scholarly journals Capillary flow-driven microfluidic device with wettability gradient and sedimentation effects for blood plasma separation

2017 ◽  
Vol 7 (1) ◽  
Author(s):  
M. Sneha Maria ◽  
P. E. Rakesh ◽  
T. S. Chandra ◽  
A. K. Sen
2019 ◽  
Vol 209 ◽  
pp. 28-34 ◽  
Author(s):  
L. Spigarelli ◽  
V. Bertana ◽  
D. Marchisio ◽  
L. Scaltrito ◽  
S. Ferrero ◽  
...  

Lab on a Chip ◽  
2016 ◽  
Vol 16 (8) ◽  
pp. 1492-1504 ◽  
Author(s):  
Mokhamad Fakhrul Ulum ◽  
Leni Maylina ◽  
Deni Noviana ◽  
Dedy Hermawan Bagus Wicaksono

Whole blood plasma separation and assay using EDTA-treated cotton thread.


2021 ◽  
Vol 8 (7) ◽  
pp. 94
Author(s):  
Yudong Wang ◽  
Bharath Babu Nunna ◽  
Niladri Talukder ◽  
Ernst Emmanuel Etienne ◽  
Eon Soo Lee

Blood plasma is the most commonly used biofluid in disease diagnostic and biomedical analysis due to it contains various biomarkers. The majority of the blood plasma separation is still handled with centrifugation, which is off-chip and time-consuming. Therefore, in the Lab-on-a-chip (LOC) field, an effective microfluidic blood plasma separation platform attracts researchers’ attention globally. Blood plasma self-separation technologies are usually divided into two categories: active self-separation and passive self-separation. Passive self-separation technologies, in contrast with active self-separation, only rely on microchannel geometry, microfluidic phenomena and hydrodynamic forces. Passive self-separation devices are driven by the capillary flow, which is generated due to the characteristics of the surface of the channel and its interaction with the fluid. Comparing to the active plasma separation techniques, passive plasma separation methods are more considered in the microfluidic platform, owing to their ease of fabrication, portable, user-friendly features. We propose an extensive review of mechanisms of passive self-separation technologies and enumerate some experimental details and devices to exploit these effects. The performances, limitations and challenges of these technologies and devices are also compared and discussed.


Lab on a Chip ◽  
2010 ◽  
Vol 10 (2) ◽  
pp. 211-219 ◽  
Author(s):  
Angeles Ivón Rodríguez-Villarreal ◽  
Martin Arundell ◽  
Manuel Carmona ◽  
Josep Samitier

Author(s):  
Sung Yang ◽  
Akif U¨ndar ◽  
Jeffrey D. Zahn

A microfluidic device for continuous, real time blood plasma separation is introduced. This device is composed of a blood inlet, a purified plasma outlet, and a concentrated blood cell outlet. It is designed to separate blood plasma from an initial blood sample of up to 45 % hematocrit (Hct). The microfluidic device is designed and analyzed using an analogous electrical circuit, analytical and numerical studies. The numerical study results show that 27 % and 25 % of plasma volume can be separated from a total inlet blood volume of 45 % and 39 % hematocrit, respectively. The functionality of this device was demonstrated using defibrinated sheep blood (Hct=36 %). During 2 hrs. of continuous blood infusion through the device, 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. The experimentally measured plasma skimming volume was about 33 % for a 36 % inlet hematocrit. Due to the device’s simple structure and control mechanism, this microdevice is expected to be used for highly efficient continuous, real time cell-free blood plasma separation device.


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