アスパラギン酸、アジピン酸、グルタミン酸、フマル酸等の有機酸およびそれらの塩類、塩酸等の無機酸、水酸化ナトリウム等の無機塩基等が挙げられ、好ましいpH調整剤は、クエン酸及び/又はその塩、塩酸、水酸化ナトリウムである。 The pH of the oral liquid composition of the present invention is not particularly limited, but from the viewpoint of being suitable for drinking, the lower limit is preferably 2.0 to 7.0, more preferably 2.5 to 4.5, and 3.0 4.0 is more preferred. The pH of the oral liquid composition of the present invention can be adjusted using commonly used pH adjusters. Specific pH adjusters include organic acids such as citric acid, malic acid, tartaric acid, succinic acid, lactic acid, acetic acid, maleic acid, gluconic acid, aspartic acid, adipic acid, glutamic acid, and fumaric acid, salts thereof, and hydrochloric acid. and inorganic bases such as sodium hydroxide. Preferred pH adjusters are citric acid and/or salts thereof, hydrochloric acid, and sodium hydroxide.
また、本発明の経口液体組成物には、本発明の効果を損なわない範囲で、その他の成分として、ビタミンB2類以外のビタミン類、ミネラル類、アルギニン以外のアミノ酸類またはその塩類、生薬類、生薬抽出物類、ローヤルゼリー等を適宜に配合することができる。さらに、本発明の経口液体組成物には、本発明の効果を損なわない範囲で、抗酸化剤、着色料、香料、矯味剤、界面活性剤、増粘剤、安定剤、保存料、甘味料、酸味料等の添加物を適宜配合することができる。 In addition, the oral liquid composition of the present invention may contain other ingredients such as vitamins other than vitamin B2, minerals, amino acids other than arginine or salts thereof, herbal medicines, as long as the effects of the present invention are not impaired. Herbal medicine extracts, royal jelly and the like can be blended as appropriate. Furthermore, the oral liquid composition of the present invention may contain antioxidants, coloring agents, flavoring agents, corrigents, surfactants, thickeners, stabilizers, preservatives, and sweeteners as long as they do not impair the effects of the present invention. , an acidulant, etc., can be added as appropriate.
本発明における経口液体組成物とは、経口摂取できる液状の組成物であれば特に制限はなく、医薬品、医薬部外品、又は食品(機能性表示食品や栄養機能食品、特定保健用食品も含む)が挙げられる。医薬品及び医薬部外品としては、例えば内服液剤、ドリンク剤等が挙げられる。食品としては、清涼飲料水、炭酸飲料、スポーツ・機能性飲料、ノンアルコール飲料、乳飲料、茶飲料、コーヒー飲料、果実・野菜系飲料、ゼリー飲料等があげられる。 The oral liquid composition in the present invention is not particularly limited as long as it is a liquid composition that can be taken orally. ). Examples of pharmaceuticals and quasi-drugs include internal liquids and drinks. Foods include soft drinks, carbonated drinks, sports/functional drinks, non-alcoholic drinks, milk drinks, tea drinks, coffee drinks, fruit/vegetable drinks, jelly drinks and the like.
本発明の経口液体組成物は、従来公知の方法により製造することができる。例えば、水に、ガランガル抽出物及びビタミンB2類を添加し、カフェイン及び/又はアルギニンを添加した後、さらに所望により前述した他の成分を添加して溶解させ、さらに水を加え容量調整する。必要に応じてpHの調整や加熱殺菌を施し、容器に充填することで持ち運びのしやすい経口液体組成物として提供することができる。 The oral liquid composition of the present invention can be produced by a conventionally known method. For example, after adding galangal extract and vitamin B2 to water and adding caffeine and/or arginine, if desired, the other components described above are added and dissolved, and water is added to adjust the volume. It can be provided as an easy-to-carry oral liquid composition by subjecting it to pH adjustment and heat sterilization as necessary and filling it in a container.
本発明の経口液体組成物を炭酸飲料とする場合、例えば、水に、ガランガル抽出物及びビタミンB2類を添加し、カフェイン及び/又はアルギニンを添加した後、さらに所望により前述した他の成分を添加して溶解させ、飲料原液を調製する。必要に応じてpHの調整や加熱殺菌をしてから冷却した後、二酸化炭素を圧入(カーボネーション)し、容器に充填して、適宜殺菌する工程により製造することができる。そのガスボリュームは0.5~4.0であることが好ましい。前記ガスボリュームとは、標準状態(1気圧、20℃)において、溶媒である液体1に対しそれに溶けている二酸化炭素の体積比である。なお、炭酸飲料の製法には、プレミックス法とポストミックス法とがあるが、本発明においてはいずれを採用してもよい。 When the oral liquid composition of the present invention is a carbonated drink, for example, water is added with galangal extract and vitamin B2, caffeine and / or arginine is added, and if desired, the other ingredients described above are added. Add and dissolve to prepare a beverage concentrate. After adjusting the pH and sterilizing by heating as necessary, after cooling, carbon dioxide is injected (carbonation), filled in a container, and sterilized as appropriate. The gas volume is preferably between 0.5 and 4.0. The gas volume is the volume ratio of carbon dioxide dissolved in liquid 1 as a solvent under standard conditions (1 atm, 20° C.). There are a premix method and a postmix method for producing carbonated beverages, and either method may be employed in the present invention.
以下に、実施例、比較例を挙げ、本発明をさらに詳細に説明するが、本発明はこれらの実施例等に何ら限定されるものではない。なお、リボフラビン5’-リン酸エステルナトリウム、カフェイン抽出物、L-アルギニンは、市販品(リボフラビン5’-リン酸エステルナトリウム:DSM製、カフェイン抽出物:白鳥製薬製、L-アルギニン:協和発酵バイオ製)を以下の実施例、比較例で用いた。
(抽出例1~2、比較例1~13、実施例1-1~13)
EXAMPLES The present invention will be described in more detail below with reference to Examples and Comparative Examples, but the present invention is not limited to these Examples and the like. Riboflavin 5'-phosphate sodium, caffeine extract, and L-arginine are commercially available products (riboflavin 5'-phosphate sodium: manufactured by DSM, caffeine extract: manufactured by Shiratori Pharmaceutical, L-arginine: Kyowa Fermented Bio) was used in the following examples and comparative examples.
(Extraction Examples 1-2, Comparative Examples 1-13, Examples 1-1-13)
ガランガル抽出物の調製:
[抽出例1:以下、本発明においてガランガル抽出物Aと記載する]
ガランガル地下茎を熱水で抽出し、常法を用いて減圧濃縮を行い、ガランガル地下茎の質量の10分の1量の乾燥粉末状(固体)の抽出物を得た。
[抽出例2:以下、本発明においてガランガル抽出物Bと記載する]
ガランガル地下茎を熱水で抽出し、常法を用いて酵素処理、ろ過、減圧濃縮を行い、Brix15(可溶性固形分含量15%)の液状(液体)の抽出物を得た。
なお、試験例の表中にはガランガル抽出物A、Bともにガランガル乾燥固形分換算量を記載した。
Preparation of galangal extract:
[Extraction Example 1: Hereinafter, referred to as galangal extract A in the present invention]
Galangal rhizomes were extracted with hot water and concentrated under reduced pressure using a conventional method to obtain a dry powdery (solid) extract of 1/10 of the mass of galangal rhizomes.
[Extraction Example 2: Hereinafter, referred to as galangal extract B in the present invention]
Galangal rhizomes were extracted with hot water, and subjected to enzymatic treatment, filtration, and concentration under reduced pressure using conventional methods to obtain a liquid (liquid) extract of Brix 15 (soluble solid content: 15%).
In the tables of test examples, both galangal extracts A and B are described in terms of galangal dry solid content.
経口液体組成物の調製:
下記表2~8に記載の処方および次の方法に従い経口液体組成物を調製した。まず、全量の90%程度の精製水に、ビタミンB2類としてリボフラビン5’-リン酸エステルナトリウム、ガランガル抽出物Aもしくはガランガル抽出物B、カフェイン又はアルギニンを添加し、十分に撹拌した。撹拌後、塩酸及び水酸化ナトリウム溶液を用いてpHを調整し、精製水を加えて全量とし、経口液体組成物を得た(実施例1-1~13)。ガランガル抽出物Aもしくはガランガル抽出物Bを添加しない経口液体組成物(比較例1~13)を対照とした。
Preparation of oral liquid composition:
Oral liquid compositions were prepared according to the formulations shown in Tables 2-8 below and the following method. First, sodium riboflavin 5′-phosphate as vitamin B2, galangal extract A or galangal extract B, caffeine or arginine was added to approximately 90% of the total amount of purified water, and the mixture was thoroughly stirred. After stirring, the pH was adjusted using hydrochloric acid and sodium hydroxide solution, and purified water was added to make up the total volume to obtain oral liquid compositions (Examples 1-1 to 1-13). Oral liquid compositions without addition of galangal extract A or galangal extract B (Comparative Examples 1-13) served as controls.
得られた経口液体組成物をスクリュー管No.6((株)マルエム製)に30ml充填し、80℃25分の殺菌を行った。上記の通り調製した経口液体組成物を、国際照明委員会 (CIE) により定義された標準光源D65を用いて3000ルクスの照度下に7日間静置した後、においを嗅ぎ、表1の基準で不快臭の軽減度合いを評価した。 The resulting oral liquid composition was passed through a screw tube no. 6 (manufactured by Maruem Co., Ltd.) was filled with 30 ml and sterilized at 80° C. for 25 minutes. After leaving the oral liquid composition prepared as described above under an illumination of 3000 lux for 7 days using a standard light source D65 defined by the International Commission on Illumination (CIE), it was smelled and measured according to the criteria in Table 1. The degree of reduction of unpleasant odor was evaluated.
表2~8から明らかなように、ガランガル抽出物及びビタミンB2類を含有し、カフェイン又はアルギニンを配合した組成物は、それぞれ比較例に対してガランガル抽出物及びビタミンB2類を含有させた時に生じる特有の不快臭の低減効果を示した。 As is clear from Tables 2 to 8, the composition containing galangal extract and vitamin B2, and containing caffeine or arginine, compared to the comparative example, when containing galangal extract and vitamin B2 It showed the effect of reducing the peculiar unpleasant odor that occurs.
(実施例14~16)
表9に記載の処方および次の方法により液体飲料及び炭酸飲料を調製した。
(Examples 14-16)
Liquid beverages and carbonated beverages were prepared according to the formulations listed in Table 9 and the following methods.
液体飲料の調製:
全量の50%程度の水にリボフラビン5’-リン酸エステルナトリウム、安息香酸ナトリウムを除く成分を添加、溶解させた。そこに別途、全量の10%程度の70℃の水にリボフラビン5’-リン酸エステルナトリウムおよび安息香酸ナトリウムを添加、溶解させたものを加え、十分に撹拌した。撹拌後、クエン酸三ナトリウムを用いてpHを調整し、精製水を加えて全量とし、経口液体組成物を得た(実施例14及び15)。得られた経口液体組成物を100mlの茶瓶に充填し、密閉した後、80℃25分の殺菌を行った。殺菌後、調製した経口液体組成物を標準光源D65、3000ルクスの照度下に7日間静置した。実施例1-1~13及び比較例1~13と同様に表1の評価基準においてガランガル抽出物及びビタミンB2類を含有させた時に生じる特有の不快臭を評価した。
Preparation of liquid beverages:
Ingredients other than sodium riboflavin 5′-phosphate and sodium benzoate were added and dissolved in about 50% of the total amount of water. Separately, about 10% of the total amount of sodium riboflavin 5′-phosphate and sodium benzoate were added and dissolved in water at 70° C., and the mixture was thoroughly stirred. After stirring, trisodium citrate was used to adjust the pH, and purified water was added to make up the total volume to obtain oral liquid compositions (Examples 14 and 15). The obtained oral liquid composition was filled in a 100 ml tea bottle, sealed, and then sterilized at 80° C. for 25 minutes. After sterilization, the prepared oral liquid composition was allowed to stand under illumination of standard light source D65, 3000 lux for 7 days. In the same manner as in Examples 1-1 to 1-13 and Comparative Examples 1-13, the evaluation criteria in Table 1 were used to evaluate the peculiar unpleasant odors produced when the galangal extract and vitamin B2 were contained.
炭酸飲料の調製:
全量の10%程度の水にリボフラビン5’-リン酸エステルナトリウム、安息香酸ナトリウムを除く成分を添加、溶解させた。そこに別途、全量の2.5%程度の70℃の水にリボフラビン5’-リン酸エステルナトリウムおよび安息香酸ナトリウムを添加、溶解させたものを加え、十分に撹拌した。撹拌後、クエン酸三ナトリウムを用いてpHを調整し、全量の25%量となるまで水を添加した飲料原液を調製した。この飲料原液を80℃で25分間殺菌し、炭酸水を加え全量とし、透明の密閉容器に250ml充填した(実施例16)。充填後、調製した経口液体組成物を標準光源D65、3000ルクスの照度下に7日間静置した。実施例1-1~13及び比較例1~13と同様に表1の評価基準においてガランガル抽出物及びビタミンB2類を含有させた時に生じる特有の不快臭を評価した。
Preparation of carbonated drinks:
Ingredients other than sodium riboflavin 5′-phosphate and sodium benzoate were added and dissolved in about 10% of the total amount of water. Separately, about 2.5% of the total amount of sodium riboflavin 5′-phosphate and sodium benzoate were added and dissolved in water at 70° C., and the mixture was thoroughly stirred. After stirring, the pH was adjusted with trisodium citrate and water was added to 25% of the total volume to prepare a beverage concentrate. This undiluted beverage was sterilized at 80° C. for 25 minutes, carbonated water was added to make up the total volume, and 250 ml was filled in a transparent sealed container (Example 16). After filling, the prepared oral liquid composition was allowed to stand under illumination of standard light source D65, 3000 lux for 7 days. In the same manner as in Examples 1-1 to 1-13 and Comparative Examples 1-13, the evaluation criteria in Table 1 were used to evaluate the peculiar unpleasant odors produced when the galangal extract and vitamin B2 were contained.
表9から明らかなように、実施例14~16では、ガランガル抽出物とビタミンB2類を配合した時の不快臭はほとんど感じられないか、わずかに感じられる程度であることが確認できた。 As is clear from Table 9, in Examples 14 to 16, it was confirmed that almost no unpleasant odor was felt when the galangal extract and vitamin B2 were blended, or only a slight odor was felt.
本発明により、経口液体組成物中にガランガル抽出物とビタミンB2類を配合した際の不快臭を抑制することが可能となったので、医薬品、医薬部外品及び食品の分野において、商品性の高い経口液体組成物を提供することが期待される。 INDUSTRIAL APPLICABILITY According to the present invention, it has become possible to suppress the unpleasant odor when a galangal extract and vitamin B2 are added to an oral liquid composition. It is expected to provide a high oral liquid composition.
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