Synchronizing degradation with regeneration: a model-driven framework for designing biodegradable biomaterials in bone tissue engineering

IF 4.7 3区 医学 Q2 ENGINEERING, BIOMEDICAL
Vahid Zarghami
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Abstract

Bone regeneration is a complex biological process, and the repair of critical-sized bone defects is often difficult, highlighting the need to develop biodegradable scaffolds that can effectively synergize with tissue repair. This paper introduces a model-based bone repair design framework that matches the kinetics of material degradation with the spatiotemporal stages of bone repair. We systematically evaluated the degradation mechanisms and tunability of four classes of biomaterials—metals (Mg, Fe, Zn), ceramics (HA, β-TCP, bioactive glass), polymers (PLGA, PCL), and composites—and mapped established mathematical models (linear partial differential equations, sigmoid curves, response-diffusion partial differential equations, and mechanobiological finite element models) to specific bone defect sizes and clinical scenarios. Based on this classification, we propose a four-step clinical design to guide researchers in completing the following steps: (1) calculating patient-specific healing timelines using first-order heuristics; (2) selecting appropriate material classes based on mechanical and biological requirements; (3) designing degradation kinetics to match the healing stages; and (4) validating scaffold-tissue alignment. To achieve quantitative assessment, we introduce the synchronization index (SI), a provisional index designed to quantify the correlation between actual implant degradation and patient-specific target curves. While the SI and the healing timeline formula are currently proposed only as conceptual design tools and require prospective experimental and clinical validation, their integration provides a structured path for scaffold development, moving it from experimental trial and error to precise, model-based engineering design. The goal of this framework is to facilitate the rational design of smart, resorbable implants that dynamically match the biological and mechanical requirements of bone regeneration.

同步降解与再生:骨组织工程中设计可生物降解生物材料的模型驱动框架。
骨再生是一个复杂的生物过程,修复临界尺寸的骨缺损往往是困难的,这突出了开发能够有效协同组织修复的可生物降解支架的必要性。本文介绍了一种基于模型的骨修复设计框架,该框架将材料降解动力学与骨修复的时空阶段相匹配。我们系统地评估了四类生物材料(金属(Mg, Fe, Zn),陶瓷(HA, β-TCP,生物活性玻璃),聚合物(PLGA, PCL)和复合材料)的降解机制和可调性,并将建立的数学模型(线性偏微分方程,s型曲线,响应-扩散偏微分方程和机械生物学有限元模型)映射到特定的骨缺损尺寸和临床情况。基于这种分类,我们提出了一个四步临床设计来指导研究人员完成以下步骤:(1)使用一阶启发式计算患者特异性愈合时间表;(2)根据机械和生物要求选择合适的材料类别;(3)设计与愈合阶段相匹配的降解动力学;(4)验证支架-组织对齐。为了实现定量评估,我们引入了同步指数(SI),这是一个临时指数,旨在量化实际种植体降解与患者特定目标曲线之间的相关性。虽然SI和愈合时间轴公式目前仅作为概念设计工具提出,需要前瞻性的实验和临床验证,但它们的整合为支架开发提供了结构化的路径,将其从实验试错转变为精确的、基于模型的工程设计。该框架的目标是促进智能,可吸收植入物的合理设计,动态匹配骨再生的生物和机械要求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Materials Science: Materials in Medicine
Journal of Materials Science: Materials in Medicine 工程技术-材料科学:生物材料
CiteScore
8.00
自引率
0.00%
发文量
73
审稿时长
3.5 months
期刊介绍: The Journal of Materials Science: Materials in Medicine publishes refereed papers providing significant progress in the application of biomaterials and tissue engineering constructs as medical or dental implants, prostheses and devices. Coverage spans a wide range of topics from basic science to clinical applications, around the theme of materials in medicine and dentistry. The central element is the development of synthetic and natural materials used in orthopaedic, maxillofacial, cardiovascular, neurological, ophthalmic and dental applications. Special biomedical topics include biomaterial synthesis and characterisation, biocompatibility studies, nanomedicine, tissue engineering constructs and cell substrates, regenerative medicine, computer modelling and other advanced experimental methodologies.
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