Orthopaedic Center, Affiliated Hospital of Guangdong Medical University, Guangdong Medical University, Zhanjiang 524002, China; School of Pharmacy and Guangdong Key Laboratory for Research and Development of Natural Drugs, Guangdong Medical University, Zhanjiang 524023, China; Department of Orthopaedics & Traumatology, Faculty of Medicine, The Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong, China.
School of Pharmacy and Guangdong Key Laboratory for Research and Development of Natural Drugs, Guangdong Medical University, Zhanjiang 524023, China.
Biomaterials. 2019 Mar;196:109-121. doi: 10.1016/j.biomaterials.2018.04.004. Epub 2018 Apr 4.
Spinal disorders often require surgical treatment called spinal fusion to restore a stabilized spine where bone grafts are implanted for the fusion of adjacent vertebras. In this study, we developed a bioactive composite scaffold incorporated with salvianolic acid B (SB), an active component extracted from Danshen. This study aimed to evaluate the effects of SB-incorporated porous scaffold on spinal fusion models. The composite scaffolds composed of poly (lactic-co-glycolic acid) and tricalcium phosphate (PLGA/β-TCP) were fabricated with low-temperature rapid prototyping technique, which incorporated SB at low (SB-L), middle (SB-M), high (SB-H) doses, and pure PLGA/β-TCP as blank control (Con). The release profile of SB from the scaffolds was determined by high performance liquid chromatography. Osteoconductive and osteoinductive properties of the scaffolds were reflected by the osteogenic differentiation ability of rat primary mesenchymal stem cells. The angiogenesis was determined by the forming of tube-like structures resembling capillaries using endothelial cell line (EA hy9.26). A well-established spinal fusion model was used to evaluate the in vivo bony fusion. Animals were transplanted with scaffolds, or autografts from iliac crest as positive controls. Micro-computed tomography (CT) analysis, CT-based angiography, manual palpation test, histomorphometry, and histology were performed after 8 weeks of transplantation. Results revealed that incorporated SB was steadily released from the scaffolds. The aliquot of released SB promoted osteogenesis and angiogenesis in vitro in a dose-dependent manner. In animal study, a dose-dependent effect of SB on new bone formation, mineral apposition rate, and vessel density within the scaffold were demonstrated. Manual palpation test showed little numerical improvement in fusion rate when compared with the blank controls. In summary, our results suggested that SB-incorporated PLGA/β-TCP composite scaffold could enhance bony fusion through the promotion of osteogenesis and angiogenesis.
脊柱疾病常需要手术治疗,称为脊柱融合术,以恢复稳定的脊柱,在相邻的椎骨中植入骨移植物进行融合。在这项研究中,我们开发了一种含有丹参提取物丹酚酸 B(SB)的生物活性复合支架。本研究旨在评估 SB 复合多孔支架对脊柱融合模型的影响。复合支架由聚乳酸-羟基乙酸共聚物(PLGA)和磷酸三钙(β-TCP)组成,采用低温快速成型技术制备,分别以低(SB-L)、中(SB-M)、高(SB-H)剂量掺入 SB,以及纯 PLGA/β-TCP 作为空白对照(Con)。通过高效液相色谱法测定 SB 从支架中的释放情况。支架的骨诱导和骨传导性能通过大鼠原代间充质干细胞的成骨分化能力来反映。通过内皮细胞系(EA hy9.26)形成类似于毛细血管的管状结构来确定血管生成。建立了成熟的脊柱融合模型来评估体内骨融合。将支架或髂嵴自体移植物作为阳性对照移植到动物体内。移植 8 周后进行微计算机断层扫描(CT)分析、基于 CT 的血管造影、手动触诊试验、组织形态计量学和组织学检查。结果表明,SB 被稳定地从支架中释放出来。释放的 SB 可促进体外成骨和成血管作用,并呈剂量依赖性。在动物研究中,SB 对支架内新骨形成、矿化沉积率和血管密度的影响呈剂量依赖性。与空白对照组相比,手动触诊试验显示融合率略有改善。综上所述,我们的结果表明,SB 复合 PLGA/β-TCP 支架可通过促进成骨和成血管作用增强骨融合。