Evidence map›Paper›PMID 28891337›Full record

ArticleDrug delivery2017

Enhanced tumor targeting effects of a novel paclitaxel-loaded polymer: PEG-PCCL-modified magnetic iron oxide nanoparticles.

Xinyi Li, Yuan Yang, Yiping Jia, Xuan Pu, Ting Yang, Yicheng Wang, Xuefei Ma, Qi Chen, Mengwen Sun, Dapeng Wei and 3 more

Abstract 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 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Targeting Strategies for Enhancing Paclitaxel Specificity in Chemotherapy.Frontiers in cell and developmental biology · 2021
    Review
  5. Review
  6. Review
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

13 authors.

Xinyi Lia Department of Microbiology, West China School of Basic Medical Sciences & Forensic Medicine , Sichuan University , Chengdu , China.
Yuan Yanga Department of Microbiology, West China School of Basic Medical Sciences & Forensic Medicine , Sichuan University , Chengdu , China.
Yiping Jiaa Department of Microbiology, West China School of Basic Medical Sciences & Forensic Medicine , Sichuan University , Chengdu , China.
Xuan Pua Department of Microbiology, West China School of Basic Medical Sciences & Forensic Medicine , Sichuan University , Chengdu , China.
Ting Yanga Department of Microbiology, West China School of Basic Medical Sciences & Forensic Medicine , Sichuan University , Chengdu , China.
Yicheng Wanga Department of Microbiology, West China School of Basic Medical Sciences & Forensic Medicine , Sichuan University , Chengdu , China.
Xuefei Maa Department of Microbiology, West China School of Basic Medical Sciences & Forensic Medicine , Sichuan University , Chengdu , China.
Qi Chena Department of Microbiology, West China School of Basic Medical Sciences & Forensic Medicine , Sichuan University , Chengdu , China.
Mengwen Suna Department of Microbiology, West China School of Basic Medical Sciences & Forensic Medicine , Sichuan University , Chengdu , China.
Dapeng Weia Department of Microbiology, West China School of Basic Medical Sciences & Forensic Medicine , Sichuan University , Chengdu , China.
Yu Kuanga Department of Microbiology, West China School of Basic Medical Sciences & Forensic Medicine , Sichuan University , Chengdu , China.
Yang Lid School of Microelectronics and Solid-state Electronics , University of Electronic Science and Technology of China , Chengdu , China.
Yu Liud School of Microelectronics and Solid-state Electronics , University of Electronic Science and Technology of China , Chengdu , China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMultifunctional magnetic nanoparticles (MNP) have been newly developed for tumor-targeted drug carriers. To address challenges including biocompatibility, stability, nontoxicity, and targeting efficiency, here we report the novel drug deliverer poly(ethylene glycol) carboxyl-poly(ɛ-caprolactone) modified MNP (PEG-PCCL-MNP) suitable for magnetic targeting based on our previous studies.

methodsTheir in vitro characterization and cytotoxicity assessments, in vivo cytotoxicity assessments, and antitumor efficacy study were elaborately investigated.

resultsThe size of PEG-PCCL-MNP was 79.6 ± 0.945 nm. PEG-PCCL-MNP showed little in vitro or in vivo cytotoxicity and good biocompatibility, as well as effective tumor-specific cell targeting for drug delivery with the presence of external magnetic field. DISCUSSION: PEG-PCCL-MNP is a potential candidate of biocompatible and tumor-specific targeting drug vehicle for hydrophobic drugs.

Indexed as

NeoplasmsCell Line, TumorDrug CarriersFerric CompoundsHumansMetal NanoparticlesPaclitaxelPolyethylene GlycolsPolymersDrug CarriersFerric Compoundsferric oxidePaclitaxelPolyethylene GlycolsPolymersbiocompatibilitycarriercytotoxicityMagnetic nanoparticletumor-target

Identifiers

PMID28891337
PMCPMC8241137

What OpenQuestion holds

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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.