Evidence map›Paper›PMID 36964439›Full record

ArticleDrug delivery and translational research2023

The development of a solid lipid nanoparticle (SLN)-based lacticin 3147 hydrogel for the treatment of wound infections.

Aoibhín Ryan, Pratikkumar Patel, Poonam Ratrey, Paula M O'Connor, Julie O'Sullivan, R Paul Ross, Colin Hill, Sarah P Hudson

Open access · hybridAbstract read
In one paragraph

Article in Drug delivery and translational research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
7.4field-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

14 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Biofilm-Responsive Nanoplatforms for Infected Wound Reconstruction.International journal of nanomedicine · 2026
    Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Review
  12. Polymeric Nanoparticles for Wound Healing.Pharmaceutical nanotechnology · 2025
    Review
  13. Review
  14. 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

8 authors at 3 institutions in 1 country.

Aoibhín RyanDepartment of Chemical Sciences, Bernal Institute, University of Limerick, Limerick, Ireland.
Pratikkumar PatelDepartment of Chemical Sciences, Bernal Institute, University of Limerick, Limerick, Ireland.
Poonam RatreyDepartment of Chemical Sciences, Bernal Institute, University of Limerick, Limerick, Ireland.
Paula M O'ConnorTeagasc Food Research Centre, Moorepark, Fermoy, Co. Cork, Ireland.
Julie O'SullivanAPC Microbiome Ireland, Cork, Ireland.
R Paul RossAPC Microbiome Ireland, Cork, Ireland.
Colin HillAPC Microbiome Ireland, Cork, Ireland.
Sarah P HudsonDepartment of Chemical Sciences, Bernal Institute, University of Limerick, Limerick, Ireland. Sarah.Hudson@ul.ie.ORCID 0000-0002-6718-2190
University of Limerick · IEUniversity College Cork · IETeagasc - The Irish Agriculture and Food Development Authority · IE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic wounds affect millions of people globally. This number is set to rise with the increasing incidence of antimicrobial-resistant bacterial infections, such as methicillin-resistant Staphylococcus aureus (MRSA), which impair the healing of chronic wounds. Lacticin 3147 is a two-peptide chain bacteriocin produced by Lactococcus lactis that is active against S. aureus including MRSA strains. Previously, poor physicochemical properties of the peptides were overcome by the encapsulation of lacticin 3147 into solid lipid nanoparticles. Here, a lacticin 3147 solid lipid nanoparticle gel is proposed as a topical treatment for S. aureus and MRSA wound infections. Initially, lacticin 3147's antimicrobial activity against S. aureus was determined before encapsulation into solid lipid nanoparticles. An optimised gel formulation with the desired physicochemical properties for topical application was developed, and the lacticin-loaded solid lipid nanoparticles and free lacticin 3147 aqueous solution were incorporated into separate gels. The release of lacticin 3147 from both the solid lipid nanoparticle and free lacticin gels was measured where the solid lipid nanoparticle gel exhibited increased activity for a longer period (11 days) compared to the free lacticin gel (9 days). Both gels displayed potent activity ex vivo against S. aureus-infected pig skin with significant bacterial eradication (> 75%) after 1 h. Thus, a long-acting potent lacticin 3147 solid lipid nanoparticle gel with the required physicochemical properties for topical delivery of lacticin 3147 to the skin for the potential treatment of S. aureus-infected chronic wounds was developed.

Indexed as

Anti-Infective AgentsMethicillin-Resistant Staphylococcus aureusWound InfectionAnimalsAnti-Bacterial AgentsHydrogelsLiposomesNanoparticlesPeptidesStaphylococcus aureusSwineAnti-Bacterial AgentsAnti-Infective AgentsHydrogelsLipid NanoparticlesLiposomesPeptidesAntimicrobial resistanceBacteriocinsDrug deliveryHydrogelsLacticin 3147Solid lipid nanoparticles

Identifiers

PMID36964439
PMCPMC10382363
OpenAlexW4360826157

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.