Evidence map›Paper›PMID 19569127›Full record

ArticleElectrophoresis2009

Chip-based immunoaffinity CE: application to the measurement of brain-derived neurotrophic factor in skin biopsies.

Terry M Phillips, Edward F Wellner

Abstract readComparative Study
In one paragraph

Article in Electrophoresis, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

9 citing papers in PubMed, 22 citations in OpenAlex.

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  9. Microfluidic, bead-based assay: Theory and experiments.Journal of chromatography. B, Analytical technologies in the biomedical and life sciences · 2010
    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

2 authors at 1 institution in 1 country.

Terry M PhillipsUltramicro Immunodiagnostics Section, Laboratory of Bioengineering and Physical Science, National Institute of Biomedical Imaging and Bioengineering, NIH, Bethesda, MD 20892, USA. phillipt@mail.nih.gov
Edward F Wellner
National Institute of Biomedical Imaging and Bioengineering · US

Funding

Development Of An Ultrasensitive Capillary Electrophoresis Detection SystemZIAEB000018 · NIBIB · NATIONAL INSTITUTE OF BIOMEDICAL IMAGING AND BIOENGINEERING · PI PHILLIPS, TERRY M. · 2009 to 2010
$139k
Development of a Static Tissue Sampling ProbeZIAEB000041 · NIBIB · NATIONAL INSTITUTE OF BIOMEDICAL IMAGING AND BIOENGINEERING · PI PHILLIPS, TERRY M. · 2009 to 2010
$120k
Development Of An Ultrasensitive Capillary Electrophoresis Detection SystemZ01EB000018 · NIBIB · NATIONAL INSTITUTE OF BIOMEDICAL IMAGING AND BIOENGINEERING · PI PHILLIPS, TERRY M. · 2007 to 2008
$74k
Intramural NIH HHS Z01 EB000018
6 · The paper itself

Abstract

A chip-based immunoaffinity CE system has been employed to measure the concentrations of brain-derived neurotrophic factor in human skin biopsies, taken during atopic inflammatory events. The device employs a replaceable immunoaffinity disk to which capture antibodies have been chemically immobilized. Homogenates obtained from micro-dissected human skin samples were injected into the system, where the analyte of interest was captured in the immunoextraction port, thus allowing non-reactive materials to be removed prior to analysis. The captured analyte was labeled in situ with a red-emitting laser dye before being released from the capture antibody, separated by electrophoresis, and the resolved peaks detected by online LIF. Comparison of this chip-based system with conventional immunoassay demonstrated good correlation when analyzing both standards and patient samples. The system was semi-automated resulting in a CE analysis within 1.5 min and a total of circa 5 min. Intra- and inter-assay CV's of 3.85 and 4.19 were achieved with circa 98.8% recovery of brain-derived neurotrophic factor at a concentration of 100 pg/mL. The assay demonstrated clear differences between clinical stages of atopic dermatitis in human patients and could run 10-15 samples per hour. This system holds the potential for being modified to be a portable unit that could be used in clinics and other biomedical screening studies.

Indexed as

AdultBiopsyBrain-Derived Neurotrophic FactorDermatitis, AtopicElectrophoresis, CapillaryEnzyme-Linked Immunosorbent AssayHumansImmunoassayInflammationMicrofluidic Analytical TechniquesReproducibility of ResultsSensitivity and SpecificitySkinBrain-Derived Neurotrophic Factor

Identifiers

PMID19569127
PMCPMC2778805
OpenAlexW2087364876

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.