Rational Surface Engineering Reduces Advanced Glycation End‐Product Adsorption and Improves Implant Integration
Year: 2026
Type: article
Abstract: Advanced glycation end-products (AGEs) accumulate in metabolic diseases such as diabetes and are closely associated with poor outcomes following implantation. However, how these molecules influence events at the biomaterial interface has remained largely unknown. Here, we identify AGEs as critical biointerfacial modifiers that adsorb onto implant surfaces, reprogram immune responses, promote fibrotic encapsulation, impair angiogenesis, and compromise osseointegration. This suggests a potential mechanism by which metabolic disease disrupts biomaterial-tissue integration. By engineering titanium surfaces enriched with amine or carboxyl functionalities, we create AGE-resistant biointerfaces that effectively suppress pro-inflammatory M1 macrophage polarization, promote an anti-inflammatory M2 macrophage phenotype, reduce fibrotic encapsulation, enhance angiogenesis, and improve osseointegration across ex vivo, in vitro, and in vivo diabetic models. These findings establish disease-informed surface chemistry as a design paradigm for next-generation implants intended for metabolically compromised and other high-risk patient populations.
Source: Advanced Science
DOI: 10.1002/advs.78507
Language: English
Subfield: Biomedical Engineering
Field: Engineering
Domain: Physical Sciences
Open Access status: gold
Estimated APC paid: $6,730
Funders: Australian Nuclear Science and Technology Organisation, Shandong University, Government of South Australia, Diabetes Australia, Flinders University, National Natural Science Foundation of China, Natural Science Foundation of Shandong Province, Australian Research Council, National Health and Medical Research Council
Awards: G404440373, G6282230199
OpenAlex ID: W7223809933
