Evidence map›Paper›PMID 31952316›Full record

ArticleInternational journal of molecular sciences2020

Enhanced Efficacy of PEGylated Liposomal Cisplatin: In Vitro and In Vivo Evaluation.

Mohsen Ghaferi, Mohammad Javad Asadollahzadeh, Azim Akbarzadeh, Hasan Ebrahimi Shahmabadi, Seyed Ebrahim Alavi

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. 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
3.6field-weighted citation impact, top 7% 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, 77 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Liposomal Formulations of Metallodrugs for Cancer Therapy.International journal of molecular sciences · 2024
    Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Development of Responsive Nanoparticles for Cancer Therapy.International journal of molecular sciences · 2023
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. 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

5 authors at 3 institutions in 2 countries.

Mohsen GhaferiDepartment of Chemical Engineering, Shahrood Branch, Islamic Azad University, Shahrood 36155-163, Iran.ORCID 0000-0002-6784-8300
Mohammad Javad AsadollahzadehDepartment of Chemical Engineering, Shahrood Branch, Islamic Azad University, Shahrood 36155-163, Iran.ORCID 0000-0001-5817-6576
Azim AkbarzadehDepartment of Pilot Nanobiotechnology, Pasteur Institute of Iran, Tehran 1316943551, Iran.
Hasan Ebrahimi ShahmabadiDepartment of Microbiology, School of Medicine, Rafsanjan University of Medical Sciences, Rafsanjan 7717933777, Iran.ORCID 0000-0001-5222-3829
Seyed Ebrahim AlaviDepartment of Pilot Nanobiotechnology, Pasteur Institute of Iran, Tehran 1316943551, Iran.ORCID 0000-0003-4009-4921
Islamic Azad University, Shahrood · IRPasteur Institute of Iran · IRRafsanjan University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study aims to evaluate the potency of cisplatin (Cispt)-loaded liposome (LCispt) and PEGylated liposome (PLCispt) as therapeutic nanoformulations in the treatment of bladder cancer (BC). Cispt was loaded into liposomes using reverse-phase evaporation method, and the formulations were characterized using dynamic light scattering, scanning electron microscopy, dialysis membrane, and Fourier-transform infrared spectroscopy (FTIR) methods. The results showed that the particles were formed in spherical monodispersed shapes with a nanoscale size (221-274 nm) and controlled drug release profile. The cytotoxicity effects of LCispt and PLCispt were assessed in an in vitro environment, and the results demonstrated that PLCispt caused a 2.4- and 1.9-fold increase in the cytotoxicity effects of Cispt after 24 and 48 h, respectively. The therapeutic and toxicity effects of the formulations were also assessed on BC-bearing rats. The results showed that PLCispt caused a 4.8-fold increase in the drug efficacy (tumor volume of 11 ± 0.5 and 2.3 ± 0.1 mm

Indexed as

AnimalsAntineoplastic AgentsButylhydroxybutylnitrosamineCell Line, TumorCell SurvivalCisplatinDrug LiberationFemaleHumansLiposomesMicroscopy, Electron, ScanningParticle SizePolyethylene GlycolsRats, WistarTreatment OutcomeTumor BurdenAntineoplastic AgentsButylhydroxybutylnitrosamineCisplatinLiposomesPolyethylene Glycolscisplatindrug deliveryliposomenanoparticlePEGPEGylated liposomepolyethylene glycol

Identifiers

PMID31952316
PMCPMC7013419
OpenAlexW2999553432

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.