Evidence map›Paper›PMID 30347857›Full record

ArticleMaterials (Basel, Switzerland)2018

Ionically Crosslinked Chitosan Membranes Used as Drug Carriers for Cancer Therapy Application.

Alecsandra Ferreira Tomaz, Sandra Maria Sobral de Carvalho, Rossemberg Cardoso Barbosa, Suédina M L Silva, Marcos Antônio Sabino Gutierrez, Antônio Gilson B de Lima, Marcus Vinícius L Fook

Open access · goldAbstract read
In one paragraph

Article in Materials (Basel, Switzerland), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

33 citing papers in PubMed, 101 citations in OpenAlex.

  1. Article
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  6. Article
  7. Article
  8. Review
  9. Regenerative therapy · 2024
    Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Chitosan: Structural and Chemical Modification, Properties, and Application.International journal of molecular sciences · 2023
    Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Review
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 at 2 institutions in 2 countries.

Alecsandra Ferreira TomazPostgraduate Program in Process Engineering, Federal University of Campina Grande, Campina Grande, PB 58429-900, Brazil. alecsandratomaz@hotmail.com.
Sandra Maria Sobral de CarvalhoPostgraduate Program in Materials Science and Engineering, Federal University of Campina Grande, Campina Grande, PB 58429-900, Brazil. sandram.carvalho@hotmail.com.
Rossemberg Cardoso BarbosaPostgraduate Program in Materials Science and Engineering, Federal University of Campina Grande, Campina Grande, PB 58429-900, Brazil. rcbvet@gmail.com.
Suédina M L SilvaDepartment of Materials Engineering, Federal University of Campina Grande, Campina Grande, PB 58429-900, Brazil. suedina.silva@ufcg.edu.br.ORCID 0000-0002-2073-0989
Marcos Antônio Sabino GutierrezB5IDA Research Group, Chemistry Department, Simon Bolivar University, Caracas 89000, Venezuela. msabino@usb.ve.
Antônio Gilson B de LimaDepartment of Mechanical Engineering, Federal University of Campina Grande, Campina Grande, PB 58429-900, Brazil. antonio.gilson@ufcg.edu.br.
Marcus Vinícius L FookDepartment of Materials Engineering, Federal University of Campina Grande, Campina Grande, PB 58429-900, Brazil. marcus.liafook@certbio.ufcg.edu.br.
Universidade Federal de Campina Grande · BRSimón Bolívar University · VE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this paper was to prepare, by the freeze-drying method, ionically crosslinked chitosan membranes with different contents of pentasodium tripolyphosphate (TPP) and loaded with 1,4-naphthoquinone (NQ14) drug, in order to evaluate how the physical crosslinking affects NQ14 release from chitosan membranes for cancer therapy application. The membranes were characterized by Fourier transform infrared spectroscopy (FTIR), wide-angle X-ray diffraction (WAXD), scanning electron microscopy (SEM), swelling degree, and through in vitro drug release and cytotoxicity studies. According to the results, the molecular structure, porosity and hydrophilicity of the chitosan membranes were affected by TPP concentration and, consequently, the NQ14 drug release behavior from the membranes was also affected. The release of NQ14 from crosslinked chitosan membranes decreased when the cross-linker TPP quantity increased. Thus, depending on the TPP amount, the crosslinked chitosan membranes would be a potential delivery system to control the release of NQ14 for cancer therapy application. Lastly, the inhibitory potential of chitosan membranes ionically crosslinked with TPP and loaded with NQ14 against the B16F10 melanoma cell line was confirmed through in vitro cytotoxicity studies assessed via MTT assay. The anti-proliferative effect of prepared membranes was directly related to the amount of cross-linker and among all membranes prepared, such that one crosslinked with 0.3% of TPP may become a potential delivery system for releasing NQ14 drug for cancer therapy.

Indexed as

1,4-naphthoquinonecancer therapychitosancontrolled releaseionic crosslinkingpentasodium tripolyphosphate

Identifiers

PMID30347857
PMCPMC6213910
OpenAlexW2897007409

What OpenQuestion holds

Textmetadata
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.