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首页> 外文期刊>Journal of Immunological Methods >Development of a rapid, sensitive, dye immunoassay for schistosomiasis diagnosis: a colloidal dye immunofiltration assay.
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Development of a rapid, sensitive, dye immunoassay for schistosomiasis diagnosis: a colloidal dye immunofiltration assay.

机译:用于血吸虫病诊断的快速,灵敏的染料免疫测定法的开发:胶体染料免疫过滤法。

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The colloidal dye immunofiltration assay (CDIFA) combines the concepts of the double-antigen sandwich assay, the Dot immunofiltration assay, and colloidal dye-linked antigen technique to produce a new dye immunoassay for antibody detection in schistosomiasis. The CDIFA consisted of soluble egg antigen (SEA) of Schistosoma japonicum coated onto nitrocellulose membrane, mounted on a flow-through test device to provide the assay capture matrix. SEA absorbed to a red colloidal dye, R-3, produced in China, served as the antigen-antibody complex detecting reagents. The results showed that the sensitivity of the CDIFA was 100% in 35 cases of acute schistosomiasis (35/35), 98% in 50 cases of chronic schistosomiasis (49/50). The specificity of the assay was 99.4% in 180 healthy individuals (179/180). The cross-reaction was 13.3% in 30 cases of paragonimiasis, 2.6% in 38 cases of clonorchiasis sinensis and 0% in 20 cases of hookworm infection, 20 cases of fasciolopsiasis and 16 cases of ascariasis. The results were similar to those detected by routine enzyme-linked immunosorbent assay (ELISA). In a field evaluation of the CDIFA kit, the positivity rate of the CDIFA was 97.5% in 157 cases of schistosomiasis, compared with 91.1% with the circumoval precipitin test (COPT). The dye-labeled SEA conjugate was stable at room temperature for at least 6 months. The results indicated that the CDIFA provided an economic, simple, rapid, robust test for the detection of schistosome infection, suitable for a wide variety of field applications without any instrumentation.
机译:胶体染料免疫过滤测定法(CDIFA)结合了双抗原夹心测定,Dot免疫过滤测定和胶体染料连接抗原技术的概念,从而为血吸虫病中的抗体检测提供了一种新的染料免疫测定法。 CDIFA由涂在硝酸纤维素膜上的日本血吸虫的可溶性卵抗原(SEA)组成,安装在流通测试设备上以提供分析捕获基质。 SEA被吸收到中国生产的红色胶体染料R-3中,用作抗原-抗体复合物检测试剂。结果显示,CDIFA敏感性在35例急性血吸虫病中为100%(35/35),在50例慢性血吸虫病中为98%(49/50)。该测定的特异性在180名健康个体中为99.4%(179/180)。 30例肺吸虫病的交叉反应为13.3%,中华支气管扩张病的交叉反应为2.6%,钩虫感染的20例为20%,筋膜软化症为16例,as虫感染为0%。结果类似于通过常规酶联免疫吸附测定(ELISA)检测到的结果。在CDIFA试剂盒的现场评估中,在157例血吸虫病病例中,CDIFA阳性率为97.5%,相比之下,经环皮沉淀试验(COPT)的阳性率为91.1%。染料标记的SEA共轭物在室温下稳定至少6个月。结果表明,CDIFA为检测血吸虫病感染提供了一种经济,简单,快速,可靠的测试方法,适用于无需任何仪器的多种现场应用。

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