Evidence map›Paper›PMID 30771234›Full record

ArticleJournal of biomedical materials research. Part A2019

Use of affinity allows anti-inflammatory and anti-microbial dual release that matches suture wound resolution.

Rebecca M Haley, Victoria R Qian, Greg D Learn, Horst A von Recum

Abstract read
In one paragraph

Article in Journal of biomedical materials research. Part A, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. A review of current advancements for wound healing: Biomaterial applications and medical devices.Journal of biomedical materials research. Part B, Applied biomaterials · 2022
    Review
  7. Article
  8. 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

4 authors.

Rebecca M HaleyDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland, Ohio 44106.ORCID 0000-0001-7322-7829
Victoria R QianDepartment of Bioengineering, University of California, Berkeley, California 94720.
Greg D LearnDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland, Ohio 44106.
Horst A von RecumDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland, Ohio 44106.

Funding

Reducing Adhesions in Hernia Repair Meshes Through a Polysaccharide CoatingR01GM121477 · NIGMS · CASE WESTERN RESERVE UNIVERSITY · PI VON RECUM, HORST A. · 2017 to 2019
$870k
NIGMS NIH HHS R01 GM121477
6 · The paper itself

Abstract

Surgical sutures are vulnerable to bacterial infections and biofilm formation. At the suture site, pain and undesirable, excess inflammation are additionally detrimental to wound healing. The development of a polymerized cyclodextrin (pCD) coated surgical suture introduces the capability to locally deliver both anti-inflammatory and anti-microbial drugs throughout the phases of acute and chronic healing. Local delivery allows for the improvement of wound healing while reducing related systemic side effects and drug resistance. Through testing, it has been shown that the fabrication of our pCD coating minimally affects the suture's mechanical properties. In vitro studies show measurable and consistent drug delivery for nearly 5 weeks. The therapeutic level of this delivery is sufficient to show inhibition of bacterial growth for 4 weeks, and free-radical scavenging (an in vitro anti-inflammatory activity approximation) for 2 weeks. With this pCD coating technique, we maintain clinical performance standards while also introducing a long-term dual delivery system relevant to the wound healing timeframe. © 2019 Wiley Periodicals, Inc. J Biomed Mater Res Part A, 2019.

Indexed as

Drug Delivery SystemsSuturesAnti-Infective AgentsAnti-Inflammatory AgentsBiphenyl CompoundsCoated Materials, BiocompatibleCyclodextrinsDrug LiberationFree Radical ScavengersMicrobial Sensitivity TestsPicratesPolymerizationResveratrolRifampinSolventsStaphylococcus aureus1,1-diphenyl-2-picrylhydrazylAnti-Infective AgentsAnti-Inflammatory AgentsBiphenyl CompoundsCoated Materials, BiocompatibleCyclodextrinsFree Radical ScavengersPicratesResveratrolRifampinSolventsanti-inflammatoryanti-microbialdrug deliverysuturewound healing

Identifiers

PMID30771234
PMCPMC6527479

What OpenQuestion holds

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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.