Bone Morphogenetic Protein-, Antimicrobial Agent-, and Analgesic-Incorporated Nanofibrous Scaffolds for the Therapy of Alveolar Clefts.
Pang-Yung ChouDemei LeeChi-Chang WengRen-Chin WuChien-Tun LiaoShih-Jung LiuPublished in: Pharmaceutics (2022)
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.
Keyphrases
- tissue engineering
- growth factor
- bone regeneration
- mesenchymal stem cells
- staphylococcus aureus
- bone mineral density
- neuropathic pain
- anti inflammatory
- oxidative stress
- bone loss
- bone marrow
- body composition
- metabolic syndrome
- emergency department
- adipose tissue
- stem cells
- replacement therapy
- big data
- deep learning
- smoking cessation
- platelet rich plasma
- glycemic control
- artificial intelligence