Evidence map›Paper›PMID 32368051›Full record

ArticleInternational journal of nanomedicine2020

Enhancing Drug Delivery for Overcoming Angiogenesis and Improving the Phototherapy Efficacy of Glioblastoma by ICG-Loaded Glycolipid-Like Micelles.

Yupeng Liu, Suhuan Dai, Lijuan Wen, Yun Zhu, Yanan Tan, Guoxi Qiu, Tingting Meng, Fangying Yu, Hong Yuan, Fuqiang Hu

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 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

13 citing papers in PubMed, 23 citations in OpenAlex.

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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

10 authors at 3 institutions in 1 country.

Yupeng LiuCollege of Pharmaceutical Science, Zhejiang University, Hangzhou 310058, People's Republic of China.ORCID 0000-0001-9544-1009
Suhuan DaiCollege of Pharmaceutical Science, Zhejiang University, Hangzhou 310058, People's Republic of China.
Lijuan WenCollege of Pharmaceutical Science, Zhejiang University, Hangzhou 310058, People's Republic of China.
Yun ZhuOcean College, Zhejiang University, Zhoushan 316021, Republic of China.
Yanan TanOcean College, Zhejiang University, Zhoushan 316021, Republic of China.
Guoxi QiuCollege of Pharmaceutical Science, Zhejiang University, Hangzhou 310058, People's Republic of China.ORCID 0000-0002-7662-9652
Tingting MengCollege of Pharmaceutical Science, Zhejiang University, Hangzhou 310058, People's Republic of China.ORCID 0000-0003-1009-1287
Fangying YuCollege of Pharmaceutical Science, Zhejiang University, Hangzhou 310058, People's Republic of China.
Hong YuanCollege of Pharmaceutical Science, Zhejiang University, Hangzhou 310058, People's Republic of China.
Fuqiang HuCollege of Pharmaceutical Science, Zhejiang University, Hangzhou 310058, People's Republic of China.
Zhejiang University · CNZhejiang Ocean University · CNGannan Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPhototherapy is a potential new candidate for glioblastoma (GBM) treatment. However inadequate phototherapy due to stability of the photosensitizer and low target specificity induces the proliferation of neovascular endothelial cells for angiogenesis and causes poor prognosis.

methodsIn this study, we constructed c(RGDfk)-modified glycolipid-like micelles (cRGD-CSOSA) encapsulating indocyanine green (ICG) for dual-targeting neovascular endothelial cells and tumor cells, and cRGD-CSOSA/ICG mediated dual effect of PDT/PTT with NIR irradiation.

resultsIn vitro, cRGD-CSOSA/ICG inhibited cell proliferation and blocked angiogenesis with NIR irradiation. In vivo, cRGD-CSOSA/ICG exhibited increased accumulation in neovascular endothelial cells and tumor cells. Compared with that of CSOSA, the accumulation of cRGD-CSOSA in tumor tissue was further improved after dual-targeted phototherapy pretreatment. With NIR irradiation, the tumor-inhibition rate of cRGD-CSOSA/ICG was 80.00%, significantly higher than that of ICG (9.08%) and CSOSA/ICG (42.42%). Histological evaluation showed that the tumor vessels were reduced and that the apoptosis of tumor cells increased in the cRGD-CSOSA/ICG group with NIR irradiation.

conclusionThe cRGD-CSOSA/ICG nanoparticle-mediated dual-targeting phototherapy could enhance drug delivery to neovascular endothelial cells and tumor cells for anti-angiogenesis and improve the phototherapy effect of glioblastoma, providing a new strategy for glioblastoma treatment.

Indexed as

Angiogenesis InhibitorsAnimalsApoptosisCell Line, TumorCell ProliferationDrug Delivery SystemsEndothelial CellsGlioblastomaGlycolipidsHumansIndocyanine GreenMicellesMice, NudeNanoparticlesNeovascularization, PathologicOligopeptidesAngiogenesis Inhibitorsarginyl-glycyl-aspartic acidGlycolipidsIndocyanine GreenMicellesOligopeptidesPhotosensitizing Agentsangiogenesisdual-targetingglioblastomaglycolipid-like micellesphototherapy

Identifiers

PMID32368051
PMCPMC7184138
OpenAlexW3018215672

What OpenQuestion holds

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Registered trials

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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.