Evidence map›Paper›PMID 25621868›Full record

ArticleACS nano2015

Preparation and in vitro antimicrobial activity of silver-bearing degradable polymeric nanoparticles of polyphosphoester-block-poly(L-lactide).

Young H Lim, Kristin M Tiemann, Gyu Seong Heo, Patrick O Wagers, Yohannes H Rezenom, Shiyi Zhang, Fuwu Zhang, Wiley J Youngs, David A Hunstad, Karen L Wooley

Abstract read
In one paragraph

Article in ACS nano, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
6.8field-weighted citation impact, top 2% 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

26 citing papers in PubMed, 94 citations in OpenAlex.

  1. Article
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  6. Review
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  11. Nanoparticles as Potential Novel Therapies for Urinary Tract Infections.Frontiers in cellular and infection microbiology · 2021
    Review
  12. Article
  13. Review
  14. Review
  15. Review
  16. Article
  17. Nanoscience-Based Strategies to Engineer Antimicrobial Surfaces.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2018
    Review
  18. Article
  19. Article
  20. 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

10 authors at 3 institutions in 1 country.

Young H LimDepartments of Chemistry, Chemical Engineering, and Materials Science and Engineering, and Laboratory for Synthetic-Biologic Interactions, Texas A&M University , P.O. Box 30012, 3255 TAMU, College Station, Texas 77842, United States.
Kristin M Tiemann
Gyu Seong Heo
Patrick O Wagers
Yohannes H Rezenom
Shiyi Zhang
Fuwu Zhang
Wiley J Youngs
David A Hunstad
Karen L Wooley
Texas A&M University · USUniversity of Akron · USWashington University in St. Louis · US

Funding

pan-Genome of E.coli in the bladder and gut of women with recurrent UTIP50DK064540 · NIDDK · WASHINGTON UNIVERSITY · PI HULTGREN, SCOTT J. · 2002 to 2017
$17.9M
ADHESIN-BASED NANOTHERAPEUTICS IN URINARY TRACT INFECTIONR01DK082546 · NIDDK · WASHINGTON UNIVERSITY · PI HUNSTAD, DAVID · 2010 to 2014
$1.6M
NHLBI NIH HHS HHSN268201000046CNIDDK NIH HHS P50 DK064540NIDDK NIH HHS R01 DK082546NIDDK NIH HHS R01-DK082546
6 · The paper itself

Abstract

The development of well-defined polymeric nanoparticles (NPs) as delivery carriers for antimicrobials targeting human infectious diseases requires rational design of the polymer template, an efficient synthetic approach, and fundamental understanding of the developed NPs, e.g., drug loading/release, particle stability, and other characteristics. Herein, we developed and evaluated the in vitro antimicrobial activity of silver-bearing, fully biodegradable and functional polymeric NPs. A series of degradable polymeric nanoparticles (dNPs), composed of phosphoester and L-lactide and designed specifically for silver loading into the hydrophilic shell and/or the hydrophobic core, were prepared as potential delivery carriers for three different types of silver-based antimicrobials-silver acetate or one of two silver carbene complexes (SCCs). Silver-loading capacities of the dNPs were not influenced by the hydrophilic block chain length, loading site (i.e., core or shell), or type of silver compound, but optimization of the silver feed ratio was crucial to maximize the silver loading capacity of dNPs, up to ca. 12% (w/w). The release kinetics of silver-bearing dNPs revealed 50% release at ca. 2.5-5.5 h depending on the type of silver compound. In addition, we undertook a comprehensive evaluation of the rates of hydrolytic or enzymatic degradability and performed structural characterization of the degradation products. Interestingly, packaging of the SCCs in the dNP-based delivery system improved minimum inhibitory concentrations up to 70%, compared with the SCCs alone, as measured in vitro against 10 contemporary epidemic strains of Staphylococcus aureus and eight uropathogenic strains of Escherichia coli. We conclude that these dNP-based delivery systems may be beneficial for direct epithelial treatment and/or prevention of ubiquitous bacterial infections, including those of the skin and urinary tract.

Indexed as

Drug DesignAnti-Bacterial AgentsEscherichia coliKineticsMicrobial Sensitivity TestsNanoparticlesOrganophosphatesPolyestersSilverStaphylococcus aureusAnti-Bacterial AgentsOrganophosphatesPolyesterspoly(lactide)Silver(bio)degradable polymeric nanoparticlesEscherichia colifunctional polymeric nanoparticlesin vitro antimicrobial efficacynanoparticle-based antimicrobial delivery systemsilver carbene complexesStaphylococcus aureus

Identifiers

PMID25621868
PMCPMC4455953
OpenAlexW2057344665

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.