Bone‐targeted hybrid extracellular vesicles for alveolar bone regeneration

Abstract Prolonged tooth loss causes a blade‐like narrowing of the alveolar bone, severely impairing chewing function and aesthetics and complicating subsequent orthodontic or restorative treatments. Bone morphogenetic protein‐2 (BMP‐2) is widely used to induce osteogenesis; however, its lack of cel...

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Main Authors: Anqi Liu, Gang Yang, Yijie Zhao, Jiajia Deng, Jialiang Liu, Kairun Zhang, Li Mei, Yan Liu, Tingjiao Liu
Format: Article
Language:English
Published: Wiley-VCH 2025-05-01
Series:Interdisciplinary Medicine
Subjects:
Online Access:https://doi.org/10.1002/INMD.20240126
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author Anqi Liu
Gang Yang
Yijie Zhao
Jiajia Deng
Jialiang Liu
Kairun Zhang
Li Mei
Yan Liu
Tingjiao Liu
author_facet Anqi Liu
Gang Yang
Yijie Zhao
Jiajia Deng
Jialiang Liu
Kairun Zhang
Li Mei
Yan Liu
Tingjiao Liu
author_sort Anqi Liu
collection DOAJ
description Abstract Prolonged tooth loss causes a blade‐like narrowing of the alveolar bone, severely impairing chewing function and aesthetics and complicating subsequent orthodontic or restorative treatments. Bone morphogenetic protein‐2 (BMP‐2) is widely used to induce osteogenesis; however, its lack of cellular targeting in complex microenvironments often results in significant side effects. Developing a safe, stable, and osteoblast‐targeted drug delivery system is crucial for precise bone regeneration. Nanoparticles, as ideal drug delivery vehicles, offer highly controllable cellular targeting. This study introduces an innovative approach using DNA nanostructure‐modified BMP‐2‐loaded hybrid extracellular vesicles (EVs) formed by fusing liposomes and EVs. Screening identified 180 nm as the optimal particle size for EVs fusion efficiency. The system achieved osteoblast‐specific targeting by attaching the DNA aptamer 19S to the hybrid EVs membrane. The hybrid EVs were further combined with a hydrogel sustained‐release system, creating a drug delivery platform that effectively repaired alveolar bone defects. This approach demonstrated significant potential for advancing bone tissue repair and regeneration.
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issn 2832-6245
language English
publishDate 2025-05-01
publisher Wiley-VCH
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series Interdisciplinary Medicine
spelling doaj-art-7b3a991863de48519985ded786bee3e72025-08-20T03:26:39ZengWiley-VCHInterdisciplinary Medicine2832-62452025-05-0133n/an/a10.1002/INMD.20240126Bone‐targeted hybrid extracellular vesicles for alveolar bone regenerationAnqi Liu0Gang Yang1Yijie Zhao2Jiajia Deng3Jialiang Liu4Kairun Zhang5Li Mei6Yan Liu7Tingjiao Liu8Department of Orthodontics School of Medicine Shanghai Ninth People's Hospital College of Stomatology Shanghai Jiao Tong University Shanghai ChinaDepartment of Multidisciplinary Consultant Center Shanghai Stomatological Hospital & School of Stomatology Shanghai ChinaShanghai Key Laboratory of Craniomaxillofacial Development and Diseases Fudan University Shanghai ChinaShanghai Key Laboratory of Craniomaxillofacial Development and Diseases Fudan University Shanghai ChinaShanghai Key Laboratory of Craniomaxillofacial Development and Diseases Fudan University Shanghai ChinaShanghai Key Laboratory of Craniomaxillofacial Development and Diseases Fudan University Shanghai ChinaDepartment of Oral Sciences Faculty of Dentistry University of Otago Dunedin New ZealandCentral Laboratory Peking University School and Hospital for Stomatology & National Center for Stomatology & National Clinical Research Center for Oral Diseases & National Engineering Research Center of Oral Biomaterials and Digital Medical Devices & Beijing Key Laboratory of Digital Stomatology & Research Center of Engineering and Technology for Computerized Dentistry Ministry of Health & NMPA Key Laboratory for Dental Materials & National Engineering Research Center of Oral Biomaterials and Digital Medical Devices Beijing ChinaShanghai Key Laboratory of Craniomaxillofacial Development and Diseases Fudan University Shanghai ChinaAbstract Prolonged tooth loss causes a blade‐like narrowing of the alveolar bone, severely impairing chewing function and aesthetics and complicating subsequent orthodontic or restorative treatments. Bone morphogenetic protein‐2 (BMP‐2) is widely used to induce osteogenesis; however, its lack of cellular targeting in complex microenvironments often results in significant side effects. Developing a safe, stable, and osteoblast‐targeted drug delivery system is crucial for precise bone regeneration. Nanoparticles, as ideal drug delivery vehicles, offer highly controllable cellular targeting. This study introduces an innovative approach using DNA nanostructure‐modified BMP‐2‐loaded hybrid extracellular vesicles (EVs) formed by fusing liposomes and EVs. Screening identified 180 nm as the optimal particle size for EVs fusion efficiency. The system achieved osteoblast‐specific targeting by attaching the DNA aptamer 19S to the hybrid EVs membrane. The hybrid EVs were further combined with a hydrogel sustained‐release system, creating a drug delivery platform that effectively repaired alveolar bone defects. This approach demonstrated significant potential for advancing bone tissue repair and regeneration.https://doi.org/10.1002/INMD.20240126alveolar bone defectbone targetingDNA nanostructureshybrid EVsliposomes
spellingShingle Anqi Liu
Gang Yang
Yijie Zhao
Jiajia Deng
Jialiang Liu
Kairun Zhang
Li Mei
Yan Liu
Tingjiao Liu
Bone‐targeted hybrid extracellular vesicles for alveolar bone regeneration
Interdisciplinary Medicine
alveolar bone defect
bone targeting
DNA nanostructures
hybrid EVs
liposomes
title Bone‐targeted hybrid extracellular vesicles for alveolar bone regeneration
title_full Bone‐targeted hybrid extracellular vesicles for alveolar bone regeneration
title_fullStr Bone‐targeted hybrid extracellular vesicles for alveolar bone regeneration
title_full_unstemmed Bone‐targeted hybrid extracellular vesicles for alveolar bone regeneration
title_short Bone‐targeted hybrid extracellular vesicles for alveolar bone regeneration
title_sort bone targeted hybrid extracellular vesicles for alveolar bone regeneration
topic alveolar bone defect
bone targeting
DNA nanostructures
hybrid EVs
liposomes
url https://doi.org/10.1002/INMD.20240126
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