JP4216013B2 - Anti-influenza virus agent - Google Patents
Anti-influenza virus agent Download PDFInfo
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- JP4216013B2 JP4216013B2 JP2002217441A JP2002217441A JP4216013B2 JP 4216013 B2 JP4216013 B2 JP 4216013B2 JP 2002217441 A JP2002217441 A JP 2002217441A JP 2002217441 A JP2002217441 A JP 2002217441A JP 4216013 B2 JP4216013 B2 JP 4216013B2
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- JP
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- Prior art keywords
- influenza virus
- extract
- infection
- present
- virus agent
- 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.)
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Description
【0001】
【発明の属する技術分野】
本発明は、インフルエンザウイルスの感染抑制作用を有する植物由来の抽出物を有効成分とすることを特徴とする抗インフルエンザウイルス剤に関するものである。
【0002】
【従来の技術】
毎年のようにインフルエンザの流行を引き起こすインフルエンザウイルスは、直径1万分の1ミリメートル程度のエンベロープ膜を有するRNAウイルスである。その抗原性の違いからA、B、Cの3つの型に分類されるが、流行的な広がりをみせるのはA型、B型である。これらのウイルスの粒子表面には、赤血球凝集素(HA)とノイラミニダーゼ(NA)という2種類の糖蛋白がスパイク状に突き出しており、内部には8本に分節した遺伝子RNAが存在する。ウイルスの表面にあるHAとNAは同一の亜型内で変異を頻繁に起こし、毎年のように新しい抗原変異株が出現する。
【0003】
咳による飛沫によって放出されたインフルエンザウイルスは、ヒトの鼻や口から侵入し、ウイルス表層のスパイク状糖蛋白質HAにより上気道の粘膜上皮細胞に吸着し、細胞へ侵入後増殖を開始する。近年の研究により、ウイルスの感染メカニズムが明らかにされている。ウイルスは、ヒトの標的細胞の表層に存在する糖鎖よりなるレセプターに結合し、エンドゾームへ取り込まれ、ウイルス膜とエンドゾーム膜の融合により細胞内に侵入し、ウイルス遺伝子の転写と複製、さらに宿主細胞膜からの出芽により子孫ウイルス粒子を形成し増殖する。
【0004】
インフルエンザウイルスの感染により数日で突然の発熱、頭痛、関節の痛み、全身倦怠感等の症状が現れ、それと前後して咳や喉の痛み、鼻水、鼻づまりなどの呼吸器症状が出現する。いわゆる風邪とは異なり、感染力が強く短期間で爆発的な流行を引き起こすのが特徴である。またインフルエンザウイルスのHA蛋白質の構造は年ごとに変異を繰り返し、過去の感染によりできた抗体があまり役に立たないことも感染を広げてしまう要因になっている。
【0005】
インフルエンザウイルスの感染を抑制するためには、上皮細胞への吸着の阻害、細胞への侵入の阻害、遺伝子の転写・複製の抑制、蛋白質の合成阻害、細胞からの放出の抑制などが考えられ、それぞれが抗ウイルス薬のターゲットになっている。現在までに、アマンタジン、リマンタジン、ザナミビル等の抗ウイルス薬が開発されているが、過敏症、精神神経症状、消化器系症状、自律神経系症状等の副作用が報告されており、その応用に関しては注意が必要である。
【0006】
またインフルエンザウイルスは気道粘膜上皮で感染、増殖することや、その年の流行型が予想できないことから、ワクチンの接種によって感染を抑えることも困難であると考えられている。頻繁なうがいと、喉の乾燥を避けること、栄養と休息を十分にとることなどが、現在最も有効な予防策と考えられている。そのため、感染抑制効果が高く、さらに安全性に問題がなく、日常的に利用できる抗インフルエンザウイルス剤の開発が望まれている。
【0007】
近年、天然物由来の抗インフルエンザ素材としてお茶や紅茶のポリフェノール成分が報告されており(感染症学雑誌, 68 (7) 824-829 (1994)、感染症学雑誌, 70 (11) 1190-1192 (1996))、人を用いた試験により紅茶のうがいが実際のウイルス感染を抑えることが明らかになっている(感染症学雑誌, 71 (6) 487-494 (1997))。またオウゴン由来のフラボノイド成分が、ウイルスのシアリダーゼ阻害活性によりインフルエンザ感染抑制効果を示すことが報告されている(Chem. Pharm. Bull. 38(5) 1329-1332 (1990))。さらに漢方製剤である桂枝二越婢一湯(特開平6−199680)、黒房すぐり抽出物(特開2000−212092)、馬鈴薯アントシアニン色素(特開2001−316399)、グァバ葉抽出物(特開2000−273048)羅布麻抽出物(特開平11−71296)等の抗ウイルス効果が報告されているが、本発明に示された植物抽出物のインフルエンザウイルス感染抑制効果に関する報告はみられず、本発明により初めて明らかにされたものである。
【0008】
【発明が解決しようとする課題】
本発明は、日常的に安心して使用できる安全性の高い植物抽出物を用いて、インフルエンザウイルスの感染に対して高い抑制効果を示し、副作用の無い抗インフルエンザウイルス剤を提供することである。
【0009】
【課題を解決するための手段】
上記課題を解決するために、本発明者らは副作用がなく安全性の高い古くより食品や香料、お茶などに利用されてきた植物や生薬、ハーブなどに着目し、これらの中から抗インフルエンザウイルス作用を有する植物抽出物を見出すため、インフルエンザウイルス(H3N2)のMDCK細胞に対する感染性の抑制効果を指標に試験を実施した。
【0010】
その結果、イチジク(Ficus carica)、アカザ(Chenopodium album)、モモ(Prunus persica)、リンゴ(Malus pumila)、ガラナ(Paullinia cupana)、ワタフジウツギ(Buddleia officinalis)、ツユクサ(Commelina communis)、ナズナ(Capsella bursa−pastoris)、マーシュマロー(Althaea officinalis)、レモンバーベナ(Aloysia triphylla)、アイスランドモス(Cetraria islandica)、アマチャヅル(Gynostemma pentaphyllum)、フキ(Petasites japonicus)の抽出物が強いインフルエンザウイルスの感染抑制効果を有することを見出し、本発明を完成させた。
【0011】
すなわち本発明は、イチジク(Ficus carica)、アカザ(Chenopodium album)、モモ(Prunus persica)、リンゴ(Malus pumila)、ガラナ(Paullinia cupana)、ワタフジウツギ(Buddleia officinalis)、ツユクサ(Commelina communis)、ナズナ(Capsella bursa−pastoris)、マーシュマロー(Althaea officinalis)、レモンバーベナ(Aloysia triphylla)、アイスランドモス(Cetraria islandica)、アマチャヅル(Gynostemma pentaphyllum)、フキ(Petasites japonicus)からなる群より選択される1種の植物から抽出することより得られる抽出物を有効成分とすることを特徴とする抗インフルエンザウイルス剤である。
【0013】
【発明の実施の形態】
本発明品の原料となる植物、イチジク(Ficus carica)、アカザ(Chenopodium album)、モモ(Prunus persica)、リンゴ(Malus pumila)、ガラナ(Paullinia cupana)、ワタフジウツギ(Buddleia officinalis)、ツユクサ(Commelina communis)、ナズナ(Capsella bursa−pastoris)、マーシュマロー(Althaea officinalis)、レモンバーベナ(Aloysia triphylla)、アイスランドモス(Cetraria islandica)、アマチャヅル(Gynostemma pentaphyllum)、フキ(Petasites japonicus)は、その全体、葉、果実、花、材、樹皮、根等の部位を使用することができるが、イチジク、モモ、ツユクサ、ナズナ、マーシュマロー、レモンバーベナ、フキについては葉を、またアカザ、アイスランドモスについてはその全体を、リンゴについてはその果実(未熟果)を、ワタフジウツギについては花を、ガラナについては種子を使用することが望ましい。
【0014】
上記植物の粉砕物から本発明の抽出物を得る方法については特に限定しないが、水、メタノール、エタノール、n−プロパノール並びにn−ブタノール等の低級アルコール、エーテル、クロロホルム、酢酸エチル、アセトン、グリセリン、プロピレングリコール等の有機溶剤またはこれらを適宜混合した溶剤を、好ましくは親水性の有機溶剤またはこれらを適宜混合した溶剤を用いて抽出することができる。しかし、本発明の抗インフルエンザウイルス剤を経口で摂取することを考慮すると、安全性の面から水、エタノールもしくはその混合液を用いて抽出することが望ましい。
【0015】
抽出条件としては特に制限はないが、50〜80℃で1〜5時間程度が望ましい。抽出液を濾過し、抽出溶剤を留去したあと、減圧下において濃縮または凍結乾燥したものを使用することができる。また、これらの抽出物を有機溶剤分画、カラムクロマトグラフィー等により分画精製したものも使用することができる。
【0016】
本発明品の投与方法については特に制限はないが、経口投与以外に気道投与、静脈内投与、直腸投与、皮下投与、皮内投与等を例示することができ、成人への投与量は各抽出物で10〜2000mg/日が好ましいが、この値に制限されるものではない。
【0017】
本発明品である抗インフルエンザウイルス剤は、有効成分として例示した植物抽出物を溶剤もしくは分散剤等で適宜希釈調製して用いることもできる。また、場合により製剤用担体、乳化剤、希釈剤、安定剤等を添加することによりうがい薬、含漱剤、吸入剤、トローチ剤、散剤、錠剤、座剤、注射剤等、任意の製剤として利用することができる。この場合、抽出物の添加量としては、その形態によって異なるが、0.001重量%以上、好ましくは約0.01重量%以上の割合になるように添加するのが好適である。
【0018】
また、本発明の抗インフルエンザウイルス剤を、マスク、エアコンフィルター、衣類、ウエットティシュ、スプレー等に吸着、含浸、添加することにより、インフルエンザ予防に寄与しうる組成物を提供することができる。これらの用途における植物抽出物の吸着、含浸、添加する量は、その組成物の形態に応じて異なり、一概に規定することは困難であるが、0.001〜5重量%の割合になるように添加するのが好適である。
【0019】
さらに、本発明の抗インフルエンザウイルス剤の有効成分である植物抽出物は安全性が高いことから、例えばチューインガム、キャンディ、錠菓、グミゼリー、チョコレート、ビスケット等の菓子、アイスクリーム、シャーベット、氷菓等の冷菓、飲料、スープ、ジャム等の飲食物に配合し、日常的に利用することが可能である。添加量としては、その利用形態および抽出物の呈味性によって異なるが、飲食品に対して0.001〜5重量%、好ましくは約0.01〜1重量%の割合になるように添加するのが好適である。
【0020】
【実施例】
以下実施例、試験例を挙げて本発明を具体的に説明するが、本発明はこれらに限定されるものではない。
【0021】
〔実施例1〕植物抽出物の調製
破砕した各種植物(ラズベリー、ストロベリー、ブラックベリー、イチジク、アカザ、アグリモニー、ユーカリ、モモ、リンゴ、ヴァイオレット、クロモジ、ガラナ、ワタフジウツギ、ツユクサ、ナズナ、エンメイソウ、ワイルドストロベリー、ホアハウンド、マーシュマロー、オオバコ、レモンバーベナ、ヤロー、アイスランドモス、アマチャヅル、フキ)それぞれ50gに500mlの抽出溶剤(水、50%エタノール、100%エタノール、アセトン、酢酸エチル)を加え、3時間還流抽出を行った。得られた抽出液を濾別し、濃縮、凍結乾燥することにより、本発明品である植物抽出物を得ることができる。各植物の使用部位、抽出溶剤及び得られた抽出物の収率を表1に示した。
【0022】
【表1】
【0023】
〔試験例1〕
実施例1で示した本発明品である抽出物を試料として、インフルエンザウイルス感染抑制効果を調べた。インフルエンザウイルスはA/Udorn/307/72(H3N2)株を用いた。試料をジメチルスルフォキシドに溶解(50mg/ml)したものを試料原液とした。試料原液をTris-Glucose-Saline(TGS)で10倍段階希釈し(106倍希釈まで)、これらの試料希釈液とウイルス液(1000PFU(plaque forming unit)/ml)を1:1に混合して室温で30分間反応させた。この0.1mlをMadin-Darby canine kidney(MDCK)細胞の単層培養(直径35mmシャーレ)に接種し、ウイルスを室温で1時間吸着させ、2mlのL−15アガロース培地を流し込み固めて34℃、3日間培養し、生じたプラーク数を計測した。プラーク数がTGS処理コントロールの50%以下となる試料の希釈倍数を感染中和価とした。実施例1で調製した本発明品である抽出物のインフルエンザウイルス感染抑制活性(感染中和価)を、以下の表2に示した。本発明品であるこれらの抽出物はいずれも感染中和価が105以上であり、強いウイルス感染抑制効果を示した。
【0024】
【表2】
【0025】
実施例1で調製した植物抽出物を用いて、うがい薬、吸入剤、トローチ剤、スプレー、チューインガム、キャンディ、錠菓、飲料を調製した。以下に実施例としてその処方を示した。
【0026】
【0027】
【0028】
【0029】
【0030】
【0031】
【0032】
【0033】
【0034】
【発明の効果】
本発明品の抗インフルエンザウイルス剤は、安全性の高い天然物の抽出物を含有することを特徴とし、インフルエンザウイルスに対して強い感染抑制作用を有するものである。また、本発明の抗インフルエンザウイルス剤は、安全性が高いことから、マスク、エアコンフィルター、衣類、ウエットティッシュ、スプレー等に吸着、含浸、添加することにより、抗インフルエンザウイルス組成物として日常生活において広く利用することができる。さらに、チューインガム、キャンディ、錠菓、飲料等の飲食物に添加し、抗インフルエンザウイルス作用を有する飲食物として日常的に利用、摂取することも可能である。そのため、本発明の抗インフルエンザウイルス剤及びそれを含む組成物並びに飲食物はインフルエンザウイルスの感染予防や、インフルエンザウイルスに起因する疾病症状の緩和に有効である。[0001]
BACKGROUND OF THE INVENTION
The present invention relates to an anti-influenza virus agent characterized by containing, as an active ingredient an extract from a plant having an infection inhibiting activity of influenza virus.
[0002]
[Prior art]
The influenza virus that causes the influenza epidemic every year is an RNA virus having an envelope membrane with a diameter of about 1 / 10,000 mm. Although it is classified into three types, A, B, and C, due to the difference in antigenicity, it is A type and B type that show a trendy spread. Two types of glycoproteins, hemagglutinin (HA) and neuraminidase (NA), protrude in the form of spikes on the surface of these virus particles, and gene RNA segmented into 8 segments exists inside. HA and NA on the surface of the virus frequently mutate within the same subtype, and new antigenic variants appear every year.
[0003]
The influenza virus released by the cough droplets enters from the human nose and mouth, adsorbs to the mucosal epithelial cells of the upper respiratory tract by the spike-like glycoprotein HA on the surface of the virus, and starts to proliferate after entering the cells. Recent research has revealed the mechanism of viral infection. A virus binds to a receptor consisting of a sugar chain on the surface of a human target cell, is taken into the endosome, enters the cell by fusion of the viral membrane and the endosomal membrane, transcription and replication of the viral gene, and further the host cell membrane Progeny virus particles form and propagate by budding.
[0004]
Infection of influenza virus causes symptoms such as sudden fever, headache, joint pain, general malaise in a few days, followed by respiratory symptoms such as cough, sore throat, runny nose and stuffy nose. Unlike the so-called cold, it is highly infectious and causes an explosive epidemic in a short period of time. In addition, the structure of the HA protein of influenza virus repeats mutations every year, and the fact that antibodies produced by past infections are not very useful is also a factor that spreads infection.
[0005]
In order to suppress infection with influenza virus, inhibition of adsorption to epithelial cells, inhibition of entry into cells, inhibition of gene transcription / replication, inhibition of protein synthesis, inhibition of release from cells, etc. are considered. Each is a target for antiviral drugs. To date, antiviral drugs such as amantadine, rimantadine, and zanamivir have been developed, but side effects such as hypersensitivity, neuropsychiatric symptoms, digestive system symptoms, and autonomic nervous system symptoms have been reported. Caution must be taken.
[0006]
In addition, influenza viruses are thought to be difficult to control by vaccination because influenza viruses infect and proliferate in the airway mucosal epithelium and the epidemic type of the year cannot be predicted. Frequent gargling, avoiding throat dryness, and adequate nutrition and rest are currently considered the most effective preventive measures. Therefore, it is desired to develop an anti-influenza virus agent that has a high infection-suppressing effect, has no safety problem, and can be used on a daily basis.
[0007]
In recent years, polyphenol components of tea and black tea have been reported as anti-influenza materials derived from natural products (Journal of Infectious Diseases, 68 (7) 824-829 (1994), Journal of Infectious Diseases, 70 (11) 1190-1192 (1996)), it has been clarified that gargle of black tea suppresses actual viral infections by human tests (Journal of Infectious Diseases, 71 (6) 487-494 (1997)). In addition, it has been reported that a flavonoid component derived from urgonum exhibits an influenza infection suppression effect due to a virus sialidase inhibitory activity (Chem. Pharm. Bull. 38 (5) 1329-1332 (1990)). Furthermore, Kameda Futoshi Koshiketsuto (Japanese Patent Laid-Open No. Hei 6-199680), Kurofu currant extract (Japanese Patent Laid-Open No. 2000-212092), potato anthocyanin pigment (Japanese Patent Laid-Open No. 2001-316399), guava leaf extract (specialty) Open 2000-273048) Rafu hemp extract (Japanese Patent Laid-Open No. 11-71296) has been reported to have an antiviral effect, but no report on the influenza virus infection inhibitory effect of the plant extract shown in the present invention has been found, This has been revealed for the first time by the present invention.
[0008]
[Problems to be solved by the invention]
An object of the present invention is to provide an anti-influenza virus agent that exhibits a high inhibitory effect against influenza virus infection and has no side effects, using a highly safe plant extract that can be used with peace of mind on a daily basis.
[0009]
[Means for Solving the Problems]
In order to solve the above problems, the present inventors have focused on plants, herbal medicines, herbs, etc. that have been used for foods, fragrances, teas, etc., since they have no side effects and are highly safe. In order to find a plant extract having an action, a test was carried out using as an index the inhibitory effect of influenza virus (H3N2) on the infectivity of MDCK cells.
[0010]
As a result, figs (Ficus carica), red crows (Chenopodium album), peaches (Prunus persica), apples (Malus pumila), guarana (Paulinia cupana), buddujia sasa (Buddleia sap) -Pastoris, Martha Mallow (Althaea officinalis), Lemon Verbena (Aloysia triphylla), Icelandic moss (Cetraria islandica), Gynostemma pentaphyllum, Jessica (Peto), pesto The present invention was completed by finding that it has an inhibitory effect on Nzavirus infection.
[0011]
That is, the present invention relates to figs (Ficus carica), akaza (Chenopodium album), peaches (Prunus persica), apples (Malus pumila), guarana (Paulinia cupana), buddulina Comma (Buddulina). From Capsella bursa-pastoris, Marshmallow (Althaea officinalis), Lemon Verbena (Aloysia triphylla), Iceland moss (Cetriaria islandica), Gammastemma pentaphyl It is an anti-influenza virus agent characterized by using an extract obtained by extracting from one selected plant as an active ingredient.
[0013]
DETAILED DESCRIPTION OF THE INVENTION
Plants from which the product of the present invention is made, figs (Ficus carica), red peas (Chenopodium album), peaches (Prunus persica), apples (Malus pumila), guarana (Paullinia cupana), cotton codice (a) ), Nazuna (Capsella bursa-pastoris), Marshmallow (Althaea officinalis), Lemon Verbena (Aloysia triphylla), Iceland moss (Cetraria islandica, et al.) Whole, leaves, fruits, flowers, timber, bark, roots, etc. can be used, but for figs, peaches, communis, nazuna, marsh mallow, lemon verbena, fuchsia leaves, akaza, iceland moss its entirety for, the fruit (unripe) for apples, flowers for Watafujiutsugi, it is desirable for the gas Rana to use seeds.
[0014]
The method for obtaining the extract of the present invention from the above pulverized plant is not particularly limited, but water, methanol, ethanol, lower alcohols such as n-propanol and n-butanol, ether, chloroform, ethyl acetate, acetone, glycerin, An organic solvent such as propylene glycol or a solvent appropriately mixed with these can be extracted, preferably using a hydrophilic organic solvent or a solvent appropriately mixed with these. However, in consideration of taking the anti-influenza virus agent of the present invention orally, it is desirable to extract using water, ethanol or a mixture thereof from the viewpoint of safety.
[0015]
There are no particular limitations on the extraction conditions, but it is preferably about 1 to 5 hours at 50 to 80 ° C. The extract can be filtered and the extraction solvent can be distilled off, followed by concentration or lyophilization under reduced pressure. Further, those obtained by fractionating and purifying these extracts by organic solvent fractionation, column chromatography or the like can also be used.
[0016]
There are no particular restrictions on the administration method of the product of the present invention, but airway administration, intravenous administration, rectal administration, subcutaneous administration, intradermal administration, etc. can be exemplified in addition to oral administration. Although 10 to 2000 mg / day is preferable, it is not limited to this value.
[0017]
The anti-influenza virus agent which is the product of the present invention can be used by appropriately diluting and preparing a plant extract exemplified as an active ingredient with a solvent or a dispersant. In some cases, it can be used as an optional preparation such as mouthwash, gargle, inhalant, troche, powder, tablet, suppository, injection, etc. by adding pharmaceutical carriers, emulsifiers, diluents, stabilizers, etc. can do. In this case, the amount of the extract to be added varies depending on the form, but it is preferable that the extract is added in an amount of 0.001 wt% or more, preferably about 0.01 wt% or more.
[0018]
Moreover, the composition which can contribute to influenza prevention can be provided by adsorb | sucking, impregnating, and adding the anti-influenza virus agent of this invention to a mask, an air-conditioner filter, clothing, wet tissue, a spray etc. The amount of adsorbed, impregnated and added plant extract in these applications varies depending on the form of the composition and is difficult to define in general, but it will be in the proportion of 0.001 to 5% by weight. It is suitable to add to.
[0019]
Furthermore, since the plant extract which is an active ingredient of the anti-influenza virus agent of the present invention has high safety, for example, chewing gum, candy, tablet confectionery, gummy jelly, chocolate, biscuits and other confectionery, ice cream, sorbet, ice confectionery etc. It can be blended into foods and drinks such as frozen desserts, beverages, soups and jams and used on a daily basis. The amount added varies depending on the form of use and the taste of the extract, but it is added in an amount of 0.001 to 5% by weight, preferably about 0.01 to 1% by weight, based on the food or drink. Is preferred.
[0020]
【Example】
EXAMPLES The present invention will be specifically described below with reference to examples and test examples, but the present invention is not limited to these examples.
[0021]
[Example 1] Preparation of plant extract Various crushed plants (raspberry, strawberry, blackberry, fig, red aza, agrimony, eucalyptus, peach, apple, violet, black moji, guarana, cotton bud, communis, nazuna, emmeiso, wild Add 500 ml of extraction solvent (water, 50% ethanol, 100% ethanol, acetone, ethyl acetate) to 50 g each of strawberry, hoahound, marsh mallow, plantain, lemon verbena, yarrow, iceland moss, amacha eel, burdock) for 3 hours Reflux extraction was performed. The obtained extract is filtered, concentrated and freeze-dried to obtain the plant extract as the product of the present invention. Table 1 shows the use site of each plant, the extraction solvent, and the yield of the extract obtained.
[0022]
[Table 1]
[0023]
[Test Example 1]
Using the extract, which is the product of the present invention shown in Example 1, as a sample, the influenza virus infection inhibitory effect was examined. As the influenza virus, A / Udon / 307/72 (H3N2) strain was used. A sample stock solution was prepared by dissolving a sample in dimethyl sulfoxide (50 mg / ml). The sample stock solution Tris-Glucose-Saline (TGS) at ten-fold serial dilutions (10 to 6 fold dilution), these sample diluent and virus solution (1000PFU (plaque forming unit) / ml) 1: mixture 1 And reacted at room temperature for 30 minutes. 0.1 ml of this was inoculated into a monolayer culture (35 mm diameter petri dish) of Madin-Darby canine kidney (MDCK) cells, the virus was adsorbed at room temperature for 1 hour, and 2 ml of L-15 agarose medium was poured and solidified at 34 ° C. After culturing for 3 days, the number of plaques produced was counted. The dilution multiple of the sample in which the number of plaques was 50% or less of the TGS-treated control was taken as the infection neutralization value. The influenza virus infection inhibitory activity (infection neutralization value) of the extract of the present invention prepared in Example 1 is shown in Table 2 below. These extracts products of the present invention is any even infection neutralization number of 10 5 or more, it showed a strong viral infection inhibiting effect.
[0024]
[Table 2]
[0025]
Using the plant extract prepared in Example 1, a mouthwash, inhalant, troche, spray, chewing gum, candy, tablet confectionery, and beverage were prepared. The prescription was shown as an Example below.
[0026]
[0027]
[0028]
[0029]
[0030]
[0031]
[0032]
[0033]
[0034]
【The invention's effect】
The anti-influenza virus agent of the present invention contains a highly safe natural product extract, and has a strong infection-suppressing action against influenza virus. Further, since the anti-influenza virus agent of the present invention has high safety, it is widely used in daily life as an anti-influenza virus composition by adsorbing, impregnating, and adding to a mask, air conditioner filter, clothing, wet tissue, spray, etc. Can be used. Furthermore, it can be added to foods and drinks such as chewing gum, candy, tablet confectionery, beverages, etc., and can be used and taken on a daily basis as foods and drinks having an anti-influenza virus action. Therefore, the anti-influenza virus agent of the present invention, the composition containing it, and food and drink are effective for preventing infection of influenza virus and alleviating disease symptoms caused by influenza virus.
Claims (1)
Priority Applications (4)
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JP2002217441A JP4216013B2 (en) | 2002-07-26 | 2002-07-26 | Anti-influenza virus agent |
KR1020030051304A KR101165592B1 (en) | 2002-07-26 | 2003-07-25 | Anti-influenza viral agent, the composition and the food containing the same |
KR1020100093459A KR101084552B1 (en) | 2002-07-26 | 2010-09-27 | Anti-influenza viral agent, the composition and the food containing the same |
KR1020120009164A KR101254168B1 (en) | 2002-07-26 | 2012-01-30 | Anti-influenza viral agent, the composition and the food containing the same |
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JP2002217441A JP4216013B2 (en) | 2002-07-26 | 2002-07-26 | Anti-influenza virus agent |
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JP4216013B2 true JP4216013B2 (en) | 2009-01-28 |
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Cited By (1)
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WO2022065983A3 (en) * | 2020-09-28 | 2022-05-19 | 한국한의학연구원 | Coronavirus infection preventing or treating composition comprising gynostemma pentaphyllum extract |
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DE10359384A1 (en) * | 2003-12-18 | 2005-07-28 | Anoxymer Gmbh | Use of an extract of Aloysia triphylla as matrix protector |
JP4669670B2 (en) * | 2004-06-04 | 2011-04-13 | 株式会社ロッテ | Anti-influenza virus agent and influenza infection suppression product obtained by adsorbing, impregnating and adding the same |
JP4306586B2 (en) | 2004-10-26 | 2009-08-05 | トヨタ自動車株式会社 | Valve characteristic control device for internal combustion engine |
JP5064731B2 (en) * | 2005-07-22 | 2012-10-31 | 株式会社ファンケル | Antihypertensive |
HUP0500947A2 (en) * | 2005-10-14 | 2007-08-28 | Mendon Trade & Commerce Lc | Composition for treatment of paradontosis |
JP5002588B2 (en) * | 2006-04-27 | 2012-08-15 | ユーハ味覚糖株式会社 | Arteriosclerosis inhibitor |
GB0808974D0 (en) * | 2008-05-16 | 2008-06-25 | Veritron Ltd | Plant extract and its therapeutic use |
JP5996837B2 (en) | 2010-05-28 | 2016-09-21 | 小林製薬株式会社 | Influenza virus infection inhibitor |
JP5776364B2 (en) * | 2011-06-22 | 2015-09-09 | ライオン株式会社 | Antimicrobial agents, oral compositions and their applications |
WO2013027245A1 (en) | 2011-08-24 | 2013-02-28 | 株式会社ロッテ | Influenza virus infection inhibitor |
KR101647323B1 (en) * | 2014-09-05 | 2016-08-11 | 경상대학교 산학협력단 | Virucidal composition containing natural products for avian inflenza virus |
RU2580305C1 (en) * | 2015-02-26 | 2016-04-10 | Федеральное бюджетное учреждение науки "Государственный научный центр вирусологии и биотехнологии "Вектор" (ФБУН ГНЦ ВБ "Вектор") | ANTIVIRAL AGENT BASED ON DRY EXTRACT OF LICHEN Cetraria islandica |
ES2811951T3 (en) * | 2015-04-01 | 2021-03-15 | Zeller Max Soehne Ag | Butterbur extract and composition to treat viral infections |
CZ307823B6 (en) * | 2016-07-14 | 2019-05-29 | DG PHARMA, s.r.o. | Herbal extract and its use |
JP2018118959A (en) * | 2017-01-20 | 2018-08-02 | 養命酒製造株式会社 | Antimicrobial composition having lindera umbellate as source material |
WO2020017619A1 (en) | 2018-07-20 | 2020-01-23 | 株式会社 資生堂 | Virus inactivating agent |
KR102386936B1 (en) * | 2020-01-15 | 2022-04-13 | 한국수목원정원관리원 | Composition containing extract of butterbur as an active ingredient for preventing, alleviating or treating sepsis |
KR102540384B1 (en) * | 2022-10-25 | 2023-06-05 | 한국 한의학 연구원 | Composition for preventing, ameliorating or treating coronavirus infectious disease comprising herbal medicine extract as effective component |
US11813287B1 (en) | 2023-03-10 | 2023-11-14 | King Faisal University | Covid-19 binding aerosols |
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JP4127875B2 (en) | 1997-06-11 | 2008-07-30 | 株式会社ロッテ | Anti-Helicobacter pylori |
JP3978517B2 (en) | 1997-07-25 | 2007-09-19 | 株式会社ロッテ | Anti-Legionella composition |
JP4013017B2 (en) * | 1999-01-22 | 2007-11-28 | 三栄源エフ・エフ・アイ株式会社 | Anti-fading agent for anthocyanin pigment and food containing the same |
JP2001328941A (en) * | 2000-05-22 | 2001-11-27 | Yanai Yoshiaki | Antiviral agent |
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WO2022065983A3 (en) * | 2020-09-28 | 2022-05-19 | 한국한의학연구원 | Coronavirus infection preventing or treating composition comprising gynostemma pentaphyllum extract |
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JP2004059463A (en) | 2004-02-26 |
KR20100121579A (en) | 2010-11-18 |
KR20040010390A (en) | 2004-01-31 |
KR101254168B1 (en) | 2013-04-18 |
KR101165592B1 (en) | 2012-07-23 |
KR20120027040A (en) | 2012-03-20 |
KR101084552B1 (en) | 2011-11-17 |
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