骨形态发生蛋白
骨形态发生蛋白2
抗菌剂
体内
医学
牙槽
生物医学工程
化学
牙科
体外
生物
生物化学
基因
生物技术
有机化学
作者
Pang‐Yun Chou,Demei Lee,Chi-Chang Weng,Ren‐Chin Wu,Chien-Tun Liao,Shih‐Jung Liu
出处
期刊:Pharmaceutics
[MDPI AG]
日期:2022-02-08
卷期号:14 (2): 374-374
被引量:2
标识
DOI:10.3390/pharmaceutics14020374
摘要
An alveolar cleft is a bone defect in the maxillary arch. Although the use of autologous iliac bone grafts to repair alveolar clefts is the preferred treatment method, donor-site morbidity remains a concern. In this study, we incorporated bone morphogenetic protein (BMP), an antimicrobial agent, and an analgesic into nanofibrous scaffolds for alveolar cleft therapy. Three-dimensional (3D) printing and coaxial electrospinning techniques were used to fabricate the scaffolds. BMP-2, ketorolac, and amoxicillin were used as the growth factor, analgesic, and antimicrobial agent, respectively. The in vitro properties of the nanofibrous scaffolds were characterized, and in vivo efficacy was evaluated in a rat alveolar-cleft model. The empirical data indicated that the biomolecule-incorporated scaffolds offered extended discharge of BMP-2, amoxicillin, and ketorolac for >4 weeks. The animal test outcomes also demonstrated favorable bone healing at the cleft site. Biomolecule- and drug-incorporated nanofibrous scaffolds demonstrated their efficacy in alveolar cleft treatment.
科研通智能强力驱动
Strongly Powered by AbleSci AI