Evidence map›Paper›PMID 29269331›Full record

ArticleActa biomaterialia2018

A bio-based pro-antimicrobial polymer network via degradable acetal linkages.

Douglas V Amato, Dahlia N Amato, Logan T Blancett, Olga V Mavrodi, William B Martin, Sarah N Swilley, Michael J Sandoz, Glenmore Shearer, Dmitri V Mavrodi, Derek L Patton

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 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 29% 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

5 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Review
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.

Douglas V AmatoSchool of Polymer Science and Engineering, The University of Southern Mississippi, Hattiesburg, MS 39406, United States.
Dahlia N AmatoSchool of Polymer Science and Engineering, The University of Southern Mississippi, Hattiesburg, MS 39406, United States.
Logan T BlancettDepartment of Biological Sciences, The University of Southern Mississippi, Hattiesburg, MS 39406, United States.
Olga V MavrodiDepartment of Biological Sciences, The University of Southern Mississippi, Hattiesburg, MS 39406, United States.
William B MartinSchool of Polymer Science and Engineering, The University of Southern Mississippi, Hattiesburg, MS 39406, United States.
Sarah N SwilleySchool of Polymer Science and Engineering, The University of Southern Mississippi, Hattiesburg, MS 39406, United States.
Michael J SandozSchool of Polymer Science and Engineering, The University of Southern Mississippi, Hattiesburg, MS 39406, United States.
Glenmore ShearerDepartment of Biological Sciences, The University of Southern Mississippi, Hattiesburg, MS 39406, United States.
Dmitri V MavrodiDepartment of Biological Sciences, The University of Southern Mississippi, Hattiesburg, MS 39406, United States.
Derek L PattonSchool of Polymer Science and Engineering, The University of Southern Mississippi, Hattiesburg, MS 39406, United States. Electronic address: derek.patton@usm.edu.
University of Southern Mississippi · US

Funding

Training and Mentoring Core P20GM103476 · NIGMS · UNIVERSITY OF SOUTHERN MISSISSIPPI · PI MICHAEL R GARRETT · 2012 to 2026
$60.2M
TOUGALOO PROTEOMICSP20RR016476 · NCRR · UNIVERSITY OF SOUTHERN MISSISSIPPI · PI SHEARER, GLEN · 2001 to 2011
$30.4M
NCRR NIH HHS P20 RR016476NIGMS NIH HHS P20 GM103476
6 · The paper itself

Abstract

The synthesis of a fully degradable, bio-based, sustained release, pro-antimicrobial polymer network comprised of degradable acetals (PANDA) is reported. The active antimicrobial agent - p-anisaldehyde (pA) (an extract from star anise) - was converted into a UV curable acetal containing pro-antimicrobial monomer and subsequently photopolymerized into a homogenous thiol-ene network. Under neutral to acidic conditions (pH < 8), the PANDAs undergo surface erosion and exhibit sustained release of pA over 38 days. The release of pA from PANDAs was shown to be effective against both bacterial and fungal pathogens. From a combination of confocal microscopy and transmission electron microscopy, we observed that the released pA disrupts the cell membrane. Additionally, we demonstrated that PANDAs have minimal cytotoxicity towards both epithelial cells and macrophages. Although a model platform, these results point to promising pathways for the design of fully degradable sustained-release antimicrobial systems with potential applications in agriculture, pharmaceuticals, cosmetics, household/personal care, and food industries. STATEMENT OF SIGNIFICANCE: With the increasing number of patients prescribed immunosuppressants coupled with the rise in antibiotic resistance - life-threatening microbial infections are a looming global threat. With limited success within the antibiotic pipeline, nature-based essential oils (EOs) are being investigated for their multimodal effectiveness against microbes. Despite the promising potential of EOs, difficulties in their encapsulation, limited water solubility, and high volatility limit their use. Various studies have shown that covalent attachment of these EO derivatives to polymers can mitigate these limitations. The current study presents the synthesis of a fully-degradable, sustained release, cytocompatible, pro-antimicrobial acetal network derived from p-anisaldehyde. This polymer network design provides a pathway toward application-specific EO releasing materials with quantitative encapsulation efficiencies, sustained release, and broad-spectrum antimicrobial activity.

Indexed as

AcetalsAnimalsAntifungal AgentsAnti-Infective AgentsBacteriaBiocompatible MaterialsCell DeathCell MembraneChlorocebus aethiopsFungiKineticsMiceMicrobial Sensitivity TestsPolymersRAW 264.7 CellsVero CellsAcetalsAntifungal AgentsAnti-Infective AgentsBiocompatible MaterialsPolymersAcetalDegradablePro-antimicrobialSustained releaseThiol-ene

Identifiers

PMID29269331
PMCPMC6064185
OpenAlexW2778318961

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.