Functionalized 3D-Printed PEI scaffolds synergize immunomodulation and cartilage regeneration to accelerate tendon–bone healing

The tendon–bone interface is a specialized transitional structure featuring a four-layered gradient organization—tendon, unmineralized fibrocartilage, mineralized fibrocartilage, and bone—that enables smooth mechanical load transfer between soft and hard tissues. Its intrinsic regenerative capacity is extremely limited, and post-injury repair is often replaced by mechanically inferior scar tissue, increasing the risk of re-injury. Conventional tissue engineering scaffolds have largely focused on structural mimicry but frequently neglect modulation of the local immune microenvironment, particularly macrophage-mediated chronic inflammation, which hinders fibrocartilaginous layer regeneration and functional integration. Here, we developed a 3D-printed multifunctional polyetherimide (PEI)-based scaffold capable of simultaneously releasing bioactive Silicate (Si), calcium (Ca), and zinc (Zn) ions(P-CaSiO 3 -ZnO). The scaffold exhibits suitable mechanical strength, interconnected porosity, and controlled ion release. In vitro, it promoted osteogenic, chondrogenic, and tenogenic differentiation while modulating inflammatory responses. In vivo experiments, P-CaSiO 3 -ZnO scaffold accelerated new bone formation, organized collagen deposition, and fibrocartilaginous layer regeneration, achieving robust tendon–bone interface integration and markedly improved mechanical performance. These findings demonstrate a promising strategy for functional tendon–bone interface repair by integrating multi-tissue regeneration and immunomodulatory capabilities. • Sequentially regulated ion release synchronizes stage-specific biological functions with the dynamic healing process. • Beyond structural mimicry, our scaffold suppresses fibrotic scarring by immunomodulating inflammation via Zn²⁺ release. • Integrating 3D printing with hybrid design and surface coatings bridges the gap between mechanical strength and biological complexity.

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Publication Details

Journal
Materials Today Advances
Published
2026-01-29
DOI
https://doi.org/10.1016/j.mtadv.2026.100695
Primary Topic
Tendon Structure and Treatment
Type
article
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article

Functionalized 3D-Printed PEI scaffolds synergize immunomodulation and cartilage regeneration to accelerate tendon–bone healing

Qingshuai Wang, Zhicheng Zhang, Minglei Liu, Yuhuan Zhang et al.
Materials Today Advances
Tendon Structure and Treatment
article

Functionalized 3D-Printed PEI scaffolds synergize immunomodulation and cartilage regeneration to accelerate tendon–bone healing

Qingshuai Wang, Zhicheng Zhang, Minglei Liu, Yuhuan Zhang, Bo Chen, Haolin Zeng, Yingzhi Li
article en

Abstract

The tendon–bone interface is a specialized transitional structure featuring a four-layered gradient organization—tendon, unmineralized fibrocartilage, mineralized fibrocartilage, and bone—that enables smooth mechanical load transfer between soft and hard tissues. Its intrinsic regenerative capacity is extremely limited, and post-injury repair is often replaced by mechanically inferior scar tissue, increasing the risk of re-injury. Conventional tissue engineering scaffolds have largely focused on structural mimicry but frequently neglect modulation of the local immune microenvironment, particularly macrophage-mediated chronic inflammation, which hinders fibrocartilaginous layer regeneration and functional integration. Here, we developed a 3D-printed multifunctional polyetherimide (PEI)-based scaffold capable of simultaneously releasing bioactive Silicate (Si), calcium (Ca), and zinc (Zn) ions(P-CaSiO 3 -ZnO). The scaffold exhibits suitable mechanical strength, interconnected porosity, and controlled ion release. In vitro, it promoted osteogenic, chondrogenic, and tenogenic differentiation while modulating inflammatory responses. In vivo experiments, P-CaSiO 3 -ZnO scaffold accelerated new bone formation, organized collagen deposition, and fibrocartilaginous layer regeneration, achieving robust tendon–bone interface integration and markedly improved mechanical performance. These findings demonstrate a promising strategy for functional tendon–bone interface repair by integrating multi-tissue regeneration and immunomodulatory capabilities. • Sequentially regulated ion release synchronizes stage-specific biological functions with the dynamic healing process. • Beyond structural mimicry, our scaffold suppresses fibrotic scarring by immunomodulating inflammation via Zn²⁺ release. • Integrating 3D printing with hybrid design and surface coatings bridges the gap between mechanical strength and biological complexity.

Materials Today AdvancesVol. 29
Weifang Medical University (CN), Weifang People's Hospital (CN), Second Affiliated Hospital of Jilin University (CN)
Openalex Percentile: Top 75%
Tendon Structure and Treatment
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