Evidence map›Paper›PMID 28371090›Full record

ArticleAngewandte Chemie (International ed. in English)2017

A Biomimetic Phosphatidylcholine-Terminated Monolayer Greatly Improves the In Vivo Performance of Electrochemical Aptamer-Based Sensors.

Hui Li, Philippe Dauphin-Ducharme, Netzahualcóyotl Arroyo-Currás, Claire H Tran, Philip A Vieira, Shaoguang Li, Christina Shin, Jacob Somerson, Tod E Kippin, Kevin W Plaxco

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing 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

52 citing papers in PubMed.

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  9. Generalizable Molecular Switch Designs forAccounts of chemical research · 2025
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  18. Real-time label-free detection of dynamic aptamer-small molecule interactions using a nanopore nucleic acid conformational sensor.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  19. Article
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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

10 authors.

Hui LiDepartment of Chemistry and Biochemistry, University of California Santa Barbara, Santa Barbara, CA, 93106, USA.ORCID 0000-0001-7849-9735
Philippe Dauphin-DucharmeDepartment of Chemistry and Biochemistry, University of California Santa Barbara, Santa Barbara, CA, 93106, USA.
Netzahualcóyotl Arroyo-CurrásDepartment of Chemistry and Biochemistry, University of California Santa Barbara, Santa Barbara, CA, 93106, USA.ORCID 0000-0002-2740-6276
Claire H TranDepartment of Chemistry and Biochemistry, University of California Santa Barbara, Santa Barbara, CA, 93106, USA.
Philip A VieiraDepartment of Psychology, California State University, Dominguez Hills, 1000 E. Victoria Ave., Carson, CA, 90747, USA.
Shaoguang LiDepartment of Chemistry and Biochemistry, University of California Santa Barbara, Santa Barbara, CA, 93106, USA.
Christina ShinDepartment of Psychological and Brain Sciences, University of California Santa Barbara, Santa Barbara, CA, 93106, USA.
Jacob SomersonInterdepartmental Program, Biomolecular Science and Engineering, University of California Santa Barbara, Santa Barbara, CA, 93106, USA.
Tod E KippinDepartment of Psychological and Brain Sciences, University of California Santa Barbara, Santa Barbara, CA, 93106, USA.
Kevin W PlaxcoDepartment of Chemistry and Biochemistry, University of California Santa Barbara, Santa Barbara, CA, 93106, USA.ORCID 0000-0003-4772-8771

Funding

A new approach to quantitative, point-of-care serologyR01AI107936 · NIAID · UNIVERSITY OF CALIFORNIA SANTA BARBARA · PI PLAXCO, KEVIN W · 2014 to 2017
$1.4M
Personalized, high-resolution pharmacokinetic measurements to improve drug dosingF31CA183385 · NCI · UNIVERSITY OF CALIFORNIA SANTA BARBARA · PI SOMERSON, JACOB · 2014 to 2016
$107k
NCI NIH HHS F31 CA183385NIAID NIH HHS R01 AI107936
6 · The paper itself

Abstract

The real-time monitoring of specific analytes in situ in the living body would greatly advance our understanding of physiology and the development of personalized medicine. Because they are continuous (wash-free and reagentless) and are able to work in complex media (e.g., undiluted serum), electrochemical aptamer-based (E-AB) sensors are promising candidates to fill this role. E-AB sensors suffer, however, from often-severe baseline drift when deployed in undiluted whole blood either in vitro or in vivo. We demonstrate that cell-membrane-mimicking phosphatidylcholine (PC)-terminated monolayers improve the performance of E-AB sensors, reducing the baseline drift from around 70 % to just a few percent after several hours in flowing whole blood in vitro. With this improvement comes the ability to deploy E-AB sensors directly in situ in the veins of live animals, achieving micromolar precision over many hours without the use of physical barriers or active drift-correction algorithms.

Indexed as

BiomimeticsBiosensing TechniquesAlgorithmsAnimalsAptamers, NucleotideBlood Chemical AnalysisCell MembraneElectrochemical TechniquesPhosphatidylcholinesAptamers, NucleotidePhosphatidylcholinesaptamersbiomimetic surfaceselectrochemical sensorsin vivo measurementsmembrane monolayers

Identifiers

PMID28371090
PMCPMC5660315

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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.