Evidence map›Paper›PMID 42920045›Full record

ArticlePharmaceutical research2026

Preclinical Evaluation of a Nanoformulated Hydrogen Sulfide-releasing Dexamethasone for Topical Treatment of Psoriasis.

Daniel A G Miranda, Anderson R A Cerqueira, Marcelo Nicolas Muscara, Angela Corvino, Antonia Scognamiglio, Rosa Sparaco, Beatrice Severino, Vincenzo Santagada, Giuseppe Caliendo, Francesco Frecentese and 2 more

Abstract read
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In one paragraph

Article in Pharmaceutical research, 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
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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

12 authors.

Daniel A G MirandaDepartment of Pharmacology, Institute of Biomedical Sciences, University of São Paulo, Av. Prof. Lineu Prestes 1524, São Paulo, SP, 05508-000, Brazil.
Anderson R A CerqueiraDepartment of Pharmacology, Institute of Biomedical Sciences, University of São Paulo, Av. Prof. Lineu Prestes 1524, São Paulo, SP, 05508-000, Brazil.
Marcelo Nicolas MuscaraDepartment of Pharmacology, Institute of Biomedical Sciences, University of São Paulo, Av. Prof. Lineu Prestes 1524, São Paulo, SP, 05508-000, Brazil.
Angela CorvinoDepartment of Pharmacy, School of Medicine, Università Degli Studi Di Napoli "Federico II", 80131, Naples, Italy.
Antonia ScognamiglioDepartment of Pharmacy, School of Medicine, Università Degli Studi Di Napoli "Federico II", 80131, Naples, Italy.
Rosa SparacoDepartment of Pharmacy, School of Medicine, Università Degli Studi Di Napoli "Federico II", 80131, Naples, Italy.
Beatrice SeverinoDepartment of Pharmacy, School of Medicine, Università Degli Studi Di Napoli "Federico II", 80131, Naples, Italy.
Vincenzo SantagadaDepartment of Pharmacy, School of Medicine, Università Degli Studi Di Napoli "Federico II", 80131, Naples, Italy.
Giuseppe CaliendoDepartment of Pharmacy, School of Medicine, Università Degli Studi Di Napoli "Federico II", 80131, Naples, Italy.
Francesco FrecenteseDepartment of Pharmacy, School of Medicine, Università Degli Studi Di Napoli "Federico II", 80131, Naples, Italy.
Soraia Katia Pereira CostaDepartment of Pharmacology, Institute of Biomedical Sciences, University of São Paulo, Av. Prof. Lineu Prestes 1524, São Paulo, SP, 05508-000, Brazil. skcosta@usp.br.
Luciana B LopesDepartment of Pharmacology, Institute of Biomedical Sciences, University of São Paulo, Av. Prof. Lineu Prestes 1524, São Paulo, SP, 05508-000, Brazil. lublopes@usp.br.ORCID http://orcid.org/0000-0001-7814-9647

Funding

CAPES 001CNPq 142029/2020-3;307928/2023-3CNPq 306294/2019-2CNPq 312514/2019-0FAPESP 2018/13877-1FAPESP 2019/21910-1FAPESP 2025/02119-2
6 · The paper itself

Abstract

purposeConcerns regarding local and systemic adverse effects associated with long-term use of corticosteroids has motivated the study of new therapeutic approaches for psoriasis treatment. This study evaluated the efficacy of a novel nanoformulation loaded with a hydrogen sulfide (H₂S)-releasing dexamethasone derivative (Dexa-TBZ) in an experimental psoriasis model.

methodsPsoriasis was induced with topical imiquimod, and mice were treated for 4 days with dexamethasone- (Dexa, control) or Dexa-TBZ-loaded nanoformulations. Erythema and scaling (assessed by a modified Psoriasis Area Severity Index), myeloperoxidase (MPO) activity, and spleen size were assessed for efficacy.

resultsDaily topical treatment with either Dexa or Dexa-TBZ reduced scaling and erythema, with the last most likely related to decreased inflammation, as suggested by a marked reduction in MPO activity and neutrophil infiltration. Both treatments also reduced epidermal thickening, indicating comparable local therapeutic effects. However, Dexa caused a greater reduction in circulating leukocytes and spleen size, suggesting higher systemic exposure despite topical administration. In contrast, Dexa-TBZ showed limited systemic effects.

conclusionsAlthough Dexa-TBZ did not demonstrate superior local efficacy, its lower systemic impact suggests an improved safety and tolerability profile, which may be advantageous for the long-term topical treatment of chronic conditions such as psoriasis.

Indexed as

dexamethasone hybridshydrogen sulfide (H2S)nanoformulationpsoriasis

Identifiers

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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.