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Related Concept Videos

DNA Microarrays02:34

DNA Microarrays

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Microarrays are high-throughput and relatively inexpensive assays that can be automated to analyze large quantities of data at a time. They are used in genome-wide studies to compare gene or protein expression under two varied conditions, such as healthy and diseased states. Microarrays consist of glass or silica slides on which probe molecules are covalently attached through surface functionalization. Most commonly, the slides are prepared through the chemisorption of silanes to silica...
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Visual Detection of Multiple Nucleic Acids in a Capillary Array
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Prospects of Microfluidic Technology in Nucleic Acid Detection Approaches.

Zilwa Mumtaz1, Zubia Rashid2, Ashaq Ali3

  • 1KAM School of Life Sciences, Forman Christian College University, Ferozpur Road, Lahore 54600, Pakistan.

Biosensors
|June 27, 2023
PubMed
Summary

Microfluidic technology enables sensitive nucleic acid detection for diseases. Paper-based devices with isothermal amplification offer cost-effective, rapid point-of-care diagnostics.

Keywords:
isothermal amplificationlab on chipmicrofluidicsmolecular diagnosticsnucleic acid detectionnucleic acid testingportable devices

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Area of Science:

  • Biomedical Engineering
  • Analytical Chemistry
  • Molecular Diagnostics

Background:

  • Conventional diagnostics require multi-step procedures, hindering rapid point-of-care (POC) testing.
  • Microfluidic platforms offer integrated, single-step solutions for analyte detection in clinical and biochemical applications.
  • Challenges in nucleic acid detection include cellular lysis, isolation, and amplification, necessitating improved on-chip methodologies.

Approach:

  • This review highlights microfluidic technology for nucleic acid detection of infectious and non-infectious diseases.
  • Explores modular microfluidics for streamlined on-chip sample preparation, amplification, and detection.
  • Discusses the integration of isothermal amplification with lateral flow assays for enhanced sensitivity and nanoparticle-biomolecule binding efficiency.

Key Points:

  • Microfluidic systems provide specific, sensitive disease detection with benefits like low cost and simple fabrication.
  • Paper-based microfluidics using cellulose reduce overall diagnostic costs.
  • CRISPR/Cas technology integration in microfluidics advances next-generation diagnostic methods.

Conclusions:

  • Microfluidic technology is crucial for advancing nucleic acid testing for various diseases.
  • Combining microfluidics with isothermal amplification and paper-based materials enhances detection limits and sensitivity.
  • Future prospects involve comparing diverse microfluidic systems, detection methods, and plasma separation techniques for improved diagnostics.