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University of Washington

Towards Rapid Measurement of Non-Nucleoside Reverse Transcriptase Inhibitors in a Portable, Low-Cost Platform

Abstract

dc:description.abstract

While antiretrovirals (ARV) for HIV prevention and treatment have become very effective over the last 40 years of development, many people living with HIV (PLWH) encounter inadequately suppressed viral loads and treatment failure. Providing drug-level feedback (DLF) can identify those with subtherapeutic ARV levels quickly to promote interventions to improve outcomes. Most DLF approaches measure drug levels via liquid chromatography-tandem mass spectrometry (LC-MS/MS), which can incur high costs and lengthy delays that make it unsuitable for near point-of-care settings. In response, we developed a rapid enzymatic assay for the measurement of non-nucleoside reverse transcriptase inhibitors (NNRTIs) based on inhibition of DNA synthesis using an inexpensive, portable instrument. This assay is entitled the REverse transcriptase ACTivity (REACT) assay. This work demonstrates proof-of-concept measurement of multiple NNRTIs in buffer and spiked plasma samples. We also demonstrate the feasibility of using a portable reader to support routine drug measurement at or near the point of care, providing prompt feedback to facilitate rapid interventions.

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Brainerd, Cara
Advisor dc:contributor.advisor
  • Olanrewaju, Ayokunle

Subjects

dc:subject × 7

Rights

dc:rights
Statement dc:rights
  • CC BY-ND
Language dc:language.iso
en_US

Identifiers

dc:identifier.*
Handle dc:identifier.uri
https://hdl.handle.net/1773/52714
OAI identifier oai:identifier
oai:digital.lib.washington.edu:1773/52714

Chain of custody

source
Harvested from
University of Washington
Base URL
digital.lib.washington.edu/server/oai/request
Last updated
2026-07-24
Source record
OAI-PMH GetRecord
citation

Brainerd, Cara. Towards Rapid Measurement of Non-Nucleoside Reverse Transcriptase Inhibitors in a Portable, Low-Cost Platform. 2025. https://hdl.handle.net/1773/52714