Evidence map›Paper›PMID 35057000›Full record

ArticlePharmaceutics2022

Quercetin Liposomal Nanoformulation for Ischemia and Reperfusion Injury Treatment.

Margarida Ferreira-Silva, Catarina Faria-Silva, Manuela C Carvalheiro, Sandra Simões, H Susana Marinho, Paulo Marcelino, Maria Celeste Campos, Josbert M Metselaar, Eduarda Fernandes, Pedro V Baptista and 2 more

Open access · goldAbstract read
In one paragraph

Article in Pharmaceutics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
8.5field-weighted citation impact, top 2% 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

24 citing papers in PubMed, 44 citations in OpenAlex.

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  17. Quercetin: A Potential Polydynamic Drug.Molecules (Basel, Switzerland) · 2023
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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 at 5 institutions in 2 countries.

Margarida Ferreira-SilvaFaculty of Pharmacy, iMed.ULisboa-Research Institute for Medicines, University of Lisbon, Av. Prof. Gama Pinto, 1649-003 Lisbon, Portugal.ORCID 0000-0002-5724-2823
Catarina Faria-SilvaFaculty of Pharmacy, iMed.ULisboa-Research Institute for Medicines, University of Lisbon, Av. Prof. Gama Pinto, 1649-003 Lisbon, Portugal.ORCID 0000-0002-8057-2548
Manuela C CarvalheiroFaculty of Pharmacy, iMed.ULisboa-Research Institute for Medicines, University of Lisbon, Av. Prof. Gama Pinto, 1649-003 Lisbon, Portugal.ORCID 0000-0002-6028-4717
Sandra SimõesFaculty of Pharmacy, iMed.ULisboa-Research Institute for Medicines, University of Lisbon, Av. Prof. Gama Pinto, 1649-003 Lisbon, Portugal.
H Susana MarinhoCQB-Centro de Química Estrutural, DQB-Departamento de Química e Bioquímica, Faculdade de Ciências, Universidade de Lisboa, 1749-016 Lisboa, Portugal.ORCID 0000-0002-4625-2516
Paulo MarcelinoCEDOC, Campo dos Mártires da Pátria 130, Nova Medical School, 1169-056 Lisboa, Portugal.
Maria Celeste CamposANATOMIK-Laboratório de Anatomia Patológica, Grupo Clara Saúde, Rua Gago Coutinho e Sacadura Cabral, 136-138, 2955-190 Palmela, Portugal.
Josbert M MetselaarInstitute for Experimental Molecular Imaging, RWTH Aachen University Clinic, 52074 Aachen, Germany.
Eduarda FernandesLAQV, REQUIMTE-Laboratory of Applied Chemistry, Department of Chemical Sciences, Faculty of Pharmacy, University of Porto, Rua de Jorge Viterbo Ferreira, 228, 4050-313 Porto, Portugal.
Pedro V BaptistaAssociate Laboratory i4HB, Campus da Caparica, Institute for Health and Bioeconomy, NOVA School of Science and Technology, NOVA University Lisbon, 2819-516 Caparica, Portugal.ORCID 0000-0001-5255-7095
Alexandra R FernandesAssociate Laboratory i4HB, Campus da Caparica, Institute for Health and Bioeconomy, NOVA School of Science and Technology, NOVA University Lisbon, 2819-516 Caparica, Portugal.ORCID 0000-0003-2054-4438
Maria Luísa CorvoFaculty of Pharmacy, iMed.ULisboa-Research Institute for Medicines, University of Lisbon, Av. Prof. Gama Pinto, 1649-003 Lisbon, Portugal.ORCID 0000-0002-6332-3937
University of Lisbon · PTUnidade em Ciências Biomoleculares AplicadasRWTH Aachen University · DEUniversidade do Porto · PTUniversidade Nova de Lisboa · PT

Funding

Fundação para a Ciência e Tecnologia PD/BD/135264/2017; UID/DTP/04138/2020; UIDP/04138/2020; UIDP/04378/2020; UIDB/04378/2020; LA/P/0140/2020; UIDB/50006/2020; UIDB/00100/2020; POCI-01-0145-FEDER-029253Phospholipid Research Center LCO-2017-052/1-1
6 · The paper itself

Abstract

Ischemia and reperfusion injury (IRI) is a common complication caused by inflammation and oxidative stress resulting from liver surgery. Current therapeutic strategies do not present the desirable efficacy, and severe side effects can occur. To overcome these drawbacks, new therapeutic alternatives are necessary. Drug delivery nanosystems have been explored due to their capacity to improve the therapeutic index of conventional drugs. Within nanocarriers, liposomes are one of the most successful, with several formulations currently in the market. As improved therapeutic outcomes have been demonstrated by using liposomes as drug carriers, this nanosystem was used to deliver quercetin, a flavonoid with anti-inflammatory and antioxidant properties, in hepatic IRI treatment. In the present work, a stable quercetin liposomal formulation was developed and characterized. Additionally, an in vitro model of ischemia and reperfusion was developed with a hypoxia chamber, where the anti-inflammatory potential of liposomal quercetin was evaluated, revealing the downregulation of pro-inflammatory markers. The anti-inflammatory effect of quercetin liposomes was also assessed in vivo in a rat model of hepatic IRI, in which a decrease in inflammation markers and enhanced recovery were observed. These results demonstrate that quercetin liposomes may provide a significant tool for addressing the current bottlenecks in hepatic IRI treatment.

Indexed as

anti-inflammatory therapydrug delivery nanosystemshepatic ischemia and reperfusion injuryinflammationliposomesliverquercetin

Identifiers

PMID35057000
PMCPMC8779145
OpenAlexW4205470122

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.