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乙型肝炎免疫球蛋白聚氰基丙烯酸正丁酯纳米粒抑制HBsAg、HBV DNA分泌的体外实验
引用本文:彭忠田,谭德明,黄顺玲,朱平安,刘菲.乙型肝炎免疫球蛋白聚氰基丙烯酸正丁酯纳米粒抑制HBsAg、HBV DNA分泌的体外实验[J].中华传染病杂志,2006,27(1):330-334.
作者姓名:彭忠田  谭德明  黄顺玲  朱平安  刘菲
作者单位:南华大学附属第一医院肝病研究中心,421001;中南大学湘雅医院传染病研究所,长沙,410008;
基金项目:湖南省长沙市科学技术局基金
摘    要:Objective To investigate the inhibitive activities of hepatitis B immunoglobulin(HBIG)poly(butylcynaoacrylate)nanoparticles(HBIG-PBCA-NP)to hepatitis B surface antigen(HBsAg)and hepatitis B virus(HBV)DNA secretions using HBV infected cell model in vitro.Methods HepG 2.2.15 cells were cultured with media containing HBIG-PBCA-NP or HBIG for several days,or cultured with HBIG-PBC-NP and HBIG for 2 days and without HBIG-PBCA-NP and HBIG from day 3.The supernatants at different time points were collected for quantitative detection of HBsAg and HBV DNA.The comparisons between groups were done by variance analysis.Resalts Secretions of HBsAg and HBV DNA in supernatants of HepG2.2.15 cultured with 0.1-10.0 IU/mL of HBIG-PBCA-NP and HBIG were inhibited significantly compared with control group.HBsAg titers and HBV DNA levels in supernatants of HBIG-PBCA-NP group and HBIG group cultured with media without HBIG-PBCA-NP and HBIG kept decreasing at day 5 and 7,then rebounded at day 9 and 11.HBsAg titera in supernatants of 0.1,1.0,5.0 IU/mL HBIG-PBCA-NP group were all significantly different from those in HBIG group at day 9(31.31±1.98)μg/L vs(40.62±2.99)μg/L,(23.79±1.31)μg/L vs(36.51±2.12)μg/L,(19.91±1.74)μg/L vs(33.03±1.65)μg/L;F=412.24,P<0.01].Couclusion HBIG-PBCA-NP can inhibit secretions of HgsAg and HBV DNA in vitro,which is more effective than HBIG.

关 键 词:肝炎  乙型    免疫球蛋白类    氰丙烯酸盐类    脂质体纳米结构    肝炎表面抗原  乙型    DNA  病毒    

Inhibition of hepatitis B surface antigen and hepatitis B virus DNA secretions by hepatitis B immunoglobulin poly(butylcynaoacrylate)nanoparticles in vitro
PENG Zhong-tian,TAN De-ming,HUANG Shun-ling,ZHU Ping-an,LIU Fei.Inhibition of hepatitis B surface antigen and hepatitis B virus DNA secretions by hepatitis B immunoglobulin poly(butylcynaoacrylate)nanoparticles in vitro[J].Chinese Journal of Infectious Diseases,2006,27(1):330-334.
Authors:PENG Zhong-tian  TAN De-ming  HUANG Shun-ling  ZHU Ping-an  LIU Fei
Abstract:
Keywords:Hepatitis BImmunoglobulinsCyanoacrylatesLiposomes  nanostructuresHepatitis B surface antigensDNA  viral
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