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首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >Development of a highly sensitive, quantitative, and rapid detection system for Plasmodium falciparum-infected red blood cells using a fluorescent blue-ray optical system
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Development of a highly sensitive, quantitative, and rapid detection system for Plasmodium falciparum-infected red blood cells using a fluorescent blue-ray optical system

机译:使用荧光蓝射线光学系统开发用于疟原虫感染的红细胞的高敏感,定量和快速检测系统

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A highly sensitive diagnostic system for determining low-density infections that are missed by conventional methods is necessary to detect the carriers of Plasmodium falciparum. A fluorescent blue-ray optical system with a polycarbonate scan disc was developed to detect P. falciparum-infected red blood cells (Pf-iRBCs), and nine samples could be analyzed simultaneously. The cultured P. falciparum strain 3D7 was used to examine the potential of the system for diagnosing malaria. After an RBC suspension had been applied to the disc, the cells were dispersed on the disc by rotation. During the 10 min standing period to allow the RBCs to settle on the disc surface, the cells were simultaneously stained with nuclear fluorescence staining dye Hoechst 34580, which was previously adsorbed on the disc surface. RBCs were arranged on the disc surface as a monolayer by removing excess cells through momentary rotation. Over 1.1 million RBCs remained on the disc for fluorescence analysis. A portable, battery-driven fluorescence image reader was employed to detect fluorescence-positive RBCs for approximately 40 min. A good correlation between examination of Giemsa-stained RBCs by light microscopy and the developed system was demonstrated in the parasitemia range of 0.0001-1.0% by linear regression analysis (R2 = 0.99993). The limit of detection of 0.00020% and good reproducibility for parasitemia determination were observed. The ability of the developed system to detect sub-microscopic low-density Pf-iRBCs and provide accurate quantitative evaluation with easy operation was demonstrated.
机译:用于测定常规方法错过的低密度感染的高敏感性诊断系统是检测疟原虫疟原虫的载体。开发了具有聚碳酸酯扫描盘的荧光蓝射线光学系统以检测P.Malciparum感染的红细胞(PF-IRBCS),并且可以同时分析九个样品。培养的P.Falciparum菌株3D7用于检查系统诊断疟疾的潜力。在将RBC悬浮液施加到盘上后,通过旋转将细胞分散在盘上。在10分钟的站点期间,允许RBC沉降在盘表面上,细胞同时用核荧光染料染料Hoechst 34580染色,所述核荧光染料Hoechst 34580预先吸附在盘表面上。通过瞬间旋转去除多余的细胞,将RBC设置为单层作为单层。超过110万RBC仍然在光盘上进行荧光分析。使用便携式电池驱动的荧光图像读取器检测荧光阳性RBC约40分钟。通过光学显微镜和发达的系统对Giemsa染色的RBC的检查与发达的系统之间的良好相关性,在寄生血症范围内,线性回归分析显示为0.0001-1.0%(R2 = 0.99993)。观察到检测限0.00020%,对寄生虫测定的良好再现性。发达系统检测亚微观低密度PF-IRBCS的能力并提供简单操作的准确定量评估。

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