Leveraging solid–liquid interaction to fabricate drug-microsphere in site encapsulated bone-repair scaffolds

Drug-encapsulated scaffolds are crucial to treat challenging bone defects, but the approach for loading drugs into scaffolds is limited. Despite microspheres as carriers that improve drug efficacy and the therapeutic window, the traditional "first preparation - then encapsulation" in drug-microsphere encapsulated scaffolds remains complicated and time-consuming. Herein, we present a facile approach for fabricating drug-microsphere in site encapsulated bone-repair scaffolds (CHP@Drug), in which a solid-liquid interaction triggered by vortex oscillation can be leveraged to realize in site preparation and simultaneous encapsulation of drug-loaded microspheres, rapidly and uniformly. Owing to the induced collision, homogenized and reinforced shear stress from the solid-liquid interaction, CHP@Drug endowed a sustained drug release and an interconnected porous structure. As a proof of concept, CHP@Drugs, were loaded with three drugs respectively, demonstrating significantly enhanced healing of critical-sized, infected, and osteoporotic bone defects <i>in vivo</i>. This study offers a facile and universal way to load drugs into tissue-repair scaffolds, with in-clinic potential.

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Publication Details

Journal
Materials Horizons
Published
2025-10-15
DOI
https://doi.org/10.1039/d5mh01359c
Primary Topic
Bone Tissue Engineering Materials
Type
article
Field-Weighted Citation Impact
0.00

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article

Leveraging solid–liquid interaction to fabricate drug-microsphere in site encapsulated bone-repair scaffolds

Fengxin Zhao, Xiangdong Zhu, Changshun Ruan, Puxin Liu et al.
Materials Horizons
Bone Tissue Engineering Materials
article

Leveraging solid–liquid interaction to fabricate drug-microsphere in site encapsulated bone-repair scaffolds

Fengxin Zhao, Xiangdong Zhu, Changshun Ruan, Puxin Liu, Dongxiao Li, Yumei Xiao, Xingdong Zhang, Jirong Yang, Xinyi Wang
article en

Abstract

Drug-encapsulated scaffolds are crucial to treat challenging bone defects, but the approach for loading drugs into scaffolds is limited. Despite microspheres as carriers that improve drug efficacy and the therapeutic window, the traditional "first preparation - then encapsulation" in drug-microsphere encapsulated scaffolds remains complicated and time-consuming. Herein, we present a facile approach for fabricating drug-microsphere in site encapsulated bone-repair scaffolds (CHP@Drug), in which a solid-liquid interaction triggered by vortex oscillation can be leveraged to realize in site preparation and simultaneous encapsulation of drug-loaded microspheres, rapidly and uniformly. Owing to the induced collision, homogenized and reinforced shear stress from the solid-liquid interaction, CHP@Drug endowed a sustained drug release and an interconnected porous structure. As a proof of concept, CHP@Drugs, were loaded with three drugs respectively, demonstrating significantly enhanced healing of critical-sized, infected, and osteoporotic bone defects <i>in vivo</i>. This study offers a facile and universal way to load drugs into tissue-repair scaffolds, with in-clinic potential.

Materials HorizonsVol. 13(3)
Shenzhen Institutes of Advanced Technology (CN), Sichuan Academy of Traditional Chinese Medicine (CN), University of Chinese Academy of Sciences (CN), Southwest Minzu University (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 72%
Bone Tissue Engineering Materials
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