Evidence map›Paper›PMID 28293102›Full record

ArticleDrug design, development and therapy2017

Paclitaxel-loaded star-shaped copolymer nanoparticles for enhanced malignant melanoma chemotherapy against multidrug resistance.

Yongsheng Su, Jian Hu, Zhibin Huang, Yubin Huang, Bingsheng Peng, Ni Xie, Hui Liu

Open access · goldAbstract read
In one paragraph

Article in Drug design, development and therapy, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.1field-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

17 citing papers in PubMed, 45 citations in OpenAlex.

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  15. Photodynamic Therapy for Metastatic Melanoma Treatment: A Review.Technology in cancer research & treatment · 2018
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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

7 authors at 2 institutions in 1 country.

Yongsheng SuDepartment of Burn and Plastic Surgery, The People's Hospital of Baoan Shenzhen Affiliated to Southern Medical University.
Jian HuDepartment of Burn and Plastic Surgery, The People's Hospital of Baoan Shenzhen Affiliated to Southern Medical University.
Zhibin HuangDepartment of Burn and Plastic Surgery, The People's Hospital of Baoan Shenzhen Affiliated to Southern Medical University.
Yubin HuangDepartment of Burn and Plastic Surgery, The People's Hospital of Baoan Shenzhen Affiliated to Southern Medical University.
Bingsheng PengDepartment of Burn and Plastic Surgery, The People's Hospital of Baoan Shenzhen Affiliated to Southern Medical University.
Ni XieCore Laboratory, Shenzhen Second People's Hospital, First Affiliated Hospital of Shenzhen University, Shenzhen, People's Republic of China.
Hui LiuDepartment of Burn and Plastic Surgery, The People's Hospital of Baoan Shenzhen Affiliated to Southern Medical University.
Southern Medical University Shenzhen Hospital · CNShenzhen Second People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Malignant melanoma (MM) is the most dangerous type of skin cancer with annually increasing incidence and death rates. However, chemotherapy for MM is restricted by low topical drug concentration and multidrug resistance. In order to surmount the limitation and to enhance the therapeutic effect on MM, a new nanoformulation of paclitaxel (PTX)-loaded cholic acid (CA)-functionalized star-shaped poly(lactide-co-glycolide) (PLGA)-D-α-tocopheryl polyethylene glycol 1000 succinate (TPGS) nanoparticles (NPs) (shortly PTX-loaded CA-PLGA-TPGS NPs) was fabricated by a modified method of nanoprecipitation. The particle size, zeta potential, morphology, drug release profile, drug encapsulation efficiency, and loading content of PTX-loaded NPs were detected. As shown by confocal laser scanning, NPs loaded with coumarin-6 were internalized by human melanoma cell line A875. The cellular uptake efficiency of CA-PLGA-TPGS NPs was higher than those of PLGA NPs and PLGA-TPGS NPs. The antitumor effects of PTX-loaded NPs were evaluated by the MTT assay in vitro and by a xenograft tumor model in vivo, demonstrating that star-shaped PTX-loaded CA-PLGA-TPGS NPs were significantly superior to commercial PTX formulation Taxol

Indexed as

Antineoplastic Agents, PhytogenicCell ProliferationCell SurvivalDose-Response Relationship, DrugDrug CarriersDrug Resistance, MultipleDrug Resistance, NeoplasmDrug Screening Assays, AntitumorHumansMelanomaNanoparticlesPaclitaxelParticle SizePolymersStructure-Activity RelationshipSurface PropertiesAntineoplastic Agents, PhytogenicDrug CarriersPaclitaxelPolymersdrug deliveryenhanced therapeutic effectsmalignant melanomananoparticlespaclitaxel

Identifiers

PMID28293102
PMCPMC5345981
OpenAlexW2591861696

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.