Evidence map›Paper›PMID 42698789›Full record

ArticleFrontiers in drug delivery2026

Harnessing liposomal delivery to boost polyphenols' potential in chronic wound therapy.

Lisa Myrseth Hemmingsen, Marte Kristensen, Cecilie Thanh Loan Dang, Mari Salamonsen, Elizabeth G Aarag Fredheim, Nataša Škalko-Basnet

Abstract read
In one paragraph

Article in Frontiers in drug delivery, 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

6 authors.

Lisa Myrseth HemmingsenDepartment of Pharmacy, Drug Transport and Delivery Research Group, University of Tromsø The Arctic University of Norway, Tromsø, Norway.
Marte KristensenDepartment of Pharmacy, Drug Transport and Delivery Research Group, University of Tromsø The Arctic University of Norway, Tromsø, Norway.
Cecilie Thanh Loan DangDepartment of Pharmacy, Drug Transport and Delivery Research Group, University of Tromsø The Arctic University of Norway, Tromsø, Norway.
Mari SalamonsenDepartment of Pharmacy, Drug Transport and Delivery Research Group, University of Tromsø The Arctic University of Norway, Tromsø, Norway.
Elizabeth G Aarag FredheimDepartment of Pharmacy, Microbial Pharmacology and Population Biology, University of Tromsø The Arctic University of Norway, Tromsø, Norway.
Nataša Škalko-BasnetDepartment of Pharmacy, Drug Transport and Delivery Research Group, University of Tromsø The Arctic University of Norway, Tromsø, Norway.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Chronic wounds pose a significant clinical challenge due to impaired healing, persistent inflammation, and susceptibility to infection, often by antimicrobial-resistant bacteria. Therefore, active compounds should ideally act both as antimicrobials with limited potential for resistance development and offer other beneficial wound-healing properties. Polyphenols, such as chlorogenic acid (CGA) and quercetin (QCT), exhibit those properties, but are limited by poor stability or low bioavailability. Methods: In this study, liposomal formulations of CGA (CGA-LP) and QCT (QCT-LP) were tailored to overcome delivery barriers to wound sites. Liposomes were characterized by size, size distribution, zeta potential, entrapment efficiency, and stability. Results and Discussion:

Indexed as

antimicrobial therapybiocompatibilitychronic woundsliposomespolyphenols

Identifiers

PMID42698789
PMCPMC13541760

What OpenQuestion holds

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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.