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康复新液HPLC指纹图谱建立及6种成分测定 被引量:6
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作者 吕娜 王钧篪 +3 位作者 陈丽华 沈连刚 李广志 斯建勇 《中成药》 CAS CSCD 北大核心 2018年第3期613-617,共5页
目的建立康复新液(美洲大蠊提取物)HPLC指纹图谱,并测定6种成分含有量。方法该药物的分析采用TOSOH TSK-GEL ODS色谱柱(250 mm×4.6 mm,5μm);流动相乙腈-水(含0.07%乙酸),梯度洗脱;体积流量1.0 mL/min;检测波长280 nm。结果 10批样... 目的建立康复新液(美洲大蠊提取物)HPLC指纹图谱,并测定6种成分含有量。方法该药物的分析采用TOSOH TSK-GEL ODS色谱柱(250 mm×4.6 mm,5μm);流动相乙腈-水(含0.07%乙酸),梯度洗脱;体积流量1.0 mL/min;检测波长280 nm。结果 10批样品(Ⅰ~Ⅹ)指纹图谱中有24个共有峰,相似度0.932~0.993(除样品Ⅰ)。尿嘧啶、次黄嘌呤、黄嘌呤、肌苷、原儿茶酸、环(甘氨酰-酪氨酸)分别在3.460~173.0、3.960~198.0、3.596~179.8、1.338~66.9、3.672~183.6、3.552~177.6μg/mL范围内线性关系良好(r>0.999 0),平均加样回收率(RSD)分别为99.8%(2.65%)、98.0%(2.55%)、99.7%(1.59%)、100.7%(2.80%)、102.0%(2.09%)、99.6%(1.88%)。结论该方法准确、稳定、简单,可用于康复新液的质量控制。 展开更多
关键词 康复新液 HPLC指纹图谱 尿嘧啶 次黄嘌呤 黄嘌呤 肌苷 原儿茶酸 环(甘氨酰-酪氨酸)
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Cryptoporic acid E from Cryptoporusvolvatus inhibits influenza virus replication in vitro
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作者 GAO Li HAN Jia-yuan +2 位作者 wang jun-chi SI Jian-yong CAO Li 《中国药理学与毒理学杂志》 CAS CSCD 北大核心 2016年第10期1091-1092,共2页
Influenza virus infection is a global public health issue.The effectiveness of antiviral agents for influenza has been limited by the emergence of drugresistant virus strains.Therefore,there is an urgent need to ident... Influenza virus infection is a global public health issue.The effectiveness of antiviral agents for influenza has been limited by the emergence of drugresistant virus strains.Therefore,there is an urgent need to identify novel antiviral therapies.Our previous studies have found that Cryptoporus volvatus extract could potently inhibit influenza virus replication in vitro and in vivo.However,the effective component of Cryptoporus volvatus which mediated the antiviral activity hasn′t been identified.Here,we identified a novel anti-influenza molecule,cryptoporic acid E(CAE),from Cryptoporus volvatus.Our results showed that CAE had broad-spectrum anti-influenza activity against 2009 pandemic strain A/Beijing/07/2009(H1N1/09),seasonal strain A/Jiangxi/262/05(H3N2),mouse adapted strains A/WSN/33(H1N1)and A/PR8/34(H1N1).We further investigated the mode of CAE action,and found that CAE directlyattenuated influenza virus infectivity.Time-course-analysis indicated that CAE exerted its inhibition mainly at middle stage of the replication cycle of influenza virus.Subsequently,we confirmed that CAE blocked virus RNA replication and transcription in MDCK cells and CAE repressed influenza virus RNA polymerase activity.In addition,we found that CAE impaired influenza virus infectivity by directly targeting virus particles.Our data suggest that CAE is a major effective component of Cryptoporus volvatus and might be a potential candidate for the development of a new anti-influenza virus therapy. 展开更多
关键词 cryptoporic acid E anti-influenza virus effective component in vitro
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