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炎症调节聚合物纳米颗粒:设计策略、作用机制及治疗应用

Inflammation-modulating polymeric nanoparticles: design strategies, mechanisms, and therapeutic applications.

作者信息

Zhang Hailin, Chen Haoxiang, Hu Xinman, Muhammad Wali, Liu Chenyu, Liu Wenxing

机构信息

MOE Key Laboratory of Macromolecular Synthesis and Functionalisation, Department of Polymer Science and Engineering, Zhejiang University, Hangzhou 310058, China; Zhejiang Engineering Research Center for Interface Technology of Medical Polymers and Devices, Shaoxing Key Laboratory of Healthcare Materials and Application Technology, and Center for Healthcare Materials, Shaoxing Institute, Zhejiang University, Shaoxing 312099, China.

MOE Key Laboratory of Macromolecular Synthesis and Functionalisation, Department of Polymer Science and Engineering, Zhejiang University, Hangzhou 310058, China.

出版信息

EBioMedicine. 2025 Jul 3;118:105837. doi: 10.1016/j.ebiom.2025.105837.


DOI:10.1016/j.ebiom.2025.105837
PMID:40614330
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12271758/
Abstract

Inflammation plays a pivotal dual role in disease pathogenesis, acting as both a protective response and a critical factor to chronic inflammatory pathologies. Traditional anti-inflammatory therapies remain constrained by adverse effects and suboptimal bioavailability, necessitating innovative therapeutic paradigms. Polymeric nanoparticles (PNPs) have emerged as a promising alternative for inflammation modulation, offering significant drug-loading capacity, precise targeting, biodegradability, and stimuli-responsive properties. This review summarises PNPs as a versatile nanomedicine platform for inflammation modulation. The physiological and pathological mechanisms underlying inflammation are elucidated, followed by a comprehensive summary of the engineering strategies, mechanistic actions, and therapeutic potential of PNPs for inflammation modulation. The clinical translation challenges, including toxicity and off-target effects, are discussed. The potential future directions for multifunctional PNPs in theranostics and AI-driven personalised inflammation modulation are finally proposed. This work seeks to bridge polymeric nanomaterials innovation and precision medicine to drive next-generation anti-inflammatory therapies.

摘要

炎症在疾病发病机制中起着关键的双重作用,既是一种保护性反应,也是慢性炎症性疾病的关键因素。传统的抗炎疗法仍然受到副作用和生物利用度不理想的限制,因此需要创新的治疗模式。聚合物纳米颗粒(PNPs)已成为一种有前途的炎症调节替代方案,具有显著的载药能力、精确靶向性、生物可降解性和刺激响应特性。本综述总结了PNPs作为一种用于炎症调节的多功能纳米医学平台。阐述了炎症背后的生理和病理机制,随后全面总结了PNPs用于炎症调节的工程策略、作用机制和治疗潜力。讨论了临床转化挑战,包括毒性和脱靶效应。最后提出了多功能PNPs在治疗诊断学和人工智能驱动的个性化炎症调节方面潜在的未来发展方向。这项工作旨在弥合聚合物纳米材料创新与精准医学之间的差距,以推动下一代抗炎疗法的发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ddf/12271758/dcc52af92a17/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ddf/12271758/388ac04e676e/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ddf/12271758/e1ee88838ca7/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ddf/12271758/ce3046dc2760/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ddf/12271758/dcc52af92a17/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ddf/12271758/388ac04e676e/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ddf/12271758/e1ee88838ca7/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ddf/12271758/ce3046dc2760/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ddf/12271758/dcc52af92a17/gr4.jpg

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Inflammation-modulating polymeric nanoparticles: design strategies, mechanisms, and therapeutic applications.

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本文引用的文献

[1]
Stimuli-Responsive Nanomedicines for the Treatment of Non-cancer Related Inflammatory Diseases.

ACS Nano. 2025-4-29

[2]
Innate immunity-modulating nanobiomaterials for controlling inflammation resolution.

Matter. 2024-11-6

[3]
Biomaterials for Modulating the Immune Microenvironment in Rheumatoid Arthritis.

BME Front. 2025-3-10

[4]
Polymer-based nanocarriers to transport therapeutic biomacromolecules across the blood-brain barrier.

Acta Biomater. 2025-4

[5]
Dual physiological responsive structural color hydrogel particles for wound repair.

Bioact Mater. 2025-1-7

[6]
pH-Responsive Polyglycerol Nanogels for Periodontitis Treatment through Antibacterial and Pro-Angiogenesis Action.

Angew Chem Int Ed Engl. 2025-2-24

[7]
Microemulsion-Inspired Polysaccharide Nanoparticles for an Advanced Targeted Thrombolytic Treatment.

ACS Nano. 2025-1-21

[8]
Tau(t)ing glucocorticoid binding.

Cell Res. 2025-1

[9]
Immunomodulatory activity of red algal galactans and their partially depolymerized derivatives in RAW264.7 macrophages.

Carbohydr Polym. 2025-1-1

[10]
Curcumin/pEGCG-encapsulated nanoparticles enhance spinal cord injury recovery by regulating CD74 to alleviate oxidative stress and inflammation.

J Nanobiotechnology. 2024-10-24

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