Evidence map›Paper›PMID 39204381›Full record

ArticlePharmaceutics2024

Chitosan-Coated Liposome Formulations for Encapsulation of Ciprofloxacin and Etoposide.

Rubén Gil-Gonzalo, D Alonzo Durante-Salmerón, Saeedeh Pouri, Ernesto Doncel-Pérez, Andrés R Alcántara, Inmaculada Aranaz, Niuris Acosta

Abstract read
In one paragraph

Article in Pharmaceutics, 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
–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

10 citing papers in PubMed.

  1. Article
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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

7 authors.

Rubén Gil-GonzaloPluridisciplinar Institute, Complutense University of Madrid, Paseo Juan XXIII, 1, E-28040 Madrid, Spain.ORCID 0009-0002-7131-7876
D Alonzo Durante-SalmerónDepartment of Chemistry in Pharmaceutical Science, Pharmacy Faculty, Complutense University of Madrid, Plaza de Ramón y Cajal s/n, E-28040 Madrid, Spain.ORCID 0009-0006-4451-3432
Saeedeh PouriPluridisciplinar Institute, Complutense University of Madrid, Paseo Juan XXIII, 1, E-28040 Madrid, Spain.
Ernesto Doncel-PérezNeural Regeneration Group, Hospital Nacional de Parapléjicos (SESCAM), E-45071 Toledo, Spain.ORCID 0000-0002-2704-9782
Andrés R AlcántaraDepartment of Chemistry in Pharmaceutical Science, Pharmacy Faculty, Complutense University of Madrid, Plaza de Ramón y Cajal s/n, E-28040 Madrid, Spain.ORCID 0000-0003-4856-4000
Inmaculada AranazPluridisciplinar Institute, Complutense University of Madrid, Paseo Juan XXIII, 1, E-28040 Madrid, Spain.ORCID 0000-0002-1495-9744
Niuris AcostaPluridisciplinar Institute, Complutense University of Madrid, Paseo Juan XXIII, 1, E-28040 Madrid, Spain.ORCID 0000-0001-5145-8781

Funding

Programa Investigo MCIN/AEI/ 10.13039/501100011033 and European Union NextGenerationEU/PRTRScience, Innovation and Universities Ministry, Spain PID2019-105337RB-C22 funded by MCIN/AEI /10.13039/501100011033
6 · The paper itself

Abstract

Cancer and bacterial infections rank among the most significant global health threats. accounting for roughly 25 million fatalities each year. This statistic underscores the urgent necessity for developing novel drugs, enhancing current treatments, and implementing systems that boost their bioavailability to achieve superior therapeutic outcomes. Liposomes have been recognised as effective carriers; nonetheless, they encounter issues with long-term stability and structural integrity, which limit their pharmaceutical applicability. Chitosomes (chitosan-coated liposomes) are generally a good alternative to solve these issues. This research aims to demonstrate the effective individual encapsulation of ciprofloxacin (antibacterial, hydrophilic) and etoposide (anticancer, hydrophobic), within chitosomes to create more effective drug delivery systems (oral administration for ciprofloxacin, parenteral administration for etoposide). Thus, liposomes and chitosomes were prepared using the thin-film hydration technique and were characterised through ATR-FTIR, Dynamic Light Scattering (DLS), zeta potential, and release profiling. In both cases, the application of chitosomes enhanced long-term stability in size and surface charge. Chitosome-encapsulated ciprofloxacin formulations exhibited a slower and sustained release profile, while the combined effect of etoposide and chitosan showed heightened efficacy against the glioblastoma cell line U373. Therefore, coating liposomes with chitosan improved the encapsulation system's properties, resulting in a promising method for drug delivery.

Indexed as

chitosanchitosomeciprofloxacinCS-coated liposomesEscherichia colietoposideglioblastomaliposomethin-film hydrationU373

Identifiers

PMID39204381
PMCPMC11359655

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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.