首页> 外文期刊>Kurume Medical Journal >Evaluation of Third Generation Anti-HCV Test Kit (SYNPEPTM HCV-EIA II) Using Sera of Inhabitants from HCV Hyperendemic Area
【24h】

Evaluation of Third Generation Anti-HCV Test Kit (SYNPEPTM HCV-EIA II) Using Sera of Inhabitants from HCV Hyperendemic Area

机译:使用HCV高流行区居民的血清评估第三代抗HCV测试试剂盒(SYNPEPTM HCV-EIA II)

获取原文
       

摘要

We examined the characteristics and usefulness of a third generation anti-HCV test kit, SYNPEPTM HCV-EIA II (Kyokuto Pharmaceutical Inc., Tokyo, Japan). The sera of inhabitants from a hepatitis C virus (HCV) hyperendemic area were used. The kit had even or more anti-HCV detection sensitivity and reproducibility than ORTHO HCVIII ELISA Test SystemTM (Ortho-Clinical Diagnostic K.K., Tokyo, Japan) or HCV PHA 2nd GenerationTM (Dinabot Co., Ltd., Tokyo, Japan). SYNPEPTM HCV-EIA II needed less total reaction time than other EIA kits, resulting in a simple procedure. Also, HCV RNA was detected in 90% of subjects who had a 7.5 or greater cut-off index (COI) of SYNPEPTM HCV-EIA II kit. In conclusion, SYNPEPTM HCV-EIA II require cheap cost and simple procedure and it could be applied to mass screening to find out HCV RNA positive persons who may need clinical care.
机译:我们检查了第三代抗HCV检测试剂盒SYNPEPTM HCV-EIA II(日本东京都京九制药公司)的特性和实用性。使用了丙型肝炎病毒(HCV)高流行区居民的血清。与ORTHO HCVIII ELISA Test SystemTM(日本东京Ortho-Clinical Diagnostic K.K.)或HCV PHA 2nd GenerationTM(日本东京的Dinabot Co.,Ltd)相比,该试剂盒具有甚至更高的抗HCV检测灵敏度和可重复性。 SYNPEPTM HCV-EIA II与其他EIA试剂盒相比,所需的总反应时间更少,因此操作步骤简单。此外,在SYNPEPTM HCV-EIA II试剂盒的7.5或更高的截断指数(COI)的受试者中,有90%的受试者检测到HCV RNA。综上所述,SYNPEPTM HCV-EIA II成本低廉且操作简单,可用于大规模筛查以发现可能需要临床护理的HCV RNA阳性患者。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号