Department of Electrical and Computer Engineering, Rutgers, The State University of New Jersey, Piscataway, NJ, 08854, USA.
Department of Biomedical Engineering, Rutgers, The State University of New Jersey, Piscataway, NJ, 08854, USA.
Sci Rep. 2020 Apr 9;10(1):6109. doi: 10.1038/s41598-020-62894-z.
Multiplexing allows quantifying multiple analytes in a single step, providing advantages over individual testing through shorter processing time, lower sample volume, and reduced cost per test. Currently, flow cytometry is the gold standard for biomedical multiplexing, but requires technical training, extensive data processing, and expensive operational and capital costs. To solve this challenge, we designed digital barcoded particles and a microfluidic architecture for multiplexed analyte quantification. In this work, we simulate and model non-fluorescence-based microfluidic impedance detection with a single excitation and detection scheme using barcoded polymer microparticles. Our barcoded particles can be designed with specific coding regions and generate numerous distinct patterns enabling digital barcoding. We found that signals based on adhered microsphere position and relative orientation were evaluated and separated based on their associated electrical signatures and had a 7 µm microsphere limit of detection. Our proposed microfluidic system can enumerate micron-sized spheres in a single assay using barcoded particles of various configurations. As representation of blood cells, the microsphere concentrations may provide useful information on disease onset and progression. Such sensors may be used for diagnostic and management of common critical care diseases like sepsis, acute kidney injury, urinary tract infections, and HIV/AIDS.
多重检测可在单个步骤中定量检测多种分析物,通过缩短处理时间、减少样本量和降低每个检测的成本,优于单个检测。目前,流式细胞术是生物医学多重检测的金标准,但需要技术培训、大量的数据处理以及昂贵的运营和资本成本。为了解决这一挑战,我们设计了数字编码颗粒和微流控架构,用于多重分析物定量。在这项工作中,我们使用编码聚合物微球,通过单一激发和检测方案模拟和建模基于非荧光的微流控阻抗检测。我们的编码颗粒可以设计有特定的编码区域,并产生许多不同的模式,实现数字编码。我们发现,基于粘附微球位置和相对取向的信号可以根据其相关的电信号特征进行评估和分离,具有 7 µm 微球的检测限。我们提出的微流控系统可以使用各种配置的编码颗粒在单个测定中对微米级球体进行计数。作为血细胞的代表,微球浓度可能提供有关疾病发作和进展的有用信息。此类传感器可用于诊断和管理常见的重症监护疾病,如脓毒症、急性肾损伤、尿路感染和 HIV/AIDS。