Evidence map›Paper›PMID 27428945›Full record

ArticleMolecules (Basel, Switzerland)2016

DNA Cleavage and Condensation Activities of Mono- and Binuclear Hybrid Complexes and Regulation by Graphene Oxide.

Shuo Li, Mingxing Dai, Chunping Zhang, Bingying Jiang, Junqiang Xu, Dewen Zhou, Zhongwei Gu

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 43% 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

1 citing paper in PubMed, 8 citations in OpenAlex.

  1. Guanidine- and purine-functionalized ligands of FeJournal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry · 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 3 institutions in 1 country.

Shuo LiNational Engineering Research Center for Biomaterials, Sichuan University, Chengdu 610064, China. lishuo@cqut.edu.cn.
Mingxing DaiSchool of Chemical Engineering, Chongqing University of Technology, Chongqing 400054, China. dai_mingxing@yeah.net.
Chunping ZhangJiangsu Key Laboratory of Target Drug and Clinical Application, Xuzhou Medical College, Xuzhou 221004, China. gaoshan210@163.com.
Bingying JiangSchool of Chemical Engineering, Chongqing University of Technology, Chongqing 400054, China. jiangby@cqut.edu.cn.
Junqiang XuSchool of Chemical Engineering, Chongqing University of Technology, Chongqing 400054, China. xujunqiang@cqut.edu.cn.
Dewen ZhouSchool of Chemical Engineering, Chongqing University of Technology, Chongqing 400054, China. dewen@cqut.edu.cn.
Zhongwei GuNational Engineering Research Center for Biomaterials, Sichuan University, Chengdu 610064, China. zwgu@scu.edu.cn.
Chongqing University of Technology · CNSichuan University · CNXuzhou Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hybrid complexes with N,N'-bis(2-benzimidazolylmethyl)amine and cyclen moieties are novel enzyme mimics and controlled DNA release materials, which could interact with DNA through three models under different conditions. In this paper, the interactions between plasmid DNA and seven different complexes were investigated, and the methods to change the interaction patterns by graphene oxide (GO) or concentrations were also investigated. The cleavage of pUC19 DNA promoted by target complexes were via hydrolytic or oxidative mechanisms at low concentrations ranging from 3.13 × 10(-7) to 6.25 × 10(-5) mol/L. Dinuclear complexes 2a and 2b can promote the cleavage of plasmid pUC19 DNA to a linear form at pH values below 7.0. Furthermore, binuclear hybrid complexes could condense DNA as nanoparticles above 3.13 × 10(-5) mol/L and partly release DNA by graphene oxide with π-π stacking. Meanwhile, the results also reflected that graphene oxide could prevent DNA from breaking down. Cell viability assays showed dinuclear complexes were safe to normal human hepatic cells at relative high concentrations. The present work might help to develop novel strategies for the design and synthesis of DNA controllable releasing agents, which may be applied to gene delivery and also to exploit the new application for GO.

Indexed as

DNA CleavageNucleic Acid ConformationCell Line, TumorDNAFree Radical ScavengersGraphiteHumansHydrogen-Ion ConcentrationOxidesPlasmidsTime FactorsDNAFree Radical ScavengersGraphiteOxidescyclenDNA condenstionDNA releaseenzyme mimicgraphene oxideN,N′-bis(2-benzimidazolylmethyl)amine

Identifiers

PMID27428945
PMCPMC6274443
OpenAlexW2469421050

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.