Evidence map›Paper›PMID 27143884›Full record

ArticleInternational journal of nanomedicine2016

c(RGDyK)-decorated Pluronic micelles for enhanced doxorubicin and paclitaxel delivery to brain glioma.

YuKun Huang, Wenchao Liu, Feng Gao, Xiaoling Fang, Yanzuo Chen

RetractedOpen access · goldAbstract readRetracted Publication
In one paragraph

Article in International journal of nanomedicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

12 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
  2. Article
  3. Indocarbocyanine nanoparticles extravasate and distribute better than liposomes in brain tumors.Journal of controlled release : official journal of the Controlled Release Society · 2022
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  4. Review
  5. Review
  6. Article
  7. Tumor Targeting by αACS nano · 2020
    Article
  8. Review
  9. Article
  10. PET imaging ofEJNMMI research · 2018
    Article
  11. Article
  12. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 2 countries.

YuKun HuangDepartment of Pharmaceutics, School of Pharmacy, East China University of Science and Technology, Shanghai, People's Republic of China.
Wenchao LiuDepartment of Pharmaceutics, School of Pharmacy, East China University of Science and Technology, Shanghai, People's Republic of China.
Feng GaoDepartment of Pharmaceutics, School of Pharmacy, East China University of Science and Technology, Shanghai, People's Republic of China.
Xiaoling FangKey Laboratory of Smart Drug Delivery, Ministry of Education & PLA, School of Pharmacy, Fudan University, Shanghai, People's Republic of China.
Yanzuo ChenDepartment of Pharmaceutics, School of Pharmacy, East China University of Science and Technology, Shanghai, People's Republic of China.
East China University of Science and Technology · CNSmart Software (Czechia) · CZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Brain glioma therapy is an important challenge in oncology. Here, doxorubicin (DOX) and paclitaxel (PTX)-loaded cyclic arginine-glycine-aspartic acid peptide (c(RGDyK))-decorated Pluronic micelles (cyclic arginine-glycine-aspartic acid peptide-decorated Pluronic micelles loaded with doxorubicin and paclitaxel [RGD-PF-DP]) were designed as a potential targeted delivery system to enhance blood-brain barrier penetration and improve drug accumulation via integrin-mediated transcytosis/endocytosis and based on integrin overexpression in blood-brain barrier and glioma cells. The physicochemical characterization of RGD-PF-DP revealed a satisfactory size of 28.5±0.12 nm with uniform distribution and core-shell structure. The transport rates across the in vitro blood-brain barrier model, cellular uptake, cytotoxicity, and apoptosis of U87 malignant glioblastoma cells of RGD-PF-DP were significantly greater than those of non-c(RGDyK)-decorated Pluronic micelles. In vivo fluorescence imaging demonstrated the specificity and efficacy of intracranial tumor accumulation of RGD-PF-DP. RGD-PF-DP displayed an extended median survival time of 39 days, with no serious body weight loss during the regimen. No acute toxicity to major organs was observed in mice receiving treatment doses via intravenous administration. In conclusion, RGD-PF-DP could be a promising vehicle for enhanced doxorubicin and paclitaxel delivery in patients with brain glioma.

Indexed as

Drug Delivery SystemsMicellesAnimalsApoptosisBiological TransportBlood-Brain BarrierBody WeightBrain NeoplasmsCell Line, TumorCell ProliferationDoxorubicinEndocytosisGliomaHumansKaplan-Meier EstimateMalecyclic arginine-glycine-aspartic acid peptideDoxorubicinMicellesPaclitaxelPeptides, CyclicPoloxamerblood–brain barrierbrain gliomaintegrinPluronic micellestargeted delivery

Identifiers

PMID27143884
PMCPMC4844271
OpenAlexW2337125676

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.