AI Article Synopsis

  • Tuberculosis (TB) remains a significant global health issue, with millions of new cases each year, largely hindered by the lack of affordable, point-of-care diagnostic tests.
  • Researchers have been exploring mannose-capped lipoarabinomannan (ManLAM), a TB biomarker, but its detection has been challenging due to interference from other components in body fluids.
  • Recent advancements include developing an automated microfluidic platform that simplifies the sample pretreatment process for ManLAM, achieving similar recovery rates as traditional methods, and plans to integrate it with a portable reader for TB diagnostics.

Article Abstract

Tuberculosis (TB) represents a major public health threat, with millions of new cases reported worldwide each year. A major hurdle to curtailing the spread of this disease is the need for low-cost, point-of-care (PoC) diagnostics. Mannose-capped lipoarabinomannan, a significant component of the bacillus, has been heavily studied as a biomarker for TB, but with little success due to its complexation with endogenous components of body fluids in a manner that sterically interferes with its detection by ELISA and other immunoassays. Recent work by our group and others has shown that complexation can be disrupted with protein-denaturing protocols. By way of followup, we recently described an enzymatic digestion (Proteinase K) sample pretreatment that enables quantitative recovery of ManLAM spiked into healthy human control serum. Herein, we report on the transfer of our benchtop sample pretreatment methodology to an automated microfluidic platform. We show that this platform can be configured to: (1) carry out the pretreatment process with very little user interaction and, (2) yield recoveries for ManLAm spiked into control serum which are statistically indistinguishable from those achieved by the benchtop process. Plans to integrate this device with a portable sample reader as a possible basis for a PoC TB diagnostic system and analyze patient samples are briefly discussed.

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Source
http://dx.doi.org/10.1039/d4ay00772gDOI Listing

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