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使用硅微结构进行核酸浓缩的快速自动化核酸探针检测。

Rapid, automated nucleic acid probe assays using silicon microstructures for nucleic acid concentration.

作者信息

Christel L A, Petersen K, McMillan W, Northrup M A

机构信息

Cepheid, Sunnyvale, CA 94089, USA.

出版信息

J Biomech Eng. 1999 Feb;121(1):22-7. doi: 10.1115/1.2798037.

Abstract

A system for rapid point-of-use nucleic acid (NA) analysis based on PCR techniques is described. The extraction and concentration of DNA from test samples has been accomplished utilizing silicon fluidic microchips with high surface-area-to-volume ratios. Short (500 bp) and medium size (48,000 bp) DNA have been captured, washed, and eluted using the silicon dioxide surfaces of these chips. Chaotropic (GuHCl) salt solutions were used as binding agents. Wash and elution agents consisted of ethanol-based solutions and water, respectively. DNA quantities approaching 40 ng/cm2 of binding area were captured from input solutions in the 100-1000 ng/mL concentration range. For dilute samples of interest for pathogen detection, PCR and gel electrophoresis were used to demonstrate extraction efficiencies of about 50 percent, and concentration factors of about 10x using bacteriophage lambda DNA as the target. Rapid, multichannel PCR thermal cycling modules with integrated solid-state detection components have also been demonstrated. These results confirm the viability of utilizing these components as elements of a compact, disposable cartridge system for the detection of NA in applications such as clinical diagnostics, biowarfare agent detection, food quality control, and environmental monitoring.

摘要

本文描述了一种基于PCR技术的用于快速现场核酸(NA)分析的系统。利用具有高表面积与体积比的硅流体微芯片完成了从测试样品中提取和浓缩DNA的工作。短片段(500 bp)和中等大小片段(48,000 bp)的DNA已通过这些芯片的二氧化硅表面进行了捕获、洗涤和洗脱。离液盐(GuHCl)溶液用作结合剂。洗涤和洗脱剂分别由乙醇基溶液和水组成。在100 - 1000 ng/mL浓度范围内的输入溶液中,从结合面积接近40 ng/cm²的区域捕获到了DNA。对于用于病原体检测的稀释样品,使用PCR和凝胶电泳证明了提取效率约为50%,以噬菌体λDNA为靶标时浓缩因子约为10倍。还展示了具有集成固态检测组件的快速多通道PCR热循环模块。这些结果证实了将这些组件用作紧凑型一次性试剂盒系统的元件用于临床诊断、生物战剂检测、食品质量控制和环境监测等应用中检测NA的可行性。

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