Evidence map›Paper›PMID 28165807›Full record

ArticleDrug delivery2017

Preparation of endostatin-loaded chitosan nanoparticles and evaluation of the antitumor effect of such nanoparticles on the Lewis lung cancer model.

Rui-Lin Ding, Fang Xie, Yue Hu, Shao-Zhi Fu, Jing-Bo Wu, Juan Fan, Wen-Feng He, Yu He, Ling-Lin Yang, Sheng Lin and 1 more

Open access · goldAbstract read
In one paragraph

Article in Drug delivery, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

11 citing papers in PubMed, 37 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

11 authors at 1 institution in 1 country.

Rui-Lin Dinga Department of Oncology , The Affiliated Hospital of Southwest Medical University , Luzhou , P.R. China.
Fang Xiea Department of Oncology , The Affiliated Hospital of Southwest Medical University , Luzhou , P.R. China.
Yue Hua Department of Oncology , The Affiliated Hospital of Southwest Medical University , Luzhou , P.R. China.
Shao-Zhi Fua Department of Oncology , The Affiliated Hospital of Southwest Medical University , Luzhou , P.R. China.
Jing-Bo Wua Department of Oncology , The Affiliated Hospital of Southwest Medical University , Luzhou , P.R. China.
Juan Fana Department of Oncology , The Affiliated Hospital of Southwest Medical University , Luzhou , P.R. China.
Wen-Feng Hea Department of Oncology , The Affiliated Hospital of Southwest Medical University , Luzhou , P.R. China.
Yu Hea Department of Oncology , The Affiliated Hospital of Southwest Medical University , Luzhou , P.R. China.
Ling-Lin Yanga Department of Oncology , The Affiliated Hospital of Southwest Medical University , Luzhou , P.R. China.
Sheng Lina Department of Oncology , The Affiliated Hospital of Southwest Medical University , Luzhou , P.R. China.
Qing-Lian Wena Department of Oncology , The Affiliated Hospital of Southwest Medical University , Luzhou , P.R. China.
Affiliated Hospital of Southwest Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The purpose of this study was to prepare ES-loaded chitosan nanoparticles (ES-NPs) and evaluate the antitumor effect of these particles on the Lewis lung cancer model. ES-NPs were prepared by a simple ionic cross-linking method. The characterization of the ES-NPs, including size distribution, zeta potential, loading efficiency and encapsulation efficiency (EE), was performed. An in vitro release test was also used to determine the release behavior of the ES-NPs. Cell viability and cell migration were assayed to detect the in vitro antiangiogenic effect of ES-NPs. In order to clarify the antitumor effect of ES-NPs in vivo, the Lewis lung cancer model was used. ES-NPs were successfully synthesized and shown to have a suitable size distribution and high EE. The nanoparticles were spherical and homogeneous in shape and exhibited an ideal releasing profile in vitro. Moreover, ES-NPs significantly inhibited the proliferation and migration of human umbilical vascular endothelial cells (HUVECs). The in vivo antiangiogenic activity was evaluated by ELISA and immunohistochemistry analyses, which revealed that ES-NPs had a stronger antiangiogenic effect for reinforced anticancer activity. Indeed, even the treatment cycle in which ES-NPs were injected every seven days, showed stronger antitumor effect than the free ES injected for 14 consecutive days. Our study confirmed that the CS nanoparticle is a feasible carrier for endostatin to be used in the treatment of lung cancer.

Indexed as

AnimalsCarcinoma, Lewis LungCell MovementCell SurvivalChitosanDrug CarriersDrug Evaluation, PreclinicalEndostatinsFemaleHumansHuman Umbilical Vein Endothelial CellsMiceMice, Inbred C57BLNanoparticlesRandom AllocationChitosanDrug CarriersEndostatinschitosandrug carrierEndostatinlung cancernanoparticles

Identifiers

PMID28165807
PMCPMC8241108
OpenAlexW2587247372

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.