JP2001122795A - Prophylactic and therapeutic agent for infectious disease - Google Patents

Prophylactic and therapeutic agent for infectious disease

Info

Publication number
JP2001122795A
JP2001122795A JP30520099A JP30520099A JP2001122795A JP 2001122795 A JP2001122795 A JP 2001122795A JP 30520099 A JP30520099 A JP 30520099A JP 30520099 A JP30520099 A JP 30520099A JP 2001122795 A JP2001122795 A JP 2001122795A
Authority
JP
Japan
Prior art keywords
echinacea
therapeutic agent
extract
prophylactic
infectious diseases
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.)
Withdrawn
Application number
JP30520099A
Other languages
Japanese (ja)
Inventor
Junji Okuma
淳司 大隈
Takayuki Kojima
隆之 小嶋
Mayumi Nakamoto
真由美 中本
Kozo Yatagai
浩三 谷田貝
Fumio Ichikawa
文雄 市川
Ikuo Hanada
郁生 花田
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nissui Pharmacetuical Co Ltd
Original Assignee
Nissui Pharmacetuical 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 Nissui Pharmacetuical Co Ltd filed Critical Nissui Pharmacetuical Co Ltd
Priority to JP30520099A priority Critical patent/JP2001122795A/en
Publication of JP2001122795A publication Critical patent/JP2001122795A/en
Withdrawn legal-status Critical Current

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Abstract

PROBLEM TO BE SOLVED: To obtain a prophylactic and therapeutic agent for infectious diseases excellent in safety and having excellent effects. SOLUTION: This prophylatic and therapeutic agent for the infectious diseases comprises Echinacea purpurea, Echinacea pallida and Echinacea angustifolia or an extract thereof and a root of Isatis tinctoria L. of the family Cruciferae and a root of Baphicacanthes cusia Bremek. of the family Acanthaceae or an extract thereof as active ingredients.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、エキナケア及び板
藍根を併用した、各種感染性疾患の予防・治療剤に関す
る。
TECHNICAL FIELD The present invention relates to a prophylactic / therapeutic agent for various infectious diseases, in which echinacea is used in combination with roots.

【0002】[0002]

【従来の技術及び発明が解決しようとする課題】インフ
ルエンザウイルス等のウイルスや細菌による感染性疾患
は、ときに大流行し、多数の死者をだすこともある。こ
のため、ウイルスや細菌によってひきおこされる感染性
疾患の予防・治療を目的とした、日常的に用いることの
できる製剤の開発が望まれている。ところで、近年薬品
や食品に対して安全性が強く求められるようになり、上
記感染性疾患予防・治療剤についても、安全性の高い成
分を有効成分とするものが望まれている。
BACKGROUND OF THE INVENTION Infectious diseases caused by viruses and bacteria, such as influenza virus, sometimes become epidemic and cause many deaths. For this reason, there is a demand for the development of a preparation that can be used on a daily basis for the purpose of preventing and treating infectious diseases caused by viruses and bacteria. By the way, in recent years, safety has been strongly demanded for medicines and foods, and for the above-mentioned infectious disease preventive / therapeutic agents, those having a highly safe component as an active ingredient are desired.

【0003】したがって、本発明は、安全性に優れると
ともに、優れた効果を有する感染性疾患予防・治療剤を
提供することを目的とする。
Accordingly, an object of the present invention is to provide a prophylactic / therapeutic agent for infectious diseases which is excellent in safety and has excellent effects.

【0004】[0004]

【課題を解決するための手段】本発明者らは、すでに安
全性が十分立証されている生薬に着目して検討を行っ
た。そして、中国等でインフルエンザ等の治療薬として
用いられている板藍根と、火傷や昆虫刺傷の際の外用
薬、あるいは歯痛、頭痛の際の内服薬として用いられて
きたエキナケアとを併用すれば、意外にも両者が相乗的
に作用し、極めて優れた感染性疾患の予防・治療効果を
示し、感染性疾患予防・治療剤として有効であることを
見出した。
Means for Solving the Problems The present inventors have focused on herbal medicines whose safety has been sufficiently proven. Surprisingly, the combination of the indigo root, which is used as a remedy for influenza in China and other countries, and the echinacea, which has been used as an external medicine for burns and insect stings, or as an oral medicine for toothache and headache, Found that both act synergistically, exhibit extremely excellent effects of preventing and treating infectious diseases, and are effective as agents for preventing and treating infectious diseases.

【0005】すなわち、本発明は、エキナケア(Echina
cea purpurea, E.pallida及びE.angustifolia)又はそ
の抽出物と、板藍根(アブラナ科菘藍 Isatis tinctor
ia L.及びキツネノゴマ科馬藍 Baphicacanthes cusia
Bremek.の根)又はその抽出物とを有効成分として含有
する感染性疾患予防・治療剤を提供するものである。
That is, the present invention relates to an echinacea (Echina
cea purpurea, E. pallida and E. angustifolia) or an extract thereof, and an indigo root (Brassicaceae Suzu indigo Isatis tinctor)
ia L. and the fox-finch horse, Ai Baphicacanthes cusia
The present invention provides a prophylactic / therapeutic agent for infectious diseases, which contains Bremek. Root) or an extract thereof as an active ingredient.

【0006】[0006]

【発明の実施の形態】エキナケアは、北アメリカの原住
民の間で、創傷、火傷、リンパ節の膨張、昆虫刺傷の外
用薬、歯痛、頸部痛、頭痛、胃痙攣等の内服薬として用
いられてきた。また、板藍根は、中国で肝炎、インフル
エンザ、日本脳炎、おたふく風邪、帯状疱疹、扁桃腺炎
等の治療薬として用いられてきた。両者とも安全性は優
れたものであるが、感染性疾患に対する予防・治療効果
は十分ではなかった。しかし、両者を併用することによ
り、インフルエンザ等の感染性疾患に対して極めて優れ
た予防・治療効果を示すことは全く知られていなかっ
た。
DETAILED DESCRIPTION OF THE INVENTION Echinacea has been used by indigenous people in North America as a topical medicine for wounds, burns, lymph node swelling, insect stings, toothache, neck pain, headache, gastric spasm, etc. Was. In addition, it is used in China as a remedy for hepatitis, influenza, Japanese encephalitis, mumps, shingles, tonsillitis and the like. Although both were excellent in safety, their preventive and therapeutic effects on infectious diseases were not sufficient. However, it has never been known that the combined use of both of them exhibits extremely excellent preventive and therapeutic effects against infectious diseases such as influenza.

【0007】本発明においては、感染性疾患予防・治療
効果を示すものであれば、エキナケア(Echinacea purp
urea, E.pallida及びE.angustifolia)の近縁植物を用
いることもできる。また、感染性疾患予防・治療効果を
示すものであれば、板藍(アブラナ科菘藍及びキツネノ
ゴマ科馬藍)の近縁植物の根を用いることもできる。
[0007] In the present invention, Echinacea purp (Echinacea purp.)
urea, E. pallida and E. angustifolia) can also be used. In addition, as long as they exhibit the effect of preventing or treating infectious diseases, roots of closely related plants of the indigo plant (Brassicaceae Suzu indigo and the foxtail Sesinaceae Indigo) can also be used.

【0008】エキナケア及び板藍根は、原生薬をそのま
ま用いてもよく、またこれらの抽出物を用いてもよい。
エキナケアの原生薬は、根、葉、葉柄、茎、種子の1も
しくは2以上の箇所もしくは全草、又はそれらを乾燥、
裁断、粉砕したものである。板藍根の原生薬は、根又は
根を乾燥、裁断、粉砕したものである。これらは、市販
品を用いてもよい。
[0008] Echinacea and lantern roots may use the crude drug as it is or an extract thereof.
Echinacea's crude drug is one or more of roots, leaves, petiole, stem, seed, or whole plant, or dried,
It is cut and crushed. The crude drug of the roots of the lantern is dried or cut and crushed. These may use a commercial item.

【0009】また、抽出物とは、エキナケアの根、葉
等、あるいは板藍の根を乾燥し又は乾燥することなく粉
砕した後、常温又は加温下で溶媒により抽出するか又は
ソックスレー抽出器等の抽出器具を用いて抽出すること
により得られる、抽出溶媒液、その希釈液もしくは濃縮
液、又はその乾燥末をいう。
[0009] The extract refers to the roots and leaves of echinacea, or the roots of the indigo plant, which are dried or pulverized without drying, and then extracted with a solvent at room temperature or under heating, or a soxhlet extractor or the like. Refers to an extraction solvent solution, a diluting solution or a concentrated solution thereof, or a dried powder thereof obtained by extraction using an extracting device described above.

【0010】抽出に用いる溶媒としては、水、メタノー
ル、エタノール、プロパノール、ブタノール等のアルコ
ール類;プロピレングリコール、ブチレングリコール等
の多価アルコール類;アセトン、メチルエチルケトン等
のケトン類;酢酸メチル、酢酸エチル等のエステル類;
テトラヒドロフラン、ジエチルエーテル等の鎖状又は環
状エーテル類;ジクロロメタン等のハロゲン化炭化水素
類;n−ヘキサン、シクロヘキサン、石油エーテル等の
炭化水素類;トルエン等の芳香族炭化水素類;ポリエチ
レングリコール等のポリエーテル類;ピリジン類等が挙
げられ、これらを1種以上用いることができる。このう
ち、水及び/又はエタノールが好ましい。
Solvents used for extraction include water, alcohols such as methanol, ethanol, propanol and butanol; polyhydric alcohols such as propylene glycol and butylene glycol; ketones such as acetone and methyl ethyl ketone; methyl acetate, ethyl acetate and the like. Esters of
Chain or cyclic ethers such as tetrahydrofuran and diethyl ether; halogenated hydrocarbons such as dichloromethane; hydrocarbons such as n-hexane, cyclohexane and petroleum ether; aromatic hydrocarbons such as toluene; Ethers; pyridines and the like, and one or more of these can be used. Of these, water and / or ethanol are preferred.

【0011】抽出は、例えば以下のように行う。エキナ
ケアの葉、根等もしくは板藍の根、又はそれらの乾燥
物、乾燥裁断物、乾燥粉砕物に溶媒を加え、好ましくは
1〜120℃、特に好ましくは5〜100℃で、好まし
くは0.1〜30日間、特に好ましくは1〜15日間抽
出する。次いで得られた液を適宜濾過、静置等すること
により抽出物を得ることができる。また、当該抽出物を
希釈、濃縮もしくは凍結乾燥した後、粉末又はペースト
状に調製し、適宜製剤化してもよい。また、必要により
公知の方法で脱臭、脱色等の精製処理を行ってもよい。
抽出物はこのようにして抽出したものを用いてもよく、
又は市販品を用いてもよい。
The extraction is performed, for example, as follows. A solvent is added to echinacea leaves, roots and the like, or roots of indigo plants, or dried, cut, and pulverized materials thereof, preferably at 1 to 120 ° C, particularly preferably 5 to 100 ° C, and preferably 0.1 to 100 ° C. Extraction is carried out for 1 to 30 days, particularly preferably for 1 to 15 days. Next, an extract can be obtained by appropriately filtering and allowing the obtained liquid to stand. Alternatively, the extract may be diluted, concentrated, or lyophilized, and then prepared in a powder or paste form and appropriately formulated. Further, if necessary, purification treatment such as deodorization and decolorization may be performed by a known method.
The extract may be used in this way,
Alternatively, a commercially available product may be used.

【0012】本発明の感染性疾患予防・治療剤は、ウイ
ルス、細菌及び真菌等に由来する感染性疾患に対して適
用することができる。このうち、気管、呼吸器、消化器
及び尿路等の感染性疾患に対してより効果的に作用す
る。さらに、インフルエンザ、流感及び感冒等に対して
特に効果的に作用する。
The agent for preventing or treating infectious diseases of the present invention can be applied to infectious diseases derived from viruses, bacteria, fungi and the like. Among them, it works more effectively against infectious diseases such as trachea, respiratory tract, digestive tract and urinary tract. In addition, it works particularly effectively against influenza, flu and cold.

【0013】本発明の感染性疾患予防・治療剤は、医薬
又は食品として用いることができる。医薬として用いる
場合、投与形態としては、内服、経腸、坐剤及び静脈内
投与等が挙げられるが、内服用が好ましい。具体的には
散剤、顆粒剤、硬カプセル剤、軟カプセル剤、丸剤、錠
剤等の固形製剤、シロップ剤、懸濁剤、乳剤等の液剤等
が挙げられる。これらの経口投与剤は、エキナケア及び
板藍根以外に、経口投与剤の形態に応じて一般に用いら
れる、セルロース及びその誘導体、デンプン及びその誘
導体、天然及び合成高分子等の賦形剤、ステアリン酸等
の高級脂肪酸及びその塩類、天然及び合成ワックス等の
滑沢剤、崩壊剤、矯味剤、結合剤、油性成分、界面活性
剤、アルコール類、水、甘味料、糖類、酸味料、香料等
を添加し、常法にしたがって製造することができる。
The agent for preventing or treating infectious diseases of the present invention can be used as a medicine or food. When used as a medicament, examples of the administration form include oral administration, enteral administration, suppositories, and intravenous administration, and internal administration is preferable. Specific examples include solid preparations such as powders, granules, hard capsules, soft capsules, pills and tablets, and liquid preparations such as syrups, suspensions and emulsions. These orally administered drugs include, in addition to echinacea and roots, excipients such as cellulose and its derivatives, starch and its derivatives, excipients such as natural and synthetic polymers, and stearic acid, which are generally used depending on the form of the orally administered drug. Add lubricants such as higher fatty acids and their salts, natural and synthetic waxes, disintegrants, flavoring agents, binders, oily components, surfactants, alcohols, water, sweeteners, sugars, acidulants, flavors, etc. Can be produced according to a conventional method.

【0014】食品としては、健康食品、機能性食品、特
定保健用食品等が挙げられる。具体的には、錠剤、顆粒
剤、粉末剤、粉末飲料、あるいはヨーグルト等のゲル状
または半ゲル状食品、乳酸菌飲料等の飲料類、チョコレ
ート等の固形状食品等が挙げられる。このうち、粉末飲
料の形態とすることが特に好ましい。これらの食品は、
エキナケア及び板藍根以外に、該食品の形態に応じて一
般に用いられる原料を添加し、常法に従って製造するこ
とができる。
Examples of the food include health foods, functional foods, foods for specified health use, and the like. Specific examples include tablets, granules, powders, powdered drinks, gel or semi-gel foods such as yogurt, drinks such as lactic acid bacteria drinks, and solid foods such as chocolate. Among them, it is particularly preferable to use a powdered beverage. These foods are
In addition to the echinacea and the indigo root, commonly used raw materials are added according to the form of the food, and the food can be produced according to a conventional method.

【0015】本発明の感染性疾患予防・治療剤中の、エ
キナケア及び板藍根の合計の配合量に特に制限はない
が、粉末剤、顆粒剤、錠剤等の形態とする場合は、未乾
燥原生薬換算で0.5〜80重量%が好ましい。また水
剤、乳濁剤、懸濁剤等の液状とする場合は、未乾燥原生
薬換算で0.1〜20重量%が好ましい。また、エキナ
ケアと板藍根の配合比に特に制限はないが、0.000
4:99.9996〜85:15が好ましい。
The total amount of echinacea and roots in the infectious disease prophylactic / therapeutic agent of the present invention is not particularly limited. It is preferably 0.5 to 80% by weight in terms of conversion. In the case of a liquid such as a solution, an emulsion, and a suspension, the content is preferably 0.1 to 20% by weight in terms of undried crude drug. There is no particular limitation on the mixing ratio of Echinacea and lantern, but 0.000
4: 99.9996 to 85:15 is preferred.

【0016】本発明の感染性疾患予防・治療剤の投与量
は、年齢、性別、病状の程度にもよるが、成人1日当た
り未乾燥原生薬換算で、エキナケアが24〜2400m
g、板藍根が0.5〜50gが好ましく、エキナケアが
50〜1500mg、板藍根が1.0〜40gが特に好
ましい。かかる量を1日1〜数回、特に2〜5回に分け
て投与することが好ましい。
The dosage of the prophylactic / therapeutic agent for infectious diseases of the present invention depends on the age, sex and degree of medical condition, but is equivalent to 24 to 2400 m / day for adults per day in terms of virgin crude drug.
g, indigo root is preferably 0.5 to 50 g, echinacea is particularly preferably 50 to 1500 mg, and indigo root is particularly preferably 1.0 to 40 g. It is preferable to administer such an amount in 1 to several times a day, especially 2 to 5 times.

【0017】[0017]

【実施例】次に実施例を示して本発明をさらに詳細に説
明するが、本発明は以下の実施例に限定されるものでは
ない。
EXAMPLES Next, the present invention will be described in more detail with reference to examples, but the present invention is not limited to the following examples.

【0018】実施例1 BALB/cマウスのインフルエンザウイルス感染に対
する本発明の感染性疾患予防・治療剤の効果の確認 エキナケアエキス末は、日本粉末薬品株式会社製「エキ
ナケアエキスパウダー」(エキナケアの根を粗切し、粗
切品に対して30%エタノールを5重量倍加え、室温で
2日間抽出し、抽出液を120メッシュのステンレス製
金網で濾過し、残留物にさらに30%エタノールを5重
量倍加え、室温で1日間抽出して同様に濾過し、次いで
両濾液を合わせ、60℃以下で減圧(150mmHg以
下)濃縮した後噴霧乾燥したもの(収率約12.5
%):該エキナケアエキス1gは未乾燥原生薬約8gに
相当する。)を使用した(以下の実施例においても同
じ)。また、板藍根エキス末は、次の方法により製造し
た。すなわち、菘藍の根を粗切し、粗切品に対して常水
を10重量倍加え、100℃で60分間抽出し、抽出液
を120メッシュのステンレス製金網で濾過した。残留
物にさらに常水を10重量倍加え、100℃で60分間
抽出し、同様に濾過した。次いで両濾液を合わせ、60
℃以下で減圧(150mmHg以下)濃縮した後、噴霧
乾燥して板藍根エキス末を製造した(収率約10%)。
該板藍根エキス末1gは未乾燥原生薬約10gに相当す
る(以下の実施例においても同じ)。
Example 1 Confirmation of Effect of Infectious Disease Prevention / Treatment Agent of the Present Invention on Influenza Virus Infection of BALB / c Mice Echinacea Extract Powder was manufactured by Nippon Shokubai Pharmaceutical Co., Ltd. “Echinacea Extract Powder” (Root of Echinacea). The mixture was roughly cut, 30% ethanol was added to the crude product 5 times by weight, and the mixture was extracted at room temperature for 2 days. The extract was filtered through a 120-mesh stainless steel wire mesh, and the residue was further 5 times by weight with 30% ethanol. In addition, the mixture was extracted at room temperature for 1 day, filtered in the same manner, then combined, concentrated under reduced pressure (150 mmHg or less) at 60 ° C. or less, and then spray-dried (yield about 12.5
%): 1 g of the echinacea extract corresponds to about 8 g of the undried crude drug. ) (The same applies to the following examples). The indigo root extract powder was produced by the following method. That is, the roots of Suzu indigo were roughly cut, and 10 parts by weight of normal water was added to the roughly cut product, extracted at 100 ° C. for 60 minutes, and the extract was filtered through a 120-mesh stainless steel wire mesh. To the residue was added 10 times by weight of ordinary water, extracted at 100 ° C. for 60 minutes, and filtered in the same manner. Then, the two filtrates were combined and 60
After concentrating under reduced pressure (150 mmHg or less) at a temperature of not more than 0 ° C., it was spray-dried to produce a root extract powder (yield: about 10%).
1 g of the indigo root extract powder corresponds to about 10 g of undried crude drug (the same applies to the following examples).

【0019】BALB/c雌マウスを1群3匹ずつ4群
に分け、第1群には水、第2群にはエキナケアエキス末
を体重1kg当たり1日50mg、第3群には板藍根エ
キス末を体重1kg当たり1日1g、並びに第4群には
エキナケアエキス末を体重1kg当たり1日25mg及
び板藍根エキス末を体重1kg当たり1日0.5g、そ
れぞれ7日間経口投与した。次いで各マウスの腹腔内に
アモバルビタールナトリウム溶液を注射して麻酔し、マ
ウス感染型インフルエンザウイルスA/PR/8/34
の懸濁液を鼻孔から滴下して感染させた。感染後さらに
4日間、上記と同様の条件で各群のマウスに水、各エキ
ス末を経口投与した。該インフルエンザウイルス感染後
5日目に、気管と肺を切除し、牛血清アルブミン(BS
A)と抗生物質を含むリン酸緩衝液で洗浄し、気管支肺
胞洗浄液を得た。次いで該洗浄液をBSAと抗生物質を
含むEagle’s最少培地で適度な濃度に希釈し、M
adin−Darbyイヌ肝(MDCK)細胞に加え、
5%CO2 存在下で37℃、3日間培養した。次いで、
ウイルスがMDCK細胞に感染し、細胞変性したものを
カウントして、ウイルス数を測定した。各群のマウスの
インフルエンザウイルス数及び第1群のマウスに対する
第2群〜第4群のマウスのウイルス減少率を表1に示
す。
BALB / c female mice were divided into four groups of three mice per group. The first group was water, the second group was Echinacea extract powder 50 mg / kg body weight per day, and the third group was a blue root extract powder. Was administered orally at a dose of 1 g / kg body weight / day, and the fourth group was orally administered with echinacea extract powder 25 mg / kg body weight / day and lantern root extract powder 0.5 g / kg body weight / day for 7 days. Subsequently, each mouse was anesthetized by injecting amobarbital sodium solution into the peritoneal cavity, and the mouse-infected influenza virus A / PR / 8/34 was injected.
Was infected by instillation through the nostrils. Water and each extract powder were orally administered to each group of mice under the same conditions as above for another 4 days after the infection. On day 5 after the influenza virus infection, the trachea and lungs were excised, and bovine serum albumin (BS
Washing was performed with a phosphate buffer containing A) and an antibiotic to obtain a bronchoalveolar lavage fluid. The wash was then diluted to an appropriate concentration with Eagle's minimal medium containing BSA and antibiotics,
adin-Darby canine liver (MDCK) cells,
The cells were cultured at 37 ° C. for 3 days in the presence of 5% CO 2 . Then
Viruses infected MDCK cells and cytopathic ones were counted to determine the number of viruses. Table 1 shows the numbers of influenza viruses in the mice of each group and the virus reduction rates of the mice in the second to fourth groups with respect to the mice in the first group.

【0020】[0020]

【表1】 [Table 1]

【0021】第2群、第3群のマウスのウイルス数は、
第1群のマウスのウイルス数より減少したが、減少率は
いずれの群も低かった。これに対し、第4群のマウスの
ウイルス数は、第1群のマウスのウイルス数の1/10
0程度に減少した。この結果から、エキナケアと板藍根
を併用すれば、インフルエンザの感染に対して予防・治
療効果が高いことが確認された。
The virus counts of the mice of the second and third groups were as follows:
Although the virus number was lower than that of the mice in the first group, the reduction rate was lower in all groups. In contrast, the number of viruses in the mice of the fourth group was 1/10 of the number of viruses in the mice of the first group.
It decreased to about 0. From these results, it was confirmed that the combined use of Echinacea and Panglai roots has a high effect of preventing and treating influenza infection.

【0022】実施例2 流感、感冒による体調不良者に対する本発明の感染性疾
患予防・治療剤の効果の確認 表2に示す配合で粉末飲料1〜4を常法に従って製造し
た。次いでこれらを、全量が120mLとなるように水
を添加して溶解し、飲料1〜4を調製した。
Example 2 Confirmation of the effect of the preventive / therapeutic agent for infectious diseases of the present invention on a person with poor physical condition due to flu or cold Powdered beverages 1 to 4 were prepared according to a conventional method using the formulations shown in Table 2. Then, these were added and dissolved by adding water so that the total amount was 120 mL, and beverages 1 to 4 were prepared.

【0023】[0023]

【表2】 [Table 2]

【0024】流感又は感冒により、のどの痛み、鼻水又
は鼻づまりの症状を有する者16名(25〜50才)
を、1群4人ずつ4群に分け、第1群には飲料1、第2
群には飲料2、第3群には飲料3、及び第4群には飲料
4を、1日3回飲用してもらった。次いで、飲用翌日の
体調の変化を、著しく改善された、改善された、変化が
なかった、悪化した、の4段階で評価してもらった。な
お、被験者には飲料の内容を知らせずに、飲用してもら
った。結果を表2に示す。
16 persons (25-50 years old) who have symptoms of sore throat, runny nose or nasal congestion due to flu or cold
Are divided into 4 groups, each group consisting of 4 people, and the first group has beverage 1 and the second
Group 2 had drink 2, group 3 had drink 3, and group 4 had drink 4 three times a day. Next, the change in physical condition on the next day of drinking was evaluated on a four-point scale: markedly improved, improved, unchanged, and worsened. In addition, the subject was asked to drink without notifying the contents of the beverage. Table 2 shows the results.

【0025】第4群は、体調が改善された者はいなかっ
た。また、第2群及び第3群は、体調の改善効果が必ず
しも十分でなかった。これに対し、第1群は、体調の改
善効果が顕著であった。かかる結果から、本発明の感染
性疾患予防・治療剤の流感、感冒に対する効果が確認さ
れた。
In the fourth group, no one improved in physical condition. In addition, the second group and the third group did not always have a sufficient effect of improving the physical condition. On the other hand, in the first group, the effect of improving the physical condition was remarkable. From these results, the effects of the agent for preventing and treating infectious diseases of the present invention on flu and cold were confirmed.

【0026】表3に示す配合で、粉末飲料を常法に従っ
て製造した。該粉末飲料は、優れた感染性疾患予防・治
療効果を示した。
Powdered beverages were prepared according to a conventional method with the composition shown in Table 3. The powdered beverage exhibited an excellent infectious disease prevention / treatment effect.

【0027】[0027]

【表3】 [Table 3]

【0028】表4に示す配合で、錠剤を常法に従って製
造した。該錠剤は、優れた感染性疾患予防・治療効果を
示した。
Tablets having the composition shown in Table 4 were produced according to a conventional method. The tablets exhibited excellent infectious disease prevention / treatment effects.

【0029】[0029]

【表4】 [Table 4]

【0030】[0030]

【発明の効果】本発明の感染性疾患予防・治療剤は、エ
キナケア及び板藍根を併用したものであり、安全性が極
めて高く、かつ種々の感染性疾患、特にインフルエン
ザ、流感、感冒等の予防・治療に有効である。
EFFECT OF THE INVENTION The infectious disease preventive / therapeutic agent of the present invention is a combination of echinacea and roots of indigo, which is extremely safe and prevents various infectious diseases, especially influenza, flu, cold and the like. Effective for treatment.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 中本 真由美 茨城県結城市北南茂呂1075−2 日水製薬 株式会社内 (72)発明者 谷田貝 浩三 茨城県結城市北南茂呂1075−2 日水製薬 株式会社内 (72)発明者 市川 文雄 茨城県結城市北南茂呂1075−2 日水製薬 株式会社内 (72)発明者 花田 郁生 茨城県結城市北南茂呂1075−2 日水製薬 株式会社内 Fターム(参考) 4C088 AB12 AB15 AC01 BA08 MA07 MA43 ZB33  ──────────────────────────────────────────────────続 き Continuing on the front page (72) Mayumi Nakamoto, Inventor 1075-2 Kita-Namiro, Yuki City, Ibaraki Prefecture Nissui Pharmaceutical Co., Ltd. Pharmaceutical Co., Ltd. (72) Inventor Fumio Ichikawa 1075-2 Kita-Namiro, Yuki City, Ibaraki Prefecture Nissui Pharmaceutical Co., Ltd. F-term (reference) 4C088 AB12 AB15 AC01 BA08 MA07 MA43 ZB33

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】 エキナケア(Echinacea purpurea, E.pa
llida及びE.angustifolia)又はその抽出物と、板藍根
(アブラナ科菘藍(Isatis tinctoria L. )及びキツネ
ノゴマ科馬藍(Baphicacanthes cusia Bremek.)の根)
又はその抽出物とを有効成分として含有する感染性疾患
予防・治療剤。
[Claim 1] Echinacea (Echinacea purpurea, E.pa)
llida and E. angustifolia) or an extract thereof, and an indigo root (the roots of Brassicaceae Suzu indigo (Isatis tinctoria L.) and the fox-flea beetle (Baphicacanthes cusia Bremek.))
Or a prophylactic / therapeutic agent for an infectious disease, comprising an extract thereof and an active ingredient thereof.
【請求項2】 内服用である請求項1記載の感染性疾患
予防・治療剤。
2. The preventive / therapeutic agent for an infectious disease according to claim 1, which is taken internally.
【請求項3】 粉末飲料である請求項2記載の感染性疾
患予防・治療剤。
3. The prophylactic / therapeutic agent according to claim 2, which is a powdered beverage.
JP30520099A 1999-10-27 1999-10-27 Prophylactic and therapeutic agent for infectious disease Withdrawn JP2001122795A (en)

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* Cited by examiner, † Cited by third party
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WO2002102308A3 (en) * 2001-06-15 2003-08-21 Sanjiu Medical & Pharmaceutica Pharmaceutical composition for the treatment of viral infection
JP2005255662A (en) * 2004-05-11 2005-09-22 Kokuhi Tei Plant component mixture for beverage extraction, mixed liquor of plant component and plant component mixture
JP2008120728A (en) * 2006-11-13 2008-05-29 Pola Chem Ind Inc Oral administration composition for arthritis/arthrosis
CN103263522A (en) * 2013-05-30 2013-08-28 钦州市钦南区人民医院 Traditional Chinese medicine for treating parotitis
JP2013539770A (en) * 2010-10-11 2013-10-28 インデナ エッセ ピ ア Formulations for the treatment of upper airway disorders
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Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002102308A3 (en) * 2001-06-15 2003-08-21 Sanjiu Medical & Pharmaceutica Pharmaceutical composition for the treatment of viral infection
JP2005255662A (en) * 2004-05-11 2005-09-22 Kokuhi Tei Plant component mixture for beverage extraction, mixed liquor of plant component and plant component mixture
JP2008120728A (en) * 2006-11-13 2008-05-29 Pola Chem Ind Inc Oral administration composition for arthritis/arthrosis
JP2013539770A (en) * 2010-10-11 2013-10-28 インデナ エッセ ピ ア Formulations for the treatment of upper airway disorders
JP2016155878A (en) * 2010-10-11 2016-09-01 インデナ エッセ ピ ア Formulations for treatment of upper respiratory tract disorders
CN103263522A (en) * 2013-05-30 2013-08-28 钦州市钦南区人民医院 Traditional Chinese medicine for treating parotitis
CN104721352A (en) * 2014-12-20 2015-06-24 熊安富 Traditional Chinese medicine for treating acute/chronic hepatitis and cholecystitis
JP2017153451A (en) * 2016-03-04 2017-09-07 有限会社アルテミス candy
CN109288930A (en) * 2018-11-26 2019-02-01 河南百年康鑫药业有限公司 A kind of preparation method of GANMAO TUIRE KELI
JP2021169444A (en) * 2019-11-29 2021-10-28 国立大学法人弘前大学 Influenza virus inhibitor

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