posted on 2021-07-16, 17:38authored byMicaela
L. Everitt, David J. Boegner, Konstantin G. Birukov, Ian M. White
Severe internal trauma results in
millions of hospitalizations
each year, including thousands of deaths caused by subsequent multiple
organ failure. The majority of these deaths occur within the first
24 h, and thus, rapid diagnosis of internal trauma severity is necessary
for immediate treatment. For early organ damage identification, diagnosis
in point-of-care settings is crucial for rapid triage and treatment.
Recent reports suggest that circulating histones may serve as a biomarker
for severe organ damage and the risk of multiple organ failure. Here,
we report a point-of-care diagnostic system that utilizes the inherent
interactions between histones and DNA for the fluorescence-based detection
of histones in whole blood. In the assay, histones within the sample
are wrapped by DNA, thus preventing an intercalating dye from binding
the DNA and fluorescing. To allow for quantitative fluorescent measurements
to be made in a point-of-care setting, we integrate a rapid, automated
blood separation step into our assay. Furthermore, we eliminate manual
reagent additions using a thermally responsive alkane partition (TRAP),
thus making the system sample-to-answer. Finally, we demonstrate the
assay in a portable fluorescence reader compatible with a point-of-care
environment. We report a limit of detection 112 ng/mL in whole blood,
suggesting that our device can be used to rapidly diagnose internal
trauma severity and the likelihood of multiple organ failure in near-patient
settings.