Evidence map›Paper›PMID 37514111›Full record

ArticlePharmaceutics2023

Polymeric Nanoparticles' Accumulation in Atopic Dermatitis: Clinical Comparison between Healthy, Non-Lesional, and Lesional Skin.

Céline Try, Mona M A Abdel-Mottaleb, Arnaud Béduneau, Brice Moulari, Lionel Pazart, Chrystelle Vidal, Gaëlle Brunotte, Florence Castelain, Alf Lamprecht, Philippe Humbert and 1 more

Open access · goldAbstract read
In one paragraph

Article in Pharmaceutics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
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  5. 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

11 authors at 5 institutions in 3 countries.

Céline TryPEPITE EA4267, (Labex LipStic ANR-11-LABX0021) Université Franche-Comté, F-25000 Besançon, France.
Mona M A Abdel-MottalebDepartment of Pharmaceutics and Industrial Pharmacy, Faculty of Pharmacy, Ain Shams University, Cairo 11566, Egypt.ORCID 0000-0002-4017-1248
Arnaud BéduneauPEPITE EA4267, (Labex LipStic ANR-11-LABX0021) Université Franche-Comté, F-25000 Besançon, France.
Brice MoulariPEPITE EA4267, (Labex LipStic ANR-11-LABX0021) Université Franche-Comté, F-25000 Besançon, France.
Lionel PazartCHU de Besançon, F-25000 Besançon, France.
Chrystelle VidalCHU de Besançon, F-25000 Besançon, France.
Gaëlle BrunotteCHU de Besançon, F-25000 Besançon, France.
Florence CastelainCHU de Besançon, F-25000 Besançon, France.
Alf LamprechtPEPITE EA4267, (Labex LipStic ANR-11-LABX0021) Université Franche-Comté, F-25000 Besançon, France.
Philippe HumbertRIGHT UMR1098 INSERM EFS BFC, Université Franche-Comté, F-25000 Besançon, France.
Yann PellequerPEPITE EA4267, (Labex LipStic ANR-11-LABX0021) Université Franche-Comté, F-25000 Besançon, France.ORCID 0000-0003-4318-974X
Inserm · FRUniversité de franche-comté · FRCentre Hospitalier Universitaire de Besançon · FRAin Shams University · EGUniversity of Bonn · DE

Funding

CHU Besançon and Région Franche-Comté APICHU RFC 2012 MicroIskinLABEX LIPSTIC (Lipoprotéines et Santé) ANR-11-LABX0021
6 · The paper itself

Abstract

A major limitation in the current topical treatment strategies for inflammatory skin disorders is the inability to selectively target the inflamed site with minimal exposure of healthy skin. Atopic dermatitis is one of the most prevalent types of dermatitis. The use of polymeric nanoparticles for targeting inflamed skin has been recently proposed, and therefore the aim of this proof-of-concept clinical study was to investigate the skin penetration and deposition of polymeric biodegradable nanoparticles in the atopic dermatitis lesions and compare the data obtained to the deposition of the particles into the healthy skin or lesion-free skin of the atopic dermatitis patients. For that, fluorescent PLGA nanoparticles in sizes of approximately 100 nm were prepared and applied to the skin of healthy volunteers and the lesional and non-lesional skin of atopic dermatitis patients. Skin biopsies were examined using confocal laser scanning microscopy to track the skin deposition and depth of penetration of the particles. Immunohistochemistry was performed to investigate the alteration in tight-junction protein distribution in the different types of skin. Results have shown that nanoparticles were found to have higher deposition into the atopic dermatitis lesions with minimal accumulation in healthy or non-lesional skin. This has been primarily correlated with the impaired barrier properties of atopic dermatitis lesions with the reduced production of Claudin-1. It was concluded that polymeric nanoparticles offer a potential tool for selective drug delivery to inflamed skin with minimal exposure risk to healthy skin.

Indexed as

altered permeabilityatopic dermatitisclinical studypolymeric nanoparticlestight junction

Identifiers

PMID37514111
PMCPMC10385499
OpenAlexW4383912389

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.