Dental Biomaterials Department, School of Dentistry, Tehran University of Medical Sciences, Tehran, Iran.
Dental Biomaterials Department, School of Dentistry, Tehran University of Medical Sciences, Tehran, Iran; Iranian Tissue Bank and Research Center, Tehran University of Medical Sciences, Tehran, Iran.
Mater Sci Eng C Mater Biol Appl. 2016 Dec 1;69:171-83. doi: 10.1016/j.msec.2016.06.033. Epub 2016 Jun 16.
The purpose of this multi-phase explorative in vivo animal/surgical and in vitro multi-test experimental study was to (1) create a 3wt%-nanostrontium hydroxyapatite-enhanced calcium phosphate cement (Sr-HA/CPC) for increasing bone formation and (2) creating a simvastatin-loaded poly(lactic-co-glycolic acid) (SIM-loaded PLGA) microspheres plus CPC composite (SIM-loaded PLGA+nanostrontium-CPC). The third goal was the extensive assessment of multiple in vitro and in vivo characteristics of the above experimental explorative products in vitro and in vivo (animal and surgical studies).
METHODS AND RESULTS PERTAINING TO SR-HA/CPC: Physical and chemical properties of the prepared Sr-HA/CPC were evaluated. MTT assay and alkaline phosphatase activities, and radiological and histological examinations of Sr-HA/CPC, CPC and negative control were compared. X-ray diffraction (XRD) indicated that crystallinity of the prepared cement increased by increasing the powder-to-liquid ratio. Incorporation of Sr-HA into CPC increased MTT assay (biocompatibility) and ALP activity (P<0.05). Histomorphometry showed greater bone formation after 4weeks, after implantation of Sr-HA/CPC in 10 rats compared to implantations of CPC or empty defects in the same rats (n=30, ANOVA P<0.05). METHODS AND RESULTS PERTAINING TO SIM-LOADED PLGA MICROSPHERES+NANOSTRONTIUM-CPC COMPOSITE: After SEM assessment, the produced composite of microspheres and enhanced CPC were implanted for 8weeks in 10 rabbits, along with positive and negative controls, enhanced CPC, and enhanced CPC plus SIM (n=50). In the control group, only a small amount of bone had been regenerated (localized at the boundary of the defect); whereas, other groups showed new bone formation within and around the materials. A significant difference was found in the osteogenesis induced by the groups sham control (16.96±1.01), bone materials (32.28±4.03), nanostrontium-CPC (24.84±2.6), nanostrontium-CPC-simvastatin (40.12±3.29), and SIM-loaded PLGA+nanostrontium-CPC (44.8±6.45) (ANOVA P<0.001). All the pairwise comparisons were significant (Tukey P<0.01), except that of nanostrontium-CPC-simvastatin and SIM-loaded PLGA+nanostrontium-CPC. This confirmed the efficacy of the SIM-loaded PLGA+nanostrontium-CPC composite, and its superiority over all materials except SIM-containing nanostrontium-CPC.
本多阶段探索性体内动物/手术和体外多试验实验研究的目的是 (1) 创造一种 3wt%-纳米锶羟基磷灰石增强磷酸钙水泥(Sr-HA/CPC)以增加骨形成,和 (2) 制造载辛伐他汀的聚(乳酸-共-乙醇酸)(SIM-载 PLGA)微球加 CPC 复合材料(SIM-载 PLGA+纳米锶-CPC)。第三个目标是广泛评估上述实验探索产品的多种体外和体内(动物和手术研究)特性。
与 Sr-HA/CPC 相关的方法和结果:评估了制备的 Sr-HA/CPC 的物理化学性质。比较了 Sr-HA/CPC、CPC 和阴性对照的 MTT 测定和碱性磷酸酶活性以及放射学和组织学检查。X 射线衍射(XRD)表明,随着粉末与液体比例的增加,水泥的结晶度增加。在 CPC 中掺入 Sr-HA 可提高 MTT 测定(生物相容性)和 ALP 活性(P<0.05)。组织形态计量学显示,在 10 只大鼠中植入 Sr-HA/CPC 后 4 周,与植入 CPC 或同一大鼠中的空缺陷相比,骨形成更多(n=30,ANOVA P<0.05)。
与 SIM-载 PLGA 微球+纳米锶-CPC 复合材料相关的方法和结果:在进行 SEM 评估后,将微球和增强 CPC 的复合材料植入 10 只兔子体内 8 周,同时设置阳性和阴性对照、增强 CPC 和增强 CPC 加 SIM(n=50)。在对照组中,仅在缺陷边界处再生了少量骨;而其他组在材料内部和周围显示出新骨形成。在诱导成骨方面,各组之间存在显著差异,假对照(16.96±1.01)、骨材料(32.28±4.03)、纳米锶-CPC(24.84±2.6)、纳米锶-CPC-辛伐他汀(40.12±3.29)和 SIM-载 PLGA+纳米锶-CPC(44.8±6.45)(ANOVA P<0.001)。所有两两比较均有显著性差异(Tukey P<0.01),除纳米锶-CPC-辛伐他汀和 SIM-载 PLGA+纳米锶-CPC 外。这证实了 SIM-载 PLGA+纳米锶-CPC 复合材料的功效,以及其优于除 SIM 载纳米锶-CPC 之外的所有材料的优势。