Injectable biomimetic hybrid nanofibers for targeting cartilage in early osteoarthritis treatment DOI
Maihemuti Yakufu, Qiyu Jia, Chunbao Li

et al.

Chemical Engineering Journal, Journal Year: 2024, Volume and Issue: 490, P. 151790 - 151790

Published: April 29, 2024

Language: Английский

Biomimetic lubricating COFs with donor–acceptor structure for osteoarthritis therapy DOI
Dandan Wang, Junyao Li,

Chenxu Niu

et al.

Journal of Colloid and Interface Science, Journal Year: 2025, Volume and Issue: 687, P. 85 - 94

Published: Feb. 5, 2025

Language: Английский

Citations

2

Current status and prospect of ZIF-based materials for breast cancer treatment DOI

Yana Zeng,

Donghui Liao,

Xiangyang Kong

et al.

Colloids and Surfaces B Biointerfaces, Journal Year: 2023, Volume and Issue: 232, P. 113612 - 113612

Published: Oct. 26, 2023

Language: Английский

Citations

27

A biomimetic lubricating nanosystem for synergistic therapy of osteoarthritis DOI
Peiwei Gong, Meng Wang, Jiangli Wang

et al.

Journal of Colloid and Interface Science, Journal Year: 2024, Volume and Issue: 672, P. 589 - 599

Published: June 3, 2024

Language: Английский

Citations

7

Synovial Lubrication Factors‐Recruiting Biomimetic Polyphenolized Hyaluronic Acid for Promoting Cartilage Repair DOI
Hui Yuan,

Pengcheng Xiao,

Bruno Sarmento

et al.

Advanced Functional Materials, Journal Year: 2024, Volume and Issue: unknown

Published: July 8, 2024

Abstract Osteoarthritis is a common degenerative disease characterized by continuous detachment of lubrication factors from damaged cartilage matrix. This study proposes paradigm that combines natural polyanionic polysaccharides (hyaluronic acid, HA) with dopamine (DA) to design synovial factors‐recruiting biomimetic polyphenolized system. The lubricants can use DA's polarity and hydrophilic groups as specific binding sites type II collagen's stably bind surface, further utilize molecular interaction recruit detached, joint endogenous or chondrocytes expressed factors, continuously forming supramolecular complex onto matrix induce lubrication. Simultaneously, the biolubricants also catechol eliminate anionic free radicals resist reactive oxygen species invasion in early stages failure. prepared exhibit low coefficient friction (µ < 0.08), which attributed fluid hydration provided HA DA side chains through dynamic effect interfacial adsorption. Cell animal experiments demonstrate polyphenolic have good biocompatibility promote regeneration. Therefore, developed lubricants‐recruiting potential for treating osteoarthritis, provide theoretical basis other biological tissues problems.

Language: Английский

Citations

6

Microenvironment-responsive nanosystems for osteoarthritis therapy DOI Creative Commons
Song Li, Yuan Xiong, Hao Zhu

et al.

Engineered Regeneration, Journal Year: 2023, Volume and Issue: 5(1), P. 92 - 110

Published: Dec. 14, 2023

Osteoarthritis (OA) represents an enduring and widespread global burden, causing significant morbidity disability, whose pathology is characterized by persistent inflammation, progressive cartilage degeneration, abnormal bone homeostasis, excessive synovial hyperplasia, resulting from its complex microenvironment. Unfortunately, current therapeutic approaches for OA remain suboptimal, prompting increased interest in advanced nanotechnology as a means to enhance effects. In recent years, progress has been made the development of versatile nanoplatforms designed specific microenvironment OA, promising results introducing concept "OA nanomedicine". Compared conventional therapies like non-steroidal anti-inflammatory drugs (NSAIDs), nanomedicine offers precise targeted, controllable personalized ways therapy, contributing better outcomes. However, comprehensive review consolidating nanomedicine" currently absent literature. Therefore, this review, we aim unravel key pathological microenvironmental characteristics while summarizing properties advantages nanosystems possessing microenvironment-reprogramming capabilities therapy. First, make retrospection features Furthermore, provide overview advances nanomedicine. Eventually, discuss present challenges associated with insights into future prospects clinical-translational lens. By doing so, can foster propel successful nanomedicine, addressing unmet needs

Language: Английский

Citations

16

Exploring the Early Molecular Pathogenesis of Osteoarthritis Using Differential Network Analysis of Human Synovial Fluid DOI Creative Commons
Martin Rydén, Amanda Sjögren, Patrik Önnerfjord

et al.

Molecular & Cellular Proteomics, Journal Year: 2024, Volume and Issue: 23(6), P. 100785 - 100785

Published: May 14, 2024

Language: Английский

Citations

4

Reprogramming Lung Redox Homeostasis by NIR Driven Ultra‐Small Pd Loaded Covalent Organic Framework Inhibits NF‐κB Pathway for Acute Lung Injury Immunotherapy DOI Creative Commons

Doudou Lei,

Lin Liao, Tao Qin

et al.

Advanced Science, Journal Year: 2025, Volume and Issue: unknown

Published: Feb. 18, 2025

Abstract Acute lung injury (ALI) refers to damage related cells, typically caused by an uncontrollable inflammatory response, and over‐generated reactive oxygen species (ROS). Increasing evidence suggests that reprogramming redox homeostasis holds significant potentials for the clinical treatment of ALI. Herein, simple synthesis ultra‐small Pd loaded covalent organic framework (COF) (TP@Pd) is reported, which, when combined with near infrared (NIR) irradiation, exhibits nanozyme functionalities, including multiple enzyme mimicking activities broad spectrum ROS scavenging, thereby promoting tissue repair ALI immunotherapy. Mechanistically, through therapeutic strategy TP@Pd+NIR, damaged cells tissues are ameliorated decreasing intracellular levels (total ROS, ·OH ·O 2 − ), downregulating cytokines (IL‐6, TNF‐α IL‐1β), upregulating antioxidant factor level (SOD2), inducing macrophage M2 directional polarization (downregulation iNOS CD86, upregulation IL‐10 CD206), activating immunoregulation (CD4 + /CD8 ratio increase), (upregulation HSP70 CD31), suppressing NF‐κB signaling pathway phosphorylated p65 IκBα). Furthermore, following intravenous (IV) injection in rats, TP@Pd accumulated 6 h, indicating promising efficacy via this administration route. Notably, TP@Pd+NIR demonstrated excellent synergistic effects alleviating inflammation storms, reducing diffuse alveolar damage, accelerating repair. Summarily, work has designed a novel enhancement amelioration, which may serve as approach other diseases.

Language: Английский

Citations

0

Theranostics of osteoarthritis: Applications and prospects of precision targeting nanotechnology DOI
Yujing Chen,

Hongyi Jiang,

Haoran Zhu

et al.

International Journal of Pharmaceutics, Journal Year: 2025, Volume and Issue: unknown, P. 125548 - 125548

Published: April 1, 2025

Language: Английский

Citations

0

Magnetic dialdehyde starch as green support for the growth of hyaluronic acid terminated covalent organic framework: A pH-controlled daunorubicin delivery system with inherent antibacterial feature DOI
Hassan Namazi, Malihe Pooresmaeil, Roya Salehi

et al.

European Polymer Journal, Journal Year: 2023, Volume and Issue: 198, P. 112428 - 112428

Published: Sept. 15, 2023

Language: Английский

Citations

10

Design of Spatial Pore Structures in Micro-Arc Oxidation Coatings of Ti Implant for Nanoparticle Drug Delivery DOI
Shuangshuang Zhang, Fang Liu, Song Xiang

et al.

Published: Jan. 1, 2025

Language: Английский

Citations

0