抗柯萨奇 B病毒性心肌炎胶囊复方新制剂对柯萨奇 B3病毒感染的人喉癌上皮细胞的影响 |
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引用本文: | 徐静,姚荣妹,马会霞,李洁,韩淑英,包巨太. 抗柯萨奇 B病毒性心肌炎胶囊复方新制剂对柯萨奇 B3病毒感染的人喉癌上皮细胞的影响[J]. 河北中医, 2013, 0(11): 1697-1699,1702 |
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作者姓名: | 徐静 姚荣妹 马会霞 李洁 韩淑英 包巨太 |
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作者单位: | 1. 河北联合大学2011级硕士研究生,河北 唐山,063000 2. 河北联合大学基础学院药理教研室,河北 唐山,063000 3. 河北联合大学中医学院,河北唐山,063000 |
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基金项目: | “重大新药创制”科技重大专项2009年课题(编号2009 ZX09103-442);河北省科学技术厅2010年度国家科技计划项目配套资金项目 |
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摘 要: | ![]() 目的:观察不同浓度抗柯萨奇B病毒性心肌炎胶囊( K-CoxB-JN)复方新制剂对柯萨奇B3病毒(CVB3)感染人喉癌上皮(Hep-2)细胞的影响。方法首先测定K-CoxB-JN复方新制剂的最大无毒浓度(TC0),再通过K-CoxB-JN复方新制剂不同的加药和加病毒方式,用溴化噻唑蓝四氮唑(MTT)法检测对CVB3感染Hep-2细胞的活性,观察K-CoxB-JN复方新制剂对CVB3感染Hep-2细胞的影响,并采用利巴韦林颗粒对照观察。结果测得K-CoxB-JN复方新制剂TC0为1.5625 mg/mL,利巴韦林颗粒TC0为6.25 mg/mL;当K-CoxB-JN复方新制剂浓度为0.78125 mg/mL、利巴韦林浓度为3.125 mg/mL时对CVB3感染Hep-2细胞保护作用最明显;当K-CoxB-JN复方新制剂浓度为1.5625 mg/mL、利巴韦林颗粒浓度为6.25 mg/mL时直接抗病毒和抑制病毒释放作用最明显,并且表现出良好的量效关系。结论不同浓度的K-CoxB-JN复方新制剂对CVB3感染的Hep-2细胞具有保护作用,能直接抗CVB3病毒,并且能抑制病毒的释放。
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关 键 词: | 心肌炎 柯萨奇病毒感染 动物,实验 |
Effect of new compound preparation of anti-Coxsackie B viral myocarditis capsules on Coxsackie virus B3 with infection of human laryngeal epithelial cells |
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Affiliation: | XU Jing, YAO Rongmei ,MA Huixia ,et al. (2011 Graduate ,Hebei United University , Hebei , Tangshan 063000) |
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Abstract: | ![]() Objective To explore the effect of different concentration new compound preparation of anti -Coxsackie B viral myocarditis capsules on Coxsackie virus B 3 ( CVB3 ) with infection of human laryngeal epithelial (Hep-2) cells.Methods Maximum non -toxic concentrations of anti -Coxsackie B viral myocarditis capsules was detected .Activity of anti-Coxsackie B viral myocarditis capsules for CVB 3 with infection of Hep -2 cells was measured using MTT Methods through different way of dosing and processing virus .The effect of different concen-tration new compound preparation of anti -Coxsackie B viral myocarditis capsules on CVB 3 with infection of Hep-2 cells was observed and the use of ribavirin particles was observed as control at same time .Results Maximum non-toxic concentrations of anti -Coxsackie B viral myocarditis capsules was 1.562 5 mg/mL.Maximum non-toxic con-centrations of ribavirin particles was 6.25 mg/mL.Protection of 0.781 25 mg/mL anti-Coxsackie B viral myocarditis capsules was more obvious on CVB 3 with infection of Hep-2 cells,protection of 3.125 mg/mL ribavirin particles was more obvious on the protection of CVB 3 with infection of Hep-2 cells.1.562 5 mg/mL anti-Coxsackie B viral myo-carditis capsules 6.25 mg/mL ribavirin particles show the most obvious direct antiviral effect and inhibition of virus release.Conclusion Different concentration new compound preparation of anti -Coxsackie B viral myocarditis cap-sules has protection on CVB 3 with infection of Hep -2 cells, can directly resist Coxsackie B 3 virus and inhibit release of the virus . |
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Keywords: | Myocarditis Coxsackie virus infec-tion Animal experiments |
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