High-throughput and label-free screening of red blood cell stiffness: A study of sickle cell disease

Understanding the morphological and mechanical changes in cells are important for diagnostic and treatment methods in various diseases. In sickle cell disease (SCD), the mutated hemoglobin (HbS) aggregates inside the red blood cells (RBCs), making them rigid and, in extreme cases, sickle-shaped, resulting in anemia, episodes of pain, and multiple organ damage. Existing techniques are too costly and insensitive since the effect of the HbS gene (heterozygous and homozygous) is variable both in prevalence and clinical manifestations. In this work, we present a label-free, cost-effective, high-throughput electro-fluidic technique to study changes in the mechanical and morphological characteristics of RBCs. We validate our device by quantitatively comparing the mechanical properties of RBCs as a function of stiffness-altering drug (Latrunculin-A) with measurements using AFM. We demonstrate the on-site application of our system by screening SCD patients based on their RBC stiffness changes. The signatures of patient-specific heterogeneity in the RBC mechanical properties may help in monitoring clinical variability and identification of high-risk patients along with targeted therapies. The versatility of our measurements opens the whole cell stiffness as a preliminary screening biomarker in other haematological conditions, tumor cell identification, in veterinary sciences as well as in evaluating hydrogel technologies. • Sickle Cell Disease caused by protein aggregation lead RBC stiffening causing pain and multiple organ damage. • Population-wide screening is vital for monitoring clinical variability and identification of high risk SCD patients. • An electro-fluidic device is presented as a label-free, high-throughput, & resolution tool for cellular stiffness detection. • Whole cell stiffness (WCS) is quantified as preliminary screening parameter for detecting hematological conditions like SCD. • The device is tested in-hospital conditions for screening SCD patients.

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Publication Details

Journal
Biosensors and Bioelectronics X
Published
2025-03-20
DOI
https://doi.org/10.1016/j.biosx.2025.100616
Primary Topic
Hemoglobinopathies and Related Disorders
Type
article
Field-Weighted Citation Impact
0.00

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article

High-throughput and label-free screening of red blood cell stiffness: A study of sickle cell disease

Sweta Srivastava, R. Ross, Abhishek Mishra, Gautam V. Soni et al.
Biosensors and Bioelectronics X
Hemoglobinopathies and Related Disorders
article

High-throughput and label-free screening of red blood cell stiffness: A study of sickle cell disease

Sweta Srivastava, R. Ross, Abhishek Mishra, Gautam V. Soni, Cecil Ross, Saurabh Kaushik
article en

Abstract

Understanding the morphological and mechanical changes in cells are important for diagnostic and treatment methods in various diseases. In sickle cell disease (SCD), the mutated hemoglobin (HbS) aggregates inside the red blood cells (RBCs), making them rigid and, in extreme cases, sickle-shaped, resulting in anemia, episodes of pain, and multiple organ damage. Existing techniques are too costly and insensitive since the effect of the HbS gene (heterozygous and homozygous) is variable both in prevalence and clinical manifestations. In this work, we present a label-free, cost-effective, high-throughput electro-fluidic technique to study changes in the mechanical and morphological characteristics of RBCs. We validate our device by quantitatively comparing the mechanical properties of RBCs as a function of stiffness-altering drug (Latrunculin-A) with measurements using AFM. We demonstrate the on-site application of our system by screening SCD patients based on their RBC stiffness changes. The signatures of patient-specific heterogeneity in the RBC mechanical properties may help in monitoring clinical variability and identification of high-risk patients along with targeted therapies. The versatility of our measurements opens the whole cell stiffness as a preliminary screening biomarker in other haematological conditions, tumor cell identification, in veterinary sciences as well as in evaluating hydrogel technologies. • Sickle Cell Disease caused by protein aggregation lead RBC stiffening causing pain and multiple organ damage. • Population-wide screening is vital for monitoring clinical variability and identification of high risk SCD patients. • An electro-fluidic device is presented as a label-free, high-throughput, & resolution tool for cellular stiffness detection. • Whole cell stiffness (WCS) is quantified as preliminary screening parameter for detecting hematological conditions like SCD. • The device is tested in-hospital conditions for screening SCD patients.

Biosensors and Bioelectronics XVol. 24
Raman Research Institute (IN), St.John's Medical College Hospital (IN)
Department of Science and Technology, Ministry of Science and Technology, India, Rotman Research Institute, Baycrest
Zero hunger
Openalex Percentile: Top 92%
Hemoglobinopathies and Related Disorders
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