Evidence map›Paper›PMID 28181827›Full record

ArticleDrug delivery2017

Magnetically triggered drug release from nanoparticles and its applications in anti-tumor treatment.

Xin Hua, Qin Yang, Zhimin Dong, Jiashuo Zhang, Wanjiang Zhang, Qiudong Wang, Shengnan Tan, Hugh D C Smyth

Open access · goldAbstract read
In one paragraph

Article in Drug delivery, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

11 citing papers in PubMed, 39 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. 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 5 institutions in 2 countries.

Xin Huaa Division of Bacterial Diseases , State Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences , Harbin , China.
Qin Yanga Division of Bacterial Diseases , State Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences , Harbin , China.
Zhimin Dongb Tianjin Animal Science and Veterinary Research Institute , Tianjin , China.
Jiashuo Zhangc College of Wildlife Resources, College of Life Science, Northeast Forestry University , Harbin , PR China , and.
Wanjiang Zhanga Division of Bacterial Diseases , State Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences , Harbin , China.
Qiudong Wanga Division of Bacterial Diseases , State Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences , Harbin , China.
Shengnan Tanc College of Wildlife Resources, College of Life Science, Northeast Forestry University , Harbin , PR China , and.
Hugh D C Smythd College of Pharmacy, The University of Texas at Austin , Austin , TX , USA.
Chinese Academy of Agricultural Sciences · CNHarbin Veterinary Research Institute · CNNortheast Forestry University · CNThe University of Texas at Austin · USTianjin Academy of Agricultural Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The objective of this study was to describe the magnetic nanoparticle-drug conjugates for improved control of drug delivery and drug release. The widely used anticancer agent Doxorubicin (DOX) was successfully conjugated via amine groups to the carboxylic functional groups coating magnetic nanoparticles (fluidMAG-CMX). Following purification of the nanoparticles, the conjugation of DOX on fluidMAG-CMX was confirmed using FTIR spectroscopy and confocal microscopy. The observed drug loading capacity of DOX was 22.3%. Studies of magnetically triggered release were performed under an oscillating magnetic field (OMF). DOX exhibited a significant release percentage of 70% under an OMF, as compared with the release in enzyme. A magnetic field turn-on and turn-off experiment was also conducted to confirm the control of drug release using this triggered system. In vivo experiments indicated that the tumor-inhibitory rate of CMX-DOX NPs under a magnetic field was higher than the other control groups. According to the toxicity assessments, CMX-DOX NPs were not noticeably toxic to mice at our tested dose.

Indexed as

Drug CarriersMagnetic FieldsMagneticsNanoparticlesAnimalsAntibiotics, AntineoplasticCell SurvivalDextransDose-Response Relationship, DrugDoxorubicinDrug CompoundingFemaleHeLa CellsHumansInhibitory Concentration 50Mice, Inbred BALB CAntibiotics, Antineoplasticcarboxymethyl dextranDextransDoxorubicinDrug Carrierscontrolled releasedoxorubicinMagnetic nanoparticlesoscillating magnetic field

Identifiers

PMID28181827
PMCPMC8253125
OpenAlexW2586112456

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.