Evidence map›Paper›PMID 29289681›Full record

ArticleActa biomaterialia2018

Reducible disulfide poly(beta-amino ester) hydrogels for antioxidant delivery.

Andrew L Lakes, Carolyn T Jordan, Prachi Gupta, David A Puleo, J Zach Hilt, Thomas D Dziubla

Abstract read
In one paragraph

Article in Acta biomaterialia, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.4field-weighted citation impact, top 22% 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

12 citing papers in PubMed, 41 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

6 authors at 1 institution in 1 country.

Andrew L LakesDepartment of Chemical and Materials Engineering, University of Kentucky, Lexington, KY 40506, USA. Electronic address: andrewllakes@gmail.com.
Carolyn T JordanDepartment of Chemical and Materials Engineering, University of Kentucky, Lexington, KY 40506, USA. Electronic address: carolyn.schumer@uky.edu.
Prachi GuptaDepartment of Chemical and Materials Engineering, University of Kentucky, Lexington, KY 40506, USA. Electronic address: guptprachi@gmail.com.
David A PuleoF. Joseph Halcomb III, M.D. Department of Biomedical Engineering, University of Kentucky, Lexington, KY 40506, USA. Electronic address: puleo@uky.edu.
J Zach HiltDepartment of Chemical and Materials Engineering, University of Kentucky, Lexington, KY 40506, USA. Electronic address: hilt@engr.uky.edu.
Thomas D DziublaDepartment of Chemical and Materials Engineering, University of Kentucky, Lexington, KY 40506, USA. Electronic address: thomas.dziubla@uky.edu.
University of Kentucky · US

Funding

The University of Kentucky Cancer Nanotechnology Training Center (UK CNTC)R25CA153954 · NCI · UNIVERSITY OF KENTUCKY · PI ANDERSON, BRADLEY D, EVERS, BERNARD MARK · 2010 to 2014
$1.6M
NCI NIH HHS R25 CA153954
6 · The paper itself

Abstract

Recently, biomaterials have been designed to contain redox-sensitive moieties, such as thiols and disulfides, to impart responsive degradation and/or controlled release. However, due to the high sensitivity of cellular redox-based systems which maintain free-radical homeostasis (e.g. glutathione/glutathione disulfide), if these biomaterials modify the cellular redox environment, they may inadvertently affect cellular compatibility and/or oxidative stress defenses. In this work, we hypothesize that the degradation products of a poly(β-amino ester) (PBAE) hydrogel formed with redox sensitive disulfide (cystamine) crosslinking could serve as a supplement to the environmental cellular antioxidant defenses. Upon introduction into a reducing environment, these disulfide-containing hydrogels cleave to present bound-thiol groups, yet remain in the bulk form at up to 66 mol% cystamine of the total amines. By controlling the molar fraction of cystamine, it was apparent that the thiol content varied human umbilical vein endothelial cell (HUVEC) viability IC STATEMENT OF SIGNIFICANCE: In this work, we demonstrate a unique property of disulfide containing degradable biomaterials. By changing the redox state of the degradation products (from oxidized to reduced), it is possible to increase the IC

Indexed as

Drug Delivery SystemsAntioxidantsCell DeathCell SurvivalDisulfidesDrug LiberationHumansHuman Umbilical Vein Endothelial CellsHydrogelsInhibitory Concentration 50MitochondriaNanoparticlesOxidation-ReductionOxidative StressOxygen ConsumptionPolymersAntioxidantsDisulfidesHydrogelspoly(beta-amino ester)PolymersSulfhydryl CompoundsAntioxidantBiocompatibilityDisulfideHydrogelOxidative stress

Identifiers

PMID29289681
PMCPMC5803326
OpenAlexW2778927268

What OpenQuestion holds

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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.