Evidence map›Paper›PMID 32959112›Full record

ArticleAnalytical and bioanalytical chemistry2020

Using a lactadherin-immobilized silicon surface for capturing and monitoring plasma microvesicles as a foundation for diagnostic device development.

Agnieszka Kamińska, Katarzyna Gajos, Olga Woźnicka, Anna Dłubacz, Magdalena E Marzec, Andrzej Budkowski, Ewa Ł Stępień

Open access · hybridAbstract read
In one paragraph

Article in Analytical and bioanalytical chemistry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 46% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Article
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

7 authors at 2 institutions in 1 country.

Agnieszka KamińskaDepartment of Medical Physics, M. Smoluchowski Institute of Physics, Jagiellonian University, 30-348, Kraków, Poland.
Katarzyna GajosDepartment of Molecular and Interfacial Biophysics, M. Smoluchowski Institute of Physics, Jagiellonian University, 30-348, Kraków, Poland. katarzyna.gajos@uj.edu.pl.
Olga WoźnickaDepartment of Cell Biology and Imaging, Institute of Zoology and Biomedical Research, Jagiellonian University, 30-387, Kraków, Poland.
Anna DłubaczDepartment of Advanced Materials Engineering, M. Smoluchowski Institute of Physics, Jagiellonian Univeristy, 30-348, Kraków, Poland.
Magdalena E MarzecInstitute of Physics, Cracow University of Technology, 30-084, Kraków, Poland.
Andrzej BudkowskiDepartment of Molecular and Interfacial Biophysics, M. Smoluchowski Institute of Physics, Jagiellonian University, 30-348, Kraków, Poland.
Ewa Ł StępieńDepartment of Medical Physics, M. Smoluchowski Institute of Physics, Jagiellonian University, 30-348, Kraków, Poland. e.stepien@uj.edu.pl.
Institute of Physics · PLJagiellonian University · PL

Funding

Ministerstwo Nauki i Szkolnictwa Wyższego 7150/E-338/M/2017Narodowe Centrum Badań i Rozwoju LIDER/9/0031/L-9/NCBR/2018Polish National Science Centre 2016/21/N/ST5/00880
6 · The paper itself

Abstract

Microvesicles (MVs) are found in several types of body fluids and are promising disease biomarkers and therapeutic targets. This study aimed to develop a novel biofunctionalized surface for binding plasma microvesicles (PMVs) based on a lab-on-a-chip (LOC) approach. A new lactadherin (LACT)-functionalized surface was prepared and examined for monitoring PMVs. Moreover, two different strategies of LACT immobilization on a silicon surface were applied to compare different LACT orientations. A higher PMV to LACT binding efficiency was observed for LACT bonded to an αvβ3 integrin-functionalized surface compared with that for LACT directly bonded to a glutaraldehyde-modified surface. Effective binding of PMVs and its components for both LACT immobilization strategies was confirmed using spectral ellipsometry and time-of-flight secondary ion mass spectrometry methods. The proposed PMV capturing system can be used as a foundation to design novel point-of-care (POC) diagnostic devices to detect and characterize PMVs in clinical samples. Graphical Abstract.

Indexed as

Point-of-Care SystemsCell-Derived MicroparticlesHumansLab-On-A-Chip DevicesMicroscopy, Atomic ForcePlasmaSiliconSpectrometry, Mass, Secondary IonSurface PropertiesSiliconBiosensorExtracellular vesiclesLactadherinMicrovesiclesNanotechnologyTime-of-flight secondary ion mass spectrometry

Identifiers

PMID32959112
PMCPMC7584542
OpenAlexW3087618848

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.