Evidence map›Paper›PMID 29258613›Full record

ArticleJournal of nanobiotechnology2017

Dual-drug loaded nanoneedles with targeting property for efficient cancer therapy.

Xiangrui Yang, Shichao Wu, Wanyi Xie, Anran Cheng, Lichao Yang, Zhenqing Hou, Xin Jin

Open access · goldAbstract read
In one paragraph

Article in Journal of nanobiotechnology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

6 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
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  6. Prussian blue nanosphere-embeddedActa pharmaceutica Sinica. B · 2019
    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

7 authors at 1 institution in 1 country.

Xiangrui YangDepartment of Basic Medical Science, Medical College, Xiamen University, Xiamen, 361102, China.
Shichao WuDepartment of Basic Medical Science, Medical College, Xiamen University, Xiamen, 361102, China. wushichao@xmu.edu.cn.ORCID http://orcid.org/0000-0001-8511-0281
Wanyi XieDepartment of Basic Medical Science, Medical College, Xiamen University, Xiamen, 361102, China.
Anran ChengDepartment of Basic Medical Science, Medical College, Xiamen University, Xiamen, 361102, China.
Lichao YangDepartment of Basic Medical Science, Medical College, Xiamen University, Xiamen, 361102, China.
Zhenqing HouResearch Center of Biomedical Engineering, College of Materials, Xiamen University, Xiamen, 361005, China. houzhenqing@xmu.edu.cn.
Xin JinDepartment of Basic Medical Science, Medical College, Xiamen University, Xiamen, 361102, China. xinjin@xmu.edu.cn.
Xiamen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSince the anticancer drugs have diverse inhibited mechanisms to the cancer cells, the use of two or more kinds of anticancer agents may achieve excellent therapeutic effects, especially to the drug-resistant tumors.

resultsIn this study, we developed a kind of dual drug [methotrexate (MTX) and 10-hydroxycamptothecine (HCPT)] loaded nanoneedles (DDNDs) with pronounced targeting property, high drug loading and prolonged drug release. The anti-solvent precipitation of the HCPT and MTX modified PEG-b-PLGA (PEG-b-PLGA-MTX, PPMTX) leads to nucleation of nanoneedles with nanocrystalline HCPT as the core wrapped with PPMTX as steric stabilizers. In vitro cell uptake studies showed that the DDNDs revealed an obviously targeting property and entered the HeLa cells easier than the nanoneedles without MTX modification. The cytotoxicity tests illustrated that the DDNDs possessed better killing ability to HeLa cells than the individual drugs or their mixture in the same dose, indicating its good synergistic effect and targeting property. The in vivo studies further confirmed these conclusions.

conclusionsThis approach led to a promising sustained drug delivery system for cancer diagnosis and treatment.

Indexed as

AnimalsAntineoplastic AgentsCamptothecinCell SurvivalDrug CarriersDrug LiberationDrug SynergismHeLa CellsHumansMethotrexateMiceMice, Inbred BALB CMice, NudeMicroscopy, ConfocalMicroscopy, Electron, ScanningNanoparticles10-hydroxycamptothecinAntineoplastic AgentsCamptothecinDrug CarriersMethotrexatePolyethylene GlycolsPolyglactin 910poly(lactic-glycolic acid)-poly(ethyleneglycol) copolymer10-HydroxycamptothecineDual-drugMethotrexateNanoneedle

Identifiers

PMID29258613
PMCPMC5735828
OpenAlexW2780219753

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.