Evidence map›Paper›PMID 30458644›Full record

ArticleDrug delivery2018

Multistage delivery of CDs-DOX/ICG-loaded liposome for highly penetration and effective chemo-photothermal combination therapy.

Xiao Xue, Ting Fang, Luyao Yin, Jianqi Jiang, Yunpeng He, Yinghui Dai, Dongkai Wang

Open access · goldAbstract read
In one paragraph

Article in Drug delivery, 2018. 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
2.6field-weighted citation impact, top 9% 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, 66 citations in OpenAlex.

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  12. Recent Advances in Functional Carbon Quantum Dots for Antitumour.International journal of nanomedicine · 2021
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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 1 institution in 1 country.

Xiao Xuea Department of Pharmaceutics, School of Pharmacy , Shenyang Pharmaceutical University , Shenyang , P.R. China.
Ting Fanga Department of Pharmaceutics, School of Pharmacy , Shenyang Pharmaceutical University , Shenyang , P.R. China.
Luyao Yina Department of Pharmaceutics, School of Pharmacy , Shenyang Pharmaceutical University , Shenyang , P.R. China.
Jianqi Jianga Department of Pharmaceutics, School of Pharmacy , Shenyang Pharmaceutical University , Shenyang , P.R. China.
Yunpeng Hea Department of Pharmaceutics, School of Pharmacy , Shenyang Pharmaceutical University , Shenyang , P.R. China.
Yinghui Daib Department of Traditional Chinese Medicine, School of Pharmacy , Shenyang Pharmaceutical University , Shenyang , P.R. China.
Dongkai Wanga Department of Pharmaceutics, School of Pharmacy , Shenyang Pharmaceutical University , Shenyang , P.R. China.ORCID http://orcid.org/0000-0002-4081-8443
Shenyang Pharmaceutical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nanoparticles (NPs) have proven to be effective drug carriers in diagnosis and therapy of cancer. But, they faced a contradictory issue that NPs with large size appear weak tumor penetration, meanwhile small size resulted in poor tumor retention. Herein, we fabricated doxorubicin conjugated carbon dots (CDs-DOX) and indocyanine green (ICG)-loaded liposomes (ICG-LPs) named CDs-ICG-LPs using a modified reverse phase evaporation process, and with high incorporation in the aqueous core. The CDs-ICG-LPs exhibited good monodispersity, excellent fluorescence/size stability, and consistent spectra characteristics compared with free ICG or DOX. Moreover, the CDs-ICG-LPs showed higher temperature response, faster DOX release under laser irradiation. In the meantime, the fluorescence of DOX and ICG in CDs-ICG-LPs was also visualized for the process of subcellular location in vitro. In comparison with chemo or photothermal treatment alone, the combined treatment of CDs-ICG-LPs with laser irradiation synergistically induced the apoptosis and death of DOX-sensitive HepG2 cells. In vivo antitumor activities demonstrated CDs-ICG-LPs could reach higher antitumor activity compared with CDs-DOX and ICG-LPs for H22 tumor cells, and suppressed H22 tumor growth in vivo. Notably, no systemic toxicity occurrence was observed after repeated dose of CDs-ICG-LPs with laser irradiation. Hence, the well-defined CDs-ICG-LPs exhibited great potential in targeting cancer imaging and chemo-photothermal therapy.

Indexed as

AnimalsAntineoplastic AgentsApoptosisCarbonCell SurvivalCombined Modality TherapyDoxorubicinDrug Delivery SystemsDrug DesignDrug LiberationDrug Therapy, CombinationHep G2 CellsHumansHyperthermia, InducedIndocyanine GreenLiposomesAntineoplastic AgentsCarbonDoxorubicinIndocyanine GreenLiposomesPhotosensitizing AgentsCarbon dotschemo-photothermaldoxorubicinhighly penetrationindocyanine greenliposome

Identifiers

PMID30458644
PMCPMC6598495
OpenAlexW2900990293

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.