Evidence map›Paper›PMID 27102110›Full record

ArticleJournal of nanobiotechnology2016

Delivery of disulfiram into breast cancer cells using folate-receptor-targeted PLGA-PEG nanoparticles: in vitro and in vivo investigations.

Hamidreza Fasehee, Rassoul Dinarvand, Ardeshir Ghavamzadeh, Mehdi Esfandyari-Manesh, Hanieh Moradian, Shahab Faghihi, Seyed Hamidollah Ghaffari

Open access · goldAbstract read
In one paragraph

Article in Journal of nanobiotechnology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed, 1 pooled it
8.6field-weighted citation impact, top 2% 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

59 citing papers in PubMed, 1 synthesis or guideline pooled it, 140 citations in OpenAlex.

  1. Pooled it
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  8. Nanotechnology Applications in Breast Cancer Immunotherapy.Small (Weinheim an der Bergstrasse, Germany) · 2024
    Review
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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 at 5 institutions in 1 country.

Hamidreza FaseheeTissue Engineering and Biomaterials Research Center, National Institute of Genetic Engineering and Biotechnology (NIGEB), Tehran, 14965/161, Iran.
Rassoul DinarvandNanotechnology Research Center, Tehran University of Medical Sciences, Tehran, Iran.
Ardeshir GhavamzadehHematology, Oncology and Stem cell Transplantation Research Center, Shariati Hospital, Tehran University of Medical Science, Tehran, Iran.
Mehdi Esfandyari-ManeshDepartment of Chemistry, Amirkabir University of Technology, Tehran, Iran.
Hanieh MoradianTissue Engineering and Biomaterials Research Center, National Institute of Genetic Engineering and Biotechnology (NIGEB), Tehran, 14965/161, Iran.
Shahab FaghihiTissue Engineering and Biomaterials Research Center, National Institute of Genetic Engineering and Biotechnology (NIGEB), Tehran, 14965/161, Iran. sfaghihi@nigeb.ac.ir.
Seyed Hamidollah GhaffariHematology, Oncology and Stem cell Transplantation Research Center, Shariati Hospital, Tehran University of Medical Science, Tehran, Iran. Shghaffari200@yahoo.com.
National Institute of Genetic Engineering and Biotechnology · IRAmirkabir University of Technology · IRShariati Hospital · IRTehran University of Medical Sciences · IRUniversity of Tehran · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundA folate-receptor-targeted poly (lactide-co-Glycolide) (PLGA)-Polyethylene glycol (PEG) nanoparticle is developed for encapsulation and delivery of disulfiram into breast cancer cells. After a comprehensive characterization of nanoparticles, cell cytotoxicity, apoptosis induction, cellular uptake and intracellular level of reactive oxygen species are analyzed. In vivo acute and chronic toxicity of nanoparticles and their efficacy on inhibition of breast cancer tumor growth is studied.

resultsThe folate-receptor-targeted nanoparticles are internalized into the cells, induce reactive oxygen species formation, induce apoptosis and inhibit cell proliferation more efficiently compared to the untargeted nanoparticles. The acute and toxicity test show the maximum dose of disulfiram equivalent of nanoparticles for intra-venous injection is 6 mg/kg while show significant decrease in the breast cancer tumor growth rate.

conclusionIt is believed that the developed formulation could be used as a potential vehicle for successful delivery of disulfiram, an old and inexpensive drug, into breast cancer cells and other solid tumors.

Indexed as

Breast NeoplasmsCell Line, TumorCell SurvivalDisulfiramDrug CarriersFemaleFolate Receptors, GPI-AnchoredFolic AcidHumansLactic AcidMCF-7 CellsNanoparticlesParticle SizePolyethylene GlycolsPolyglycolic AcidPolylactic Acid-Polyglycolic Acid CopolymerDisulfiramDrug CarriersFolate Receptors, GPI-AnchoredFolic AcidLactic Acidpoly(ethylene glycol)-folatePolyethylene GlycolsPolyglycolic AcidPolylactic Acid-Polyglycolic Acid CopolymerApoptosisBreast cancer cellsDisulfiramFolate receptorPLGA nanoparticlesTargeted drug delivery

Identifiers

PMID27102110
PMCPMC4839071
OpenAlexW2338671196

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.