Evidence map›Paper›PMID 38491077›Full record

ArticleScientific reports2024

Microfluidic production of amiodarone loaded nanoparticles and application in drug repositioning in ovarian cancer.

Asia Saorin, Gloria Saorin, Fahriye Duzagac, Pietro Parisse, Ni Cao, Giuseppe Corona, Enrico Cavarzerani, Flavio Rizzolio

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

10 citing papers in PubMed, 16 citations in OpenAlex.

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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

8 authors at 4 institutions in 2 countries.

Asia Saorin *Department of Molecular Sciences and Nanosystems, Ca'Foscari University of Venice, Venezia-Mestre, Italy.
Gloria Saorin *Department of Molecular Sciences and Nanosystems, Ca'Foscari University of Venice, Venezia-Mestre, Italy.
Fahriye DuzagacDepartment of Clinical Cancer Prevention, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Pietro ParisseElettra-Sincrotrone Trieste S.C.p.A., Area Science Park, Strada Statale 14 km 163.5, Basovizza, 34149, Trieste, Italy.
Ni CaoDepartment of Molecular Sciences and Nanosystems, Ca'Foscari University of Venice, Venezia-Mestre, Italy.
Giuseppe CoronaImmunopathology and Cancer Biomarkers Unit, Centro di Riferimento Oncologico di Aviano (CRO), IRCCS, Aviano, Italy.
Enrico CavarzeraniDepartment of Molecular Sciences and Nanosystems, Ca'Foscari University of Venice, Venezia-Mestre, Italy.
Flavio RizzolioDepartment of Molecular Sciences and Nanosystems, Ca'Foscari University of Venice, Venezia-Mestre, Italy. flavio.rizzolio@unive.it.
Ca' Foscari University of Venice · ITAREA Science Park · ITCentro di Riferimento Oncologico · ITThe University of Texas MD Anderson Cancer Center · US

Funding

Fondazione AIRC per la ricerca sul cancro ETS F.R.: I.G.23566Italian Ministry of University and Research ECS00000041 - VITALITY. P.P.
6 · The paper itself

Abstract

Amiodarone repositioning in cancer treatment is promising, however toxicity limits seem to arise, constraining its exploitability. Notably, amiodarone has been investigated for the treatment of ovarian cancer, a tumour known for metastasizing within the peritoneal cavity. This is associated with an increase of fatty acid oxidation, which strongly depends on CPT1A, a transport protein which has been found overexpressed in ovarian cancer. Amiodarone is an inhibitor of CPT1A but its role still has to be explored. Therefore, in the present study, amiodarone was tested on ovarian cancer cell lines with a focus on lipid alteration, confirming its activity. Moreover, considering that drug delivery systems could lower drug side effects, microfluidics was employed for the development of drug delivery systems of amiodarone obtaining simultaneously liposomes with a high payload and amiodarone particles. Prior to amiodarone loading, microfluidics production was optimized in term of temperature and flow rate ratio. Moreover, stability over time of particles was evaluated. In vitro tests confirmed the efficacy of the drug delivery systems.

Indexed as

AmiodaroneNanoparticlesOvarian NeoplasmsDrug Delivery SystemsDrug RepositioningFemaleHumansLiposomesMicrofluidicsAmiodaroneLiposomesAmiodaroneCPT1ALipidic nanoparticlesMicrofluidicsOvarian cancer

Identifiers

PMID38491077
PMCPMC10943008
OpenAlexW4392850197

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.