Evidence map›Paper›PMID 32110017›Full record

ArticleInternational journal of nanomedicine2020

Celastrol Self-Stabilized Nanoparticles for Effective Treatment of Melanoma.

Jinran Li, Yuxi Jia, Peng Zhang, Huailin Yang, Xianling Cong, Lin An, Chunsheng Xiao

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.0field-weighted citation impact, top 10% 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

21 citing papers in PubMed, 30 citations in OpenAlex.

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  8. Targeted liposomes for macrophages-mediated pulmonary fibrosis therapy.Drug delivery and translational research · 2024
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  18. Decreased expression ofFrontiers in oncology · 2023
    Article
  19. Antifungal Activity of ToAP2D Peptide AgainstFrontiers in bioengineering and biotechnology · 2021
    Article
  20. 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

7 authors at 3 institutions in 1 country.

Jinran LiDepartment of Dermatology, China-Japan Union Hospital, Jilin University, Changchun 130033, People's Republic of China.
Yuxi JiaDepartment of Dermatology, China-Japan Union Hospital, Jilin University, Changchun 130033, People's Republic of China.
Peng ZhangKey Laboratory of Polymer Ecomaterials, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, People's Republic of China.
Huailin YangKey Laboratory of Polymer Ecomaterials, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, People's Republic of China.
Xianling CongDepartment of Dermatology, China-Japan Union Hospital, Jilin University, Changchun 130033, People's Republic of China.ORCID 0000-0002-5790-4188
Lin AnDepartment of Hand Surgery, China-Japan Union Hospital of Jilin University, Changchun 130033, People's Republic of China.
Chunsheng XiaoKey Laboratory of Polymer Ecomaterials, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, People's Republic of China.ORCID 0000-0001-7936-4146
Chinese Academy of Sciences · CNJilin University · CNUnion Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCelastrol (CEL), a triterpene extracted from the Chinese herb PURPOSE: We proposed a facile "in situ drug conjugation-induced self-assembly" strategy to prepare CEL-loaded nanoparticles (CEL-NPs) that exhibited enhanced antitumor activity against melanoma.

methodsFirst, the CEL was chemically conjugated onto a methoxyl poly(ethylene glycol)-

resultsThe CEL-NPs exhibited sustained drug release behavior and were effectively endocytosed by B16F10 cells. Furthermore, the in vivo antitumor evaluation demonstrated that the CEL-NPs had remarkably higher tumor growth inhibition rates and lower systemic side effects than free CEL.

conclusionIn summary, our present work not only demonstrates the generation of stable CEL-loaded nanoparticles for the efficient treatment of melanoma but also describes a general way to prepare drug self-stabilized nanomedicine for anticancer therapy.

Indexed as

AnimalsAntineoplastic Agents, PhytogenicDelayed-Action PreparationsDynamic Light ScatteringHydrophobic and Hydrophilic InteractionsMaleMelanomaMelanoma, ExperimentalMice, Inbred C57BLMicellesMicroscopy, Electron, TransmissionNanoparticlesPentacyclic TriterpenesPolyethylene GlycolsPolylysineTriterpenesAntineoplastic Agents, PhytogeniccelastrolDelayed-Action PreparationsMicellesmPEG-block-PLLPentacyclic TriterpenesPolyethylene GlycolsPolylysineTriterpenescelastrolmelanomananomedicineself-assemblyself-stabilization

Identifiers

PMID32110017
PMCPMC7037082
OpenAlexW3008939207

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.