Literature DB >> 16322722

Blood plasma separation in microfluidic channels using flow rate control.

Sung Yang1, Akif Undar, Jeffrey D Zahn.   

Abstract

Several studies have clearly shown that cardiac surgery induces systemic inflammatory responses, particularly when cardiopulmonary bypass (CPB) is used. CPB induces complex inflammatory responses. Considerable evidence suggests that systemic inflammation causes many postoperative complications. Currently, there is no effective method to prevent this systemic inflammatory response syndrome in patients undergoing CPB. The ability to clinically intervene in inflammation, or even study the inflammatory response to CPB, is limited by the lack of timely measurements of inflammatory responses. In this study, a microfluidic device for continuous, real-time blood plasma separation, which may be integrated with downstream plasma analysis device, is introduced. This device is designed to have a whole blood inlet, a purified plasma outlet, and a concentrated blood cell outlet. The device is designed to separate plasma with up to 45% hematocrit of the inlet blood and is analyzed using computational fluid dynamics simulation. The simulation results show that 27% and 25% of plasma can be collected from the total inlet blood volume for 45% and 39% hematocrit, respectively. The device's functionality was demonstrated using defibrinated sheep blood (hematocrit=39%). During the experiment, all the blood cells traveled through the device toward the concentrated blood outlet while only the plasma flowed towards the plasma outlet without any clogging or lysis of cells. Because of its simple structure and control mechanism, this microdevice is expected to be used for highly efficient, realtime, continuous cell-free plasma separation.

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Year:  2005        PMID: 16322722     DOI: 10.1097/01.mat.0000178962.69695.b0

Source DB:  PubMed          Journal:  ASAIO J        ISSN: 1058-2916            Impact factor:   2.872


  7 in total

1.  International conference on pediatric mechanical circulatory support systems and pediatric cardiopulmonary perfusion: outcomes and future directions.

Authors:  Akif Undar
Journal:  ASAIO J       Date:  2008 Mar-Apr       Impact factor: 2.872

2.  Microfluidic blood plasma separation via bulk electrohydrodynamic flows.

Authors:  Dian R Arifin; Leslie Y Yeo; James R Friend
Journal:  Biomicrofluidics       Date:  2007-01-01       Impact factor: 2.800

3.  OPTIMIZATION OF A MICROFLUIDIC DEVICE FOR DIFFUSION-BASED EXTRACTION OF DMSO FROM A CELL SUSPENSION.

Authors:  K K Fleming Glass; E K Longmire; A Hubel
Journal:  Int J Heat Mass Transf       Date:  2008-11       Impact factor: 5.584

4.  High-throughput particle separation and concentration using spiral inertial filtration.

Authors:  Jeffrey M Burke; Rebecca E Zubajlo; Elisabeth Smela; Ian M White
Journal:  Biomicrofluidics       Date:  2014-04-01       Impact factor: 2.800

5.  Multiphoton flow cytometry to assess intrinsic and extrinsic fluorescence in cellular aggregates: applications to stem cells.

Authors:  David G Buschke; Jayne M Squirrell; Hidayath Ansari; Michael A Smith; Curtis T Rueden; Justin C Williams; Gary E Lyons; Timothy J Kamp; Kevin W Eliceiri; Brenda M Ogle
Journal:  Microsc Microanal       Date:  2010-08-05       Impact factor: 4.127

Review 6.  Microfluidics geometries involved in effective blood plasma separation.

Authors:  Anamika Maurya; Janani Srree Murallidharan; Atul Sharma; Amit Agarwal
Journal:  Microfluid Nanofluidics       Date:  2022-09-04       Impact factor: 3.090

Review 7.  Nanomedicine--challenge and perspectives.

Authors:  Kristina Riehemann; Stefan W Schneider; Thomas A Luger; Biana Godin; Mauro Ferrari; Harald Fuchs
Journal:  Angew Chem Int Ed Engl       Date:  2009       Impact factor: 15.336

  7 in total

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