Evidence map›Paper›PMID 30323587›Full record

ArticleInternational journal of nanomedicine2018

Graphene quantum dots-gated hollow mesoporous carbon nanoplatform for targeting drug delivery and synergistic chemo-photothermal therapy.

Junfeng Fang, Yanqing Liu, Yiwen Chen, Dimei Ouyang, Guangji Yang, Tao Yu

Abstract read
In one paragraph

Article in International journal of nanomedicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

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  16. Nanoparticle Systems for Cancer Phototherapy: An Overview.Nanomaterials (Basel, Switzerland) · 2021
    Review
  17. Article
  18. Review
  19. Article
  20. Conventional Nanosized Drug Delivery Systems for Cancer Applications.Advances in experimental medicine and biology · 2021
    Article
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

6 authors.

Junfeng FangDepartment of Gynecology, The First People's Hospital of Yunnan Province, Kunming University of Science and Technology, Kunming, P.R. China, yutao13987659711@163.com.
Yanqing LiuDepartment of Gynecology, The First People's Hospital of Yunnan Province, Kunming University of Science and Technology, Kunming, P.R. China, yutao13987659711@163.com.
Yiwen ChenDepartment of Gynecology, The First People's Hospital of Yunnan Province, Kunming University of Science and Technology, Kunming, P.R. China, yutao13987659711@163.com.
Dimei OuyangDepartment of Gynecology, The First People's Hospital of Yunnan Province, Kunming University of Science and Technology, Kunming, P.R. China, yutao13987659711@163.com.
Guangji YangDepartment of Gynecology, The First People's Hospital of Yunnan Province, Kunming University of Science and Technology, Kunming, P.R. China, yutao13987659711@163.com.
Tao YuDepartment of Gynecology, The First People's Hospital of Yunnan Province, Kunming University of Science and Technology, Kunming, P.R. China, yutao13987659711@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCarbon-based drug delivery systems have attracted great interest because of their excellent photothermal conversion capability and high specific surface area for drug loading. Herein, we report a multifunctional nanoplatform based on hyaluronic acid (HA)-modified and graphene quantum dot (GQD)-gated hollow mesoporous carbon nanoparticle (HMCN) for anticancer drug encapsulation and targeted chemo-photothermal therapy of CD44 receptor-overexpressed cancer cells.

methodsIn this design, HMCN was not only used as a nanocarrier with high drug loading content to achieve chemotherapy, but also as a near-infrared absorbing agent to realize photothermal therapy. GQDs could not only prevent premature drug release during blood circulation, but also enhance the chemo-photothermal therapeutic efficacy for complete tumor growth suppression. After being modified with HA, the HA-HMCN(DOX)@GQDs could specifically target cancer cells.

resultsAs expected, the as-prepared HMCN exhibited high doxorubicin (DOX)-loading capacity of 410 mg/g and excellent light-to-heat conversion property. The DOX was released from HA-HMCN(DOX)@GQDs in a near-infrared laser and pH stimuli-responsive manner, which could enhance the therapeutic effect. In vitro cell biological experimental results confirmed that the nanoplatform possesses excellent biocompatibility, specifically target CD44 receptor-overexpressing human cervical carcinoma HeLa cells, and has remarkable synergistic chemo-photothermal killing capacity. The in vivo therapeutic studies in HeLa xenografts also showed negligible toxicity of HA-HMCN@GQDs and complete inhibition of tumor growth of HA-HMCN(DOX) @GQDs with near-infrared irradiation.

conclusionThe excellent therapeutic effects demonstrated in vitro and in vivo suggested the HMCN-based nanoplatform holds potential for efficient dual-responsive targeting drug delivery and synergistic chemo-photothermal therapy.

Indexed as

Drug Delivery SystemsHyperthermia, InducedPhototherapyAnimalsAntineoplastic AgentsApoptosisCell SurvivalDoxorubicinDrug LiberationFemaleGraphiteHeLa CellsHumansHyaluronic AcidMice, NudeNanoparticlesAntineoplastic AgentsDoxorubicinGraphiteHyaluronic AcidCD44 receptor targetingchemo-photothermal therapygraphene quantum dotshollow mesoporous carbon nanoparticles

Identifiers

PMID30323587
PMCPMC6177379

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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.