Evidence map›Paper›PMID 22652024›Full record

ArticleBiomaterials2012

Lipid nanoparticles for hepatic delivery of small interfering RNA.

Bo Yu, Shu-Hao Hsu, Chenguang Zhou, Xinmei Wang, Megan C Terp, Yun Wu, Lesheng Teng, Yicheng Mao, Feng Wang, Weiming Xue and 4 more

Abstract read
In one paragraph

Article in Biomaterials, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

21 citing papers in PubMed, 71 citations in OpenAlex.

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  14. Selective targeting of alveolar type II respiratory epithelial cells by anti-surfactant protein-C antibody-conjugated lipoplexes.Journal of controlled release : official journal of the Controlled Release Society · 2015
    Article
  15. Article
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  18. Enhanced hepatic delivery of siRNA and microRNA using oleic acid based lipid nanoparticle formulations.Journal of controlled release : official journal of the Controlled Release Society · 2013
    Article
  19. 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

14 authors at 2 institutions in 2 countries.

Bo YuDepartment of Chemical and Biomolecular Engineering, The Ohio State University, Columbus, OH, USA.
Shu-Hao Hsu
Chenguang Zhou
Xinmei Wang
Megan C Terp
Yun Wu
Lesheng Teng
Yicheng Mao
Feng Wang
Weiming Xue
Samson T Jacob
Kalpana Ghoshal
Robert J Lee
Ly J Lee
The Ohio State University · USJilin University · CN

Funding

The Ohio State University Center for Clinical and Translational Science (UL1)UL1TR000090 · NCATS · OHIO STATE UNIVERSITY · PI JACKSON, REBECCA D · 2012 to 2013
$7.9M
Role of microRNA-122 in hepatocarcinogenesis using conditional knock out miceR01DK088076 · NIDDK · OHIO STATE UNIVERSITY · PI GHOSHAL, KALPANA · 2010 to 2013
$1.3M
Novel Micro/nanofluidic Electroporation Devices for DNA&Oligonucleotide DeliveryR21EB008247 · NIBIB · OHIO STATE UNIVERSITY · PI LEE, LY JAMES · 2007 to 2008
$383k
Therapeutic delivery of anti-miR oligos to hepatocellular cancerR21CA152969 · NCI · OHIO STATE UNIVERSITY · PI GHOSHAL, KALPANA, JACOB, SAMSON T · 2011 to 2012
$365k
NCATS NIH HHS UL1 TR000090NCI NIH HHS R21 CA152969NCI NIH HHS R21CA152969NIBIB NIH HHS R21 EB008247NIDDK NIH HHS R01 DK088076NIDDK NIH HHS R01DK088076
6 · The paper itself

Abstract

Clinical application of small interfering RNA (siRNA) requires safe and efficient delivery in vivo. Here, we report the design and synthesis of lipid nanoparticles (LNPs) for siRNA delivery based on cationic lipids with multiple tertiary amines and hydrophobic linoleyl chains. LNPs incorporating the lipid containing tris(2-aminoethyl)amine (TREN) and 3 linoleyl chains, termed TRENL3, were found to have exceptionally high siRNA transfection efficacy that was markedly superior to lipofectamine, a commercial transfection agent. In addition, inclusion of polyunsaturated fatty acids, such as linoleic acid and linolenic acid in the formulation further enhanced the siRNA delivery efficiency. TRENL3 LNPs were further shown to transport siRNA into the cytosol primarily via macropinocytosis rather than clathrin-mediated endocytosis. The new LNPs have demonstrated preferential uptake by the liver and hepatocellular carcinoma in mice, thereby leading to high siRNA gene-silencing activity. These data suggest potential therapeutic applications of TRENL3 mediated delivery of siRNA for liver diseases.

Indexed as

AnimalsCell LineColloidsDown-RegulationDrug Delivery SystemsEthylenediaminesFatty Acids, UnsaturatedHumansLipidsLiverLiver NeoplasmsMiceMice, Inbred ICRNanoparticlesRNA, Small InterferingRNA StabilityColloidsEthylenediaminesFatty Acids, UnsaturatedLipidsRNA, Small Interferingtris(2-aminoethyl)amine

Identifiers

PMID22652024
PMCPMC3374058
OpenAlexW1967484306

What OpenQuestion holds

Textmetadata
LicenceTDM
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.