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用于基于惯性分选的微通道内流动评估:迈向微流控医疗设备的步骤

Assessment of Flow through Microchannels for Inertia-Based Sorting: Steps toward Microfluidic Medical Devices.

作者信息

Natu Rucha, Guha Suvajyoti, Dibaji Seyed Ahmad Reza, Herbertson Luke

机构信息

Division of Applied Mechanics, Office of Science and Engineering Laboratories, Center for Devices and Radiological Health, U.S. Food and Drug Administration, Silver Spring, MD 20993, USA.

出版信息

Micromachines (Basel). 2020 Sep 24;11(10):886. doi: 10.3390/mi11100886.

Abstract

The development of new standardized test methods would allow for the consistent evaluation of microfluidic medical devices and enable high-quality products to reach the market faster. A comprehensive flow characterization study was conducted to identify regulatory knowledge gaps using a generic inertia-based spiral channel model for particle sorting and facilitate standards development in the microfluidics community. Testing was performed using 2-20 µm rigid particles to represent blood elements and flow rates of 200-5000 µL/min to assess the effects of flow-related factors on overall system performance. Two channel designs were studied to determine the variability associated with using the same microchannel multiple times (coefficient of variation (CV) of 27% for Design 1 and 18% for Design 2, respectively). The impact of commonly occurring failure modes on device performance was also investigated by simulating progressive and complete channel outlet blockages. The pressure increased by 10-250% of the normal channel pressure depending on the extent of the blockage. Lastly, two common data analysis approaches were compared-imaging and particle counting. Both approaches were similar in terms of their sensitivity and consistency. Continued research is needed to develop standardized test methods for microfluidic systems, which will improve medical device performance testing and drive innovation in the biomedical field.

摘要

新的标准化测试方法的开发将允许对微流控医疗设备进行一致的评估,并使高质量的产品能够更快地进入市场。进行了一项全面的流动特性研究,以使用基于惯性的通用螺旋通道模型进行颗粒分选来识别监管知识差距,并促进微流控领域的标准制定。使用2 - 20微米的刚性颗粒来代表血液成分,并以200 - 5000微升/分钟的流速进行测试,以评估与流动相关的因素对整个系统性能的影响。研究了两种通道设计,以确定多次使用同一微通道所产生的变异性(设计1的变异系数(CV)为27%,设计2为18%)。还通过模拟渐进性和完全性通道出口堵塞来研究常见故障模式对设备性能的影响。根据堵塞程度,压力会比正常通道压力增加10% - 250%。最后,比较了两种常见的数据分析方法——成像和颗粒计数。两种方法在灵敏度和一致性方面相似。需要持续开展研究以开发微流控系统的标准化测试方法,这将改善医疗设备性能测试并推动生物医学领域的创新。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb78/7598645/d76df145f8f9/micromachines-11-00886-g001.jpg

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