Evidence map›Paper›PMID 31574945›Full record

ArticleMolecules (Basel, Switzerland)2019

Cell-Penetrating Peptide and Transferrin Co-Modified Liposomes for Targeted Therapy of Glioma.

Xi Wang, Yarong Zhao, Shiyan Dong, Robert J Lee, Dongsheng Yang, Huan Zhang, Lesheng Teng

Erratum issuedAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing 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

30 citing papers in PubMed.

  1. Article
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  8. Progress of nanoparticle drug delivery system for the treatment of glioma.Frontiers in bioengineering and biotechnology · 2024
    Review
  9. Liposomal Nanomaterials: A Rising Star in Glioma Treatment.International journal of nanomedicine · 2024
    Review
  10. Transferrin-Targeted Liposomes in Glioblastoma Therapy: A Review.International journal of molecular sciences · 2023
    Review
  11. Review
  12. Review
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  16. Review
  17. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Xi WangSchool of Life Sciences, Jilin University, Changchun 130012, China. wangxi1976@126.com.
Yarong ZhaoSchool of Life Sciences, Jilin University, Changchun 130012, China. zhaoyr16@mails.jlu.edu.cn.ORCID 0000-0003-3622-6303
Shiyan DongSchool of Life Sciences, Jilin University, Changchun 130012, China. sydong16@mails.jlu.edu.cn.
Robert J LeeDivision of Pharmaceutics and Pharmacology, College of Pharmacy, The Ohio State University, Columbus, OH 43210, USA. lee.1339@osu.edu.ORCID 0000-0002-5981-5867
Dongsheng YangDepartment of Chemistry and Pharmacy, Zhuhai College of Jilin University, Zhuhai 519041, China. yds@jluzh.edu.cn.
Huan ZhangSchool of Life Sciences, Jilin University, Changchun 130012, China. zhang_huan1020@163.com.
Lesheng TengSchool of Life Sciences, Jilin University, Changchun 130012, China. tenglesheng@jlu.edu.cn.ORCID 0000-0003-1623-5384

Funding

Jilin Province Industrial Innovation Special Fund Project 2019C050-4Key Platform and Major Research Program of Guangdong Provincial University 2017GXJK221National Natural Science Foundation of China 81502999
6 · The paper itself

Abstract

Glioma is one of the most aggressive and common malignant brain tumors. Due to the presence of the blood-brain barrier (BBB), the effectiveness of therapeutics is greatly affected. In this work, to develop an efficient anti-glioma drug with targeting and which was able to cross the BBB, cell-penetrating peptides (R8) and transferrin co-modified doxorubicin (DOX)-loaded liposomes (Tf-LPs) were prepared. Tf-LPs possessed a spherical shape and uniform size with 128.64 nm and their ξ-potential was 6.81 mV. Tf-LPs were found to be stable in serum within 48 h. Uptake of Tf-LPs in both U87 and GL261 cells was analyzed by confocal laser scanning microscopy and by flow cytometry. Tf-LPs were efficiently taken up by both U87 and GL261 cells. Moreover, Tf-LPs exhibited sustained-release. The cumulative release of DOX from Tf-LPs reached ~50.0% and showed excellent anti-glioma efficacy. Histology of major organs, including brain, heart, liver, spleen, lungs and kidney, and the bodyweight of mice, all indicated low toxicity of Tf-LPs. In conclusion, Tf-LPs showed great promise as an anti-glioma therapeutic agent.

Indexed as

AnimalsAntineoplastic AgentsBlood-Brain BarrierCell Line, TumorCell-Penetrating PeptidesCell SurvivalDisease Models, AnimalDoxorubicinDrug Delivery SystemsGliomaHumansLiposomesMicePolyethylene GlycolsTransferrinXenograft Model Antitumor AssaysAntineoplastic AgentsCell-Penetrating PeptidesDoxorubicinliposomal doxorubicinLiposomesPolyethylene GlycolsTransferrinblood-brain barriercell-penetrating peptidesgliomatargeting

Identifiers

PMID31574945
PMCPMC6804123

What OpenQuestion holds

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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.