Evidence map›Paper›PMID 26812966›Full record

ArticlePharmaceutical research2016

Nanoparticle Attachment to Erythrocyte Via the Glycophorin A Targeted ERY1 Ligand Enhances Binding without Impacting Cellular Function.

Kaustuv Sahoo, Rangika S Hikkaduwa Koralege, Nicholas Flynn, Samyukta Koteeswaran, Peter Clark, Steve Hartson, Jing Liu, Joshua D Ramsey, Carey Pope, Ashish Ranjan

Abstract read
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In one paragraph

Article in Pharmaceutical research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

13 citing papers in PubMed, 26 citations in OpenAlex.

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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 at 1 institution in 1 country.

Kaustuv SahooDepartment of Physiological Sciences, Oklahoma State University, Stillwater, Oklahoma, 74078, USA.
Rangika S Hikkaduwa KoralegeSchool of Chemical Engineering, Oklahoma State University, Stillwater, Oklahoma, 74078, USA.
Nicholas FlynnSchool of Chemical Engineering, Oklahoma State University, Stillwater, Oklahoma, 74078, USA.
Samyukta KoteeswaranSchool of Chemical Engineering, Oklahoma State University, Stillwater, Oklahoma, 74078, USA.
Peter ClarkSchool of Chemical Engineering, Oklahoma State University, Stillwater, Oklahoma, 74078, USA.
Steve HartsonDepartment of Biochemistry and Molecular Biology, Oklahoma State University, Stillwater, Oklahoma, 74078, USA.
Jing LiuDepartment of Physiological Sciences, Oklahoma State University, Stillwater, Oklahoma, 74078, USA.
Joshua D RamseySchool of Chemical Engineering, Oklahoma State University, Stillwater, Oklahoma, 74078, USA.
Carey PopeDepartment of Physiological Sciences, Oklahoma State University, Stillwater, Oklahoma, 74078, USA.
Ashish RanjanDepartment of Physiological Sciences, Oklahoma State University, Stillwater, Oklahoma, 74078, USA. ashish.ranjan@okstate.edu.
Oklahoma State University · US

Funding

ZFC3H1 Regulation of Host Defense and Influenza A Virus PathogenesisP20GM103648 · NIGMS · OKLAHOMA STATE UNIVERSITY STILLWATER · PI CHANNAPPANAVAR, RUDRAGOUDA · 2013 to 2022
$22.3M
NIGMS NIH HHS GM103648
6 · The paper itself

Abstract

purposeNanoparticle (NP) attachment to biocompatible secondary carriers such as red blood cell (RBC) can prolong blood residence time of drug molecules and help create next-generation nanotherapeutics. However, little is known about the impact of RBC-targeted NPs on erythrocyte function.

methodsThe objectives of this study were to develop and characterize in vitro a novel poly-L-lysine (PLL) and polyethylene glycol (PEG) copolymer-based NP containing fluorescent-tagged bovine serum albumin (BSA), and conjugated with ERY1, a 12 amino acid peptide with high affinity for the RBC membrane protein glycophorin A (ENP).

resultsConfocal and flow cytometry data suggest that ENPs efficiently and irreversibly bind to RBC, with approximately 70% of erythrocytes bound after 24 h in a physiologic flow loop model compared to 10% binding of NPs without ERY1. Under these conditions, synthesized ENPs were not toxic to the RBCs. The rheological parameters at the applied shear. (0-15 Pa) were not influenced by ENP attachment to the RBCs. However, at high concentration, the strong affinity of ENPs to the glycophorin-A reduced the deformability of the RBC.

conclusionsENPs can be efficiently attached to the RBCs without adversely affecting cellular function, and this may potentially enhance circulatory half-life of drug molecules.

Indexed as

Drug Delivery SystemsAnimalsCattleErythrocyte DeformabilityErythrocyte MembraneErythrocytesGlycophorinsMiceNanoparticlesPeptidesPolyethylene GlycolsPolylysineSerum Albumin, BovineGlycophorinsPeptidesPolyethylene GlycolsPolylysineSerum Albumin, BovineERY1-ligandglycophorin A targetingnanoparticlered blood cellrheology

Identifiers

PMID26812966
OpenAlexW2290745151

What Socratic 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 Socratic graph.