Evidence map›Paper›PMID 24285484›Full record

ArticleScience translational medicine2013

Real-time, aptamer-based tracking of circulating therapeutic agents in living animals.

Brian Scott Ferguson, David A Hoggarth, Dan Maliniak, Kyle Ploense, Ryan J White, Nick Woodward, Kuangwen Hsieh, Andrew J Bonham, Michael Eisenstein, Tod E Kippin and 2 more

Abstract read
In one paragraph

Article in Science translational medicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 157 papers.

0numbers the graph read from it
0cells of the map it votes in
157citing papers in PubMed
7.2field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

157 citing papers in PubMed, 392 citations in OpenAlex.

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  15. Continuous, Week-Long, Seconds-ResolvedJournal of the American Chemical Society · 2026
    Article
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97 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 1 country.

Brian Scott FergusonInstitute for Collaborative Biotechnologies, University of California, Santa Barbara, Santa Barbara, CA 93106, USA.
David A Hoggarth
Dan Maliniak
Kyle Ploense
Ryan J White
Nick Woodward
Kuangwen Hsieh
Andrew J Bonham
Michael Eisenstein
Tod E Kippin
Kevin W Plaxco
Hyongsok Tom Soh
University of California, Santa Barbara · USMetropolitan State University of Denver · USUniversity of Maryland, Baltimore County · US

Funding

Midwest Progenitor Cell ConsortiumU01HL099773 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI THOMSON, JAMES ALEXANDER · 2009 to 2015
$7.8M
QPASS: Quantitative Parallel Aptamer Selection SystemU54DK093467 · NIDDK · UNIVERSITY OF CALIFORNIA SANTA BARBARA · PI SMITH, LLOYD M, SOH, HYONGSOK TOM · 2011 to 2013
$3.2M
Rapid detection of diagnostic chemokinesR01AI076899 · NIAID · UNIVERSITY OF CALIFORNIA SANTA BARBARA · PI PLAXCO, KEVIN W · 2010 to 2014
$1.7M
Interactions between prenatal stress and genetics in cocaine responsiveness.R01DA027525 · NIDA · UNIVERSITY OF CALIFORNIA SANTA BARBARA · PI KIPPIN, TOD EDWARD · 2010 to 2014
$1.6M
Electrochemical arrays for the detection of small molecule drugsR01EB007689 · NIBIB · UNIVERSITY OF CALIFORNIA SANTA BARBARA · PI PLAXCO, KEVIN W · 2008 to 2011
$1.3M
Two-Photon Microscopy for Biomedical ResearchS10RR022585 · NCRR · UNIVERSITY OF CALIFORNIA SANTA BARBARA · PI REESE, BENJAMIN E · 2007 to 2007
$500k
NCRR NIH HHS 1S10RR022585-01A1NCRR NIH HHS S10 RR022585NHLBI NIH HHS U01HL099773-01NIAID NIH HHS R01 AI076899NIBIB NIH HHS R01 EB007689NIDA NIH HHS R01 DA027525NIDDK NIH HHS U54 DK093467PHS HHS R01A1076899
6 · The paper itself

Abstract

A sensor capable of continuously measuring specific molecules in the bloodstream in vivo would give clinicians a valuable window into patients' health and their response to therapeutics. Such technology would enable truly personalized medicine, wherein therapeutic agents could be tailored with optimal doses for each patient to maximize efficacy and minimize side effects. Unfortunately, continuous, real-time measurement is currently only possible for a handful of targets, such as glucose, lactose, and oxygen, and the few existing platforms for continuous measurement are not generalizable for the monitoring of other analytes, such as small-molecule therapeutics. In response, we have developed a real-time biosensor capable of continuously tracking a wide range of circulating drugs in living subjects. Our microfluidic electrochemical detector for in vivo continuous monitoring (MEDIC) requires no exogenous reagents, operates at room temperature, and can be reconfigured to measure different target molecules by exchanging probes in a modular manner. To demonstrate the system's versatility, we measured therapeutic in vivo concentrations of doxorubicin (a chemotherapeutic) and kanamycin (an antibiotic) in live rats and in human whole blood for several hours with high sensitivity and specificity at subminute temporal resolution. We show that MEDIC can also obtain pharmacokinetic parameters for individual animals in real time. Accordingly, just as continuous glucose monitoring technology is currently revolutionizing diabetes care, we believe that MEDIC could be a powerful enabler for personalized medicine by ensuring delivery of optimal drug doses for individual patients based on direct detection of physiological parameters.

Indexed as

Aptamers, NucleotideAnimalsBiosensing TechniquesDiabetes MellitusDoxorubicinHumansKanamycinMaleMicrofluidicsRatsRats, Sprague-DawleyAptamers, NucleotideDoxorubicinKanamycin

Identifiers

PMID24285484
PMCPMC4010950
OpenAlexW2119638450

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.