Evidence map›Paper›PMID 35056063›Full record

ArticlePharmaceuticals (Basel, Switzerland)2021

Co-Delivery of Letrozole and Cyclophosphamide via Folic Acid-Decorated Nanoniosomes for Breast Cancer Therapy: Synergic Effect, Augmentation of Cytotoxicity, and Apoptosis Gene Expression.

Hamidreza Sahrayi, Elham Hosseini, Sara Karimifard, Nazanin Khayam, Seyed Mohammadmahdi Meybodi, Sahar Amiri, Mahsa Bourbour, Bahareh Farasati Far, Iman Akbarzadeh, Mohammed Bhia and 2 more

Abstract read
In one paragraph

Article in Pharmaceuticals (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
–field-weighted citation impact
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

20 citing papers in PubMed.

  1. Review
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  15. Niosomes: a novel targeted drug delivery system for cancer.Medical oncology (Northwood, London, England) · 2022
    Review
  16. 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

12 authors.

Hamidreza SahrayiDepartment of Chemical and Petrochemical Engineering, Sharif University of Technology, Tehran 1458889694, Iran.
Elham HosseiniDepartment of Biomedical Engineering, Science and Research Branch, Islamic Azad University, Tehran 1477893855, Iran.
Sara KarimifardDepartment of Chemical and Petrochemical Engineering, Sharif University of Technology, Tehran 1458889694, Iran.
Nazanin KhayamDepartment of Chemical and Petrochemical Engineering, Sharif University of Technology, Tehran 1458889694, Iran.
Seyed Mohammadmahdi MeybodiDepartment of Veterinary Medicine, Tabriz Branch, Islamic Azad University, Tabriz 5157344533, Iran.
Sahar AmiriDepartment of Chemical and Petrochemical Engineering, Sharif University of Technology, Tehran 1458889694, Iran.
Mahsa BourbourDepartment of Biotechnology, Alzahra University, Tehran 1993893973, Iran.ORCID 0000-0001-5951-5090
Bahareh Farasati FarDepartment of Chemistry, Iran University of Science and Technology, Tehran 1684613114, Iran.
Iman AkbarzadehDepartment of Chemical and Petrochemical Engineering, Sharif University of Technology, Tehran 1458889694, Iran.ORCID 0000-0001-5136-2122
Mohammed BhiaStudent Research Committee, Department of Pharmaceutics and Nanotechnology, School of Pharmacy, Shahid Beheshti University of Medical Sciences, Tehran 1996835113, Iran.ORCID 0000-0002-0706-2058
Clare HoskinsDepartment of Pure and Applied Chemistry, University of Strathclyde, Technology Innovation Centre, 99 George Street, Glasgow G1 1RD, UK.ORCID 0000-0002-7200-0566
Chaiyavat ChaiyasutInnovation Center for Holistic Health, Nutraceuticals, and Cosmeceuticals, Faculty of Pharmacy, Chiang Mai University, Chiang Mai 50200, Thailand.ORCID 0000-0002-1633-2419

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer is one of the most prevalent causes of cancer mortality in women. In order to increase patient prognosis and survival rates, new technologies are urgently required to deliver therapeutics in a more effective and efficient manner. Niosome nanoparticles have been recently employed as therapeutic platforms capable of loading and carrying drugs within their core for both mono and combination therapy. Here, niosome-based nanoscale carriers were investigated as a targeted delivery system for breast cancer therapy. The platform developed consists of niosomes loaded with letrozole and cyclophosphamide (NLC) and surface-functionalized with a folic-acid-targeting moiety (NLCPFA). Drug release from the formulated particles exhibited pH-sensitive properties in which the niosome showed low and high release in physiological and cancerous conditions, respectively. The results revealed a synergic effect in cytotoxicity by co-loading letrozole and cyclophosphamide with an efficacy increment in NLCPFA use in comparison with NLC. The NLCPFA resulted in the greatest drug internalization compared to the non-targeted formulation and the free drug. Additionally, downregulation of

Indexed as

breast cancercyclophosphamidedrug deliveryfolic acidletrozolenanomedicinenanoparticlesneoplasmsniosomes

Identifiers

PMID35056063
PMCPMC8780158

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Registered trials

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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.