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Related Concept Videos

Enzyme-Linked Immunosorbent Assay01:33

Enzyme-Linked Immunosorbent Assay

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In 1971, Peter Perlman and Eva Engvall developed an Enzyme-linked immunosorbent assay (ELISA or EIA). ELISA differs from western blot in that the assays are conducted in microtiter plates or in vivo rather than on an absorbent membrane.
There are many different types of ELISAs, but they all involve an antibody molecule whose constant region binds an enzyme, leaving the variable region free to bind its specific antigen.  Enzyme-substrate reaction allows the antigen to be visualized or...
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Related Experiment Video

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Development of a Lateral Flow Immunochromatographic Strip for Rapid and Quantitative Detection of Small Molecule Compounds
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An integrated device for fast and sensitive immunosuppressant detection.

Sara Tombelli1, Cosimo Trono2, Simone Berneschi1

  • 1Institute of Applied Physics "Nello Carrara", CNR-IFAC, Via Madonna del Piano 10, 50019, Sesto Fiorentino, Italy.

Analytical and Bioanalytical Chemistry
|December 22, 2021
PubMed
Summary

This study introduces a novel optical device for point-of-care therapeutic drug monitoring. The compact system uses a microfluidic chip and fluorescent magnetic particles for rapid, sensitive detection of immunosuppressants.

Keywords:
Cyclosporine AFluorescenceImmunosuppressantMycophenolic acidPOCT

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Rapid Homogeneous Detection of Biological Assays Using Magnetic Modulation Biosensing System
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Area of Science:

  • Biomedical Engineering
  • Analytical Chemistry
  • Clinical Diagnostics

Background:

  • Therapeutic Drug Monitoring (TDM) is crucial for optimizing immunosuppressant dosages.
  • Existing TDM methods can be time-consuming and require specialized laboratory settings.
  • There is a need for rapid, point-of-care (POC) diagnostic tools for TDM.

Purpose of the Study:

  • To develop and validate a compact optical device for POC TDM.
  • To enable simultaneous, sensitive detection of immunosuppressants.
  • To utilize microfluidics and advanced particle technology for improved assay performance.

Main Methods:

  • Design and integration of a disposable plastic microfluidic chip with ten parallel microchannels.
  • Incorporation of a microfluidic system for automated sample and reagent handling.
  • Utilization of submicrometric fluorescent magnetic particles for enhanced immunoassay efficiency.
  • Development of integrated thin-film amorphous silicon photodiodes for fluorescence detection.

Main Results:

  • Demonstration of a compact, integrated optical device for TDM.
  • Successful simultaneous detection of multiple analytes with replicate measurements.
  • Achieved enhanced assay sensitivity and lower limit of detection using fluorescent magnetic particles.
  • Validated the device's performance by detecting mycophenolic acid and cyclosporine A in spiked solutions and patient microdialysate samples.

Conclusions:

  • The developed optical POC device offers a promising solution for rapid TDM.
  • The use of microfluidics and fluorescent magnetic particles significantly improves assay speed and sensitivity.
  • This technology has the potential to enhance patient management through timely drug level monitoring.