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The development of flow cytometry techniques began in 1934 with initial attempts by Andrew Moldavan, a bacteriologist who counted the cells in a flowing capillary system. Moldavan pumped cells through a capillary tube focused under a microscope for visualization. The invention of photometry allowed the measurement of differentially-stained cells, and Louis Kamentsky developed the first multiparameter flow cytometer in 1965 to identify and count the cancer cells in cervical tissue specimens.
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Development of a cloud-based flow rate tool for eNAMPT biomarker detection.

Bailey C Buchanan1, Yisha Tang1, Hannah Lopez2

  • 1Department of Biomedical Engineering, The University of Arizona, 1127 E. James E. Rogers Way, Tucson, AZ 85721, USA.

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|May 7, 2024
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Summary
This summary is machine-generated.

A rapid point-of-care test using particle immunoagglutination on paper microfluidics can detect extracellular nicotinamide phosphoribosyltransferase (eNAMPT) levels in under a minute. This assay aids in assessing inflammatory disease severity and guiding therapeutic decisions.

Keywords:
Google Colabacute respiratory distress syndromecapillary actionpaper microfluidicssmartphone

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Area of Science:

  • Biochemistry
  • Biomarker Discovery
  • Point-of-Care Diagnostics

Background:

  • Extracellular nicotinamide phosphoribosyltransferase (eNAMPT) is a biomarker for inflammatory diseases.
  • Neutralizing eNAMPT with monoclonal antibodies shows therapeutic potential in preclinical models.
  • Rapid point-of-care (POC) detection of eNAMPT is needed to assess anti-eNAMPT therapy efficacy.

Purpose of the Study:

  • To develop and validate a rapid POC assay for quantifying eNAMPT in human samples.
  • To assess the feasibility of using a paper microfluidic platform for eNAMPT detection.
  • To enable timely patient stratification and therapeutic guidance.

Main Methods:

  • Particle immunoagglutination assay on a paper microfluidic platform.
  • Quantification via flow rate measurement analyzed by smartphone and Google Colab.
  • Optimization using horizontal flow and immunoagglutination binding models.

Main Results:

  • Assay detected eNAMPT in whole blood and plasma within 1 minute.
  • Limit of detection: 1-20 pg/mL (0.1-0.2 ng/mL undiluted).
  • Linear range: 5-40 pg/mL; distinguished low, mid, and high eNAMPT concentrations.

Conclusions:

  • A low-cost, rapid POC assay for eNAMPT levels was successfully developed.
  • The assay enables quick determination of eNAMPT in blood/plasma.
  • This technology can aid clinical trial patient stratification and therapeutic decision-making for anti-eNAMPT treatments.