Evidence map›Paper›PMID 36531115›Full record

ArticleInternational journal of nanomedicine2022

In vitro Development of Controlled-Release Nanoniosomes for Improved Delivery and Anticancer Activity of Letrozole for Breast Cancer Treatment.

Saeedeh Ahmadi, Mahmoud Seraj, Mohsen Chiani, Seyedayin Hosseini, Saba Bazzazan, Iman Akbarzadeh, Samaneh Saffar, Ebrahim Mostafavi

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

12 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
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  6. Review
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  11. Toxicity of Carboplatin-Niosomal Nanoparticles in a Brain Cancer Cell Line.Asian Pacific journal of cancer prevention : APJCP · 2023
    Article
  12. Article
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

8 authors at 4 institutions in 2 countries.

Saeedeh AhmadiDepartment of Nano Biotechnology, New Technology Research Group, Pasteur Institute of Iran, Tehran, Iran.
Mahmoud SerajIntegrative Research Laboratory, Islamic Azad University of Medical Sciences, Tehran, Iran.
Mohsen ChianiDepartment of Nano Biotechnology, New Technology Research Group, Pasteur Institute of Iran, Tehran, Iran.ORCID 0000-0001-6413-8752
Seyedayin HosseiniSchool of Medicine, Sh Beheshti University of Medical Sciences, Tehran, Iran.ORCID 0000-0003-3221-2270
Saba BazzazanCore Facility Lab, Pasteur Institute of Iran, Tehran, Iran.
Iman AkbarzadehDepartment of Nano Biotechnology, New Technology Research Group, Pasteur Institute of Iran, Tehran, Iran.
Samaneh SaffarCore Facility Lab, Pasteur Institute of Iran, Tehran, Iran.
Ebrahim MostafaviStanford Cardiovascular Institute, Stanford University School of Medicine, Stanford, CA, 94305, USA.ORCID 0000-0003-3958-5002
Pasteur Institute of Iran · IRCardiovascular Institute of the South · USIslamic Azad University Medical Branch of Tehran · IRShahid Beheshti University of Medical Sciences · IR

Funding

Multi-Disciplinary Training Program in Cardiovascular Imaging at StanfordT32EB009035 · NIBIB · STANFORD UNIVERSITY · PI Koen Nieman, John M. Pauly · 2008 to 2026
$4.3M
NIBIB NIH HHS T32 EB009035
6 · The paper itself

Abstract

Introduction: Breast cancer is among the most prevalent mortal cancers in women worldwide. In the present study, an optimum formulation of letrozole, letrozole-loaded niosome, and empty niosome was developed, and the anticancer effect was assessed in in vitro MCF-7, MCF10A and MDA-MB-231 breast cancer cell lines. Materials and Methods: Various niosomal formulations of letrozole were fabricated through thin-film hydration method and characterized in terms of size, polydispersity index (PDI), morphology, entrapment efficiency (EE%), release kinetics, and stability. Optimized niosomal formulation of letrozole was achieved by response surface methodology (RSM). Antiproliferative activity and the mechanism were assessed by MTT assay, quantitative real-time PCR, and flow cytometry. Furthermore, cellular uptake of optimum formulation was evaluated by confocal electron microscopy. Results: The formulated letrozole had a spherical shape and showed a slow-release profile of the drug after 72 h. The size, PDI, and eEE% of nanoparticles showed higher stability at 4°C compared with 25°C. The drug release from niosomes was in accordance with Korsmeyer-Peppa's kinetic model. Confocal microscopy revealed the localization of drug-loaded niosomes in the cancer cells. MTT assay revealed that all samples exhibited dose-dependent cytotoxicity against breast cancer cells. The IC Conclusion: Results indicated that niosomes could be a promising drug carrier for the delivery of letrozole to breast cancer cells.

Indexed as

Breast NeoplasmsLiposomesDelayed-Action PreparationsFemaleHumansLetrozoleMCF-7 CellsDelayed-Action PreparationsLetrozoleLiposomesanticancerbreast cancerdrug delivery systemletrozoleniosome

Identifiers

PMID36531115
PMCPMC9753765
OpenAlexW4311260165

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.