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基于表面张力阀的低资源 RNA 提取盒的开发。

Development of a low-resource RNA extraction cassette based on surface tension valves.

机构信息

Department of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee 37235, USA.

出版信息

ACS Appl Mater Interfaces. 2011 Jun;3(6):2161-8. doi: 10.1021/am2004009. Epub 2011 May 31.

Abstract

Nucleic acid-based diagnostics are highly sensitive and specific, but are easily disrupted by the presence of interferents in biological samples. In a laboratory or hospital setting, the influence of these interferents can be minimized using an RNA or DNA extraction procedure prior to analysis. However, in low-resource settings, limited access to specialized instrumentation and trained personnel presents challenges that impede sample preparation. We have developed a self-contained nucleic acid extraction cassette suitable for operation in a low-resource setting. This simple design contains processing solutions preloaded within a continuous length of 1.6 mm inner diameter Tygon tubing. Processing solutions are separated by air gaps and held in place during processing by the surface tension forces at the liquid-air interface, viz. surface tension valves. Nucleic acids preferentially adsorbed to silica-coated magnetic particles are separated from sample interferents using an external magnet to transfer the nucleic acid biomarker through successive solutions to precipitate, wash and elute in the final cassette solution. The efficiency of the extraction cassette was evaluated using quantitative reverse transcriptase PCR (qRT-PCR) following extraction of respiratory syncytial virus (RSV) RNA. RNA was recovered from TE buffer or from lysates of RSV infected HEp-2 cells with 55 and 33% efficiency, respectively, of the Qiagen RNeasy kit. Recovery of RSV RNA from RSV infected HEp-2 cells was similar at 30% of the RNeasy kit. An overall limit of detection after extraction was determined to be nearly identical (97.5%) to a laboratory-based commercially available kit. These results indicate that this extraction cassette design has the potential to be an effective sample preparation device suitable for use in a low-resource setting.

摘要

核酸诊断具有高度的敏感性和特异性,但很容易受到生物样本中干扰物的影响。在实验室或医院环境中,可以在分析之前使用 RNA 或 DNA 提取程序来最小化这些干扰物的影响。然而,在资源有限的环境中,缺乏专用仪器和训练有素的人员会带来阻碍样本制备的挑战。我们开发了一种适用于资源有限环境的独立核酸提取盒。这种简单的设计包含预先加载在 1.6 毫米内径 Tygon 管内的处理溶液。处理溶液通过气隙分离,并在处理过程中通过液体-空气界面的表面张力保持在适当位置,即表面张力阀。优先吸附到硅涂层磁性颗粒上的核酸与样品干扰物分离,然后使用外部磁铁将核酸生物标志物转移通过连续溶液,在最终的试剂盒溶液中沉淀、洗涤和洗脱。使用定量逆转录酶 PCR(qRT-PCR)评估提取盒的效率,方法是提取呼吸道合胞病毒(RSV)RNA。从 TE 缓冲液或 RSV 感染的 Hep-2 细胞裂解物中回收 RNA 的效率分别为 Qiagen RNeasy 试剂盒的 55%和 33%。从 RSV 感染的 Hep-2 细胞中回收 RSV RNA 的效率与 RNeasy 试剂盒的 30%相似。提取后的总检测限确定为与基于实验室的市售试剂盒几乎相同(97.5%)。这些结果表明,这种提取盒设计有可能成为一种有效的样本制备装置,适用于资源有限的环境。

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