Poly(lactic acid/caprolactone) bilayer membrane achieves bone regeneration through a prolonged barrier function

• Published in: Journal of biomedical materials research. Part B, Applied biomaterials Applied biomaterials, 2024-01, Vol.112 (1), p.e35365-n/a
• Main Authors: Abe, Gabriela L., Sasaki, Jun‐Ichi, Tsuboi, Ririko, Kohno, Tomoki, Kitagawa, Haruaki, Imazato, Satoshi
• Format: Article
• Language: English
• Subjects: Alveolar bone; Animal models; Animals; barrier membrane; bilayer membrane; Biocompatible Materials; Biodegradability; Biodegradation; Biomaterials; Biomedical materials; Bone biomaterials; Bone growth; Bone Regeneration; Calvaria; Caproates; Collagen (type I); Copolymers; Defects; Degradation; Dogs; Glycolic acid; guided bone regeneration; Lactic acid; Lactic Acid - pharmacology; Lactones; Materials research; Materials science; Membranes; polycaprolactone; polylactic acid; Polylactide-co-glycolide; Polymers; Rats; Regeneration; Regeneration (physiology); Surgical implants
• ISSN: 1552-4973; 1552-4981
• DOI: 10.1002/jbm.b.35365

Guided bone regeneration (GBR) is a treatment strategy used to recover bone volume. Barrier membranes are a key component of GBR protocols, and their properties can impact treatment outcomes. This study investigated the efficacy of an experimental, slow‐degrading, bilayer barrier membrane for application in GBR using in vivo animal models. A synthetic copolymer of poly(lactic acid/caprolactone) (PLCL) was used to prepare a slow‐degrading bilayer membrane. The biodegradability of PLCL was evaluated by subcutaneous implantation in a rat model. The barrier function of the PLCL membrane was investigated in a rat calvaria defect model and compared with commercially available membranes composed of type I collagen (Col) and poly(lactic‐co‐glycolic acid) (PLGA). An alveolar bone defect model in beagle dogs was used to simulate GBR protocols to evaluate the bone regeneration ability of the experimental PLCL membrane. The PLCL membrane showed slow biodegradation, resulting in an efficient and prolonged barrier function compared with commercial materials. In turn, this barrier function enabled the space‐making ability of PLCL membrane and facilitated bone regeneration. In the alveolar bone defect model, significantly greater regeneration was achieved by treatment with PLCL membrane compared with Col and PLGA membranes. Additionally, a continuous alveolar ridge contour was observed in PLCL‐treated bone defects. In conclusion, the PLCL bilayer membrane is a promising biomaterial for use in GBR given its slow degradation and prolonged barrier function.