Biocompatible design of bioresorbable electronics and materials.

IF 2.8 4区 医学 Q2 ENGINEERING, BIOMEDICAL
Biomedical Engineering Letters Pub Date : 2026-04-15 eCollection Date: 2026-05-01 DOI:10.1007/s13534-026-00576-x
Minki Hong, Gilmo Kim, Seunghun Han, Jahyun Koo
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引用次数: 0

Abstract

Biocompatibility is the defining determinant for the clinical translation of implantable biomedical devices. As bioelectronics evolve toward softer, electroactive, and bioresorbable systems, traditional definitions of biocompatibility-largely focused on cytotoxicity and gross inflammation-are no longer sufficient. Instead, emerging bioresorbable devices demand multidimensional biocompatibility, encompassing immune modulation, mechanical and electrical matching, controlled degradation, and functional stability over clinically relevant time windows. This review offers a biocompatibility-focused overview of recent advances in bioresorbable materials and electronics, known as transient devices. Emphasis is placed on how material selection, device architecture, and degradation pathways jointly govern immune responses and tissue integration. A comparative framework is introduced to relate material classes to immune outcomes and degradation behaviors, and current biocompatibility evaluation metrics and international standards (ISO 10993) are critically discussed. Finally, we propose design guidelines and future research directions to accelerate the translation of next-generation bioresorbable electronics.

生物可吸收电子和材料的生物相容性设计。
生物相容性是植入式生物医学器械临床翻译的决定性因素。随着生物电子学向更柔软、电活性和生物可吸收的系统发展,传统的生物相容性定义——主要集中在细胞毒性和严重炎症——不再足够。相反,新兴的生物可吸收设备需要多维生物相容性,包括免疫调节、机械和电气匹配、可控降解和临床相关时间窗内的功能稳定性。本综述以生物相容性为重点概述了生物可吸收材料和电子器件的最新进展,称为瞬态器件。重点放在材料选择、设备结构和降解途径如何共同控制免疫反应和组织整合。介绍了一个比较框架,将材料类别与免疫结果和降解行为联系起来,并批判性地讨论了当前的生物相容性评价指标和国际标准(ISO 10993)。最后,我们提出了设计指南和未来的研究方向,以加速下一代生物可吸收电子产品的转化。
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
Biomedical Engineering Letters
Biomedical Engineering Letters ENGINEERING, BIOMEDICAL-
CiteScore
6.80
自引率
0.00%
发文量
34
期刊介绍: Biomedical Engineering Letters (BMEL) aims to present the innovative experimental science and technological development in the biomedical field as well as clinical application of new development. The article must contain original biomedical engineering content, defined as development, theoretical analysis, and evaluation/validation of a new technique. BMEL publishes the following types of papers: original articles, review articles, editorials, and letters to the editor. All the papers are reviewed in single-blind fashion.
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