Evidence map›Paper›PMID 42205870›Full record

ReviewInternational journal of nanomedicine2026

Natural Compound-Loaded PLGA Nanocarriers for Infected Wound Management: A Review.

Elahe Norouzi, Jaber Hemmati, Mohammad Chehelgerdi, Mohammad Reza Arabestani

Abstract readReview
In one paragraph

Review in International journal of nanomedicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Elahe NorouziDepartment of Microbiology, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.
Jaber HemmatiDepartment of Microbiology, Faculty of Medicine, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.
Mohammad ChehelgerdiYoung Researchers and Elite Club, Shahrekord Branch, Islamic Azad University, Shahrekord, Iran.ORCID 0000-0002-3483-9424
Mohammad Reza ArabestaniDepartment of Microbiology, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.ORCID 0000-0001-9991-8193

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Infected wounds remain a significant clinical challenge due to persistent microbial colonization, biofilm formation, delayed tissue regeneration, and prolonged healing processes. Poly (lactic-co-glycolic acid) (PLGA), a biodegradable and biocompatible polymer approved by the FDA, has gained increasing attention as a carrier for natural compounds because of its ability to provide controlled and sustained drug release, improve compound stability, and enhance therapeutic efficacy. This review summarizes recent advances in PLGA-based formulations loaded with natural compounds for the treatment of infected wounds. Findings from various studies demonstrate that these nanostructures promote wound healing through antimicrobial and anti-biofilm activities, antioxidant and anti-inflammatory effects, stimulation of angiogenesis, collagen deposition, and re-epithelialization. In addition, this review discusses different aspects of PLGA-based nanostructures, including fabrication and synthesis strategies, drug release behaviors, and bacterial biofilm-targeting mechanisms, which may play an important role in the development of novel nanoparticle-based therapeutic approaches for overcoming current challenges associated with infected wound management. Overall, the delivery of natural compounds through PLGA-based systems represents a promising strategy for the effective treatment of infected wounds and the advancement of next-generation wound care therapies. This review, with a focus on PLGA-natural compound systems for the treatment of infected wounds, provides a coherent synthesis of dispersed studies and, by emphasizing antibiofilm mechanisms and controlled drug release, offers an integrated perspective for a better understanding of the therapeutic potential of these nanoplatforms.

Indexed as

Biological ProductsDrug CarriersLactic AcidNanoparticlesPolyglycolic AcidWound InfectionAnimalsAnti-Infective AgentsBiofilmsHumansNanoparticle Drug Delivery SystemPolylactic Acid-Polyglycolic Acid CopolymerWound HealingAnti-Infective AgentsBiological ProductsDrug CarriersLactic AcidNanoparticle Drug Delivery SystemPolyglycolic AcidPolylactic Acid-Polyglycolic Acid Copolymeranti-inflammatoryantioxidantnatural compoundsPLGAwound

Identifiers

PMID42205870
PMCPMC13207919

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

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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.