Luo C, Chen J, Zhang Q, Yu X, Zhang S
Third Affiliated Hospital of Southern Medical University//Guangdong Key Laboratory of Bone and Joint Degenerative Diseases, Guangzhou 510630, China.
School of Pharmacy, Southern Medical University// NMPA Key Laboratory of Drug Metabolism Research and Evaluation, Guangzhou 510515, China.
Nan Fang Yi Ke Da Xue Xue Bao. 2024 Feb 20;44(2):370-380. doi: 10.12122/j.issn.1673-4254.2024.02.20.
To investigate the release kinetics of Zn from nZCP-loaded polylactic acid/hydroxyapatite (PLA/HA) composite scaffold (PHZ) and determine the optimal nZCP content in the scaffold.
The particle size of nZCP was measured by DLS measurement, and PXRD, FTIR, and SEM were used to characterize the scaffolds and nZCP distribution; EDS was used to analyze element composition of the scaffold. Compression strength of the scaffold was determined, and ion release profile was investigated using ICP-MS. The biocompatibility of the materials was evaluated by CCK-8 assay and dead/alive staining of rat bone marrow stem cells (BMSCs) incubated with their aqueous extracts. ALP staining, alizarin red staining, RT-qPCR, and Western blotting were used to assess the osteogenic potential of the treated cells. In a rat model of bilateral ovariectomy (OVX) with femoral condylar bone defect, PHZ-1, PHZ-2, PHZ-3 or PLA/HA scaffold was implanted into the bone defect, and bone repair was observed using a microCT scanner and histological staining at 6 and 12 weeks.
DLS, PXRD, SEM, FTIR, and EDS confirmed successful synthesis of 10-nm ZCP and efficient nZCP loading in the scaffold. PHZ-2 and PHZ-3 had significantly greater compression strength than PLA/HA. ICP-MS showed that Zn release from PHZ-1, PHZ-2 and PHZ-3 were all optimal for promoting osteogenesis. In rat BMSCs, all the 4 scaffolds showed good biocompatibility, and their extracts enhanced ALP activity and extracellular matrix mineralization and promoted expressions of ALP, RUNX2, and OCN in the cells. In the rat models, nZCP in the implants improved bone graft integration at 6 weeks, and PHZ-2 and PHZ-3 more effectively induced new bone formation at 12 weeks ( < 0.05).
PHZ scaffold is capable of stable Zn release to promote osteoporotic bone defect healing, and PHZ-2 and PHZ-3 scaffolds with nZCP mass fraction of 4.5%-7.5% have better osteogenic activity.
研究载有纳米零价铜(nZCP)的聚乳酸/羟基磷灰石(PLA/HA)复合支架(PHZ)中锌的释放动力学,并确定支架中nZCP的最佳含量。
通过动态光散射(DLS)测量nZCP的粒径,采用粉末X射线衍射(PXRD)、傅里叶变换红外光谱(FTIR)和扫描电子显微镜(SEM)对支架及nZCP分布进行表征;利用能谱仪(EDS)分析支架的元素组成。测定支架的抗压强度,并使用电感耦合等离子体质谱(ICP-MS)研究离子释放曲线。通过CCK-8法以及用大鼠骨髓间充质干细胞(BMSCs)与材料水提取物共孵育后的死活染色评估材料的生物相容性。采用碱性磷酸酶(ALP)染色、茜素红染色、逆转录定量聚合酶链反应(RT-qPCR)和蛋白质免疫印迹法评估处理后细胞的成骨潜能。在双侧卵巢切除(OVX)伴股骨髁骨缺损的大鼠模型中,将PHZ-1、PHZ-2、PHZ-3或PLA/HA支架植入骨缺损处,在6周和12周时使用微型计算机断层扫描(microCT)扫描仪和组织学染色观察骨修复情况。
DLS、PXRD、SEM、FTIR和EDS证实成功合成了10纳米的零价铜(ZCP)并在支架中有效负载了nZCP。PHZ-2和PHZ-3的抗压强度明显高于PLA/HA。ICP-MS显示,PHZ-1、PHZ-2和PHZ-3中锌的释放均最有利于促进成骨。在大鼠BMSCs中,所有4种支架均表现出良好的生物相容性,其提取物增强了ALP活性和细胞外基质矿化,并促进了细胞中ALP、RUNX2和骨钙素(OCN)的表达。在大鼠模型中,植入物中的nZCP在6周时改善了骨移植融合,PHZ-2和PHZ-3在12周时更有效地诱导了新骨形成(P<0.05)。
PHZ支架能够稳定释放锌以促进骨质疏松性骨缺损愈合,nZCP质量分数为4.5%-7.5%的PHZ-2和PHZ-3支架具有更好的成骨活性。