Evidence map›Paper›PMID 20880576›Full record

ArticleBiomaterials2011

Eradication of drug resistant Staphylococcus aureus by liposomal oleic acids.

Chun-Ming Huang, Chao-Hsuan Chen, Dissaya Pornpattananangkul, Li Zhang, Michael Chan, Ming-Fa Hsieh, Liangfang Zhang

Abstract read
In one paragraph

Article in Biomaterials, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
6.3field-weighted citation impact, top 3% 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

67 citing papers in PubMed, 187 citations in OpenAlex.

  1. Review
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  5. Encapsulation of Flucytosine into nanoliposomes for enhanced antifungal activity against Candida glabrata and Candida albicans.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2025
    Article
  6. Review
  7. The Inhibitory Effect of Niosome Containing Myrtenol as an Innovative Approach to Combat Methicillin-ResistantThe Canadian journal of infectious diseases & medical microbiology = Journal canadien des maladies infectieuses et de la microbiologie medicale · 2025
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7 more citing papers are in PubMed but not listed here.

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

7 authors at 2 institutions in 2 countries.

Chun-Ming HuangDivision of Dermatology, University of California, San Diego, La Jolla, CA 92093, USA. chunming@ucsd.edu
Chao-Hsuan Chen
Dissaya Pornpattananangkul
Li Zhang
Michael Chan
Ming-Fa Hsieh
Liangfang Zhang
University of California San Diego · USChung Yuan Christian University · TW

Funding

Immunological Secretomes of the Early Anthrax InfectionR01AI067395 · NIAID · VETERANS MEDICAL RESEARCH FDN/SAN DIEGO · PI HUANG, CHUN-MING · 2006 to 2010
$1.2M
Secretomes captured in vivo via ultrafiltration probesR21RR022754 · NCRR · VETERANS MEDICAL RESEARCH FDN/SAN DIEGO · PI HUANG, CHUN-MING · 2006 to 2008
$506k
Indigenous Free Fatty Oleic acid Against MRSA Skin InfectionR21AI088147 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI HUANG, CHUN-MING · 2010 to 2011
$460k
Acne Vaccines Targeting a Surface Sialidase and a Secreted CAMP Factor ToxinR41AR056169 · NIAMS · VAXIN INC. · PI HUANG, CHUN-MING · 2008 to 2008
$100k
NCRR NIH HHS R21 RR022754NIAID NIH HHS 5R21AI088147-02NIAID NIH HHS R01 AI067395NIAID NIH HHS R01-AI067395E01NIAID NIH HHS R21 AI088147NIAMS NIH HHS 1R41AR056169-01NIAMS NIH HHS R41 AR056169PHS HHS R21-R022754-01
6 · The paper itself

Abstract

Staphylococcus aureus (S. aureus) represents a major threat to a broad range of healthcare and community associated infections. This bacterium has rapidly evolved resistance to multiple drugs throughout its antibiotic history and thus it is imperative to develop novel antimicrobial strategies to enrich the currently shrinking therapeutic options against S. aureus. This study evaluated the antimicrobial activity and therapeutic efficacy of oleic acid (OA) in a liposomal formulation as an innate bactericide against methicillin-resistant S. aureus (MRSA). In vitro studies showed that these OA-loaded liposomes (LipoOA) could rapidly fuse into the bacterial membranes, thereby significantly improving the potency of OA to kill MRSA compared with the use of free OA. Further in vivo tests demonstrated that LipoOA were highly effective in curing skin infections caused by MRSA bacteria and preserving the integrity of the infected skin using a mouse skin model. Moreover, a preliminary skin toxicity study proved high biocompatibility of LipoOA to normal skin tissues. These findings suggest that LipoOA hold great potential to become a new, effective, and safe antimicrobial agent for the treatment of MRSA infections.

Indexed as

AnimalsAnti-Bacterial AgentsApoptosisDrug Resistance, BacterialFluorescenceIn Situ Nick-End LabelingLiposomesMethicillin-Resistant Staphylococcus aureusMiceMice, Inbred ICRMicrobial Sensitivity TestsOleic AcidsSkinAnti-Bacterial AgentsLiposomesOleic Acids

Identifiers

PMID20880576
PMCPMC2987540
OpenAlexW2106046373

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.