Evidence map›Paper›PMID 26417350›Full record

ArticleEXCLI journal2015

pH-sensitive, polymer modified, plasma stable niosomes: promising carriers for anti-cancer drugs.

Dena Tila, Seyede Narjes Yazdani-Arazi, Saeed Ghanbarzadeh, Sanam Arami, Zhaleh Pourmoazzen

Abstract read
In one paragraph

Article in EXCLI journal, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

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  16. Review of Curcumin Physicochemical Targeting Delivery System.International journal of nanomedicine · 2020
    Review
  17. 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

5 authors.

Dena TilaTabriz University of Medical Sciences, Tabriz, Iran, Research Center for Pharmaceutical Nanotechnology.
Seyede Narjes Yazdani-AraziTabriz University of Medical Sciences, Tabriz, Iran, Research Center for Pharmaceutical Nanotechnology.
Saeed GhanbarzadehTabriz University of Medical Sciences, Tabriz, Iran, Research Center for Pharmaceutical Nanotechnology ; Tabriz University of Medical Sciences, Tabriz, Iran, Department of Pharmaceutics, Faculty of Pharmacy ; Tabriz University of Medical Sciences, Tabriz, Iran, Student Research Committee, Faculty of Pharmacy.
Sanam AramiTabriz University of Medical Sciences, Tabriz, Iran, Research Center for Pharmaceutical Nanotechnology ; Tabriz University of Medical Sciences, Tabriz, Iran, Student Research Committee, Faculty of Pharmacy.
Zhaleh PourmoazzenChemistry Department, Science Faculty, Azarbaijan Shahid Madani University,Tabriz, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study was the design and evaluation of a novel plasma stable, pH-sensitive niosomal formulation of Mitoxantrone by a modified ethanol injection method. Cholesterol hemisuccinate was added instead of cholesterol in order to produce pH-sensitivity property and using PEG-Poly (monomethyl itaconate)-CholC6 (PEG-PMMI-CholC6) copolymer introduced simultaneously pH-sensitivity and plasma stability properties in prepared niosomes. The pH-sensitivity and cytotoxicity of Mitoxantrone niosomes were evaluated in vitro in phosphate buffer with different pHs as well as using human ovarian cancer cell line (OVCAR-3), human breast cancer cell line (MCF-7) and human umbilical vein endothelial cells (HUVEC). Results showed that both cholesterol derivatives bearing formulations had pH-sensitive property and were found to release their contents under mild acidic conditions rapidly. In addition, the PEG-PMMI-CholC6-based niosomes could reserve the pH-sensitivity after incubation in plasma. Both Mitoxantrone-loaded pH-sensitive niosomes showed higher cytotoxicity than the conventional niosomes on OVCAR-3 and MCF-7 cell lines. However, both pH-sensitive niosomes exhibited lower cytotoxic effect on HUVEC cell line. Plasma stable, pH-sensitive niosomes could improve the cytotoxic effect and reduce the side effects of anti-tumor drugs.

Indexed as

cytotoxic effectMitoxantronepH-sensitive plasma stable niosome

Identifiers

PMID26417350
PMCPMC4553888

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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.