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首页> 外文期刊>Malaria Journal >Label-free microfluidic enrichment of ring-stage Plasmodium falciparum-infected red blood cells using non-inertial hydrodynamic lift
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Label-free microfluidic enrichment of ring-stage Plasmodium falciparum-infected red blood cells using non-inertial hydrodynamic lift

机译:使用非惯性流体动力提升技术无标记地微循环富集环期恶性疟原虫感染的红细胞

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摘要

Background Understanding of malaria pathogenesis caused by Plasmodium falciparum has been greatly deepened since the introduction of in vitro culture system, but the lack of a method to enrich ring-stage parasites remains a technical challenge. Here, a novel way to enrich red blood cells containing parasites in the early ring stage is described and demonstrated. Methods A simple, straight polydimethylsiloxane microchannel connected to two syringe pumps for sample injection and two height reservoirs for sample collection is used to enrich red blood cells containing parasites in the early ring stage (8-10 h p.i.). The separation is based on the non-inertial hydrodynamic lift effect, a repulsive cell-wall interaction that enables continuous and label-free separation with deformability as intrinsic marker. Results The possibility to enrich red blood cells containing P. falciparum parasites at ring stage with a throughput of ~12,000 cells per hour and an average enrichment factor of 4.3?±?0.5 is demonstrated. Conclusion The method allows for the enrichment of red blood cells early after the invasion by P. falciparum parasites continuously and without any need to label the cells. The approach promises new possibilities to increase the sensitivity of downstream analyses like genomic- or diagnostic tests. The device can be produced as a cheap, disposable chip with mass production technologies and works without expensive peripheral equipment. This makes the approach interesting for the development of new devices for field use in resource poor settings and environments, e.g. with the aim to increase the sensitivity of microscope malaria diagnosis.
机译:背景自从引入体外培养系统以来,对恶性疟原虫引起的疟疾发病机理的了解已大大加深,但是缺乏富集环状阶段寄生虫的方法仍然是一项技术挑战。在这里,描述并展示了一种在环形早期富集含有寄生虫的红细胞的新方法。方法使用简单,直的聚二甲基硅氧烷微通道连接两个注射泵以进行样品注射,并使用两个高度容器进行样品收集,以富集早期寄生虫阶段(8-10 h p.i.)中含有寄生虫的红细胞。分离基于非惯性流体动力提升效应,这种排斥性的细胞壁相互作用可实现连续且无标签的分离,并具有可变形性作为内在标记。结果证明了在环形阶段富集含有恶性疟原虫寄生虫的红细胞的可能性,吞噬能力约为每小时12,000个细胞,平均富集因子为4.3?±?0.5。结论该方法可在恶性疟原虫入侵后连续不断地富集红细胞,而无需标记这些细胞。该方法为提高下游分析(如基因组或诊断测试)的灵敏度提供了新的可能性。该器件可以通过批量生产技术制成廉价的一次性芯片,并且无需昂贵的外围设备即可工作。这使得该方法对于开发用于资源贫乏的设置和环境中的现场使用的新设备很有趣。目的是提高显微镜疟疾诊断的敏感性。

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