Evidence map›Paper›PMID 34068129›Full record

ArticlePharmaceutics2021

Ferri-Liposomes: Preformulation and Selective Cytotoxicity against A549 Lung Cancer Cells.

Marina Guedes Fonseca de Souza, Fabrícia Nunes de Jesus Guedes, Marli Luiza Tebaldi, Éverton do Nascimento Alencar, Lucas Amaral-Machado, Eryvaldo Sócrates Tabosa do Egito, André Luis Branco de Barros, Daniel Crístian Ferreira Soares

Open access · goldAbstract read
In one paragraph

Article in Pharmaceutics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.1field-weighted citation impact, top 26% 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

8 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 3 institutions in 1 country.

Marina Guedes Fonseca de SouzaBioengineering Laboratory, Federal University of Itajubá, Rua Irmã Ivone Drumond, 200, Distrito Industrial II, Itabira 35903-087, Brazil.
Fabrícia Nunes de Jesus GuedesBioengineering Laboratory, Federal University of Itajubá, Rua Irmã Ivone Drumond, 200, Distrito Industrial II, Itabira 35903-087, Brazil.
Marli Luiza TebaldiBioengineering Laboratory, Federal University of Itajubá, Rua Irmã Ivone Drumond, 200, Distrito Industrial II, Itabira 35903-087, Brazil.
Éverton do Nascimento AlencarLaboratory of Dispersed Systems (LaSiD), Department of Pharmacy, Federal University of Rio Grande do Norte (UFRN), Rua Gal. Gustavo Cordeiro de Farias, s/n, Petropolis, Natal 59010-180, Brazil.ORCID 0000-0002-6148-6804
Lucas Amaral-MachadoLaboratory of Dispersed Systems (LaSiD), Department of Pharmacy, Federal University of Rio Grande do Norte (UFRN), Rua Gal. Gustavo Cordeiro de Farias, s/n, Petropolis, Natal 59010-180, Brazil.ORCID 0000-0002-8996-189X
Eryvaldo Sócrates Tabosa do EgitoLaboratory of Dispersed Systems (LaSiD), Department of Pharmacy, Federal University of Rio Grande do Norte (UFRN), Rua Gal. Gustavo Cordeiro de Farias, s/n, Petropolis, Natal 59010-180, Brazil.ORCID 0000-0002-2180-3991
André Luis Branco de BarrosFaculty of Pharmacy, Federal University of Minas Gerais, Avenida Presidente Antônio Carlos, 6627, Pampulha, Belo Horizonte 31270-901, Brazil.
Daniel Crístian Ferreira SoaresBioengineering Laboratory, Federal University of Itajubá, Rua Irmã Ivone Drumond, 200, Distrito Industrial II, Itabira 35903-087, Brazil.ORCID 0000-0002-2204-6881
Universidade Federal de Itajubá · BRUniversidade Federal do Rio Grande do Norte · BRUniversidade Federal de Minas Gerais · BR

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 001Coordenação de Aperfeiçoamento de Pessoal de Nível Superior 001Fundação de Amparo à Pesquisa do Estado de Minas Gerais PPM-00125-18
6 · The paper itself

Abstract

Liposomes have become successful nanostructured systems used in clinical practices. These vesicles are able to carry important drug loadings with noteworthy stability. The aim of this work was to develop iron oxide-loaded stealth liposomes as a prospective alternative for the treatment of lung cancer. In this study, citric acid iron oxide nanoparticles (IONPs-Ac) were synthesized and encapsulated in stealth liposomes. Their cytotoxicity and selectivity against lung tumor cells were assessed. Stealth liposomal vesicles, with relevant content of IONPs-Ac, named ferri-liposomes (SL-IONPs-Ac), were produced with an average size of 200 nm. They displayed important cytotoxicity in a human lung cancer cells model (A549 cells), even at low concentrations, whereas free IONPs-Ac displayed adequate biocompatibility. Nevertheless, the treatment at the same concentration of ferri-liposomes against HEK-293 cells, a normal human cell lineage, was not significantly cytotoxic, revealing a probable lung tumor selectiveness of the fabricated formulation. Furthermore, from the flow cytometry studies, it was possible to infer that ferri-liposomes were able to induce A549 tumor cells death through apoptosis/ferroptosis processes, evidenced by a significant reduction of the mitochondrial membrane potential.

Indexed as

A549 cellsiron oxide liposomeslung cancer treatmentselective therapy

Identifiers

PMID34068129
PMCPMC8152733
OpenAlexW3160988284

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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.