Evidence map›Paper›PMID 32166677›Full record

ArticleCurrent medical science2020

Application of Paclitaxel-loaded EGFR Peptide-conjugated Magnetic Polymeric Liposomes for Liver Cancer Therapy.

Zhen-Lv Lin, Jian Ding, Guo-Ping Sun, Dan Li, Shan-Shan He, Xiao-Fei Liang, Xun-Ru Huang, Jie Xie

Abstract read
PubMed Publisher
In one paragraph

Article in Current medical science, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

14 citing papers in PubMed, 34 citations in OpenAlex.

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  6. Application of mPEG-CS-cRGD/Drug delivery · 2023
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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 1 country.

Zhen-Lv LinDepartment of Emergency, The First Affiliated Hospital of Fujian Medical University, Fuzhou, 350005, China.
Jian DingDepartment of Gastroenterology, The First Affiliated Hospital of Fujian Medical University, Fuzhou, 350005, China. dingjian@fjmu.edu.cn.
Guo-Ping SunDepartment of Pharmacy, Qingdao Seventh People's Hospital, Qingdao, 266034, China.
Dan LiDepartment of Gastroenterology, Union Hospital of Fujian Medical University, Fuzhou, 350001, China. doctorlidan@163.com.
Shan-Shan HeDepartment of Gastroenterology, The First Affiliated Hospital of Fujian Medical University, Fuzhou, 350005, China.
Xiao-Fei LiangState Key Laboratory of Oncogenes and Related Genes, Shanghai Cancer Institute, Shanghai Jiaotong University School of Medicine, Shanghai, 200032, China.
Xun-Ru HuangDepartment of Gastroenterology, The First Affiliated Hospital of Fujian Medical University, Fuzhou, 350005, China.
Jie XieDepartment of Emergency, The First Affiliated Hospital of Fujian Medical University, Fuzhou, 350005, China.
First Affiliated Hospital of Fujian Medical University · CNFujian Medical University · CNFujian Normal University · CNQingdao Eighth People's Hospital · CNState Key Laboratory of Oncogene and Related Genes · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Developing the methodologies that allow for safe and effective delivery of therapeutic drugs to target sites is a very important research area in cancer therapy. In this study, polyethylene glycol (PEG)-coated magnetic polymeric liposome (MPL) nanoparticles (NPs) assembled from octadecyl quaternized carboxymethyl chitosan (OQC), PEGylated OQC, cholesterol, and magnetic NPs, and functionalized with epithelial growth factor receptor (EGFR) peptide, were successfully prepared for in-vivo liver targeting. The two-step liver targeting strategy, based on both magnetic force and EGFR peptide conjugation, was evaluated in a subcutaneous hepatocellular carcinoma model of nude mouse. The results showed that EGFR-conjugated MPLs not only accumulated in the liver by magnetic force, but could also diffuse into tumor cells as a result of EGFR targeting. In addition, paclitaxel (PTX) was incorporated into small EGFR-conjugated MPLs (102.0±0.7 nm), resulting in spherical particles with high drug encapsulation efficiency (>90%). The use of the magnetic targeting for enhancing the transport of PTX-loaded EGFR-conjugated MPLs to the tumor site was further confirmed by detecting PTX levels. In conclusion, PTX-loaded EGFR-conjugated MPLs could potentially be used as an effective drug delivery system for targeted liver cancer therapy.

Indexed as

AnimalsAntineoplastic Agents, PhytogenicCarcinoma, HepatocellularCell Line, TumorErbB ReceptorsHumansLiposomesLiverLiver NeoplasmsMagnetite NanoparticlesMicePaclitaxelParticle SizePeptidesPolymersXenograft Model Antitumor AssaysAntineoplastic Agents, PhytogenicEGFR protein, humanErbB ReceptorsLiposomesMagnetite NanoparticlesPaclitaxelPeptidesPolymersdrug deliveryliver cancermagnetic nanoparticlesquaternized chitosantargeted therapy

Identifiers

PMID32166677
OpenAlexW3011585224

What OpenQuestion holds

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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.