TW201501718A - Cordyceps formosana extract used for preparation of medicament for resisting respiratory viruses - Google Patents

Cordyceps formosana extract used for preparation of medicament for resisting respiratory viruses Download PDF

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TW201501718A
TW201501718A TW102123785A TW102123785A TW201501718A TW 201501718 A TW201501718 A TW 201501718A TW 102123785 A TW102123785 A TW 102123785A TW 102123785 A TW102123785 A TW 102123785A TW 201501718 A TW201501718 A TW 201501718A
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cordyceps
extract
formosana
respiratory
taiwan
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TWI541018B (en
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Zhen-Xiang Gao
Sheng-Hong Cai
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Mucho Biotech Co Ltd
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Abstract

The present invention discloses a Cordyceps formosana extract used for the preparation of medicament for resisting respiratory viruses. As proved by experiments, Cordyceps formosana extract shows significant inhibitory effects on respiratory viruses. This indicates that the Cordyceps formosana extract has potential applications in the field of treating respiratory virus infectious diseases and is endowed with major significance for the treatment of respiratory virus infectious diseases. This invention provides experimental basis for using Cordyceps formosana in the clinical treatment of virus infectious disease, which gives a certain guiding significance for the development of anti-respiratory virus drugs and has important reference value.

Description

臺灣蟲草提取物用於製備抗呼吸道病毒的藥物之用途 Use of Taiwan Cordyceps extract for the preparation of anti-respiratory virus drugs

本發明涉及臺灣蟲草提取物用於製備抗呼吸道病毒的藥物之用途 The invention relates to the use of Taiwan Cordyceps extract for preparing anti-respiratory virus medicine

臺灣蟲草(Cordyceps formosana Kobayasi & Shimizu)是1976年7月由日本的小林義雄等在臺灣溪頭的鳳凰山的倒木上首次發現,並於1981年正式命名為臺灣蟲草(Cordyceps formosana Kobayasi & Shimizu),中國大陸也有報導,2002年安徽農大有人在中國大陸黃山發現有臺灣蟲草。2009年7月臺灣慕求生技股份有限公司研發人員在臺灣溪頭採到了臺灣蟲草並進行分離,經有關專家鑒定為臺灣蟲草。申請人成立了臺灣蟲草研究課題組,對臺灣蟲草進行了深入研究,成功地進行了臺灣蟲草菌種的人工發酵,順利地在人工培養基生長子實體,同時利用活的鞘翅目的甲蟲的幼蟲(例如大麥蟲的幼蟲)人工培育出了臺灣蟲草。 Cordyceps formosana Kobayasi & Shimizu was first discovered in July 1976 by Japanese Kobayashi and other males on the fallen wood of Fenghuang Mountain in Xitou, Taiwan. In 1981, it was officially named Cordyceps formosana Kobayasi & Shimizu . There have also been reports in mainland China that in 2002, Anhui Agricultural University discovered that there were Taiwan Cordyceps in Huangshan, China. In July 2009, the research and development personnel of Taiwan Muqi Biotech Co., Ltd. acquired the Cordyceps sinensis in Xitou, Taiwan and separated it. It was identified as Taiwan Cordyceps by relevant experts. The applicant established the Taiwan Cordyceps Research Group to conduct an in-depth study on Cordyceps sinensis, and successfully carried out artificial fermentation of Cordyceps species in Taiwan, successfully growing fruiting bodies in artificial medium, and using live larvae of beetle-like beetles (for example) The larvae of barley worms have artificially cultivated Cordyceps sinensis.

經研究臺灣蟲草中含有較多的生物活性成分,有腺苷、甘露醇、蟲草素、醌茜素、油酸、麥角甾醇、硬脂酸、軟脂酸等化學成份。經研究發現,臺灣蟲草能明顯增強機體免疫功能;具有較強的清除自由基的活性物質;具有較強抗腫瘤活性,還具有抗菌、抗炎、抗氧化等 作用。 It has been studied that Cordyceps sinensis contains more bioactive components, such as adenosine, mannitol, cordycepin, alizarin, oleic acid, ergosterol, stearic acid, palmitic acid and other chemical components. Studies have found that Cordyceps sinensis can significantly enhance the body's immune function; it has strong free radical scavenging active substances; it has strong anti-tumor activity, and also has antibacterial, anti-inflammatory, anti-oxidant, etc. effect.

呼吸道合胞病毒(respiratory syncytial virus,RSV)是世界範圍的引起嬰幼兒毛細支氣管炎和肺炎的常見病原,幾乎所有兒童2歲時都經歷過1次或多次感染,感染的高峰年齡為2個月至8個月。是嬰兒、小齡兒童下呼吸道感染的首要原因,也是年幼兒童因呼吸道疾病住院的首要原因,而且多項研究還表明,嬰兒嚴重RSV感染是以後發生哮喘的高危因素,其嚴重性遠遠超出其他微生物病原。同時還發現RSV感染也是免疫抑制的成年人和老年人的重要病原。 Respiratory syncytial virus (RSV) is a common cause of bronchiolitis and pneumonia in infants worldwide. Almost all children have experienced one or more infections at the age of 2, and the peak age of infection is 2 Month to 8 months. It is the leading cause of lower respiratory tract infection in infants and young children, and the primary cause of hospitalization for young children due to respiratory diseases. Many studies have also shown that severe RSV infection in infants is a risk factor for asthma later, and its severity far exceeds other Microbial pathogens. It has also been found that RSV infection is also an important cause of immunosuppression in adults and the elderly.

而目前對RSV感染缺乏特異有效的治療方法。抗病毒藥物病毒唑(利巴韋林,Ribavirin)是目前FDA批准的唯一用於防治RSV感染的化學治療藥物,但該藥物由於存在骨髓細胞毒性,可引起頭痛、白細胞減少、不可逆貧血、血清膽紅素升高等副作用,其臨床應用受到限制,只嚴格用於高危和病情嚴重的患兒,且近年來其療效倍受爭議。人類單株抗體palivizumab(Synagis®)和靜脈用免疫球蛋白(RSV-IGIV)雖已經註冊使用,療效較好,但由於存在治療費用和血清製品的安全問題,在預防和治療RSV感染時,仍需謹慎考慮,而不能普遍應用於臨床。迄今臨床還沒有疫苗用於預防RSV感染。因此開發研製藥效可靠、毒副作用小的防治RSV感染的藥物,仍是目前國際上有待解決的重要課題之一。 Currently, there is no specific and effective treatment for RSV infection. The antiviral drug ribavirin (ribavirin) is currently the only chemotherapeutic drug approved by the FDA for the prevention and treatment of RSV infection, but it can cause headache, leukopenia, irreversible anemia, serum bile due to bone marrow cytotoxicity. Side effects such as elevated erythropoietin are limited in clinical application, and are only strictly used in high-risk and severely ill children, and their efficacy has been controversial in recent years. Human monoclonal antibodies palivizumab (Synagis ® ) and intravenous immunoglobulin (RSV-IGIV) have been registered for use with good efficacy, but due to the cost of treatment and the safety of serum products, in the prevention and treatment of RSV infection, Careful consideration is needed, but not universally. To date, no vaccine has been used clinically to prevent RSV infection. Therefore, the development of drugs with reliable efficacy and small side effects to prevent and treat RSV infection is still one of the important issues to be solved in the world.

申請人研究發現,臺灣蟲草提取物具有良好的抗RSV作用,目前,未見臺灣蟲草提取物抗RSV作用的相 關研究報導和專利文獻。 Applicant's research found that Taiwan Cordyceps extract has a good anti-RSV effect. At present, there is no anti-RSV effect of Taiwan Cordyceps extract. Research reports and patent documents.

本發明涉及一種臺灣蟲草提取物用於製備抗呼吸道病毒的藥物之用途。 The present invention relates to the use of a Cordyceps sinensis extract for the preparation of a medicament against respiratory viruses.

本發明的目的在於提供一種臺灣蟲草提取物用於製備抗呼吸道病毒的藥物之用途。 It is an object of the present invention to provide a use of a Cordyceps sinensis extract for the preparation of a medicament against respiratory viruses.

本發明的目的是通過如下技術手段實現的:本發明臺灣蟲草提取物是用臺灣蟲草的人工發酵菌絲體或在人工培養基生長子實體或利用鞘翅目的甲蟲的幼蟲人工培育臺灣蟲草,進行乙醇提取,旋轉蒸發得到膏狀物。將以上所得提取物,進行乾燥等方法處理,然後加入常規輔料,按常規的製劑工藝製成藥劑學可接受的任意常規劑型,包括,但不限於膠囊劑、片劑、顆粒劑、凝膠劑、緩釋劑及口服液。 The object of the present invention is achieved by the following technical means: the extract of Taiwan Cordyceps sinensis is artificially fermented mycelium of Cordyceps sinensis or artificially growing fruit body in artificial medium or larvae of coleoptera by artificially cultivating Taiwan Cordyceps for ethanol extraction Rotate to obtain a paste. The above obtained extract is subjected to a treatment such as drying, and then a conventional excipient is added, and any conventional dosage form acceptable for pharmacy is prepared according to a conventional preparation process, including, but not limited to, a capsule, a tablet, a granule, and a gel. , sustained release and oral liquid.

本發明臺灣蟲草提取物為臺灣蟲草的人工發酵菌絲體、利用人工培養基生長子實體或利用鞘翅目的甲蟲的幼蟲人工培育臺灣蟲草經乙醇提取得到的,經抗呼吸道合胞病毒活性實驗表明,具有良好的抑制呼吸道合胞病毒活性的作用。 The Taiwan Cordyceps extract is an artificial fermented mycelium of Cordyceps militaris, an artificial medium for growing fruit bodies or a larva of a coleoptera, and the larvae of the coleoptera are artificially cultivated by ethanol extraction, and the anti-respiratory syncytial virus activity test shows that Good inhibition of respiratory syncytial virus activity.

實驗例1臺灣蟲草的人工發酵菌絲體提取物抑制呼吸道合胞病毒活性實驗Experimental Example 1 Inhibition of Respiratory Syncytial Virus Activity by Artificial Fermentation Mycelium Extract of Cordyceps sinensis

1.細胞毒性試驗 Cytotoxicity test

HEp-2細胞(人喉癌上皮細胞)接種於96孔細胞培養板,置37℃,5% CO2培養箱中培養,待細胞長成單層後,去掉培養液,PBS清洗兩遍,加入0.1 mL以維持液對半稀釋的供試品溶液,同時設0.1 mL維持液為空白對照。繼續置37℃,5% CO2培養箱培養2至5天,每天在顯微鏡下觀察細胞病變情況,包括細胞單層的脫落、變圓、皺縮、胞漿中顆粒和空泡的形成,記錄結果後計算半毒性濃度(TC50)。 HEp-2 cells (human laryngeal carcinoma epithelial cells) were inoculated into a 96-well cell culture plate, cultured at 37 ° C in a 5% CO 2 incubator. After the cells were grown into a single layer, the culture solution was removed, washed twice with PBS, and added. 0.1 mL was used to maintain the liquid half-dilution test solution, and 0.1 mL of the maintenance solution was set as a blank control. Continue to incubate at 37 ° C, 5% CO 2 incubator for 2 to 5 days, observe the cytopathic condition under the microscope every day, including the shedding, rounding, shrinkage, formation of granules and vacuoles in the cytoplasm, record After the results, the half toxicity concentration (TC 50 ) was calculated.

2.抗病毒試驗 2. Antiviral test

HEp-2細胞培養方法同上,去培養液,PBS清洗,加入0.1 mL(1OOTCID50/0.1 mL病毒)病毒懸液和0.1 mL的最大細胞無毒濃度(指在光鏡下觀察檢測到的對細胞不產生毒性的供試品最大濃度)為最高濃度對半稀釋後的供試品溶液,同時以維持液為空白對照。細胞置37℃,5%CO2培養箱中培養2至5天。鏡下檢測病毒引起的細胞病變情況並記錄。以病毒唑為陽性對照藥物。 The HEp-2 cell culture method was the same as above, the culture medium was removed, washed with PBS, and 0.1 mL (1OOTCID 50 /0.1 mL virus) virus suspension and 0.1 mL of the maximum cell non-toxic concentration were added (the cells detected under light microscope were not observed). The maximum concentration of the test product that produces toxicity is the highest concentration of the test solution after the half-dilution, and the maintenance solution is used as a blank control. The cells were cultured at 37 ° C for 2 to 5 days in a 5% CO 2 incubator. The pathological changes caused by the virus were detected under the microscope and recorded. Ribavirin was used as a positive control drug.

計算半數抑制濃度(EC50)和治療指數TI=TC50/EC50Calculate the median inhibitory concentration (EC 50) and a therapeutic index TI = TC 50 / EC 50.

3.臺灣蟲草的人工發酵菌絲體提取物抗呼吸道合胞病毒活性 3. Anti-respiratory syncytial virus activity of artificial fermentation mycelium extract of Cordyceps sinensis

臺灣蟲草的人工發酵菌絲體提取物:取臺灣蟲草的人工發酵菌絲體,經含20%的乙醇提取,旋轉蒸發得膏狀物,即為臺灣蟲草的人工發酵菌絲體提取物。 Artificial fermented mycelium extract of Cordyceps sinensis: The artificial fermented mycelium of Cordyceps sinensis was extracted by 20% ethanol and rotary evaporated to obtain a paste, which is an artificial fermentation mycelium extract of Cordyceps sinensis.

具體結果見表1 表1臺灣蟲草人工發酵菌絲體提取物對呼吸道合胞病毒的抑制作用 The specific results are shown in Table 1. Table 1 Inhibition of Respiratory Syncytial Virus by Extract of Mycelium of Cordyceps Artificial Fermentation

實驗例2臺灣蟲草的子實體提取物抑制呼吸道合胞病毒活性實驗Experimental Example 2 Inhibition of respiratory syncytial virus activity by fruiting body extract of Cordyceps sinensis

1.細胞毒性試驗 Cytotoxicity test

HEp-2細胞(人喉癌上皮細胞)接種於96孔細胞培養板,置37℃,5% CO2培養箱中培養,待細胞長成單層後,去掉培養液,PBS清洗兩遍,加入0.1 mL以維持液對半稀釋的供試品溶液,同時設0.1 mL維持液為空白對照。繼續置37℃,5% CO2培養箱培養2至5天,每天在顯微鏡下觀察細胞病變情況,包括細胞單層的脫落、變圓、皺縮、胞漿中顆粒和空泡的形成,記錄結果後計算半毒性濃度(TC50)。 HEp-2 cells (human laryngeal carcinoma epithelial cells) were inoculated into a 96-well cell culture plate, cultured at 37 ° C in a 5% CO 2 incubator. After the cells were grown into a single layer, the culture solution was removed, washed twice with PBS, and added. 0.1 mL was used to maintain the liquid half-dilution test solution, and 0.1 mL of the maintenance solution was set as a blank control. Continue to incubate at 37 ° C, 5% CO 2 incubator for 2 to 5 days, observe the cytopathic condition under the microscope every day, including the shedding, rounding, shrinkage, formation of granules and vacuoles in the cytoplasm, record After the results, the half toxicity concentration (TC 50 ) was calculated.

2.抗病毒試驗 2. Antiviral test

HEp-2細胞培養方法同上,去培養液,PBS清洗,加入0.1 mL(1OOTCID50/0.1 mL病毒)病毒懸液和0.1 mL的最大細胞無毒濃度(指在光鏡下觀察檢測到的對細胞不產生 毒性的供試品最大濃度)為最高濃度對半稀釋後的供試品溶液,同時以維持液為空白對照。細胞置37℃,5%CO2培養箱中培養2至5天。鏡下檢測病毒引起的細胞病變情況並記錄。以病毒唑為陽性對照藥物。 The HEp-2 cell culture method was the same as above, the culture medium was removed, washed with PBS, and 0.1 mL (1OOTCID 50 /0.1 mL virus) virus suspension and 0.1 mL of the maximum cell non-toxic concentration were added (the cells detected under light microscope were not observed). The maximum concentration of the test product that produces toxicity is the highest concentration of the test solution after the half-dilution, and the maintenance solution is used as a blank control. The cells were cultured at 37 ° C for 2 to 5 days in a 5% CO 2 incubator. The pathological changes caused by the virus were detected under the microscope and recorded. Ribavirin was used as a positive control drug.

計算半數抑制濃度(EC50)和治療指數TI=TC50/EC50Calculate the median inhibitory concentration (EC 50) and a therapeutic index TI = TC 50 / EC 50.

3.臺灣蟲草的子實體提取物抗呼吸道合胞病毒活性 3. Anti-respiratory syncytial virus activity of fruit extracts of Cordyceps sinensis

臺灣蟲草的子實體提取物:取人工培養基上長出臺灣蟲草的子實體,經含50%的乙醇提取,旋轉蒸發得膏狀物,即為臺灣蟲草的子實體提取物。 Fruit body extract of Cordyceps sinensis: Take the fruiting body of Taiwan Cordyceps grown on artificial medium, extract it with 50% ethanol, and spin to obtain the paste, which is the fruiting body extract of Taiwan Cordyceps.

具體結果見表2 The specific results are shown in Table 2.

實驗例3利用鞘翅目的甲蟲的幼蟲(例如大麥蟲幼蟲)人工培育的臺灣蟲草(蟲、草結合體)提取物 抑制呼吸道合胞病毒活性實驗1.細胞毒性試驗 Experimental Example 3 Inhibition of Respiratory Syncytial Virus Activity by Extract of Taiwan Cordyceps (Insect, Grass Combination) Artificially Raised by Coleoptera of the Coleoptera (eg, Barley Larvae) 1. Cytotoxicity Test

HEp-2細胞(人喉癌上皮細胞)接種於96孔細胞培養板,置37℃,5% CO2培養箱中培養,待細胞長成單層後,去掉培養液,PBS清洗兩遍,加入0.1 mL以維持液對半稀釋的供試品溶液,同時設0.1 mL維持液為空白對照。繼續置37℃,5% CO2培養箱培養2至5天,每天在顯微鏡下觀察細胞病變情況,包括細胞單層的脫落、變圓、皺縮、胞漿中顆粒和空泡的形成,記錄結果後計算半毒性濃度(TC50)。 HEp-2 cells (human laryngeal carcinoma epithelial cells) were inoculated into a 96-well cell culture plate, cultured at 37 ° C in a 5% CO 2 incubator. After the cells were grown into a single layer, the culture solution was removed, washed twice with PBS, and added. 0.1 mL was used to maintain the liquid half-dilution test solution, and 0.1 mL of the maintenance solution was set as a blank control. Continue to incubate at 37 ° C, 5% CO 2 incubator for 2 to 5 days, observe the cytopathic condition under the microscope every day, including the shedding, rounding, shrinkage, formation of granules and vacuoles in the cytoplasm, record After the results, the half toxicity concentration (TC 50 ) was calculated.

2.抗病毒試驗 2. Antiviral test

HEp-2細胞培養方法同上,去培養液,PBS清洗,加入0.1 mL(1OOTCID50/0.1 mL病毒)病毒懸液和0.1 mL的最大細胞無毒濃度(指在光鏡下觀察檢測到的對細胞不產生毒性的供試品最大濃度)為最高濃度對半稀釋後的供試品溶液,同時以維持液為空白對照。細胞置37℃,5% CO2培養箱中培養2至5天。鏡下檢測病毒引起的細胞病變情況並記錄。以病毒唑為陽性對照藥物。 The HEp-2 cell culture method was the same as above, the culture medium was removed, washed with PBS, and 0.1 mL (1OOTCID 50 /0.1 mL virus) virus suspension and 0.1 mL of the maximum cell non-toxic concentration were added (the cells detected under light microscope were not observed). The maximum concentration of the test product that produces toxicity is the highest concentration of the test solution after the half-dilution, and the maintenance solution is used as a blank control. The cells were cultured at 37 ° C for 2 to 5 days in a 5% CO 2 incubator. The pathological changes caused by the virus were detected under the microscope and recorded. Ribavirin was used as a positive control drug.

計算半數抑制濃度(EC50)和治療指數TI=TC50/EC50Calculate the median inhibitory concentration (EC 50) and a therapeutic index TI = TC 50 / EC 50.

3.大麥蟲臺灣蟲草提取物抗呼吸道合胞病毒活性 3. Anti-respiratory syncytial virus activity of barley worm Cordyceps sinensis extract

大麥蟲臺灣蟲草提取物:取大麥蟲臺灣蟲草(蟲、草結合體),經含80%的乙醇提取,旋轉蒸發得膏狀物,即為大麥蟲臺灣蟲草提取物。 Barley Cordyceps sinensis extract: Take the barley worm, Taiwan Cordyceps (worm, grass combination), extract it with 80% ethanol, and spin to obtain a paste, which is the barley worm and Taiwan Cordyceps extract.

具體結果見表3 The specific results are shown in Table 3.

從以上實驗結果重複多次都一樣,從以上實驗結果可以看出,臺灣蟲草提取物具有顯著的抗呼吸道合胞病毒(RSV)作用。可以用於藥品的開發與應用。 It is the same from the above experimental results. From the above experimental results, it can be seen that the Cordyceps extract of Taiwan has a significant anti-respiratory syncytial virus (RSV) effect. Can be used in the development and application of pharmaceuticals.

Claims (9)

一種臺灣蟲草(Cordyceps formosana Kobayasi & Shimizu)提取物用於製備抗呼吸道病毒的藥物之用途。 A use of Cordyceps formosana Kobayasi & Shimizu extract for the preparation of a medicament against respiratory viruses. 如請求項1所述之用途,其中呼吸道病毒係指呼吸道合胞病毒(respiratory syncytial virus,RSV)。 The use of claim 1, wherein the respiratory virus is respiratory syncytial virus (RSV). 如請求項1所述之用途,其中臺灣蟲草是用臺灣蟲草的人工發酵菌絲體、利用人工培養基生長子實體或利用鞘翅目的甲蟲的幼蟲人工培育的臺灣蟲草。 The use according to claim 1, wherein the Cordyceps sinensis is an artificially fermented mycelium of Cordyceps militaris, a larvae artificially grown by an artificial medium, or artificially bred by a larva of a coleoptera. 如請求項1所述之用途,其中臺灣蟲草提取物是用含量10%~90%的乙醇提取。 The use according to claim 1, wherein the Cordyceps extract of Taiwan is extracted with ethanol in an amount of 10% to 90%. 如請求項1所述之用途,其中臺灣蟲草提取物是用含量20%~80%的乙醇提取。 The use according to claim 1, wherein the Cordyceps extract of Taiwan is extracted with ethanol in an amount of 20% to 80%. 如請求項3所述之用途,其中臺灣蟲草提取物是用含量10%~90%的乙醇提取。 The use according to claim 3, wherein the Cordyceps extract of Taiwan is extracted with ethanol in an amount of 10% to 90%. 如請求項3所述之用途,其中臺灣蟲草提取物是用含量20%~80%的乙醇提取。 The use according to claim 3, wherein the Cordyceps extract of Taiwan is extracted with ethanol in an amount of 20% to 80%. 如請求項1所述之用途,其中抗呼吸道病毒的藥物為膠囊劑、片劑、顆粒劑、凝膠劑、緩釋劑或口服液。 The use according to claim 1, wherein the anti-respiratory virus drug is a capsule, a tablet, a granule, a gel, a sustained release or an oral solution. 如請求項1至8任一項所述之用途,其中抗呼吸道病毒的藥物的施用劑量係介於1.5 ug/mL至50.0 ug/mL。 The use according to any one of claims 1 to 8, wherein the anti-respiratory virus drug is administered at a dose of from 1.5 ug/mL to 50.0 ug/mL.
TW102123785A 2013-07-03 2013-07-03 Taiwan Cordyceps extract for the manufacture of anti-respiratory virus drugs TWI541018B (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI577383B (en) * 2015-03-24 2017-04-11 慕求生技股份有限公司 Ophiocordyceps formosana isolate and uses thereof

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI577383B (en) * 2015-03-24 2017-04-11 慕求生技股份有限公司 Ophiocordyceps formosana isolate and uses thereof

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