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Development and validation of a low cost blood filtration element separating plasma from undiluted whole blood

机译:低成本血液过滤元件的开发和验证该元件可从未稀释的全血中分离血浆

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摘要

Clinical point of care testing often needs plasma instead of whole blood. As centrifugation is labor intensive and not always accessible, filtration is a more appropriate separation technique. The complexity of whole blood is such that there is still no commercially available filtration system capable of separating small sample volumes (10-100 μl) at the point of care. The microfluidics research in blood filtration is very active but to date nobody has validated a low cost device that simultaneously filtrates small samples of whole blood and reproducibly recovers clinically relevant biomarkers, and all this in a limited amount of time with undiluted raw samples. In this paper, we show first that plasma filtration from undiluted whole blood is feasible and reproducible in a low-cost microfluidic device. This novel microfluidic blood filtration element (BFE) extracts 12 μl of plasma from 100 μl of whole blood in less than 10 min. Then, we demonstrate that our device is valid for clinical studies by measuring the adsorption of interleukins through our system. This adsorption is reproducible for interleukins IL6, IL8, and IL10 but not for TNFα. Hence, our BFE is valid for clinical diagnostics with simple calibration prior to performing any measurement.
机译:临床护理点测试通常需要血浆而不是全血。由于离心是劳动密集型的并且并非总是可及的,因此过滤是更合适的分离技术。全血的复杂性使得在护理时仍没有可分离小样本量(10-100μl)的市售过滤系统。血液过滤中的微流体研究非常活跃,但迄今为止,没有人验证过一种低成本的设备,该设备可同时过滤少量全血样品并可再现地回收临床相关的生物标志物,而所有这些在有限的时间内用未稀释的原始样品进行。在本文中,我们首先表明,在低成本的微流控设备中从未稀释的全血中进行血浆过滤是可行且可重现的。这种新型的微流体血液过滤元件(BFE)可以在不到10分钟的时间内从100微升全血中提取12微升血浆。然后,我们通过测量系统中白介素的吸附量来证明我们的设备可用于临床研究。这种吸附对于白介素IL6,IL8和IL10是可重现的,但对于TNFα则不可重现。因此,我们的BFE在进行任何测量之前,只需简单的校准即可用于临床诊断。

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