scholarly journals Acoustic Cell Separation Based on Density and Mechanical Properties

2020 ◽  
Vol 142 (3) ◽  
Author(s):  
Yuliang Xie ◽  
Zhangming Mao ◽  
Hunter Bachman ◽  
Peng Li ◽  
Peiran Zhang ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Blood Cells ◽  
Recovery Rate ◽  
Cell Separation ◽  
White Blood Cells ◽  
Acoustic Properties ◽  
Biological Research ◽  
Microfluidic Channels ◽  
Fluid Media ◽  
Solution Surface

Abstract Density and mechanical properties (e.g., compressibility or bulk modulus) are important cellular biophysical markers. As such, developing a method to separate cells directly based on these properties can benefit various applications including biological research, diagnosis, prognosis, and therapeutics. As a potential solution, surface acoustic wave (SAW)-based cell separation has demonstrated advantages in terms of biocompatibility and compact device size. However, most SAW-reliant cell separations are achieved using an entangled effect of density, various mechanical properties, and size. In this work, we demonstrate SAW-based separation of cells/particles based on their density and compressibility, irrespective of their sizes, by manipulating the acoustic properties of the fluidic medium. Using our platform, SAW-based separation is achieved by varying the dimensions of the microfluidic channels, the wavelengths of acoustic signals, and the properties of the fluid media. Our method was applied to separate paraformaldehyde-treated and fresh Hela cells based on differences in mechanical properties; a recovery rate of 85% for fixed cells was achieved. It was also applied to separate red blood cells (RBCs) and white blood cells (WBCs) which have different densities. A recovery rate of 80.5% for WBCs was achieved.

scholarly journals Magnetic Microfluidic Linear Halbach Array Configuration for Cell Separation

2018 ◽  
Vol 153 ◽  
pp. 06008
Author(s):  
Omer Saeed ◽  
Iucienne Duru ◽  
Deng Yulin
Keyword(s):  
Blood Cell ◽  
Critical Point ◽  
Tumor Cells ◽  
Blood Cells ◽  
Recovery Rate ◽  
Cell Separation ◽  
Comsol Multiphysics ◽  
Array Configuration ◽  
Medical Tests ◽  
Halbach Array

The different type of blood entities like red blood cells (RBCs), white blood cell (WBCs) and platelets counts is a critical point in routine medical tests. Circulating tumor cells (CTCs) counting and analysing in the blood is indicative of the stage and origin of cancer in particular time. Here we are describing a proposed microfluidic device, used a magnetic means for CTCs separation from a blood or buffer sample. The device characterizations were simulated using COMSOL MULTIPHYSICS software as well as practically validated. Using a known spiked number of CTCs in the sample, the purity and recovery rate were calculated to be 93% and respectively.

scholarly journals Sheathless High-Throughput Circulating Tumor Cell Separation Using Viscoelastic non-Newtonian Fluid

Micromachines ◽  
2019 ◽  
Vol 10 (7) ◽  
pp. 462 ◽  
Author(s):  
Hyunjung Lim ◽  
Seung Min Back ◽  
Min Ho Hwang ◽  
Dae-Hee Lee ◽  
Hyuk Choi ◽  
...  
Keyword(s):  
High Throughput ◽  
Blood Cells ◽  
Cell Separation ◽  
Separation Efficiency ◽  
White Blood Cells ◽  
Flow Characteristics ◽  
Circulating Tumor Cell ◽  
Size Difference ◽  
Biological Applications ◽  
Mcf 7

Circulating tumor cells (CTCs) have attracted increasing attention as important biomarkers for clinical and biological applications. Several microfluidic approaches have been demonstrated to separate CTCs using immunoaffinity or size difference from other blood cells. This study demonstrates a sheathless, high-throughput separation of CTCs from white blood cells (WBCs) using a viscoelastic fluid. To determine the fluid viscoelasticity and the flow rate for CTC separation, and to validate the device performance, flow characteristics of 6, 13, and 27 μm particles in viscoelastic fluids with various concentrations were estimated at different flow rates. Using 0.2% hyaluronic acid (HA) solution, MCF-7 (Michigan Cancer Foundation-7) cells mimicking CTCs in this study were successfully separated from WBCs at 500 μL/min with a separation efficiency of 94.8%. Small amounts of MCF-7 cells (~5.2%) were found at the center outlet due to the size overlap with WBCs.

scholarly journals Dynamic blood flow phantom for in vivo liquid biopsy standardization

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Anastasiia Kozlova ◽  
Daniil Bratashov ◽  
Oleg Grishin ◽  
Arkadii Abdurashitov ◽  
Ekaterina Prikhozhdenko ◽  
...  
Keyword(s):  
Flow Cytometry ◽  
Blood Cells ◽  
Liquid Biopsy ◽  
High Speed ◽  
White Blood Cells ◽  
High Sensitivity ◽  
Acoustic Properties ◽  
Detection Methods ◽  
In Vivo Flow Cytometry

AbstractIn vivo liquid biopsy, especially using the photoacoustic (PA) method, demonstrated high clinical potential for early diagnosis of deadly diseases such as cancer, infections, and cardiovascular disorders through the detection of rare circulating tumor cells (CTCs), bacteria, and clots in the blood background. However, little progress has been made in terms of standardization of these techniques, which is crucial to validate their high sensitivity, accuracy, and reproducibility. In the present study, we addressed this important demand by introducing a dynamic blood vessel phantom with flowing mimic normal and abnormal cells. The light transparent silica microspheres were used as white blood cells and platelets phantoms, while hollow polymeric capsules, filled with hemoglobin and melanin, reproduced red blood cells and melanoma CTCs, respectively. These phantoms were successfully used for calibration of the PA flow cytometry platform with high-speed signal processing. The results suggest that these dynamic cell flow phantoms with appropriate biochemical, optical, thermal, and acoustic properties can be promising for the establishment of standardization tool for calibration of PA, fluorescent, Raman, and other detection methods of in vivo flow cytometry and liquid biopsy.

scholarly journals Blood-Cell Separation: Deterministic Migration-Based Separation of White Blood Cells (Small 37/2016)

Small ◽  
2016 ◽  
Vol 12 (37) ◽  
pp. 5101-5101
Author(s):  
Byeongyeon Kim ◽  
Young Joon Choi ◽  
Hyekyung Seo ◽  
Eui-Cheol Shin ◽  
Sungyoung Choi
Keyword(s):  
Blood Cell ◽  
Blood Cells ◽  
Cell Separation ◽  
White Blood Cells

scholarly journals Design and Simulation of a Point-of-Care Microfluidic Device for Acoustic Blood Cell Separation

2020 ◽  
Vol 2 (1) ◽  
pp. 76
Author(s):  
Fatemeh Sharifi ◽  
Armin Sedighi ◽  
Mubashar Rehman
Keyword(s):  
Blood Cell ◽  
Red Blood Cells ◽  
Blood Cells ◽  
Cell Separation ◽  
Numerical Study ◽  
Point Of Care ◽  
Surface Acoustic Waves ◽  
White Blood Cells ◽  
Microfluidic Channel ◽  
Diagnostic Process

Hematology tests, considered as an initial step in the patient diagnostic process, require laboratory equipment and technicians which is a time- and labor-consuming procedure. Such facilities may be available in a few central laboratories in under-resourced countries. The growing need for low cost and rapid diagnostic tests contributes to point-of-care (POC) medical diagnostic devices providing convenient and rapid test tools particularly in areas with limited medical resources. In the present study, a comprehensive numerical simulation of a POC blood cell separation device (POC-BCS) has been modeled using a finite element method. Tag-less separation of blood cells, i.e., platelets, red blood cells, and white blood cells, was carried out using standing surface acoustic waves (SSAWs) generated by interdigital transducers (IDTs) located at lateral sides of the microfluidic channel. Blood sample intake along with sheath flow was introduced via two symmetrical tilted angle inlets and a middle inlet, respectively. Superposition of acoustic radiation force applied by SSAWs accompanied by drag force caused by medium flow drove the blood cells toward different path lines correlated to their size. White blood cells were sorted out in the middle outlet and red blood cells and platelets were sorted out through the separate locations of the side outlets. Each cell was then guided to their respected visualization chamber for further image processing analysis. The results of the presented numerical study would be very promising in designing and optimizing the POC blood testing device.

Ultrastructural changes in murine lymphoma cells exposed to ultraviolet-A radiation

1991 ◽  
Vol 49 ◽  
pp. 104-105
Author(s):  
Delma P. Thomas ◽  
Dianne E. Godar
Keyword(s):  
Medical Devices ◽  
Blood Cells ◽  
White Blood Cells ◽  
Consumer Products ◽  
Ultrastructural Changes ◽  
Ultraviolet A ◽  
Uv Spectrum ◽  
Lymphoma Cells ◽  
Murine Lymphoma ◽  
Transmission Electron

Ultraviolet radiation (UVR) from all three waveband regions of the UV spectrum, UVA (320-400 nm), UVB (290-320 nm), and UVC (200-290 nm), can be emitted by some medical devices and consumer products. Sunlamps can expose the blood to a considerable amount of UVR, particularly UVA and/or UVB. The percent transmission of each waveband through the epidermis to the dermis, which contains blood, increases in the order of increasing wavelength: UVC (10%) < UVB (20%) < UVA (30%). To investigate the effects of UVR on white blood cells, we chose transmission electron microscopy to examine the ultrastructure changes in L5178Y-R murine lymphoma cells.

The Effect of Red Blood Cells on the ADP-induced Aggregation of Human Platelets in Flow Through Tubes

1990 ◽  
Vol 63 (01) ◽  
pp. 112-121 ◽  
Author(s):  
David N Bell ◽  
Samira Spain ◽  
Harry L Goldsmith
Keyword(s):  
Platelet Aggregation ◽  
Shear Rate ◽  
Red Blood Cells ◽  
Blood Cells ◽  
Platelet Rich Plasma ◽  
Mean Transit Time ◽  
White Blood Cells ◽  
Aggregate Size ◽  
Human Platelets ◽  
Induced Aggregation

SummaryThe effect of red blood cells, rbc, and shear rate on the ADPinduced aggregation of platelets in whole blood, WB, flowing through polyethylene tubing was studied using a previously described technique (1). Effluent WB was collected into 0.5% glutaraldehyde and the red blood cells removed by centrifugation through Percoll. At 23°C the rate of single platelet aggregtion was upt to 9× greater in WB than previously found in platelet-rich plasma (2) at mean tube shear rates Ḡ = 41.9,335, and 1,920 s−1, and at both 0.2 and 1.0 µM ADP. At 0.2 pM ADP, the rate of aggregation was greatest at Ḡ = 41.9 s−1 over the first 1.7 s mean transit time through the flow tube, t, but decreased steadily with time. At Ḡ ≥335 s−1 the rate of aggregation increased between t = 1.7 and 8.6 s; however, aggregate size decreased with increasing shear rate. At 1.0 µM ADP, the initial rate of single platelet aggregation was still highest at Ḡ = 41.9 s1 where large aggregates up to several millimeters in diameter containing rbc formed by t = 43 s. At this ADP concentration, aggregate size was still limited at Ḡ ≥335 s−1 but the rate of single platelet aggregation was markedly greater than at 0.2 pM ADP. By t = 43 s, no single platelets remained and rbc were not incorporated into aggregates. Although aggregate size increased slowly, large aggregates eventually formed. White blood cells were not significantly incorporated into aggregates at any shear rate or ADP concentration. Since the present technique did not induce platelet thromboxane A2 formation or cause cell lysis, these experiments provide evidence for a purely mechanical effect of rbc in augmenting platelet aggregation in WB.

White blood cells levels and PCOS: direct and indirect relationship with insulin resistance, but not with hyperandogenemia

2013 ◽  
Author(s):  
Olga Papalou ◽  
Sarantis Livadas ◽  
Athanasios Karachalios ◽  
Nektarios Benetatos ◽  
George Boutzios ◽  
...  
Keyword(s):  
Insulin Resistance ◽  
Blood Cells ◽  
White Blood Cells ◽  
Indirect Relationship

Endogenous Heparinoids Detected by anti-Xa Activity are Present in Blood during Acute Variceal Bleeding in Cirrhosis. A Prospective Study

2014 ◽  
Vol 23 (2) ◽  
pp. 187-194 ◽  
Author(s):  
Christos Triantos ◽  
Emmanuel Louvros ◽  
Maria Kalafateli ◽  
Anne Riddell ◽  
Ulrich Thalheimer ◽  
...  
Keyword(s):  
Hepatocellular Carcinoma ◽  
Variceal Bleeding ◽  
Blood Cells ◽  
Venous Pressure ◽  
White Blood Cells ◽  
International Normalized Ratio ◽  
Ulcer Bleeding ◽  
Factor X ◽  
Packed Red Blood Cells ◽  
Bacterial Peritonitis

Background & Aims: Endogenous heparinoids have been detected by thromboelastography and quantified by clotting based anti-Xa activity assays in patients with cirrhosis, but their presence in variceal bleeding has not been established yet.Methods: Clotting based anti-Xa activity was measured in A) 30 cirrhotics with variceal bleeding, B) 15 noncirrhotics with peptic ulcer bleeding, C) 10 cirrhotics without infection or bleeding, and D) 10 cirrhotics with hepatocellular carcinoma (HCC).Results: Anti-Xa activity was not detected in ulcer bleeders or in cirrhotics without infection or bleedingbut was present in seven (23%) variceal bleeders (median levels: 0.03 u/mL (0.01-0.07)) and was quantifiable for 3 days in six of seven patients. Four of seven variceal bleeders with anti-Xa activity present had HCC (p=0.023). Age, creatinine, platelet count and total infections the second day from admission were significantly correlated with the presence of measureable anti-Xa levels (p=0.014, 0.032, 0.004 and 0.019, respectively). In the HCC group, anti-Xa activity was present in three patients (30%) [median levels: 0.05 u/mL (0.01-0.06)].Conclusions: In this study, variceal bleeders and 30% of the patients with HCC had endogenous heparinoids that were detected by a clotting based anti-Xa activity assay, whereas there was no anti Xa activity present in patients with cirrhosis without infection, or bleeding or HCC, nor in those with ulcer bleeding. Thus, the anti-Xa activity is likely to be a response to bacterial infection and/or presence of HCC in cirrhosis.List of abbreviations: AFP, alpha-fetoprotein; aPTT, activated partial thromboplastin time; CP, Child-Pugh; FXa, activated factor X; GAGS, glycosaminoglycans; Hb, hemoglobin; HCC, hepatocellular carcinoma; HVPG, hepatic venous pressure gradient; INR, International normalized ratio; LMWHs, low molecular weight heparins; MELD, Model for End-stage Liver Disease; PPP, platelet-poor plasma; PRBC, packed red blood cells; PT, prothrombin time; SBP, sponataneous bacterial peritonitis; TEG, thromboelastography; WBC, white blood cells.

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