Evidence map›Paper›PMID 29399627›Full record

ArticleACS biomaterials science & engineering2015

Simulation and Experimental Assembly of DNA-Graft Copolymer Micelles with Controlled Morphology.

Zonghui We, Yong Ren, John-Michael Williford, Wei Qu, Kevin Huang, Shirley Ng, Hai-Quan Mao, Erik Luijten

Abstract read
In one paragraph

Article in ACS biomaterials science & engineering, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
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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.

Zonghui WeGraduate Program in Applied Physics, Northwestern University, Evanston, Illinois 60208, United States.
Yong RenDepartment of Materials Science and Engineering, Whiting School of Engineering, Johns Hopkins University, Baltimore, Maryland 21218, United States.
John-Michael WillifordDepartment of Biomedical Engineering, Johns Hopkins School of Medicine, Baltimore, Maryland 21205, United States.
Wei QuDepartment of Materials Science and Engineering, Northwestern University, Evanston, Illinois 60208, United States.
Kevin HuangDepartment of Chemical and Biomolecular Engineering, Johns Hopkins University, Baltimore, Maryland 21218, United States.
Shirley NgDepartment of Materials Science and Engineering, Whiting School of Engineering, Johns Hopkins University, Baltimore, Maryland 21218, United States.
Hai-Quan MaoDepartment of Materials Science and Engineering, Whiting School of Engineering, Johns Hopkins University, Baltimore, Maryland 21218, United States.
Erik LuijtenDepartment of Materials Science and Engineering, Northwestern University, Evanston, Illinois 60208, United States.

Funding

Shape Control and Transport Properties of DNA-Copolymer MicellesR01EB018358 · NIBIB · JOHNS HOPKINS UNIVERSITY · PI LUIJTEN, ERIK, MAO, HAI-QUAN · 2015 to 2018
$2.1M
Biodegradable Micelles for Liver-Targeted Gene DeliveryR01GM073937 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI MAO, HAI-QUAN · 2008 to 2011
$1.4M
Shape Control and Transfection of Self-assembled Polymer-DNA NanoparticlesR21EB013274 · NIBIB · JOHNS HOPKINS UNIVERSITY · PI MAO, HAI-QUAN · 2012 to 2013
$431k
NIBIB NIH HHS R01 EB018358NIBIB NIH HHS R21 EB013274NIGMS NIH HHS R01 GM073937
6 · The paper itself

Abstract

Nanoparticles formed through complexation of plasmid DNA and copolymers are promising gene-delivery vectors, offering a wide range of advantages over alternative delivery strategies. Notably, recent research has shown that the shape of these particles can be tuned, which makes it possible to gain understanding of their shape-dependent transfection properties. Whereas earlier methods achieved shape tuning through the use of block copolymers and variation of solvent polarity, here we demonstrate through a combined experimental and computational approach that the same degree of shape control can be achieved through the use of graft copolymers that are easier to synthesize and provide a wider range of parameters for shape control. Moreover, the approach presented here does not require the use of organic solvents. The simulation work provides insight into the mechanism governing the shape variation as well as an effective model to guide further design of non-viral gene-delivery vectors. Our experimental findings offer important opportunities for the facile and large-scale synthesis of biocompatible gene-delivery vectors with well-controlled shape and tunable transfection properties. The

Indexed as

DNA packagingmicellesself-assemblyshape controltransfection

Identifiers

PMID29399627
PMCPMC5796780

What OpenQuestion holds

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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.