4.7 Article

Separation of ctDNA by superparamagnetic bead particles in microfluidic platform for early cancer detection

Journal

JOURNAL OF ADVANCED RESEARCH
Volume 33, Issue -, Pages 109-116

Publisher

ELSEVIER
DOI: 10.1016/j.jare.2021.03.001

Keywords

Circulating tumor DNA (ctDNA) detection; Cancer biomarker; Liquid biopsy Magnetic manipulation; COMSOL Multiphysics Simulation study

Funding

  1. Ministry of Higher Educa-tion of Malaysia
  2. Universiti Teknologi Malaysia [Q. J130000.2851.00L23, Q.J130000.21A2.04E82]
  3. Ministry of Education, Youth, and Sports ofthe Czech Republic
  4. European Union (European Structural and Investment Funds Operational Program Research, Develop-ment, and Education) [CZ.02.1.01/0.0/0.0/16_025/0007293]

Ask authors/readers for more resources

This study aims to simulate the extraction and separation of ctDNA from the blood plasma of cancer patients for early and effective cancer detection. The results showed efficient separation of ctDNA for early cancer management, with a high sensitivity and specificity in tracing ctDNA using a microfluidics platform and SPM bead particles.
Introduction: Conventional biopsy, based on extraction from a tumor of a solid tissue specimen requiring needles, endoscopic devices, excision or surgery, is at risk of infection, internal bleeding or prolonged recovery. A non-invasive liquid biopsy is one of the greatest axiomatic consequences of the identification of circulating tumor DNA (ctDNA) as a replaceable surgical tumor bioQpsy technique. Most of the literature studies thus far presented ctDNA detection at almost final stage III or IV of cancer, where the treatment option or cancer management is nearly impossible for diagnosis. Objective: Hence, this paper aims to present a simulation study of extraction and separation of ctDNA from the blood plasma of cancer patients of stage I and II by superparamagnetic (SPM) bead particles in a microfluidic platform for early and effective cancer detection. Method: The extraction of ctDNA is based on microfiltration of particle size to filter some impurities and thrombocytes plasma, while the separation of ctDNA is based on magnetic manipulation to high yield that can be used for the upstream process. Result: Based on the simulation results, an average of 5.7 ng of ctDNA was separated efficiently for every 10 mL blood plasma input and this can be used for early analysis of cancer management. The particle tracing module from COMSOL Multiphysics traced ctDNA with 65.57% of sensitivity and 95.38% of specificity. Conclusion: The findings demonstrate the ease of use and versatility of a microfluidics platform and SPM bead particles in clinical research related to the preparation of biological samples. As a sample preparation stage for early analysis and cancer diagnosis, the extraction and separation of ctDNA is most important, so precision medicine can be administered. (C) 2021 The Authors. Published by Elsevier B.V. on behalf of Cairo University.

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