Evidence map›Paper›PMID 29615615›Full record

ArticleNature communications2018

Towards an arthritis flare-responsive drug delivery system.

Nitin Joshi, Jing Yan, Seth Levy, Sachin Bhagchandani, Kai V Slaughter, Nicholas E Sherman, Julian Amirault, Yufeng Wang, Logan Riegel, Xueyin He and 9 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 80 papers.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed
21.2field-weighted citation impact, top 1% 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

80 citing papers in PubMed, 245 citations in OpenAlex.

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20 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 2 institutions in 2 countries.

Nitin JoshiCenter for Nanomedicine and Division of Engineering in Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, MA, 02115, USA.
Jing YanHarvard Medical School, Boston, MA, 02115, USA.
Seth LevyHarvard Medical School, Boston, MA, 02115, USA.
Sachin BhagchandaniCenter for Nanomedicine and Division of Engineering in Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, MA, 02115, USA.
Kai V SlaughterCenter for Nanomedicine and Division of Engineering in Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, MA, 02115, USA.
Nicholas E ShermanCenter for Nanomedicine and Division of Engineering in Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, MA, 02115, USA.
Julian AmiraultCenter for Nanomedicine and Division of Engineering in Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, MA, 02115, USA.
Yufeng WangCenter for Nanomedicine and Division of Engineering in Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, MA, 02115, USA.
Logan RiegelCenter for Nanomedicine and Division of Engineering in Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, MA, 02115, USA.
Xueyin HeCenter for Nanomedicine and Division of Engineering in Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, MA, 02115, USA.
Tan Shi RuiCenter for Nanomedicine and Division of Engineering in Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, MA, 02115, USA.
Michael ValicCenter for Nanomedicine and Division of Engineering in Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, MA, 02115, USA.
Praveen K VemulaCenter for Nanomedicine and Division of Engineering in Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, MA, 02115, USA.
Oscar R MirandaCenter for Nanomedicine and Division of Engineering in Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, MA, 02115, USA.
Oren LevyCenter for Nanomedicine and Division of Engineering in Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, MA, 02115, USA.
Ellen M GravalleseDivision of Rheumatology, Department of Medicine, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Antonios O AliprantisHarvard Medical School, Boston, MA, 02115, USA.
Joerg ErmannHarvard Medical School, Boston, MA, 02115, USA. jermann@bwh.harvard.edu.ORCID http://orcid.org/0000-0003-3836-9404
Jeffrey M KarpCenter for Nanomedicine and Division of Engineering in Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, MA, 02115, USA. jmkarp@bwh.harvard.edu.
Brigham and Women's Hospital · USUniversity of Massachusetts Chan Medical School · US

Funding

Analyzing Disease Mechanisms in a Mouse Model of SpondyloarthritisR03AR066357 · NIAMS · BRIGHAM AND WOMEN'S HOSPITAL · PI ERMANN, JOERG · 2014 to 2016
$236k
A Drug Delivery Platform For Near-Term Treatment of Proteolytic DiseaseR56AR063866 · NIAMS · BRIGHAM AND WOMEN'S HOSPITAL · PI KARP, JEFFREY MICHAEL · 2013 to 2013
$200k
NIAMS NIH HHS R03 AR066357NIAMS NIH HHS R56 AR063866
6 · The paper itself

Abstract

Local delivery of therapeutics for the treatment of inflammatory arthritis (IA) is limited by short intra-articular half-lives. Since IA severity often fluctuates over time, a local drug delivery method that titrates drug release to arthritis activity would represent an attractive paradigm in IA therapy. Here we report the development of a hydrogel platform that exhibits disassembly and drug release controlled by the concentration of enzymes expressed during arthritis flares. In vitro, hydrogel loaded with triamcinolone acetonide (TA) releases drug on-demand upon exposure to enzymes or synovial fluid from patients with rheumatoid arthritis. In arthritic mice, hydrogel loaded with a fluorescent dye demonstrates flare-dependent disassembly measured as loss of fluorescence. Moreover, a single dose of TA-loaded hydrogel but not the equivalent dose of locally injected free TA reduces arthritis activity in the injected paw. Together, our data suggest flare-responsive hydrogel as a promising next-generation drug delivery approach for the treatment of IA.

Indexed as

Drug Delivery SystemsAnimalsAnti-Inflammatory AgentsArthritis, RheumatoidBiocompatible MaterialsChondrocytesDrug LiberationHumansHydrogelsInflammationMaleMiceMice, Inbred C57BLMonocytesSymptom Flare UpSynovial FluidAnti-Inflammatory AgentsBiocompatible MaterialsHydrogelsTriamcinolone Acetonide

Identifiers

PMID29615615
PMCPMC5882944
OpenAlexW2796008581

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.