Evidence map›Paper›PMID 41904460›Full record

ReviewJournal of translational medicine2026

Nanocomposite hydrogels: benefits and attributes for osteoarthritis therapy.

Jinyan He, Yujing Chen, Haoran Zhu, Saleem Hunzla, Ziqi Zhang, Duoyao Zhang, Shunyu Yao, Jiawei Liu, Hongyi Jiang, Liang Chen

Abstract readReview
In one paragraph

Review in Journal of translational medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

10 authors.

Jinyan HeDepartment of Orthopaedics, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, 325027, China.
Yujing ChenDepartment of Orthopaedics, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, 325027, China.
Haoran ZhuDepartment of Orthopaedics, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, 325027, China.
Saleem HunzlaDepartment of Orthopaedics, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, 325027, China.
Ziqi ZhangDepartment of Orthopaedics, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, 325027, China.
Duoyao ZhangDepartment of Orthopaedics, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, 325027, China.
Shunyu YaoDepartment of Orthopaedics, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, 325027, China.
Jiawei LiuDepartment of Orthopaedics, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, 325027, China.
Hongyi JiangDepartment of Orthopaedics, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, 325027, China.
Liang ChenDepartment of Orthopaedics, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, 325027, China. Breakingsunshine@163.com.ORCID 0000-0002-9684-1669

Funding

Innovative Research Group Project of the National Natural Science Foundation of China number 82272564
6 · The paper itself

Abstract

backgroundOsteoarthritis (OA) is a prevalent and debilitating chronic joint disease, creating an urgent need for therapeutic strategies that move beyond symptomatic relief toward disease modification. Nanocomposite hydrogels, which incorporate nanoparticles into a three-dimensional (3D) polymeric network, have emerged as a promising class of biomaterials due to their enhanced and tailorable physical, chemical, and biological properties compared to conventional hydrogels. MAIN BODY: This review provides a systematic analysis of nanocomposite hydrogels for OA therapy. It begins by outlining the epidemiological burden of OA and limitations of current treatments, establishing the rationale for advanced local drug delivery systems. We then comprehensively examine the preparation strategies of nanocomposite hydrogels, encompassing physical encapsulation, electrostatic assembly, hydrogen bonding, covalent crosslinking, DNA origami, and advanced co-assembly platforms. Subsequently, the resulting systems are classified into three therapeutic paradigms based on their primary action, namely microenvironment-modulating, cartilage-reparative, and target-inhibiting or activating hydrogels. A dedicated section on structure-function engineering deconstructs the design of these materials, focusing on the construction of mechanical networks, the design of pore architectures for mass transport, interface functionalization, and the integration of stimuli-responsive bonds for intelligent therapy. Finally, the review critically evaluates the key translational challenges, including manufacturing scalability, long-term safety, and regulatory pathways.

conclusionsNanocomposite hydrogels represent a transformative platform capable of integrating multiple therapeutic functions, ranging from sustained drug release and anti-inflammatory action to active tissue regeneration and precise molecular targeting. By rationally engineering their structure across multiple scales, these advanced biomaterials hold significant potential to shift OA management from palliative care to curative and disease-modifying interventions. Overcoming the identified translational hurdles through interdisciplinary collaboration will be crucial for their successful clinical adoption.

Indexed as

HydrogelsNanocompositesOsteoarthritisAnimalsDrug Delivery SystemsHumansHydrogelsCartilage regenerationNanocomposite hydrogelsOsteoarthritis therapyRational designStructure-function relationship

Identifiers

PMID41904460
PMCPMC13151263

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.