Evidence map›Paper›PMID 26141437›Full record

ArticleColloids and surfaces. B, Biointerfaces2015

Comparative study of antibody immobilization mediated by lipid and polymer fibers.

Celine Cohn, Siu Ling Leung, Zhengbao Zha, Jessica Crosby, Weibing Teng, Xiaoyi Wu

Abstract readComparative Study
In one paragraph

Article in Colloids and surfaces. B, Biointerfaces, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. 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

6 authors at 1 institution in 1 country.

Celine CohnBiomedical Engineering GIDP, University of Arizona, Thomas W. Keating Bioresearch Building, 1657 E Helen Street, Tucson, AZ 85721, USA.
Siu Ling LeungDepartment of Aerospace and Mechanical Engineering, University of Arizona, 1130N Mountain Ave, Tucson, AZ 85721, USA.
Zhengbao ZhaDepartment of Aerospace and Mechanical Engineering, University of Arizona, 1130N Mountain Ave, Tucson, AZ 85721, USA.
Jessica CrosbyBiomedical Engineering GIDP, University of Arizona, Thomas W. Keating Bioresearch Building, 1657 E Helen Street, Tucson, AZ 85721, USA.
Weibing TengDepartment of Aerospace and Mechanical Engineering, University of Arizona, 1130N Mountain Ave, Tucson, AZ 85721, USA.
Xiaoyi WuBiomedical Engineering GIDP, University of Arizona, Thomas W. Keating Bioresearch Building, 1657 E Helen Street, Tucson, AZ 85721, USA; Department of Aerospace and Mechanical Engineering, University of Arizona, 1130N Mountain Ave, Tucson, AZ 85721, USA. Electronic address: xwu@email.arizona.edu.
University of Arizona · US

Funding

Cardiovascular Biomedical Engineering Training GrantT32HL007955 · NHLBI · UNIVERSITY OF ARIZONA · PI BARTON, JENNIFER KEHLET · 2001 to 2020
$5.1M
Protein-cell assemblies as tissue-mimicsR21EB009160 · NIBIB · UNIVERSITY OF ARIZONA · PI WU, XIAOYI · 2009 to 2010
$409k
NHLBI NIH HHS T32 HL007955NHLBI NIH HHS T32HL007955NIBIB NIH HHS R21 EB009160NIBIB NIH HHS R21EB009160
6 · The paper itself

Abstract

Antibody immobilization and function retention are important to a variety of applications, including proteomics, drug discovery, diagnostics, and biosensors. The present study investigates antibody immobilization mediated by cholesteryl succinyl silane (CSS) fibers, in comparison to hydrophobic polycaprolactone (PCL) fibers and hydrophilic plasma-treated PCL fibers. When incubated with a model protein, the formation of protein aggregates is observed on hydrophobic PCL fibers but not on the more hydrophobic CSS fibers, indicating that CSS fibers immobilize proteins through mechanisms other than hydrophobic interaction. When exposed to a limited amount of antibody, CSS fibers immobilize more antibodies than plasma-treated PCL fibers and no fewer antibodies than PCL fibers. The function retention of antibodies immobilized on the fibers is analyzed using a cell-capture assay, which shows that the antibody-functionalized CSS fibrous matrices capture 6- or 7-fold more cells than the antibody-functionalized PCL or plasma-treated PCL fibrous matrices, respectively. Data collected from the study show that the lipid fiber-mediated immobilization of antibody not only maintains the advantages of physical immobilization such as easiness and rapidness of operation but also improves function retention.

Indexed as

PolymersAntibodiesLipidsAntibodiesLipidsPolymersAntibody immobilizationCholesterolFunction retentionLipid fibersPhysical adsorption

Identifiers

PMID26141437
PMCPMC7067562
OpenAlexW584345664

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.