Inertial blood fractionation using cascaded spiral microfluidics

Blood consists of many components with different sizes, such as bacteria (~ 1 μm), platelets (~ 2 – 3 μm), red blood cells (RBCs, 6 – 8 μm) and neutrophils (~ 10 – 12 μm). In clinical diagnosis, isolating dysfunctional blood components requires manual and laborious centrifugation, which is not frien...

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Main Author: Lim, Bing Qian
Other Authors: Hou Han Wei
Format: Final Year Project
Language:English
Published: Nanyang Technological University 2022
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Online Access:https://hdl.handle.net/10356/158767
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Institution: Nanyang Technological University
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spelling sg-ntu-dr.10356-1587672022-06-05T23:56:44Z Inertial blood fractionation using cascaded spiral microfluidics Lim, Bing Qian Hou Han Wei School of Mechanical and Aerospace Engineering hwhou@ntu.edu.sg Engineering::Mechanical engineering Blood consists of many components with different sizes, such as bacteria (~ 1 μm), platelets (~ 2 – 3 μm), red blood cells (RBCs, 6 – 8 μm) and neutrophils (~ 10 – 12 μm). In clinical diagnosis, isolating dysfunctional blood components requires manual and laborious centrifugation, which is not friendly to point-of-care applications. Herein, we have developed an automatable blood fractionation microfluidic device which can fractionate bacteria, RBCs, and neutrophils simultaneously. Two types of 2-staged cascaded spiral microfluidic devices were designed based on principles of Hi-Resolution (HiDFF) and Dean Flow Fractionation (DFF) reported previously. In design 1, small particles (e.g. bacteria) laterally migrated to inner wall of stage 1 junction were first sorted based on the HiDFF principle. At stage 2 junction, medium-sized particles (e.g. RBCs) migrating relatively slower were separated from the slowest large particles (e.g. neutrophils). In design 2, the stage 2 junction was modified based on the DFF principles, where larger particles were inertially focused at the inner wall while the medium-sized particles continued recirculating towards the outer wall at higher flowrates. Device characterisation was conducted using microscopic imaging of fluorescent microbeads, diluted blood, lysed blood, and purified neutrophils. In design 1, RBCs slightly overflowed into the neutrophil outlet due to high cell concentration in blood. In design 2, separation resolution was relatively lower due to reduced size difference between RBCs and deformed neutrophils under high flowrates. In future work, increasing stage 2 channel length of design 2 can improve separation resolution by reducing flowrates and minimizing neutrophil deformation. Bachelor of Engineering (Mechanical Engineering) 2022-06-04T11:56:03Z 2022-06-04T11:56:03Z 2022 Final Year Project (FYP) Lim, B. Q. (2022). Inertial blood fractionation using cascaded spiral microfluidics. Final Year Project (FYP), Nanyang Technological University, Singapore. https://hdl.handle.net/10356/158767 https://hdl.handle.net/10356/158767 en B081 application/pdf Nanyang Technological University
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Engineering::Mechanical engineering
spellingShingle Engineering::Mechanical engineering
Lim, Bing Qian
Inertial blood fractionation using cascaded spiral microfluidics
description Blood consists of many components with different sizes, such as bacteria (~ 1 μm), platelets (~ 2 – 3 μm), red blood cells (RBCs, 6 – 8 μm) and neutrophils (~ 10 – 12 μm). In clinical diagnosis, isolating dysfunctional blood components requires manual and laborious centrifugation, which is not friendly to point-of-care applications. Herein, we have developed an automatable blood fractionation microfluidic device which can fractionate bacteria, RBCs, and neutrophils simultaneously. Two types of 2-staged cascaded spiral microfluidic devices were designed based on principles of Hi-Resolution (HiDFF) and Dean Flow Fractionation (DFF) reported previously. In design 1, small particles (e.g. bacteria) laterally migrated to inner wall of stage 1 junction were first sorted based on the HiDFF principle. At stage 2 junction, medium-sized particles (e.g. RBCs) migrating relatively slower were separated from the slowest large particles (e.g. neutrophils). In design 2, the stage 2 junction was modified based on the DFF principles, where larger particles were inertially focused at the inner wall while the medium-sized particles continued recirculating towards the outer wall at higher flowrates. Device characterisation was conducted using microscopic imaging of fluorescent microbeads, diluted blood, lysed blood, and purified neutrophils. In design 1, RBCs slightly overflowed into the neutrophil outlet due to high cell concentration in blood. In design 2, separation resolution was relatively lower due to reduced size difference between RBCs and deformed neutrophils under high flowrates. In future work, increasing stage 2 channel length of design 2 can improve separation resolution by reducing flowrates and minimizing neutrophil deformation.
author2 Hou Han Wei
author_facet Hou Han Wei
Lim, Bing Qian
format Final Year Project
author Lim, Bing Qian
author_sort Lim, Bing Qian
title Inertial blood fractionation using cascaded spiral microfluidics
title_short Inertial blood fractionation using cascaded spiral microfluidics
title_full Inertial blood fractionation using cascaded spiral microfluidics
title_fullStr Inertial blood fractionation using cascaded spiral microfluidics
title_full_unstemmed Inertial blood fractionation using cascaded spiral microfluidics
title_sort inertial blood fractionation using cascaded spiral microfluidics
publisher Nanyang Technological University
publishDate 2022
url https://hdl.handle.net/10356/158767
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