Evidence map›Paper›PMID 39351157›Full record

ReviewBiomaterials translational2024

Advanced nanoparticles in osteoarthritis treatment.

Qiushi Liang, Zhiliang Cheng, Ling Qin

Abstract readReview
In one paragraph

Review in Biomaterials translational, 2024. 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
–field-weighted citation impact
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.

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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.

Qiushi LiangDepartment of Bioengineering, University of Pennsylvania, Philadelphia, PA, USA.
Zhiliang ChengDepartment of Bioengineering, University of Pennsylvania, Philadelphia, PA, USA.
Ling QinDepartment of Orthopaedic Surgery, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

Funding

Treating knee osteoarthritis by sPLA2 inhibitor-loaded micellar nanoparticlesR01AR080820 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI Zhiliang Cheng · 2022 to 2026
$2.3M
EGFR signaling in osteoarthritis and treatmentR01AG067698 · NIA · UNIVERSITY OF PENNSYLVANIA · PI QIN, LING · 2020 to 2024
$2.3M
Activation of endogenous progenitors via a nanoparticle-conjugated fibrous system to enhance meniscus repairR01AR079875 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI Robert L Mauck, Ling Qin · 2023 to 2026
$2.0M
Fat and synovial tissue remodeling in joint osteoarthritisR21AR078650 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI QIN, LING, SEALE, PATRICK · 2021 to 2021
$393k
NIAMS NIH HHS R01 AR079875NIAMS NIH HHS R01 AR080820NIAMS NIH HHS R21 AR078650NIA NIH HHS R01 AG067698
6 · The paper itself

Abstract

Osteoarthritis (OA) is the most prevalent degenerative joint disorder, affecting hundreds of millions of people globally. Current clinical approaches are confined to providing only symptomatic relief. Research over the past two decades has established that OA is not merely a process of wear and tear of the articular cartilage but involves abnormal remodelling of all joint tissues. Although many new mechanisms of disease have been identified in the past several decades, the efficient and sustainable delivery of drugs targeting these mechanisms in joint tissues remains a major challenge. Nanoparticles recently emerged as favoured delivery vehicles in OA treatment, offering extended drug retention, enhanced drug targeting, and improved drug stability and solubility. In this review, we consider OA as a disease affecting the entire joint and initially explore the pathophysiology of OA across multiple joint tissues, including the articular cartilage, synovium, fat pad, bone, and meniscus. We then classify nanoparticles based on their composition and structure, such as lipids, polymers, inorganic materials, peptides/proteins, and extracellular vesicles. We summarise the recent advances in their use for treatment and diagnosis of OA. Finally, we discuss the current challenges and future directions in this field. In conclusion, nanoparticle-based nanosystems are promising carriers that advance OA treatment and diagnosis.

Indexed as

cartilageliposomemicellenanoparticlesosteoarthritissynovium

Identifiers

PMID39351157
PMCPMC11438607

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.