Evidence map›Paper›PMID 29719394›Full record

ArticleInternational journal of nanomedicine2018

Preparation, characterization, in vitro and in vivo anti-tumor effect of thalidomide nanoparticles on lung cancer.

Long Xia Chen, Xiao Ling Ni, Heng Zhang, Min Wu, Jing Liu, Shan Xu, Ling Lin Yang, Shao Zhi Fu, Jingbo Wu

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

13 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
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  4. Review
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  8. Repurpose but also (nano)-reformulate! The potential role of nanomedicine in the battle against SARS-CoV2.Journal of controlled release : official journal of the Controlled Release Society · 2021
    Review
  9. Article
  10. Article
  11. Amphiphilic Polymer-Modified Uniform CuFeSeContrast media & molecular imaging · 2020
    Article
  12. Article
  13. 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

9 authors at 1 institution in 1 country.

Long Xia Chen *Department of Oncology, the Affiliated Hospital of Southwest Medical University, Luzhou, People's Republic of China.
Xiao Ling Ni *Department of Oncology, the Affiliated Hospital of Southwest Medical University, Luzhou, People's Republic of China.
Heng ZhangDepartment of Oncology, the Affiliated Hospital of Southwest Medical University, Luzhou, People's Republic of China.
Min WuDepartment of Oncology, the Affiliated Hospital of Southwest Medical University, Luzhou, People's Republic of China.
Jing LiuDepartment of Oncology, the Affiliated Hospital of Southwest Medical University, Luzhou, People's Republic of China.
Shan XuDepartment of Oncology, the Affiliated Hospital of Southwest Medical University, Luzhou, People's Republic of China.
Ling Lin YangDepartment of Oncology, the Affiliated Hospital of Southwest Medical University, Luzhou, People's Republic of China.
Shao Zhi FuDepartment of Oncology, the Affiliated Hospital of Southwest Medical University, Luzhou, People's Republic of China.
Jingbo WuDepartment of Oncology, the Affiliated Hospital of Southwest Medical University, Luzhou, People's Republic of China.
Affiliated Hospital of Southwest Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThalidomide (THA) is an angiogenesis inhibitor and an efficient inhibitor of the tumor necrosis factor-α (TNF-α). However, the clinical application of THA has been limited due to hydrophobicity of the compound. MATERIALS AND

methodsTo increase the water solubility of THA and in order to evaluate the anticancer abilities of this material on human lung carcinoma, methoxy poly(ethylene glycol)-poly(ε-caprolactone) nanoparticles loaded with THA (THA-NPs) were prepared. The synthesis of THA-NPs was carried out via a dialysis method with relative satisfactory encapsulation efficiency, loading capacity, size distribution, and zeta potential.

resultsA cytotoxicity assay demonstrated that THA-NPs inhibited the growth of cells in a dose-dependent manner. The evaluation of anti-tumor activity in vivo showed that THA-NPs could inhibit tumor growth and prolong the survival rate of tumor-bearing mice. Immunohistochemical analysis indicated that THA-NPs inhibited cell proliferation (Ki-67 positive rate, 32.8%±4.2%,

conclusionIn general, the drug delivery system reported herein may shed light on future targeted therapy in lung cancer treatment.

Indexed as

AnimalsAntineoplastic AgentsCell Line, TumorDrug Delivery SystemsDrug LiberationHumansHydrophobic and Hydrophilic InteractionsLung NeoplasmsMice, NudeNanoparticlesParticle SizePolyestersPolyethylene GlycolsPositron-Emission TomographySolubilitySurvival RateAntineoplastic Agentsmethoxy poly(ethylene glycol-co-epsilon-caprolactone)PolyestersPolyethylene GlycolsThalidomidelung cancerMPEG-PCLnanoparticlesthalidomide

Identifiers

PMID29719394
PMCPMC5922239
OpenAlexW2800737337

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.