Abstract

Bacterial culture methods, e.g. Plate Counting Method (PCM), are a gold standard in the assessment of microbial contamination in multitude of human industries. They are however slow, labor intensive, and prone to manual errors. Dielectrophoresis (DEP) has shown great promise for particle separation for decades; however, it has not yet been widely applied in routine laboratory setting. This paper provides an overview of a new DEP microbial capture and separation method called Fluid-Screen (FS), that achieves very fast, efficient, reliable and repeatable capture and separation of microbial cells. Method verification experiments demonstrated that the FS system captured 100% of bacteria in test samples, a capture efficiency much higher than previously reported for similar technology. Data generated supports the superiority of the FS method as compared to the established Plate Counting Method (PCM), that is routinely used to detect bacterial contamination in healthcare, pharmacological and food industries. We demonstrate that the FS method is universal and can capture and separate different species of bacteria and fungi to viruses, from various sample matrices (i.e. human red blood cells, mammalian cells).

Highlights

  • Bacterial culture methods, e.g. Plate Counting Method (PCM), are a gold standard in the assessment of microbial contamination in multitude of human industries

  • We provide a brief overview of the design of the FS system followed a detailed verification of the FS method (“Verification of the fluid-screen method” section)

  • We have presented Fluid-Screen (FS)—a new dielectrophoretic method for universal microbial capture

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Summary

Introduction

E.g. Plate Counting Method (PCM), are a gold standard in the assessment of microbial contamination in multitude of human industries. They are slow, labor intensive, and prone to manual errors. Data generated supports the superiority of the FS method as compared to the established Plate Counting Method (PCM), that is routinely used to detect bacterial contamination in healthcare, pharmacological and food industries. We establish that the FS method is universal and captures very diverse particles from different cells to viruses (“The repeatability of bacterial capture with the fluid screen system” section), and can separate bacteria from physiologically relevant fluids (i.e. human red blood cells) We summarize and discuss our results and the applications of the Fluid-Screen system in “Discussion” section

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