Evidence map›Paper›PMID 32019879›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2020

Real-time particle-by-particle detection of erythrocyte-camouflaged microsensor with extended circulation time in the bloodstream.

Wenjun Di, Xuefei Tan, Isen Andrew C Calderon, Ashlyn E Neal Reilly, Mark Niedre, Heather A Clark

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
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

14 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Wenjun DiDepartment of Pharmaceutical Sciences, Northeastern University, Boston, MA 02115.ORCID 0000-0002-1662-311X
Xuefei TanDepartment of Electrical and Computer Engineering, Northeastern University, Boston, MA 02115.
Isen Andrew C CalderonDepartment of Bioengineering, Northeastern University, Boston, MA 02115.ORCID 0000-0001-8910-1083
Ashlyn E Neal ReillyDepartment of Bioengineering, Northeastern University, Boston, MA 02115.
Mark NiedreDepartment of Electrical and Computer Engineering, Northeastern University, Boston, MA 02115.
Heather A ClarkDepartment of Bioengineering, Northeastern University, Boston, MA 02115; h.clark@northeastern.edu.ORCID 0000-0002-2628-9194

Funding

Circulating Red Blood Cell Based Nanosensors for Continuous, Real-Time Drug MonitoringR01EB024186 · NIBIB · NORTHEASTERN UNIVERSITY · PI CLARK, HEATHER A, NIEDRE, MARK JONATHAN · 2018 to 2021
$1.6M
Ultra-Rare Cell In Vivo Flow CytometryR01HL124315 · NHLBI · NORTHEASTERN UNIVERSITY · PI NIEDRE, MARK JONATHAN · 2015 to 2018
$1.5M
NHLBI NIH HHS R01 HL124315NIBIB NIH HHS R01 EB024186
6 · The paper itself

Abstract

Personalized medicine offers great potential benefits for disease management but requires continuous monitoring of drugs and drug targets. For instance, the therapeutic window for lithium therapy of bipolar disorder is very narrow, and more frequent monitoring of sodium levels could avoid toxicity. In this work, we developed and validated a platform for long-term, continuous monitoring of systemic analyte concentrations in vivo. First, we developed sodium microsensors that circulate directly in the bloodstream. We used "red blood cell mimicry" to achieve long sensor circulation times of up to 2 wk, while being stable, reversible, and sensitive to sodium over physiologically relevant concentration ranges. Second, we developed an external optical reader to detect and quantify the fluorescence activity of the sensors directly in circulation without having to draw blood samples and correlate the measurement with a phantom calibration curve to measure in vivo sodium. The reader design is inherently scalable to larger limbs, species, and potentially even humans. In combination, this platform represents a paradigm for in vivo drug monitoring that we anticipate will have many applications in the future.

Indexed as

AnimalsBlood CirculationDrug MonitoringErythrocytesFluorescenceMiceMice, NudeMolecular MimicryRatsSodiumSodiumdiffuse in vivo flow cytometryerythrocytesmicrosensorssodium monitoring

Identifiers

PMID32019879
PMCPMC7035616

What OpenQuestion holds

Textmetadata
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.