Evidence map›Paper›PMID 23036951›Full record

ArticleActa biomaterialia2013

Controlling fibrous capsule formation through long-term down-regulation of collagen type I (COL1A1) expression by nanofiber-mediated siRNA gene silencing.

Pim-on Rujitanaroj, Brian Jao, Junghoon Yang, Feng Wang, James M Anderson, Jun Wang, Sing Yian Chew

Open access · greenAbstract read
In one paragraph

Article in Acta biomaterialia, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
3.2field-weighted citation impact, top 9% 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

43 citing papers in PubMed, 101 citations in OpenAlex.

  1. Article
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  8. Oral delivery of RNAi for cancer therapy.Cancer metastasis reviews · 2023
    Review
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  10. Article
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  18. Electrospun Nanofibers for Cancer Therapy.Advances in experimental medicine and biology · 2021
    Review
  19. Article
  20. 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 3 countries.

Pim-on RujitanarojSchool of Chemical and Biomedical Engineering, Nanyang Technological University, 637459 Singapore, Singapore.
Brian Jao
Junghoon Yang
Feng Wang
James M Anderson
Jun Wang
Sing Yian Chew
Case Western Reserve University · USNanyang Technological University · SGUniversity of Science and Technology of China · CN

Funding

Microchip Drug Delivery SystemR01EB006365 · NIBIB · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI LANGER, ROBERT SAMUEL · 2007 to 2011
$5.8M
LYMPHOCYTE/MACROPHAGE INTERACTIONS ON BIOMATERIALSR01EB000282 · NIBIB · CASE WESTERN RESERVE UNIVERSITY · PI ANDERSON, JAMES MORLEY · 2002 to 2013
$3.3M
NIBIB NIH HHS EB006365-07-A2NIBIB NIH HHS R01 EB000282NIBIB NIH HHS R01 EB006365
6 · The paper itself

Abstract

The foreign body reaction often interferes with the long-term functionality and performance of implanted biomedical devices through fibrous capsule formation. While many implant modification techniques have been adopted in attempts to control fibrous encapsulation, the outcomes remained sub-optimal. Nanofiber scaffold-mediated RNA interference may serve as an alternative approach through the localized and sustained delivery of siRNA at implant sites. In this study, we investigated the efficacy of siRNA-poly(caprolactone-co-ethylethylene phosphate) nanofibers in controlling fibrous capsule formation through the down-regulation of collagen type I (COL1A1) in vitro and in vivo. By encapsulating complexes of COL1A1 siRNA with a transfection reagent (Transit TKO) or the cell penetrating peptides CADY or MPG within the nanofibers (550-650 nm in diameter), a sustained release of siRNA was obtained for at least 28 days (loading efficiency ~60-67%). Scaffold-mediated transfection significantly enhanced cellular uptake of oligonucleotides and prolonged in vitro gene silencing duration by at least 2-3 times as compared to conventional bolus delivery of siRNA (14 days vs. 5-7 days by bolus delivery). In vivo subcutaneous implantation of siRNA scaffolds revealed a significant decrease in fibrous capsule thickness at weeks 2 and 4 as compared to plain nanofibers (p<0.05). Taken together, the results demonstrated the efficacy of scaffold-mediated siRNA gene-silencing in providing effective long-term control of fibrous capsule formation.

Indexed as

Down-RegulationGene SilencingNanofibersBase SequenceCollagen Type IDNA PrimersElectrophoresis, Agar GelImmunohistochemistryKineticsMicroscopy, Electron, ScanningOrganophosphatesPolyestersReal-Time Polymerase Chain ReactionRNA, Small InterferingCollagen Type IDNA PrimersOrganophosphatespoly(caprolactone-co-ethylethylene phosphate)PolyestersRNA, Small Interfering

Identifiers

PMID23036951
PMCPMC3523808
OpenAlexW2053995348

What OpenQuestion holds

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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.