scholarly journals High-Throughput, Label-Free Isolation of White Blood Cells From Whole Blood Using Parallel Spiral Microchannels With U-Shaped Cross-Section

2021 ◽  
Author(s):  
Amirhossein Mehran ◽  
Peyman Rostami ◽  
Mohammad Said Saidi ◽  
Bahar Firoozabadi ◽  
Navid Kashaninejad
Keyword(s):  
Cross Section ◽  
High Throughput ◽  
Whole Blood ◽  
Blood Cells ◽  
High Efficiency ◽  
Rectangular Cross Section ◽  
White Blood Cells ◽  
Label Free ◽  
Entire Cross Section ◽  
Shaped Cross Section

Rapid isolation of white blood cells (WBCs) from whole blood is an essential part of any WBC examination platform. However, most conventional cell separation techniques are labor-intensive and low throughput, require large volumes of samples, need extensive cell manipulation, and have low purity. To address these challenges, we report the design and fabrication of a passive, label-free microfluidic device with a unique U-shaped cross-section to separate WBCs from whole blood using hydrodynamic forces that exist in a microchannel with curvilinear geometry. It is shown that the spiral microchannel with a U-shaped cross-section concentrates larger blood cells (e.g., WBCs) in the inner cross-section of the microchannel by moving smaller blood cells (e.g., red blood cells (RBCs) and platelets) to the outer microchannel section and preventing them from returning to the inner microchannel section. Therefore, it overcomes the major limitation of a rectangular cross-section where secondary Dean vortices constantly enforce particles throughout the entire cross-section and decrease its isolation efficiency. Under optimal settings, more than 95% of WBCs can be isolated from whole blood under high-throughput (6 ml/min), high-purity (88%), and high-capacity (180 ml of sample in 1 hour) conditions. High efficiency, fast processing time, and non-invasive WBC isolation from large blood samples without centrifugation, RBC lysis, cell biomarkers, and chemical pre-treatments make this method an ideal choice for downstream cell study platforms.

scholarly journals High-Throughput, Label-Free Isolation of White Blood Cells from Whole Blood Using Parallel Spiral Microchannels with U-Shaped Cross-Section

Biosensors ◽  
2021 ◽  
Vol 11 (11) ◽  
pp. 406
Author(s):  
Amirhossein Mehran ◽  
Peyman Rostami ◽  
Mohammad Said Saidi ◽  
Bahar Firoozabadi ◽  
Navid Kashaninejad
Keyword(s):  
Cross Section ◽  
High Throughput ◽  
Whole Blood ◽  
Blood Cells ◽  
High Efficiency ◽  
Rectangular Cross Section ◽  
White Blood Cells ◽  
Label Free ◽  
Entire Cross Section ◽  
Shaped Cross Section

Rapid isolation of white blood cells (WBCs) from whole blood is an essential part of any WBC examination platform. However, most conventional cell separation techniques are labor-intensive and low throughput, require large volumes of samples, need extensive cell manipulation, and have low purity. To address these challenges, we report the design and fabrication of a passive, label-free microfluidic device with a unique U-shaped cross-section to separate WBCs from whole blood using hydrodynamic forces that exist in a microchannel with curvilinear geometry. It is shown that the spiral microchannel with a U-shaped cross-section concentrates larger blood cells (e.g., WBCs) in the inner cross-section of the microchannel by moving smaller blood cells (e.g., RBCs and platelets) to the outer microchannel section and preventing them from returning to the inner microchannel section. Therefore, it overcomes the major limitation of a rectangular cross-section where secondary Dean vortices constantly enforce particles throughout the entire cross-section and decrease its isolation efficiency. Under optimal settings, we managed to isolate more than 95% of WBCs from whole blood under high-throughput (6 mL/min), high-purity (88%), and high-capacity (360 mL of sample in 1 h) conditions. High efficiency, fast processing time, and non-invasive WBC isolation from large blood samples without centrifugation, RBC lysis, cell biomarkers, and chemical pre-treatments make this method an ideal choice for downstream cell study platforms.

scholarly journals High-Throughput Separation of White Blood Cells From Whole Blood Using Inertial Microfluidics

2017 ◽  
Vol 11 (6) ◽  
pp. 1422-1430 ◽  
Author(s):  
Jun Zhang ◽  
Dan Yuan ◽  
Ronald Sluyter ◽  
Sheng Yan ◽  
Qianbin Zhao ◽  
...  
Keyword(s):  
High Throughput ◽  
Whole Blood ◽  
Blood Cells ◽  
White Blood Cells ◽  
Inertial Microfluidics

EFFECTS OF BLOOD CELLS ON PLATELET AGGREGATION BY IMPEDANCE METHOD

1987 ◽  
Author(s):  
L Mannucci ◽  
R Redaelli ◽  
E Tremoll
Keyword(s):  
Platelet Aggregation ◽  
Whole Blood ◽  
Blood Cells ◽  
White Blood Cells ◽  
Normal Subjects ◽  
Impedance Method ◽  
Induced Aggregation ◽  
Vitro Data ◽  
In Vitro Data

To evaluate the effects of blood cells on the response of platelets to aggregating agents using whole blood impedance aggregometer, studies were carried out on whole blood (WB) of normal subjects and of patients with: polycythemia vera (PV), iatrogenic anemia (IA), primary thrombocytosis (PT), idiopathic thrombotic purpura (ITP), myeloid chronic leukemia (MCL), iatrogenic leukopenia (IL). The in vitro effects of red blood cells (RBC) and of white blood cells (WBC) on platelet rich plasma (PRP) aggregation were also evaluated. WB, PRP, WBC and RBC were prepared by conventional methods. Aggregation was performed using the impedance aggregometer (mod. 540, Chrono Log Corp). In normal subjects the concentration of collagen giving 50 % aggregation (AC50 ) found in PRP did not differ from that of WB, indicating that hematocrit values within the normal range did not appreciably affect platelet aggregation. The results obtained in WB of patients are summarized in the table: In vitro data showed that aggregation in prp in wb of normal subjects was related to the number of platelets present in the sample. RBC added to PRP significant reduced aggregation only when the RBC number was greater than 4.101 cells. No effect of WBC on collagen induced aggregation of PRP was observed, whereas significant inhibition was detected after ADP. It is concluded that the aggregation evaluated in WB with impedance method is dependent on the platelet number. Also, in vitro data and studies in WB of patients indicate that aggregation is significantly affected by the presence of cells other than platelets only in conditions of changes of the ratio between platelets and leukocytes and/or red cells.

Direct freezing of whole blood enables analysis of leucocyte markers by flow cytometry: a proof-of-concept study

2021 ◽  
Author(s):  
Pénélope Bourgoin ◽  
Inès Ait Belkacem ◽  
Isabelle Arnoux ◽  
Pierre-Emmanuel Morange ◽  
Fabrice Malergue
Keyword(s):  
Flow Cytometry ◽  
Whole Blood ◽  
Blood Cells ◽  
White Blood Cells ◽  
Proof Of Concept ◽  
Fresh Blood ◽  
Blood Samples ◽  
Step Flow ◽  
Freezing Method ◽  
One Step

Aim: A new one-step flow cytometry procedure has been recently demonstrated for identifying subjects with infections, but only for fresh whole blood samples. The goal of this study was to assess its applicability on frozen samples, by proposing a new method to perform the sample freezing directly and easily. Methods: Fresh blood was tested, then frozen either directly or with dimethylsulfoxide and serum. Common markers of white blood cells as well as infection-related biomarkers were tested. Results: All percentages of leucocyte subsets and levels of infection-related biomarkers were significantly correlated between frozen and fresh samples. Conclusion: The direct freezing method enables an accurate assessment of common cellular sub-populations and of levels of important infectious biomarkers via flow cytometry.

scholarly journals Analysis of the dynamics of Staphylococcus aureus binding to white blood cells using whole blood assay and geno-to-pheno mapping

2020 ◽  
Vol 310 (3) ◽  
pp. 151411
Author(s):  
Daria Gaidar ◽  
Alice Jonas ◽  
Ruslan Akulenko ◽  
Ulla Ruffing ◽  
Mathias Herrmann ◽  
...  
Keyword(s):  
Staphylococcus Aureus ◽  
Whole Blood ◽  
Blood Cells ◽  
White Blood Cells ◽  
Whole Blood Assay ◽  
Blood Assay

Smoothed Particle Hydrodynamics Simulations of Whole Blood in Three-Dimensional Shear Flow

2020 ◽  
Vol 17 (10) ◽  
pp. 2050009
Author(s):  
Sisi Tan ◽  
Mingze Xu
Keyword(s):  
Shear Flow ◽  
Smoothed Particle Hydrodynamics ◽  
Whole Blood ◽  
Blood Cells ◽  
White Blood Cells ◽  
Three Dimensional ◽  
Immersed Boundary ◽  
Particle Hydrodynamics ◽  
Sph Model ◽  
Smoothed Particle

Numerical modeling of whole blood still faces great challenges although significant progress has been achieved in recent decades, because of the large differences of physical and geometric properties among blood components, including red blood cells (RBCs), platelets (PLTs) and white blood cells (WBCs). In this work, we develop a three-dimensional (3D) smoothed particle hydrodynamics (SPH) model to study the whole blood in shear flow. The immersed boundary method (IBM) is used to deal with the interaction between the fluid and cells, which provides a possibility to model the RBCs, PLTs and WBCs simultaneously. The deformation of a small capsule, comparable to a PLT in size, is first examined to show the feasibility of SPH model for the PLTs’ behaviors. The motion of a single RBC in shear flow is then studied, and three typical modes, tank-treading, swinging and tumbling motions, are reproduced, which further confirm the reliability of the SPH model. After that, a simulation of the whole blood in shear flow is carried out, in which the margination trend is observed for both PLTs and WBC. This shows the capability of SPH model with IBM for the simulation of whole blood.

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