Evidence map›Paper›PMID 36175809›Full record

ReviewMedical oncology (Northwood, London, England)2022

Niosomes: a novel targeted drug delivery system for cancer.

Maryam Moghtaderi, Kamand Sedaghatnia, Mahsa Bourbour, Mahdi Fatemizadeh, Zahra Salehi Moghaddam, Faranak Hejabi, Fatemeh Heidari, Sameer Quazi, Bahareh Farasati Far

RetractedAbstract readReviewRetracted Publication
PubMed Publisher
In one paragraph

Review in Medical oncology (Northwood, London, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
7.8field-weighted citation impact, top 1% 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

35 citing papers in PubMed, 1 synthesis or guideline pooled it, 92 citations in OpenAlex.

  1. Pooled it
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  14. Optimization andAnti-inflammatory & anti-allergy agents in medicinal chemistry · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 8 institutions in 3 countries.

Maryam MoghtaderiDepartment of Chemical Engineering, College of Engineering, University of Tehran, Tehran, Iran.
Kamand SedaghatniaDepartment of Applied Chemistry, Azad University of Tehran South Branch, Tehran, Iran.
Mahsa BourbourDepartment of Biotechnology, Alzahra University, Tehran, Iran.
Mahdi FatemizadehDepartment of Neuroscience and Addiction Studies, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Zahra Salehi MoghaddamDepartment of Microbial Biotechnology, School of Biology, College of Science, University of Tehran, Tehran, Iran.
Faranak HejabiDepartment of Cell and Molecular Biology, Faculty of Biological Sciences, Kharazmi University, Tehran, Iran.
Fatemeh HeidariDepartment of Cellular and Molecular Biology, Islamic Azad University, Tehran Medical Branch, Tehran, Iran.
Sameer QuaziGenLab Biosolutions Private Limited, Bangalore, Karnataka, India. colonel.quazi@gmail.com.ORCID http://orcid.org/0000-0002-1258-4088
Bahareh Farasati FarDepartment of Chemistry, Iran University of Science and Technology, Tehran, Iran.
University of Tehran · IRAlzahra University · IRIran University of Science and Technology · IRIslamic Azad University Medical Branch of Tehran · IRIslamic Azad University South Tehran Branch · IRKharazmi University · IRManchester Academic Health Science Centre · GBTehran University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recently, nanotechnology is involved in various fields of science, of which medicine is one of the most obvious. The use of nanoparticles in the process of treating and diagnosing diseases has created a novel way of therapeutic strategies with effective mechanisms of action. Also, due to the remarkable progress of personalized medicine, the effort is to reduce the side effects of treatment paths as much as possible and to provide targeted treatments. Therefore, the targeted delivery of drugs is important in different diseases, especially in patients who receive combined drugs, because the delivery of different drug structures requires different systems so that there is no change in the drug and its effectiveness. Niosomes are polymeric nanoparticles that show favorable characteristics in drug delivery. In addition to biocompatibility and high absorption, these nanoparticles also provide the possibility of reducing the drug dosage and targeting the release of drugs, as well as the delivery of both hydrophilic and lipophilic drugs by Niosome vesicles. Since various factors such as components, preparation, and optimization methods are effective in the size and formation of niosomal structures, in this review, the characteristics related to niosome vesicles were first examined and then the in silico tools for designing, prediction, and optimization were explained. Finally, anticancer drugs delivered by niosomes were compared and discussed to be a suitable model for designing therapeutic strategies. In this research, it has been tried to examine all the aspects required for drug delivery engineering using niosomes and finally, by presenting clinical examples of the use of these nanocarriers in cancer, its clinical characteristics were also expressed.

Indexed as

Antineoplastic AgentsNeoplasmsDrug Delivery SystemsHumansLiposomesPrecision MedicineAntineoplastic AgentsLiposomesCharacterizationIn silicoNiosomesPreparationStructureTargeted drug delivery

Identifiers

PMID36175809
OpenAlexW4297989875

What OpenQuestion holds

Textmetadata
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.