Kim Kee D, Batchelder Cynthia A, Koleva Plamena, Ghaffari-Rafi Arash, Karnati Tejas, Goodrich Dylan, Castillo Jose, Lee Charles
Department of Neurological Surgery, University of California Davis Medical Center, Sacramento, CA 95816, USA.
Molecular Matrix, Inc., 11121 Sun Center Drive Suite C, Rancho Cordova, CA 95670, USA.
Bioengineering (Basel). 2025 Feb 27;12(3):243. doi: 10.3390/bioengineering12030243.
Bone graft materials are essential for achieving arthrodesis after spine surgery. Safe bone graft products, with osteoinductive, osteoconductive properties and the ability to monitor fusion in real-time, are highly desirable. A novel hyper-crosslinked carbohydrate polymer (HCCP) bone graft substitute was shown to aid in bone regeneration in critical-size defect studies in a rabbit model. These studies further evaluated the in vivo application of HCCP as a bone graft substitute in an ovine model of spinal fusion and a retrospective study in adult human spine surgery patients. Sheep studies demonstrated the safety and efficacy of HCCP with no evidence of adverse histopathology over 6 months of follow-up. In human studies, patients (N = 63) underwent posterolateral fusion with HCCP, with follow-up to assess fusion success. No adverse reaction related to the HCCP bone graft substitute was identified. Fusion success was noted to be non-inferior to other bone graft substitutes. HCCP appears to be a safe bone void filler adjunct for use in spinal fusion surgery for both trauma and degenerative disease. It has a good degradation profile for forming bone with the ability to provide new vasculature and may also function as a scaffold to carry cells, medications, and growth factors. Given the safety profile experienced in our preclinical and clinical studies, future investigation into its efficacy to achieve solid fusion is currently ongoing.
骨移植材料对于脊柱手术后实现关节融合至关重要。具有骨诱导性、骨传导性且能够实时监测融合情况的安全骨移植产品非常理想。一种新型的超交联碳水化合物聚合物(HCCP)骨移植替代物在兔模型的临界尺寸缺损研究中显示有助于骨再生。这些研究进一步评估了HCCP作为骨移植替代物在绵羊脊柱融合模型中的体内应用以及在成年人类脊柱手术患者中的一项回顾性研究。绵羊研究证明了HCCP的安全性和有效性,在6个月的随访中没有不良组织病理学证据。在人类研究中,患者(N = 63)接受了使用HCCP的后外侧融合术,并进行随访以评估融合成功率。未发现与HCCP骨移植替代物相关的不良反应。融合成功率被认为不低于其他骨移植替代物。HCCP似乎是一种安全的骨缺损填充辅助材料,可用于创伤和退行性疾病的脊柱融合手术。它具有良好的降解特性以形成骨,能够提供新的血管,还可能作为携带细胞、药物和生长因子的支架。鉴于我们在临床前和临床研究中观察到的安全性,目前正在对其实现牢固融合的疗效进行进一步研究。