Evidence map›Paper›PMID 22750740›Full record

ArticleActa biomaterialia2012

Intra-articular controlled release of anti-inflammatory siRNA with biodegradable polymer microparticles ameliorates temporomandibular joint inflammation.

Paschalia M Mountziaris, Stephanie N Tzouanas, David C Sing, Phillip R Kramer, F Kurtis Kasper, Antonios G Mikos

Open access · bronzeAbstract read
In one paragraph

Article in Acta biomaterialia, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

16 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Biomaterials: Foreign Bodies or Tuners for the Immune Response?International journal of molecular sciences · 2019
    Review
  8. Review
  9. Review
  10. Article
  11. Technologies for controlled, local delivery of siRNA.Journal of controlled release : official journal of the Controlled Release Society · 2015
    Review
  12. siRNA Versus miRNA as Therapeutics for Gene Silencing.Molecular therapy. Nucleic acids · 2015
    Review
  13. Biomaterial-mediated modification of the local inflammatory environment.Frontiers in bioengineering and biotechnology · 2015
    Review
  14. Article
  15. Article
  16. 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

6 authors at 2 institutions in 1 country.

Paschalia M MountziarisDepartment of Bioengineering, Rice University, Houston, TX 77251, USA.
Stephanie N Tzouanas
David C Sing
Phillip R Kramer
F Kurtis Kasper
Antonios G Mikos
Rice University · USTexas A&M University System · US

Funding

BIOTECHNOLOGY RESEARCH TRAINING GRANTT32GM008362 · NIGMS · RICE UNIVERSITY · PI WEST, JENNIFER L · 1990 to 2010
$3.6M
PROMOTION OF ALVEOLAR SOCKET HEALING WITH BIOPOLYMERSR01DE015164 · NIDCR · RICE UNIVERSITY · PI MIKOS, ANTONIOS G. · 2004 to 2008
$1.4M
NIDCR NIH HHS R01 DE015164NIDCR NIH HHS R01 DE15164NIGMS NIH HHS 5 T32 GM008362-19NIGMS NIH HHS T32 GM008362
6 · The paper itself

Abstract

We investigated the in vivo therapeutic efficacy of an intra-articular controlled release system consisting of biodegradable poly(dl-lactic-co-glycolic acid) (PLGA) microparticles (MPs) encapsulating anti-inflammatory small interfering RNA (siRNA), together with branched poly(ethylenimine) (PEI) as a transfecting agent, in a rat model of painful temporomandibular joint (TMJ) inflammation. The in vivo effects of PLGA MP dose and siRNA-PEI polyplex delivery were examined via non-invasive meal pattern analysis and by quantifying the protein level of the siRNA target as well as of several downstream inflammatory cytokines. Controlled release of siRNA-PEI from PLGA MPs significantly reduced inflammation-induced changes in meal patterns compared to untreated rats with inflamed TMJs. These changes correlated to decreases in tissue-level protein expression of the siRNA target to 20-50% of the amount present in the corresponding control groups. Similar reductions were also observed in the expression of downstream inflammatory cytokines, e.g. interleukin-6, whose tissue levels in the siRNA-PEI PLGA MP groups were 50% of the values for the corresponding controls. This intra-articular sustained release system has significant implications for the treatment of severe TMJ pain, and also has the potential to be readily adapted and applied to mitigate painful, chronic inflammation in a variety of conditions.

Indexed as

MicrospheresAnimalsAnti-Inflammatory AgentsCytokinesDelayed-Action PreparationsFeeding BehaviorGenetic TherapyInflammationInflammation MediatorsLactic AcidMaleParticle SizePolyethyleneiminePolyglycolic AcidPolylactic Acid-Polyglycolic Acid CopolymerPolymersAnti-Inflammatory AgentsCytokinesDelayed-Action PreparationsInflammation MediatorsLactic AcidPolyethyleneiminePolyglycolic AcidPolylactic Acid-Polyglycolic Acid CopolymerPolymersReceptors, IgGRNA, Small Interfering

Identifiers

PMID22750740
PMCPMC3429637
OpenAlexW1972031548

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.