Evidence map›Paper›PMID 19943805›Full record

ReviewTissue engineering. Part B, Reviews2010

Evaluating intra-articular drug delivery for the treatment of osteoarthritis in a rat model.

Kyle D Allen, Samuel B Adams, Lori A Setton

Abstract readReview
In one paragraph

Review in Tissue engineering. Part B, Reviews, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 13% 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

33 citing papers in PubMed, 1 synthesis or guideline pooled it, 65 citations in OpenAlex.

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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

3 authors at 1 institution in 1 country.

Kyle D AllenDivision of Orthopaedic Surgery, Department of Surgery, Duke University Medical Center, Duke University, Durham, North Carolina 27708-0281, USA.
Samuel B Adams
Lori A Setton
Duke University · US

Funding

Thermally-Triggered Intra-articular Drug Delivery for OAP01AR050245 · NIAMS · DUKE UNIVERSITY · PI GUILAK, FARSHID · 2003 to 2012
$11.5M
Genetically Designed/Tissue-Engineered Meniscal RepairR01EB002263 · NIBIB · DUKE UNIVERSITY · PI SETTON, LORI A. · 2003 to 2010
$3.2M
Thermally-Induced Intra-Articular Drug Delivery SystemR21AR052745 · NIAMS · DUKE UNIVERSITY · PI SETTON, LORI A. · 2006 to 2007
$372k
Function and Behavior Phenotype of Inflammatory Arthritis in the Rat Knee and TMJK99AR057426 · NIAMS · DUKE UNIVERSITY · PI ALLEN, KYLE D · 2009 to 2010
$163k
Symptomatic and Functional Biomarkers of IVD Degeneration in a Small Animal ModelF32AR056190 · NIAMS · DUKE UNIVERSITY · PI ALLEN, KYLE D · 2008 to 2008
$51k
NIAMS NIH HHS F32AR056190NIAMS NIH HHS K99 AR057426NIAMS NIH HHS K99AR057426NIAMS NIH HHS P01AR050245NIAMS NIH HHS R21 AR052745NIAMS NIH HHS R21AR052745NIBIB NIH HHS R01 EB002263NIBIB NIH HHS R01EB002263
6 · The paper itself

Abstract

Osteoarthritis (OA) is a degenerative joint disease that can result in joint pain, loss of joint function, and deleterious effects on activity levels and lifestyle habits. Current therapies for OA are largely aimed at symptomatic relief and may have limited effects on the underlying cascade of joint degradation. Local drug delivery strategies may provide for the development of more successful OA treatment outcomes that have potential to reduce local joint inflammation, reduce joint destruction, offer pain relief, and restore patient activity levels and joint function. As increasing interest turns toward intra-articular drug delivery routes, parallel interest has emerged in evaluating drug biodistribution, safety, and efficacy in preclinical models. Rodent models provide major advantages for the development of drug delivery strategies, chiefly because of lower cost, successful replication of human OA-like characteristics, rapid disease development, and small joint volumes that enable use of lower total drug amounts during protocol development. These models, however, also offer the potential to investigate the therapeutic effects of local drug therapy on animal behavior, including pain sensitivity thresholds and locomotion characteristics. Herein, we describe a translational paradigm for the evaluation of an intra-articular drug delivery strategy in a rat OA model. This model, a rat interleukin-1beta overexpression model, offers the ability to evaluate anti-interleukin-1 therapeutics for drug biodistribution, activity, and safety as well as the therapeutic relief of disease symptoms. Once the action against interleukin-1 is confirmed in vivo, the newly developed anti-inflammatory drug can be evaluated for evidence of disease-modifying effects in more complex preclinical models.

Indexed as

Disease Models, AnimalEvaluation Studies as TopicAnimalsDrug Delivery SystemsInjections, Intra-ArticularOsteoarthritisRatsTissue Distribution

Identifiers

PMID19943805
PMCPMC2817653
OpenAlexW1994922556

What OpenQuestion holds

Textmetadata
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.