Evidence map›Paper›PMID 33061366›Full record

ArticleInternational journal of nanomedicine2020

In vivo Glioblastoma Therapy Using Targeted Liposomal Cisplatin.

Maryam Sadat Ashrafzadeh, Azim Akbarzadeh, Amir Heydarinasab, Mehdi Ardjmand

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 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
4.0field-weighted citation impact, top 5% 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, 88 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Article
  11. Progress of nanoparticle drug delivery system for the treatment of glioma.Frontiers in bioengineering and biotechnology · 2024
    Review
  12. Review
  13. Article
  14. Review
  15. Review
  16. Review
  17. Article
  18. Review
  19. Review
  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

4 authors at 3 institutions in 1 country.

Maryam Sadat AshrafzadehDepartment of Chemical Engineering, Science and Research Branch, Islamic Azad University, Tehran, Iran.
Azim AkbarzadehDepartment of Pilot Nanobiotechnology, Pasteur Institute of Iran, Tehran, Iran.
Amir HeydarinasabDepartment of Chemical Engineering, Science and Research Branch, Islamic Azad University, Tehran, Iran.ORCID 0000-0002-0417-4863
Mehdi ArdjmandDepartment of Chemical Engineering, South Tehran Branch, Islamic Azad University, Tehran, Iran.ORCID 0000-0003-1587-6892
Islamic Azad University, Science and Research Branch · IRIslamic Azad University South Tehran Branch · IRPasteur Institute of Iran · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDrug delivery systems have demonstrated promising results to cross blood-brain barrier (BBB) and deliver the loaded therapeutics to the brain tumor. This study aims to utilize the transferrin receptor (TR)-targeted liposomal cisplatin (Cispt) for transporting Cispt across the BBB and deliver Cispt to the brain tumor.

methodsTargeted pegylated liposomal cisplatin (TPL-Cispt) was synthesized using reverse phase evaporation method and thiolated OX26 monoclonal antibody. The formulation was characterized in terms of size, size distribution, zeta potential, drug encapsulation and loading efficiencies, bioactivity, drug release profile, stability and cellular uptake using dynamic light scattering, flame atomic absorption spectroscopy (AAS), ELISA, dialysis membrane, and fluorescence assay. Next, the potency of the formulation to increase the therapeutic effects of Cispt and decrease its toxicity effects was evaluated in the brain tumor-bearing rats through measuring the mean survival time (MST), blood factors and histopathological studies.

resultsThe results showed that TPL-Cispt with a size of 157±8 nm and drug encapsulation efficiency of 24%±1.22 was synthesized, that was biologically active and released Cispt in a slow-controlled manner. The formulation compared to Cispt-loaded PEGylated liposome nanoparticles (PL-Cispt) caused an increase in the cellular uptake by 1.43-fold, as well as an increase in the MST of the brain tumor-bearing rats by 1.7-fold compared to the PL-Cispt (

conclusionOverall, the results suggest that targeting the Cispt-loaded PEGylated liposome is a promising approach to develop formulation with enhanced efficacy and reduced toxicity for the treatment of brain tumor.

Indexed as

AnimalsAntibodies, MonoclonalAntineoplastic AgentsBlood-Brain BarrierBlood Urea NitrogenBrain NeoplasmsCisplatinDrug Delivery SystemsDrug LiberationDynamic Light ScatteringEnzymesGlioblastomaLiposomesMaleNanoparticlesRats, WistarAntibodies, MonoclonalAntineoplastic AgentsCisplatinEnzymesLiposomesReceptors, Transferrinblood brain barrierbrain tumorcisplatinliposometargeted drug delivery

Identifiers

PMID33061366
PMCPMC7522301
OpenAlexW3088559224

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.