Evidence map›Paper›PMID 24708312›Full record

ArticleACS nano2014

Molecular recognition enables nanosubstrate-mediated delivery of gene-encapsulated nanoparticles with high efficiency.

Jinliang Peng, Mitch André Garcia, Jin-sil Choi, Libo Zhao, Kuan-Ju Chen, James R Bernstein, Parham Peyda, Yu-Sheng Hsiao, Katherine W Liu, Wei-Yu Lin and 4 more

Abstract read
In one paragraph

Article in ACS nano, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Review
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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

14 authors.

Jinliang PengSchool of Biomedical Engineering, MED-X Research Institute, Shanghai Jiao Tong University , Shanghai 200030, China.
Mitch André Garcia
Jin-sil Choi
Libo Zhao
Kuan-Ju Chen
James R Bernstein
Parham Peyda
Yu-Sheng Hsiao
Katherine W Liu
Wei-Yu Lin
April D Pyle
Hao Wang
Shuang Hou
Hsian-Rong Tseng

Funding

Reprogramming and Directed Differentiation of Skeletal Muscle Cells from hPSCs.R01AR064327 · NIAMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI April D Pyle · 2013 to 2026
$6.4M
UCLA Muscular Dystrophy Core CenterP30AR057230 · NIAMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SPENCER, MELISSA JAN · 2009 to 2018
$6.2M
Generation of hPSCs Using Reprogramming Proteins-Encapsulated NanoparticlesR21GM098982 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI TSENG, HSIAN-RONG · 2011 to 2012
$410k
Supramolecular Nanoparticle-Based PET Probes for Pretargeted Tumor ImagingR21EB016270 · NIBIB · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI TSENG, HSIAN-RONG · 2013 to 2014
$400k
NIAMS NIH HHS P30 AR057230NIAMS NIH HHS R01 AR064327NIAMS NIH HHS R01AR064327NIBIB NIH HHS R21 EB016270NIGMS NIH HHS R21 GM098982
6 · The paper itself

Abstract

Substrate-mediated gene delivery is a promising method due to its unique ability to preconcentrate exogenous genes onto designated substrates. However, many challenges remain to enable continuous and multiround delivery of the gene using the same substrates without depositing payloads and immobilizing cells in each round of delivery. Herein we introduce a gene delivery system, nanosubstrate-mediated delivery (NSMD) platform, based on two functional components with nanoscale features, including (1) DNA⊂SNPs, supramolecular nanoparticle (SNP) vectors for gene encapsulation, and (2) Ad-SiNWS, adamantane (Ad)-grafted silicon nanowire substrates. The multivalent molecular recognition between the Ad motifs on Ad-SiNWS and the β-cyclodextrin (CD) motifs on DNA⊂SNPs leads to dynamic assembly and local enrichment of DNA⊂SNPs from the surrounding medium onto Ad-SiNWS. Subsequently, once cells settled on the substrate, DNA⊂SNPs enriched on Ad-SiNWS were introduced through the cell membranes by intimate contact with individual nanowires on Ad-SiNWS, resulting in a highly efficient delivery of exogenous genes. Most importantly, sequential delivery of multiple batches of exogenous genes on the same batch cells settled on Ad-SiNWS was realized by sequential additions of the corresponding DNA⊂SNPs with equivalent efficiency. Moreover, using the NSMD platform in vivo, cells recruited on subcutaneously transplanted Ad-SiNWS were also efficiently transfected with exogenous genes loaded into SNPs, validating the in vivo feasibility of this system. We believe that this nanosubstrate-mediated delivery platform will provide a superior system for in vitro and in vivo gene delivery and can be further used for the encapsulation and delivery of other biomolecules.

Indexed as

Gene Transfer TechniquesAmino Acid MotifsAnimalsbeta-CyclodextrinsFemaleGenetic VectorsHEK293 CellsHeLa CellsHumansJurkat CellsLightMCF-7 CellsMiceMice, Inbred BALB CMicroscopy, Electron, ScanningMicroscopy, Electron, Transmissionbeta-Cyclodextrinsbetadex

Identifiers

PMID24708312
PMCPMC4046775

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.