Evidence map›Paper›PMID 34202407›Full record

ArticleCells2021

Targeted Drug Delivery Technologies Potentiate the Overall Therapeutic Efficacy of an Indole Derivative in a Mouse Cystic Fibrosis Setting.

Matteo Puccetti, Marilena Pariano, Giorgia Renga, Ilaria Santarelli, Fiorella D'Onofrio, Marina M Bellet, Claudia Stincardini, Andrea Bartoli, Claudio Costantini, Luigina Romani and 2 more

Abstract read
In one paragraph

Article in Cells, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Biodrug Delivery Systems: Do mRNA Lipid Nanoparticles Come of Age?International journal of molecular sciences · 2023
    Review
  9. Article
  10. Impact ofInternational journal of molecular sciences · 2022
    Review
  11. Review
  12. Article
  13. 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

12 authors.

Matteo PuccettiDepartment of Pharmaceutical Sciences, University of Perugia, 06123 Perugia, Italy.ORCID 0000-0003-3007-0475
Marilena ParianoDepartment of Medicine and Surgery, University of Perugia, 06132 Perugia, Italy.
Giorgia RengaDepartment of Medicine and Surgery, University of Perugia, 06132 Perugia, Italy.ORCID 0000-0002-9762-6493
Ilaria SantarelliDepartment of Medicine and Surgery, University of Perugia, 06132 Perugia, Italy.
Fiorella D'OnofrioDepartment of Medicine and Surgery, University of Perugia, 06132 Perugia, Italy.
Marina M BelletDepartment of Medicine and Surgery, University of Perugia, 06132 Perugia, Italy.
Claudia StincardiniDepartment of Medicine and Surgery, University of Perugia, 06132 Perugia, Italy.
Andrea BartoliDepartment of Medicine and Surgery, University of Perugia, 06132 Perugia, Italy.
Claudio CostantiniDepartment of Medicine and Surgery, University of Perugia, 06132 Perugia, Italy.ORCID 0000-0002-1433-7830
Luigina RomaniDepartment of Medicine and Surgery, University of Perugia, 06132 Perugia, Italy.
Maurizio RicciDepartment of Pharmaceutical Sciences, University of Perugia, 06123 Perugia, Italy.ORCID 0000-0002-3373-9771
Stefano GiovagnoliDepartment of Pharmaceutical Sciences, University of Perugia, 06123 Perugia, Italy.ORCID 0000-0001-5043-7233

Funding

Fondazione per la Ricerca sulla Fibrosi Cistica FFC#24/2018FP7 Ideas: European Research Council ERC-2018-PoC-813099
6 · The paper itself

Abstract

Inflammation plays a major role in the pathophysiology of cystic fibrosis (CF), a multisystem disease. Anti-inflammatory therapies are, therefore, of interest in CF, provided that the inhibition of inflammation does not compromise the ability to fight pathogens. Here, we assess whether indole-3-aldehyde (3-IAld), a ligand of the aryl hydrocarbon receptor (AhR), may encompass such an activity. We resorted to biopharmaceutical technologies in order to deliver 3-IAld directly into the lung, via dry powder inhalation, or into the gut, via enteric microparticles, in murine models of CF infection and inflammation. We found the site-specific delivery of 3-IAld to be an efficient strategy to restore immune and microbial homeostasis in CF organs, and mitigate lung and gut inflammatory pathology in response to fungal infections, in the relative absence of local and systemic inflammatory toxicity. Thus, enhanced delivery to target organs of AhR agonists, such as 3-IAld, may pave the way for the development of safe and effective anti-inflammatory agents in CF.

Indexed as

Drug Delivery SystemsAdministration, InhalationAerosolsAnimalsCystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorDisease Models, AnimalGastrointestinal TractIndolesLigandsLungMiceMice, Inbred C57BLReceptors, Aryl HydrocarbonAerosolsCystic Fibrosis Transmembrane Conductance RegulatorindoleIndolesLigandsReceptors, Aryl Hydrocarbon3-IAldaryl hydrocarbon receptorcystic fibrosisdrug deliveryinflammation

Identifiers

PMID34202407
PMCPMC8305708

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.