Abstract

Recent advances in inertial microfluidics designs have enabled high throughput, label-free separation of cells for a variety of bioanalytical applications. Various device configurations have been proposed for binary separation with a focus on enhancing the separation distance between particle streams to improve the efficiency of separate particle collection. These configurations have not demonstrated scaling beyond 3 particle streams either because the channel width is a constraint at the collection outlets or particle streams would be too closely spaced to be collected separately. We propose a method to design collection outlets for inertial focusing and separation devices which can collect closely-spaced particle streams and easily scale to an arbitrary number of collection channels without constraining the outlet channel width, which is the usual cause of clogging or cell damage. According to our approach, collection outlets are a series of side-branching channels perpendicular to the main channel of egress. The width and length of the outlets can be chosen subject to constraints from the position of the particle streams and fluidic resistance ratio computed from fluid dynamics simulations. We show the efficacy of this approach by demonstrating a successful collection of upto 3 particle streams of 7μm, 10μm and 15μm fluorescent beads which have been focused and separated by a spiral inertial device with a separation distance of only 10μm -15μm. With a throughput of 1.8mL/min, we achieved collection efficiency exceeding 90% for each particle at the respective collection outlet. The flexibility to use wide collection channels also enabled us to fabricate the microfluidic device with an epoxy mold that was created using xurography, a low cost, and imprecise fabrication technique.

Highlights

  • Separation of microparticles and cells by size is a key processing step in many microbiological studies and clinical assays.[1]

  • The main contribution of this paper is a method of designing outlets to collect focused, separated and closely-spaced particle streams

  • We have proposed a method for designing microfluidic outlets to collect closelyspaced particle streams from inertial separation devices

Read more

Summary

Introduction

Separation of microparticles and cells by size is a key processing step in many microbiological studies and clinical assays.[1] Microfluidics-based separation methods have been applied to the particle separation task in a myriad of creative ways such as dielectrophoresis,[2] magnetophoresis,[3] acoustic based,[4] fluorescence based,[5] selective trapping with interdigitated channels[6] and deterministic lateral displacement (DLD)[7] with micropillar arrays These techniques do not require special expertise for handling and gained popularity because of low sample volume and reagent consumption. Inertial microfluidics are a recent technological advancement which overcomes the rate-limiting constraints by utilizing microscale fluidic forces at high flow rates to manipulate particles while providing high efficiency

Methods
Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.