Evidence map›Paper›PMID 30400634›Full record

ArticleNanomaterials (Basel, Switzerland)2018

Magnetic Alginate/Chitosan Nanoparticles for Targeted Delivery of Curcumin into Human Breast Cancer Cells.

Wenxing Song, Xing Su, David Alexander Gregory, Wei Li, Zhiqiang Cai, Xiubo Zhao

Open access · goldAbstract read
In one paragraph

Article in Nanomaterials (Basel, Switzerland), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
4.2field-weighted citation impact, top 4% 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

44 citing papers in PubMed, 151 citations in OpenAlex.

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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

6 authors at 2 institutions in 2 countries.

Wenxing SongDepartment of Chemical and Biological Engineering, University of Sheffield, Sheffield S1 3JD, UK. wsong4@sheffield.ac.uk.
Xing SuDepartment of Materials Science and Engineering, University of Sheffield, Sheffield S1 3JD, UK. whitesnowleopard@126.com.
David Alexander GregoryDepartment of Chemical and Biological Engineering, University of Sheffield, Sheffield S1 3JD, UK. d.a.gregory@sheffield.ac.uk.ORCID 0000-0003-2489-5462
Wei LiDepartment of Electronic and Electrical Engineering, University of Sheffield, Sheffield S3 7HQ, UK. WLi27@sheffield.ac.uk.
Zhiqiang CaiSchool of Pharmaceutical Engineering and Life Science, Changzhou University, Changzhou 213164, China. zhqcai@cczu.edu.cn.
Xiubo ZhaoDepartment of Chemical and Biological Engineering, University of Sheffield, Sheffield S1 3JD, UK. xiubo.zhao@sheffield.ac.uk.ORCID 0000-0002-4620-2893
Changzhou University · CNUniversity of Sheffield · GB

Funding

TRANSFORMATION OF B LYMPHOCYTES BY EPSTEIN-BARR VIRUSF32CA007174 · NCI · DANA-FARBER CANCER INSTITUTE · PI SPECK, SAMUEL H · 1985 to 1985
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Engineering and Physical Sciences Research Council EP/N007174/1Engineering and Physical Sciences Research Council EP/N023579/1Royal Society RG160662
6 · The paper itself

Abstract

Curcumin is a promising anti-cancer drug, but its applications in cancer therapy are limited, due to its poor solubility, short half-life and low bioavailability. In this study, curcumin loaded magnetic alginate/chitosan nanoparticles were fabricated to improve the bioavailability, uptake efficiency and cytotoxicity of curcumin to Human Caucasian Breast Adenocarcinoma cells (MDA-MB-231). Alginate and chitosan were deposited on Fe₃O₄ magnetic nanoparticles based on their electrostatic properties. The nanoparticle size ranged from 120⁻200 nm, within the optimum range for drug delivery. Controllable and sustained release of curcumin was obtained by altering the number of chitosan and alginate layers on the nanoparticles. Confocal fluorescence microscopy results showed that targeted delivery of curcumin with the aid of a magnetic field was achieved. The fluorescence-activated cell sorting (FACS) assay indicated that MDA-MB-231 cells treated with curcumin loaded nanoparticles had a 3⁻6 fold uptake efficiency to those treated with free curcumin. The 3-(4,5-Dimethylthiazol-2-yl)-2,5-Diphenyltetrazolium Bromide (MTT) assay indicated that the curcumin loaded nanoparticles exhibited significantly higher cytotoxicity towards MDA-MB-231 cells than HDF cells. The sustained release profiles, enhanced uptake efficiency and cytotoxicity to cancer cells, as well as directed targeting make MACPs promising candidates for cancer therapy.

Indexed as

alginatecancerchitosancurcumindrug deliverylayer-by-layermagnetic nanoparticles

Identifiers

PMID30400634
PMCPMC6267575
OpenAlexW2892405094

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.