Evidence map›Paper›PMID 41731650›Full record

ReviewACS infectious diseases2026

Targeting of the Gram-Negative Outer Membrane for Antibiotic Discovery and Potentiation.

Margot Draveny, Muriel Masi

Abstract readReview
In one paragraph

Review in ACS infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. TheInternational journal of molecular sciences · 2026
    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

2 authors.

Margot DravenyAix Marseille Univ, INSERM, SSA, MCT, Marseille 13005, France.
Muriel MasiAix Marseille Univ, INSERM, SSA, MCT, Marseille 13005, France.ORCID 0000-0002-1444-7511

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The emergence of multidrug resistance underscores the urgent need to develop new classes of antibiotics with novel mechanisms of action. The majority of antibiotics currently in use are designed to target Gram-positive bacteria. However, Gram-negative bacteria can circumvent the effects of the majority of drug molecules due to the unique composition of their outer membrane. This additional layer functions as a formidable barrier, impeding the penetration of compounds into the cell. In this context, several strategies have been identified to facilitate the accumulation of compounds in Gram-negative bacteria. This review provides a concise overview of the physicochemical properties that can assist in the entry and accumulation of compounds in Gram-negative bacteria, and it also covers various approaches for targeting or circumventing the outer membrane-mediated barrier of Gram-negative pathogenic bacteria.

Indexed as

Anti-Bacterial AgentsBacterial Outer MembraneDrug DiscoveryGram-Negative BacteriaBacterial Outer Membrane ProteinsHumansAnti-Bacterial AgentsBacterial Outer Membrane Proteinsantibiotic potentiationcompound accumulationGram-negative outer membranelipopolysaccharide transport (Lpt)outer membrane biogenesisβ-barrel assembly machinery (BAM)

Identifiers

PMID41731650
PMCPMC12993857

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.