自愈水凝胶
化学
药物输送
体内
共聚物
聚合
生物医学工程
纳米技术
药品
碳酸三甲烯
生物物理学
阳离子聚合
毒品携带者
钛
控制释放
生物相容性材料
组织工程
开环聚合
靶向给药
体外
粘弹性
高分子化学
作者
Jinsu Baek,Wonjoon Moon,Shin Hye Chung,Byeong‐Su Kim
出处
期刊:Biomacromolecules
[American Chemical Society]
日期:2025-12-15
卷期号:27 (1): 930-937
标识
DOI:10.1021/acs.biomac.5c02307
摘要
Herein, we present a novel implant-mediated drug delivery platform that integrates dexamethasone (DEX)-loaded injectable hydrogels with 3D-printed titanium implants. A hydrophobic monomer, (cyclohexyloxy)ethyl glycidyl ether, was designed and polymerized into ABA-type triblock copolymers via anionic ring-opening polymerization initiated by a poly(ethylene oxide) midblock. Tailoring the A block length optimized the viscoelasticity of the hydrogels, enabling shear-thinning flow for injectability and providing suitable stress relaxation for postdeformation recovery. Incorporation into customized 3D-printed titanium implants allowed controlled DEX release through engineered cavities and hole geometries. In vitro assays confirmed cytocompatibility across multiple cell types, while DEX release effectively suppressed lipopolysaccharide-induced tumor necrosis factor-α and interleukin-6 secretion in macrophages. In vivo evaluation in a rabbit mandibular model further validated surgical feasibility, mechanical integrity, and sustained drug release. Collectively, these findings underscore the translational potential of combining injectable hydrogels with patient-specific 3D-printed implants for localized, sustained anti-inflammatory therapy.
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