Microfluidic Platform for Bio-Sample Preparation and Analysis

A special issue of Micromachines (ISSN 2072-666X). This special issue belongs to the section "B:Biology and Biomedicine".

Deadline for manuscript submissions: closed (31 January 2024) | Viewed by 768

Special Issue Editors


E-Mail Website
Guest Editor
Mechanical Engineering, Chosun University, 146 Chosundae-gil, Seoseok-dong, Dong-gu, Gwangju, Republic of Korea
Interests: biomicrofluidics; blood rheology; blood dynamics; lab-on-a-chip

E-Mail Website
Guest Editor
Shu Chien-Gene Lay Department of Bioengineering, University of California, La Jolla, San Diego, CA 92023, USA
Interests: microfluidics; organs-on-chips; biomaterials; bioengineering; aging

Special Issue Information

Dear Colleagues,

Biofluid (i.e., blood, saliva, urine, or sweat) gives clinical information on the status of a patient’s health and disease. For example, red blood cells (RBCs) play an important role in transporting gases and removing wastes between peripheral tissues and capillary vessels. When blood flows in micron-sized capillary channels (i.e., microcirculation), blood flow is determined by fluidic resistance-related factors under certain pressure drop conditions. The fluidic resistance is varied and influenced by biomechanical properties (i.e., hematocrit, viscosity or viscoelasticity, aggregation, deformability, and surface adhesion). These biomechanical properties of blood have been regarded as clinical important biomarkers for screening or diagnosing diseases under in situ or laboratory conditions. For this reason, consistent quantification of blood flow is being considered as an important issue in blood biophysics fields. Recently, microfluidics has been employed to quantify blood flows under blood vessel-mimicking microfluidic channels. When red blood cells are altered into an abnormal physiological state, biophysical properties or morphology parameters (i.e., surface area, volume, or density) become significantly and heterogeneously varied. For early detection, novel microfluidic platforms or medical devices should be addressed to detect small variations or subpopulations in whole blood. This Special Issue welcomes manuscripts related to the following topics, but is not limited to them:

  1. Blood-on-a-chip for quantification of hemorheological properties;
  2. Single cell morphology analysis of bio-sample;
  3. Mathematical modeling under micro-scale physics;
  4. Disposable microfluidic device for POCT test;
  5. Experimental visualization technique under microfluidic platform;
  6. Microfluidic device for quantifying heterogeneity of red blood cells;
  7. Microfluidic device for handing or analyzing biofluids;
  8. Blood-on-a-chip;
  9. Disposable POCT device;
  10. Heterogeneity of RBCs;
  11. On-chip detection of hemorheological properties of blood;
  12. POCT device to evaluate RBCs’ flow properties;
  13. Microfluidic systems with integrated sensors for single-red-blood-cell analysis;

Prof. Dr. Yang Jun Kang
Dr. Ami Mehta-Doshi
Guest Editors

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Keywords

  • blood-on-a-chip for quantification of hemorheological properties
  • single cell morphology analysis of bio-sample
  • mathematical modeling under micro-scale physics
  • disposable microfluidic device for POCT test
  • experimental visualization technique under microfluidic platform
  • microfluidic device for quantifying heterogeneity of red blood cells
  • microfluidic device for handing or analyzing biofluids
  • blood-on-a-chip
  • disposable POCT device
  • heterogeneity of RBCs
  • on-chip detection of hemorheological properties of blood
  • POCT device to evaluate RBCs’ flow properties
  • microfluidic systems with integrated sensors for single-red-blood-cell analysis

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Published Papers

There is no accepted submissions to this special issue at this moment.
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