期刊文献+
共找到2篇文章
< 1 >
每页显示 20 50 100
放射免疫法研究重组人集成干扰素α的猕猴药动学 被引量:2
1
作者 李红侠 张莉玲 +5 位作者 徐冰 李岱 蔡永明 曾勇 陈拯民 刘昌孝 《中国药学杂志》 CAS CSCD 北大核心 2006年第7期532-534,共3页
目的用放射免疫技术测定血药浓度的方法研究猕猴皮下注射重组人集成干扰素α注射液后的药动学。方法6只健康猕猴皮下注射10μg·kg^-1的重组人集成干扰素α注射液,用放射免疫法检测动物血清中的药物浓度,测定猕猴体内血药浓度并... 目的用放射免疫技术测定血药浓度的方法研究猕猴皮下注射重组人集成干扰素α注射液后的药动学。方法6只健康猕猴皮下注射10μg·kg^-1的重组人集成干扰素α注射液,用放射免疫法检测动物血清中的药物浓度,测定猕猴体内血药浓度并计算药动学参数。结果重组人集成干扰素α在猕猴体内代谢符合一室模型。其药动学参数是:t1/2e(2.67±0.70)h;tmax(4.69±0.84)h,其中雌性猕猴的达峰时间明显比雄性动物短[雌性(3.99±0.23)h;雄性(5.38±0.49)h;P〈0.01];ρmax(3.07±1.77)g·L^-1;AUC0-21h(27.58±13.50)μg·h·L^-1.结论用放射免疫法测定猕猴皮下注射重组人集成干扰素α注射液血药浓度的方法稳定、灵敏度高、特异性强、准确性好,可用于动物和以后临床的药动学研究, 展开更多
关键词 重组人集成干扰素α 药动学 放射免疫法 猕猴
下载PDF
Activity of superior interferon α against HIV-1 in severe combined immunodeficient mice reconstituted with human peripheral blood leukocytes
2
作者 ZHANG Wei TONG Xiao +4 位作者 Tadashi Nakasone YUE Xue-tian Naoki Yamamoto LIU Xin-yuan YANG Rong-ge 《Chinese Medical Journal》 SCIE CAS CSCD 2011年第3期396-400,共5页
Background Interferon (IFN) can inhibit human immunodeficiency virus type 1 (HIV-1) replication in vitro and in clinic.However, IFN therapy for HIV infection was limited by its moderate antiviral efficacy and its ... Background Interferon (IFN) can inhibit human immunodeficiency virus type 1 (HIV-1) replication in vitro and in clinic.However, IFN therapy for HIV infection was limited by its moderate antiviral efficacy and its frequent adverse effects. In the present study we evaluated the anti-HIV efficacy of a novel synthesized superior interferon α (slFNα).Methods We performed in vitro experiments with HIV-1 IIB infected MT4 cells, and evaluated in vivo anti-HIV efficacy of slFNα in severe combined immunodeficient (SClD) mice reconstituted with human peripheral blood leukocytes (hu-PBL-SClD mice).Results We found that the 50% effective concentrations (EC5o) of slFNα against the replication of HIV-1 in MT4 cells was 0.06 ng/ml, representing stronger antiviral activity than interferon-α in vitro. In the hu-PBL-SCID mice, a dose-dependent protection pattern was observed: with 0.45 μg and 1.35 μg slFNα daily treatments, parts of SCID mice were protected from HIV infection, whereas 2.25 μg sIFNα daily treatments resulted in a terminally complete protection.Conclusions slFNα shows good anti-HIV activity both in vitro and in SCID mice, may be a promising anti-HIV agent deserving clinical investigation, especially considering the potential of IFN-α to inhibit HIV replication in patients infected with drug-resistant variants or co-infected with hepatitis C virus (HCV). 展开更多
关键词 human immunodeficiency virus type 1 severe combined immunodeficient mouse interferon-α
原文传递
上一页 1 下一页 到第
使用帮助 返回顶部