Erythrocyte Sedimentation Rate: A Physics-Driven Characterization in a Medical Context

Alexis Darras; Thomas John; Christian Wagner; Lars Kaestner

doi:10.3791/64502

Medicine

Erythrocyte Sedimentation Rate: A Physics-Driven Characterization in a Medical Context

Published: March 24, 2023 doi: 10.3791/64502

Alexis Darras¹, Thomas John¹, Christian Wagner^1,2, Lars Kaestner^1,3

¹Experimental Physics, Saarland University, ²Department of Physics and Materials Science, University of Luxembourg, ³Theoretical Medicine and Biosciences, Saarland University

Summary

Erythrocyte sedimentation rate (ESR) is a physical parameter, often used in routine health checks and medical diagnosis. A theoretical model that allows to extract physically-meaningful parameters from the whole sedimentation curve, based on modern colloidal knowledge, has recently been developed. Here, we present a protocol to automatically collect the ESR over time, and extract the parameters of this recent model from this automated data collection. These refined parameters are also likely to improve the medical testimony.

Abstract

Erythrocyte (or red blood cell) sedimentation rate (ESR) is a physical derived parameter of blood which is often used in routine health checks and medical diagnosis. For instance, in the case of inflammation, a higher ESR is observed due to the associated increase in fibrinogen and other plasma proteins. It was believed that this increase was due to the formation of larger aggregates of red blood cells (RBCs) caused by the increase in fibrinogen. Indeed, fibrinogen is an agent-fostering aggregation of RBCs and in the Stokes regime-assumed to be observed in blood-larger aggregates sediment faster. However, all models of ESR measurements based on this hypothesis require further specific physical assumptions, not required in any other system. Besides, modern studies in the field of colloidal suspensions have established that attractive particles form percolating aggregates (i.e. aggregates as wide as the container). The sedimentation of these colloids then follows a so-called "colloidal gel collapse". Recently, it has been shown that RBCs actually follow the same behavior. This hypothesis also allows to efficiently and analytically model the sedimentation curve of RBCs, from which robust and physically-meaningful descriptors can be extracted. This manuscript describes how to perform such an analysis, and discusses the benefits of this approach.

Introduction

The erythrocyte sedimentation rate (ESR) is a medical in vitro clinical tool, formally introduced in evidenced-based medicine during the twentieth century¹^,²^,³^,⁴. It is currently used worldwide as a nonspecific inflammatory test, or to monitor the evolution of some specific conditions⁵^,⁶^,⁷^,⁸. This is mainly due to an increase in the fibrinogen concentration, but also in other plasma components such as IgM¹^,⁹^,¹⁰^,¹¹. According to the current Westergren standard protocol, ESR values are reported as the measurement of the cell-free plasma layer at a given time point (30 min or 1 h) after leaving a vertical tube of a typical size of 20 cm vertically at rest¹². However, this measurement method has been criticized since qualitatively different stages in the sedimentation process have been reported, including a delay before reaching the maximum settling velocity¹³. This delay lasts more than 1 h in approximately half of healthy samples¹⁴. The velocity during this phase obeys a different scaling than during the second, faster phase of the sedimentation¹⁵. Restricting the readout to the average settling velocity during the first hour then compares a different mix of various blood properties between different individuals.

Moreover, it has recently been demonstrated that the usual theoretical considerations behind this protocol were erroneous¹⁶^,¹⁷^,¹⁸. At physiological hematocrit (above approximately 25%), red blood cells (RBCs) do not sediment as separate aggregates, but rather as a continuous, so-called percolating, network of RBCs¹⁷^,¹⁸, obeying a different set of physical equations than the usually mentioned Stokes sedimentation¹⁶^,¹⁷. It has been shown that considering a physical description based on the time-resolved measurements of the sedimentation (whole curve) was more robust in some novel medical contexts¹⁹^,²⁰. Moreover, these measurements could be used to shed light on the physical mechanisms altering the ESR in pathologies in which cell shapes are altered¹⁹^,²⁰. Additionally, a slow ESR can have a useful medical interpretation, as indicated in the measurements of a cohort of neuroacanthocytosis syndrome patients¹⁹^,²⁰. This article reviews how to practically implement the measurement of physically-meaningful parameters, based on the whole ESR kinetics. More accurately, the method presented here extracts the maximum sedimentation speed U_m, the value of which can be corrected to consider the effect of the hematocrit of the donor¹⁶^,¹⁷. This parameter is more accurate and thus more reliable than the traditional measurement¹⁶^,¹⁷^,¹⁹^,²⁰.

In addition, in some fundamental research, instead of monitoring the inflammation state of a given patient, it is interesting to exclude the effect of hematocrit on the ESR²¹^,²²^,²³, or to investigate the role of RBCs in a modified ESR¹⁹^,²⁰^,²⁴^,²⁵ between different donors. It might be useful to compare samples which are not directly full blood samples from patients. Therefore, resuspending RBCs with a controlled hematocrit in the autologous plasma, or in a plasma-substituent, might be used as the first step of ESR measurement. For instance, solutions of Dextran 70 kDa with a concentration of 55 mg/mL in phosphate buffered saline (PBS) produces a sedimentation range within the control range for healthy cells¹⁹. This manuscript also shows how such steps should be conducted, and that the presented analysis is also relevant in these cases.

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Protocol

Blood sample collection and experiments were approved by the "Ärztekammer des Saarlandes", ethics votum 51/18, and performed after informed consent was obtained according to the Declaration of Helsinki. Standard measurements should be performed with ethylenediaminetetraacetic acid (EDTA)-anticoagulated blood (standard EDTA concentration of 1.6 mg/mL blood, European norm NF EN ISO 6710), in Westergren tubes. The volume required to fill the Westergren tube depends on the manufacturer (as lower parts sometimes contain a wider reservoir); The volume should be about 1 mL of full blood, and 800 µL for the tubes indicated in the Table of Materials. The method described below is however valid no matter the specific suspension and container shape, as long as the hematocrit of the probed samples is higher than 25%¹⁶. Volumes, containers, suspending medium, and additives should therefore be selected according to the specific objectives of the performed research.

1. Experiments and measurements

NOTE: Record the sedimentation rate of the sample every minute.

Sample preparation (if required): If a control hematocrit or suspending liquid is required, start by washing the cells and preparing the samples (as an example, we show how to prepare samples with various fibrinogen levels, by mixing autologous serum and plasma). Serum can indeed be approximated as fibrinogen-free plasma²⁶^,²⁷, and can be used in order to decrease the aggregation of RBCs, in otherwise physiological conditions. In order to prepare several samples, collect the blood in standard EDTA tubes of 9 mL and the serum in standard serum tubes (with silica beads as clotting activators) of 9 mL.
1. Centrifuge the blood samples (i.e., 9 mL of standard EDTA and serum tubes in the chosen example) at 3,000 x g for at least 7 min, for optimal compaction of the packed erythrocytes. Replace the supernatant with PBS or the desired suspending liquid, if a sufficient quantity is available. If it is simply required to control the hematocrit in autologous plasma, proceed directly to step 1.1.3. Otherwise, gently mix after inclusion of the supernatant for washing.
2. Repeat three times. Perform the last wash with the desired suspending liquid in any case.
  1. In the chosen example, prepare mixtures of autologous plasma and serum with determined proportions (e.g., 25%/75%, 50%/50%, or 75%/25% of plasma-serum volume fraction). For example, when preparing 2.5 mL of the 25%/75% plasma-serum mixture, add 0.625 mL of plasma to 1.875 mL of serum.
3. Extract the required volume of packed cells and suspend it in the desired liquid. Process the packed cells as a highly viscous liquid (using standard pre-pipetting and/or reverse-pipetting or a positive displacement pipette²⁸). In the chosen example, for a 4 mL sample at a hematocrit of 45%, suspend 1.8 mL of packed cells within 2.2 mL of the plasma-serum mixture.
If the hematocrit of the sample is not controlled, determine it by high-speed microcentrifugation (other standard methods are also suitable).
1. Extract the required amount of sample for hematocrit determination: fill the micro-hematocrit capillaries by immersing its lower tip in the liquid. Stop it by covering the top opening when the required amount of sample rises in the tube by capillary suction.
2. Seal the capillaries with sealing wax. Place them in the micro-hematocrit centrifuge and run it at 15,000 x g(12,000 rpm) for 5 min, or according to the manufacturer's instructions.
3. Read the hematocrit level on the capillary and write it down for reference.
Set up a camera for recording the samples' sedimentation. To avoid overloading the memory or draining the battery, power the device from the mains and save the pictures directly to a computer or external hard drive.
1. Set up a steady camera in front of the holder where the ESR tubes will be left at rest. Use a white, illuminated background (white sheets of paper in the background work perfectly).
2. Using empty Westergren tubes, preferably without markings, set the focus and the field of view of the camera to obtain the highest resolution where the samples will be placed. Preferably, ensure that the borders of the pictures are aligned in the vertical and horizontal direction.
3. Take a picture of a scaled tube to extract the pixel resolution. The use of RGB pictures is recommended.
4. Set the light and the exposure time of the camera to have a white background, but no saturation. The example in Figure 1 has been obtained using a Canon EOS M50, with an exposure time of 1/15s, an aperture of F8.0, Tungsten white balance, in single shot mode with manual focus, and an ISO speed of 1,000.
Prepare and place the ESR tubes.
1. Fill the bottom container of the Westergren tube with the volume corresponding to the manufacturer's instructions. Insert the Westergren tube in the bottom container as indicated by the manufacturer.
2. As soon as the first tube is ready, place it in the holder and start the camera recording. Recording one picture every minute usually gives a good resolution of the ESR kinetic curve.
3. Prepare and place the next samples. Make sure not to stand in front of any sample when a picture is taken.
4. Let the measurements run for at least 2 h, in order to compare with standard measurements at 30 min, 1 h, and 2 h. However, it is also better to see the saturation and arrest of the sedimentation. For healthy samples, or in case of inflammation, recording the samples overnight, between 12 h and 24 h, is more than sufficient since the curvature of the fastest samples is visible within 3 h¹³^,¹⁹. However, if a condition decreases the sedimentation velocity, as a decrease in fibrinogen concentration does (i.e., in the chosen example, high serum volume fraction), recordings of 50 h or more might be required to obtain the most accurate information¹⁶^,¹⁹.

2. Image analysis

NOTE: Once the images are recorded, extract the ESR curve. An example of Matlab code is provided as Supplementary File 1 (MatlabCodeImageAnalysisSampled.m).

Select or identify a region of interest (ROI) where only one tube is visible, the lower border being located under the lowest position of the erythrocyte cell-free plasma interface but within the sample (see Figure 1A, B). If required, rotate the picture so that the vertical direction is aligned along the first component of the picture.
Convert the ROI of the RGB picture into a gray-scale picture or matrix Gr. Usually, combining the three-color channels (red [R], green [G] and blue [B]) as Gr = 2 * R - B - G is very efficient with a clear background (see Figure 1C and MatlabCodeImageAnalysisSampled.m lines 121-128).
Binarize the picture. For a healthy sample, using the Otsu threshold²⁹ usually gives a consistent result (see Figure 1D and line 133 of MatlabCodeImageAnalysisSampled.m). For samples with a high hematocrit or with some hemolysis, it might be better to adjust it manually or use another automatic method (as done in lines 129-131 of MatlabCodeImageAnalysisSampled.m), depending on the exact contrast obtained between the various phases inside the tube.
Obtain the average of the pixel (or elements) values of Gr along the horizontal direction. This step minimizes the noise and efficiently averages the possible interface irregularities (see Figure 1E and MatlabCodeImageAnalysisSampled.m line 137).
Before computing the variations, smooth the curve with a moving average, especially if the tubes contain some horizontal markings (see Figure 1F). For the provided examples, a moving window of ~2.5 mm (50 pixels) was used for this process (see line 138 of MatlabCodeImageAnalysisSampled.m). Then, identify the interface position as the point with the highest intensity variation (see Figure 1G).
Repeat for each picture and each sample. For each sample, save the positions of the interface along time in an appropriate format to fit the physical model with any suitably fit software.

3. Fitting of the physical model

Using any suitably fit software, knowing the hematocrit and the initial height of the blood column h₀, find the values of the delay time t₀, the dimensionless time γ, and the final packed volume fraction Φ_m of the erythrocytes that minimizes the sum of squared residual deviations for the physical model¹⁷. A Matlab code (ShapeAnalyzerIntegrated.m) is provided as Supplementary File 2 as an example of how to perform such a fit. See Supplementary File 2 for further instructions. As described elsewhere¹⁶^,¹⁷, erythrocytes at physiological hematocrit sediment as a soft particle gel, where the important physical parameters are the difference in density between the plasma and RBCs of the donor Δρ, the RBC characteristic diameter r_RBC, the plasma viscosity at room temperature η, and the donor's hematocrit Φ. Using these parameters, and assuming that the gravitational stress is the main driving process for the plasma to flow upward through the porous network formed by the erythrocytes after a delay time t₀, one obtains the temporal evolution¹⁶^,¹⁷:

with , , and being the average disk radius of an erythrocyte. An example of a Matlab code performing this is provided as an attachment (ShapeAnalyzerIntegrated.m fits the function defined in SedimFit.m [Supplementary File 3]). Alternatively, G/γ can also be used directly as a fit parameter with units of 1/t.
Once the quantitative curve is extracted from the picture, save the physical parameters of the sample. Traditional ESR values at 30 min, 1 h, or 2 h can still be extracted from the curve for reference (see ShapeAnalyzerIntegrated.m lines 123-132).

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Representative Results

An example of an image sequence correctly acquired is provided as Supplementary Movie 1 (MovieS1.avi). A series of characteristic fits of the model is shown for various conditions in Figure 2. Fibrinogen concentration was determined from the fibrinogen concentration in the plasma Fib₀, assuming that the serum does not have any fibrinogen at all. Hence, Fib = C Fib₀, where C is the plasma volume fraction in the plasma-serum mixture. In previous studies¹⁶, Fib₀ was determined by standard methods in the Clinical Chemistry Laboratory of Saarland University Hospital (Homburg, Germany). If it is necessary to measure such a quantity independently, a convenient method to determine fibrinogen concentration includes (semi-)automated ball coagulometers, which might also require obtaining a citrate-anticoagulated sample of blood from the donor³⁰. The ESR curves from the studies which generated these curves could be fitted with a Pearson coefficient R² Equation 11 [0.974, 0.9996], with an average of 0.996 and a standard deviation of 0.004 (only one curve out of 35 gave a R² < 0.99). The parameters eventually extracted are the final hematocrit in the RBC phase Φ_m, the delay time t₀-required for the gel to fracture and start to collapse-and the maximum instantaneous velocity Equation 6 , reached at the start of the collapse. The dimensionless parameter γ is associated with the inverse of the pore area in the compacting network of RBCs (expressed in multiples of particle radius), Δρ is the difference in density between the plasma and RBCs of the donor, a is the RBC characteristic diameter, η is the plasma viscosity at room temperature, and Φ is the donor's hematocrit. The fit is actually performed by fixing Δρ,a,η and Φ and then determining the best γ, Φ_m and t₀. The hematocrit should be determined independently via another standard method, while the other can be fixed at standard values (Δρ Equation 100 80kg/m³³¹^,³², η1.5 mPa s ³³, and a4 μm). Any deviation of the other parameters would simply modify the determined value of γ by a corresponding factor, but would not change the final determination of U_m, which is then a robust parameter in that regard.

Collections of parameter values collected in previous fundamental studies, showing the trends of the parameters as a function of the hematocrit and fibrinogen levels, are shown in Figure 3 and Figure 4.

Figure 1: Image processing. (A) Ideal view of several samples, with relevant ROIs, highlighted for one sample. (B) Zoom on the selected ROI. (C) Conversion of the colored ROI into grey-level. (D) Binarized picture obtained with the Otsu threshold. (E) The horizontally-averaged intensity of the binary picture as a function of the height (per the usual convention in image processing, the origin is considered to be on the top of the picture; see also step 2.4 of the protocol.) (F) Smoothed intensity by performing a moving average on a 50 pixel vertical neighborhood (see also step 2.5 of the protocol). (G) Variations of the smoothed intensity along the vertical direction. The position of the absolute maximal value is taken as the position of the interface (see also step 2.5 of the protocol). Please click here to view a larger version of this figure.

Figure 2: Characteristic fits. (A) Curves and fits obtained for a healthy donor, with various adjusted hematocrits. The curves are adapted from a previous study¹⁷. (B) Curves and fits obtained for a healthy donor, with various fibrinogen concentrations. Various fibrinogen concentrations were obtained by mixing autologous plasma and serum in various proportions. The curves and data are from a previous study¹⁶. Error bars (obtained from pixel resolution or fit statistics) are smaller than the symbol size. The figures have been reprinted with permission from Dasanna et al.¹⁶ (18 samples from four independent blood drawings) and Darras et al.¹⁷(16 samples from seven independent blood drawings). Please click here to view a larger version of this figure.

Figure 3: Characteristic values of the extracted parameters for various hematocrits. (A) Variation of the extracted maximal sedimentation velocity U_m as a function of the sample hematocrit Φ. Circles are individual measurements; different colors are related to different healthy donors. The continuous red line is the trend predicted by the model, obtained with the average values of Φ_mand γ. The corrected value of U_m for a hematocrit of Φ = 0.45 is also shown, both as triangles for individual values and as a straight line for the predicted constant of the model. This corrected value has been computed according to the model as Equation 10 . (B) Values obtained for the parameter γ. (C) Values obtained for the parameter Φ_m. (D) Values obtained for the parameter t₀. Error bars for individual data obtained from fit statistics are smaller than the symbol size. This figure has been adapted with permission from Darras et al.¹⁷. Please click here to view a larger version of this figure.

Figure 4: Characteristic values of the extracted parameters for various fibrinogen concentrations. (A) Variation of the extracted maximal sedimentation velocity U_m as a function of the sample fibrinogen concentration. Different colors are related to different healthy donors. (B) Values obtained for the parameter γ. (C) Values obtained for the parameter Φ_m. (D) Values obtained for the parameter t₀. Error bars for individual data obtained from fit statistics are smaller than the symbol size. This figure has been reprinted with permission from Dasanna et al.¹⁶. Please click here to view a larger version of this figure.

Supplementary Movie 1: Example of a properly acquired image sequence. Various sample types are shown in these pictures from two different donors (same blood group). From left to right, all samples having duplicates: full blood from donor 1, suspension of RBCs from donor 1 in Dextran 70 kDa (55 mg/mL PBS) with controlled hematocrit at 45%, full blood from donor 2, suspension of RBCs from donor 2 in Dextran (45% hematocrit), suspension of RBCs from donor 1 in plasma of donor 2 (45% hematocrit), and suspension of RBCs from donor 2 in plasma of donor 1 (45% hematocrit). The samples have a wide range of sedimentation speeds, and the suspensions in Dextran also show some hemolysis. However, the provided code MatlabCodeImageAnalysisSampled.m efficiently analyzes all of them. Please click here to download this Movie.

Supplementary File 1: MatlabCodeImageAnalysisSampled.m. Main code used for the image analysis (step 2 of the protocol). In order to run the code on a specific device, line 8 should be modified. It should contain the path to the folder containing the pictures of the Westergren tubes to analyze, ending with the prefix of the pictures, if any. A set of compressed pictures is available for open-access download on Zenodo (DOI: 10.5281/zenodo.7290177). The code, and in particular the properties of each sample (defined in lines 14-61), has already been adapted to analyze these pictures. For this picture set, the prefix used was 'IMG_'. Therefore, the string line 8 should end with '\IMG_' (or '/IMG_' on Linux systems). The last part of the code (lines 166-179) also automatically plots the extracted sedimentation curves for each sample. Please click here to download this File.

Supplementary File 2: ShapeAnalyzerIntegrated.m. Main code used to fit the physical model (step 3 of the protocol). To run this code, simply copy and paste it into the folder containing the output text files from MatlabCodeImageAnalysisSampled.m, along with SedimFit.m. The names of the files to analyze (without the .txt extension) should be listed in line 9. The initial hematocrit and height of the tube should also be contained in lines 12 and 15, respectively. This code is already prepared to analyze the curves extracted from the open-access pictures on Zenodo (DOI: 10.5281/zenodo.7290177). Once the aforementioned line codes have been modified, simply click on the 'Run' button in the Matlab Editor toolbar. Please click here to download this File.

Supplementary File 3: SedimFit.m. Physical model adjusted by ShapeAnalyzerIntegrated.m. This file is a Matlab function, defining the functions that are fitted to the experimental curves to extract the physical parameters. It should be in the same folder as ShapeAnalyzerIntegrated.m when the analysis is run. Please click here to download this File.

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Discussion

For the automated protocol to work efficiently, it is important to have a clear background and proper illumination. A dark background might prevent the existence of an efficient binarization threshold. For samples with some hemolysis, which usually occurs (increases) over time, it is important to verify first that the chosen binarization threshold is relevant for both the initial and final pictures.

When it comes to the binarization process of the picture, the choice of the ROI and binarization threshold is the most sensitive step. It might be useful to manually test different threshold values on three different pictures (at the beginning, middle, and end of the sedimentation process) to ensure that the choice of the threshold indeed provides the relevant binarization for the whole process. If the sample experiences strong hemolysis, it might be necessary to restrict the analysis of the sample to the beginning of the process, when a clear interface can still be observed. As for any ESR measurement, it is also essential to avoid the presence of any bubbles in the tube. However, if some small bubbles are observed at the top of the tube, a ROI starting below the bubbles and right on top of the initial interface might still provide the relevant measurement. In this case, however, it is important to include some background space on the right and left of the tube so that the Otsu threshold can be determined while always considering a significant amount of pixels with the grey level of the background.

The method, as with all ESR measurements, relies on the assumption that a clear interface between packed erythrocytes and cell-free plasma can be seen. If the sample experiences some significant amount of hemolysis, or if the hematocrit of the sample is too diluted (under 25%¹⁷), such an interface will not be observed anymore. An ESR measurement in these conditions is then impossible to perform.

As stated earlier, this method ensures to provide the relevant speed of the gel collapse U_m, which can be corrected according to the initial hematocrit of the patient¹⁷. Figure 3A, along with the raw measurements of U_m, also shows the corrected values for a normalized hematocrit of Φ₀ = 0.45. It can be seen that the correction removes the overall dependency on Φ₀, as well as most of the data dispersion. Determining U_m based directly on the relevant physical model also implies that the technique is more objective than an arbitrary curve smoothing, with arbitrary choices of smoothing parameters. Amongst others, this method has been shown to be more robust in medical contexts where abnormally low ESR values are observed¹⁹^,²⁰.

Another intrinsic interest of this measurement is that it gives more robust and physically interpretable data. For instance, in the case of a lowered ESR, it allows distinguishing whether the delay time t₀ of the collapse is prolonged, if the network of RBCs is unusually disordered through γ, or if the final compaction Φ_m of the cells is somehow hindered¹⁶^,¹⁹^,²⁰.

Interestingly, the measurement of the maximum sedimentation velocity is also more robust and sensitive to fibrinogen levels, as already highlighted in previous studies¹³^,¹⁴^,¹⁵. This is an important feature, as the ESR is often used to monitor inflammation, which is associated with elevated levels of fibrinogen. This sensitivity essentially arises from uncoupling U_mfrom the time of gel collapse, which is known to have an important random component³⁴^,³⁵^,³⁶. More accurately, as highlighted in Figure 4D¹⁶, for higher concentrations of fibrinogen, the intrinsic random variation of the delay time (in which measurements above 150 mg/mL are between 12 min and 30 min, even among a single donor) has the same order of magnitude as its underlying dependency on this parameter (between 150 mg/dL and 300 mg/dL; the average trend of the measurements only decrease from 0.45 h to 0.4 h [i.e., 27 min to 24 min]). Since this delay time is actually included in the traditional height measurement at 30 min or 1 h (durations that this delay time can sometimes reach or exceed), extracting the maximum velocity U_m (presenting a systematic and significant trend for each donor) then provides a more robust and meaningful parameter¹³^,¹⁴^,¹⁵^,³⁴^,³⁵^,³⁶.

Moreover, the parameter U_m can efficiently be corrected for the initial hematocrit, according to the practical result Equation 11 described earlier¹⁷. When combining data for all the healthy donors in a previous study¹⁷, values of γ = 0.50 ± 0.06 and Φ_m = 0.86 ± 0.04 are obtained, which nicely reproduce the trend of U_m as a function of the donor hematocrit Φ, as shown in Figure 3. However, in practical cases, it might be more rigorous to correct the ESR with the γ and Φ_m values obtained for a specific donor, since fibrinogen levels can also significantly change between donors and have a significant influence on these parameters (Figure 4).

Considering the points discussed and including them in routine medical procedures, the accuracy and versatility of the ESR as an in vitro clinical tool will further improve.

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Disclosures

The authors have no conflicts of interest to declare relevant to the content of this article.

Acknowledgments

This work was supported by the research unit FOR 2688 - Wa1336/12 of the German Research Foundation and by the Marie Skłodowska-Curie grant agreement No. 860436-EVIDENCE. T. J. and C. W. acknowledge funding from French German University (DFH/UFA). A. D. acknowledges funding by the Young Investigator Grant of Saarland University.

Materials

Name	Company	Catalog Number	Comments
Anticoagulant (EDTA or Heparin) tube (for blood sample)	SARSTEDT	267001 or 265	Anticoagulated blood sample to characterize
Camera EOS M50	Canon	Kit EF-M18-150 IS STM	Any camera should work, provided that sector alimentation, connection to computer for automated shooting and adapted objective are available
Centrifuge	HERMLE	302.00 V03 - Z 36 HK	Requirements: at least 3000 x g ofr 7 min.
Micro-centrifuge	MLW	TH21	or any other way to determine the hematocrit
Micro-hematocrit capilaries	Fisher scientific	11884040	or other capillaries/containers for hematocrit determination
Phosphate Buffered Saline (PBS)	ThermoFisher	10010023	1x PBS, pH 7.4, 298 Osm
Pipettes (e.g. positive displacement pipette)	Gilson	FD10006	Pipette required to manipulate blood and/or packed cells.Other models are of course suitable, but be careful to treat blood and pakced cells as highly viscous fluids.
Wax sealing plate	Hirschmann	9120101	Sealing wax for the micro-hematocrit capillaries
Westergren tubes	Praxindo	A9244560	Any other standard Wetsergren tube should work too
White background with illumination	/	/	White sheet(s) of paper behind the samples, with usual room light is perfcetly sufficient.

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