Evidence map›Paper›PMID 31849468›Full record

ArticleInternational journal of nanomedicine2019

Synergistic Anti-Staphylococcal Activity Of Niosomal Recombinant Lysostaphin-LL-37.

Somayeh Sadeghi, Haleh Bakhshandeh, Reza Ahangari Cohan, Afshin Peirovi, Parastoo Ehsani, Dariush Norouzian

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2019. 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
4.2field-weighted citation impact, top 5% 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, 51 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Niosome-loaded Tet-Amp against S. aureus, K. pneumoniae, and P. aeruginosa.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2024
    Article
  8. Surface-functionalized UIO-66-NHBMC microbiology · 2024
    Article
  9. Article
  10. Article
  11. New Weapons to Fight againstAntibiotics (Basel, Switzerland) · 2023
    Review
  12. Article
  13. Frontiers in microbiology · 2023
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Advances and perspectives for antimicrobial peptide and combinatory therapies.Frontiers in bioengineering and biotechnology · 2022
    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

6 authors at 1 institution in 1 country.

Somayeh SadeghiDepartment of Nano Biotechnology, New Technology Research Group, Pasteur Institute of Iran, Tehran, Iran.
Haleh BakhshandehDepartment of Nano Biotechnology, New Technology Research Group, Pasteur Institute of Iran, Tehran, Iran.ORCID 0000-0002-3335-4847
Reza Ahangari CohanDepartment of Nano Biotechnology, New Technology Research Group, Pasteur Institute of Iran, Tehran, Iran.ORCID 0000-0002-0490-4184
Afshin PeiroviDepartment of Nano Biotechnology, New Technology Research Group, Pasteur Institute of Iran, Tehran, Iran.
Parastoo EhsaniDepartment of Molecular Biology, Pasteur Institute of Iran, Tehran, Iran.ORCID 0000-0003-3592-2008
Dariush NorouzianDepartment of Nano Biotechnology, New Technology Research Group, Pasteur Institute of Iran, Tehran, Iran.ORCID 0000-0002-3553-3048
Pasteur Institute of Iran · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purpose

methodsIn the current study, for the first time, the synergistic activity of recombinant lysostaphin and LL-37 peptide was studied against

resultsThe optimal niosomal formulation was obtained by mixing the surfactants (span60 and tween60; 2:1 w/w), cholesterol, and dicetylphosphate at a ratio of 47:47:6, respectively. They showed uniform spherical shapes with the size of 565 and 325 nm for lysostaphin and LL-37, respectively. This formulation showed high entrapment efficiency for the peptide, protein, and a slow-release profile over time. Release kinetic was best fitted by Higuchi model indicating a diffusion-based release of the drugs. The lysostaphin/LL-37 niosomal formulation synergistically inhibited growth of

conclusionThis study indicated that the use of lysostaphin in combination with LL-37, either in niosomal or free forms, synergistically inhibited growth of

Indexed as

AnimalsAnti-Bacterial AgentsAntimicrobial Cationic PeptidesCathelicidinsDrug LiberationDrug SynergismFibroblastsLiposomesLysostaphinMiceMicrobial Sensitivity TestsParticle SizeRecombinant ProteinsStaphylococcal InfectionsStaphylococcus aureusAnti-Bacterial AgentsAntimicrobial Cationic PeptidesCathelicidinsLiposomesLysostaphinRecombinant ProteinsLL-37lysostaphinStaphylococcus aureussustained releasesynergy

Identifiers

PMID31849468
PMCPMC6911324
OpenAlexW2991989248

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.