Evidence map›Paper›PMID 29200852›Full record

ArticleInternational journal of nanomedicine2017

Natural material-decorated mesoporous silica nanoparticle container for multifunctional membrane-controlled targeted drug delivery.

Yan Hu, Lei Ke, Hao Chen, Ma Zhuo, Xinzhou Yang, Dan Zhao, Suying Zeng, Xincai Xiao

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

14 citing papers in PubMed, 38 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

8 authors at 2 institutions in 1 country.

Yan HuDepartment of Pharmaceutics, School of Pharmaceutical Science, South-Central University for Nationalities.
Lei KeDepartment of Medicinal Chemistry, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, People's Republic of China.
Hao ChenDepartment of Pharmaceutics, School of Pharmaceutical Science, South-Central University for Nationalities.
Ma ZhuoDepartment of Pharmaceutics, School of Pharmaceutical Science, South-Central University for Nationalities.
Xinzhou YangDepartment of Pharmaceutics, School of Pharmaceutical Science, South-Central University for Nationalities.
Dan ZhaoDepartment of Pharmaceutics, School of Pharmaceutical Science, South-Central University for Nationalities.
Suying ZengDepartment of Pharmaceutics, School of Pharmaceutical Science, South-Central University for Nationalities.
Xincai XiaoDepartment of Pharmaceutics, School of Pharmaceutical Science, South-Central University for Nationalities.
South Central Minzu University · CNInstitute of Medicinal Plant Development · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To avoid the side effects caused by nonspecific targeting, premature release, weak selectivity, and poor therapeutic efficacy of current nanoparticle-based systems used for drug delivery, we fabricated natural material-decorated nanoparticles as a multifunctional, membrane-controlled targeted drug delivery system. The nanocomposite material coated with a membrane was biocompatible and integrated both specific tumor targeting and responsiveness to stimulation, which improved transmission efficacy and controlled drug release. Mesoporous silica nanoparticles (MSNs), which are known for their biocompatibility and high drug-loading capacity, were selected as a model drug container and carrier. The membrane was established by the polyelectrolyte composite method from chitosan (CS) which was sensitive to the acidic tumor microenvironment, folic acid-modified CS which recognizes the folate receptor expressed on the tumor cell surface, and a CD

Indexed as

Drug Delivery SystemsMembranes, ArtificialBiocompatible MaterialsCell DeathChitosanDrug LiberationEndocytosisFolic AcidHep G2 CellsHumansNanoparticlesParticle SizePorositySilicon DioxideSpectroscopy, Fourier Transform InfraredStatic ElectricityBiocompatible MaterialsChitosanFolic AcidMembranes, ArtificialSilicon Dioxidemembrane-controlledmesoporous silica nanoparticlesmultifunctionalnatural materialstargeted drug delivery

Identifiers

PMID29200852
PMCPMC5702528
OpenAlexW2770688707

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.