细胞外小泡
动力学
细胞外
再生(生物学)
小泡
多孔性
生物物理学
胞外囊泡
材料科学
化学
纳米技术
化学工程
细胞生物学
生物化学
微泡
膜
生物
小RNA
有机化学
量子力学
基因
物理
工程类
作者
Yike Gao,Xiaojing Yuan,Ruoheng Gu,Nan Wang,Huihui Ren,Rui Song,Zhuo Wan,Jianyong Huang,Kaikai Yi,Chunyang Xiong,Zuoying Yuan,Yuming Zhao
出处
期刊:ACS Nano
[American Chemical Society]
日期:2025-04-30
标识
DOI:10.1021/acsnano.5c03297
摘要
Biomaterials functionalized with small extracellular vesicles (sEVs) hold great regenerative potential, and their therapeutic efficacy hinges on the delivery kinetics of the sEVs. Achieving rapid and stable loading, along with precisely controlled release of sEVs, necessitates affinity modifications of biomaterials. Here, we provide a quantitative description of the interaction between sEVs and various affinity molecules (i.e., polydopamine (PDA), tannic acid (TA), heparin, polyethylenimine (PEI), and calcium phosphate (CaP)) through molecular dynamics simulation. The interaction strengths followed the order of PDA < heparin < TA < CaP < PEI. To tailor the delivery kinetics of stem cells from human exfoliated deciduous teeth (SHED)-derived sEVs with concentration-dependent bioactivities, we employed two representative affinity molecules, namely PDA and CaP, to modify PLGA porous microscaffolds (PLGA MS), resulting in PDA-modified PLGA MS (PDA@MS) and biomineralized PDA-modified PLGA MS (B/PDA@MS). The B/PDA@MS exhibited the highest loading efficiency (>20 μg/mg microscaffolds) and optimized the release profile of sEVs over 21 days. Upon injection into a 5 mm defect in the rat cranial bone, sEV-loaded B/PDA@MS demonstrated the highest level of bone regeneration, with the new bone volume fraction (BV/TV) and bone mineral density (BMD) reaching 64.0% and 604.5 mg/cm3 within 8 weeks, respectively. This work not only presents a biomineralized microscaffold with sustained sEVs release and high osteogenic potential but also offers guidance on the further design and translation of sEV-functionalized biomaterials with broader applications.
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