Evidence map›Paper›PMID 27213305›Full record

ArticleMolecules (Basel, Switzerland)2016

Low-Molecular Weight Polyethylenimine Modified with Pluronic 123 and RGD- or Chimeric RGD-NLS Peptide: Characteristics and Transfection Efficacy of Their Complexes with Plasmid DNA.

Jing Hu, Wenfang Zhao, Kehai Liu, Qian Yu, Yuan Mao, Zeyu Lu, Yaguang Zhang, Manman Zhu

Abstract 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 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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.

  1. Article
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  6. Review
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.

Jing HuDepartment of Biopharmaceutics, College of Food Science and Technology, Shanghai Ocean University, Shanghai 201306, China. 15821787592@163.com.
Wenfang ZhaoDepartment of Biopharmaceutics, College of Food Science and Technology, Shanghai Ocean University, Shanghai 201306, China. wfzhao0504@163.com.
Kehai LiuDepartment of Biopharmaceutics, College of Food Science and Technology, Shanghai Ocean University, Shanghai 201306, China. khliu@shou.edu.cn.
Qian YuDepartment of Biopharmaceutics, College of Food Science and Technology, Shanghai Ocean University, Shanghai 201306, China. 15001970365@163.com.
Yuan MaoDepartment of Biopharmaceutics, College of Food Science and Technology, Shanghai Ocean University, Shanghai 201306, China. 13262975153@163.com.
Zeyu LuDepartment of Biopharmaceutics, College of Food Science and Technology, Shanghai Ocean University, Shanghai 201306, China. m18701881332@163.com.
Yaguang ZhangDepartment of Biopharmaceutics, College of Food Science and Technology, Shanghai Ocean University, Shanghai 201306, China. edwarddo@163.com.
Manman ZhuDepartment of Biopharmaceutics, College of Food Science and Technology, Shanghai Ocean University, Shanghai 201306, China. zhu_manman7526@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To solve the problem of transfection efficiency vs. cytotoxicity and tumor-targeting ability when polyethylenimine (PEI) was used as a nonviral gene delivery vector, new degradable PEI polymers were synthesized via cross-linking low-molecular-weight PEI with Pluronic P123 and then further coupled with a targeting peptide R4 (RGD) and a bifunctional R11 (RGD-NLS), which were termed as P123-PEI-R4 and P123-PEI-R11, respectively. Agarose gel electrophoresis showed that both P123-PEI-R4 and P123-PEI-R11 efficaciously condense plasmid DNA at a polymer-to-pDNA w/w ratio of 3.0 and 0.4, respectively. The polyplexes were stable in the presence of serum and could protect plasmid DNA against DNaseI. They had uniform spherical nanoparticles with appropriate sizes around 100-280 nm and zeta-potentials about +40 mV. Furthermore, in vitro experiments showed that these polyplexes had lower cytotoxicity at any concentration compared with PEI 25 kDa, thus giving promise to high transfection efficiency as compared with another P123-PEI derivate conjugated with trifunctional peptide RGD-TAT-NLS (P123-PEI-R18). More importantly, compared with the other polymers, P123-PEI-R11 showed the highest transfection efficiency with relatively lower cytotoxicity at any concentration, indicating that the new synthetic polymer P123-PEI-R11 could be used as a safe and efficient gene deliver vector.

Indexed as

Gene Transfer TechniquesDNAElectrophoresis, Agar GelGenetic TherapyGreen Fluorescent ProteinsHeLa CellsHumansMolecular WeightNanoparticlesNuclear Localization SignalsOligopeptidesPlasmidsPolyethyleneiminePolymersTransfectionarginyl-glycyl-aspartic acidDNAGreen Fluorescent ProteinsNuclear Localization SignalsOligopeptidesPolyethyleneiminePolymersnuclear localization signalphysico-chemical propertiespolycationsRGDtransfection efficiency

Identifiers

PMID27213305
PMCPMC6273895

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Registered trials

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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.