Li D X, Fan H S, Zhu X D, Tan Y F, Xiao W Q, Lu J, Xiao Y M, Chen J Y, Zhang X D
National Engineering Research Center for Biomaterials, Sichuan University, Chengdu, China.
J Mater Sci Mater Med. 2007 Nov;18(11):2225-31. doi: 10.1007/s10856-007-3084-8. Epub 2007 Jul 10.
The aim of this research is to study the effect of the controlled releasing character of the salmon calcitonin (S-CT) loaded injectable calcium phosphate cement (CPC) modified by adding organic phase, chitosan oligosaccharide (CO) and collagen polypeptide (CP). The uniform design was used to determine the basic formulation with suitable injectable time for clinical application, and then the changes of the physical characters, the controlled releasing character of the modified CPC along with the ratio of the organic phase were also evaluated in vitro. The surface morphous of the modified CPC been implanted in the abdominal cavity or soaked into the serum of rat was also observed by scanning electron microscope (SEM). The result shows that a suitable formulation of modified CPC could be got, and the injectable time is 12 min, the compressive strength is 12 MPa, and the final setting time is 40 min. Comparing with the CPC without organic phase, the releasing rate of S-CT would increase along with the increase of the organic phase after 7th day. Therefore, a novel S-CT loaded bioactive injectable CPC for treating osteoporosis induced bone defect was obtained, and the release of the containing S-CT was controlled easily through adjusting the ratio of CO and CP.
本研究旨在探讨添加有机相壳寡糖(CO)和胶原多肽(CP)对载有鲑鱼降钙素(S-CT)的可注射磷酸钙骨水泥(CPC)控释特性的影响。采用均匀设计法确定适合临床应用的具有适宜可注射时间的基本配方,然后在体外评估改性CPC的物理特性变化、改性CPC随有机相比例的控释特性。还通过扫描电子显微镜(SEM)观察植入大鼠腹腔或浸泡在大鼠血清中的改性CPC的表面形态。结果表明,可获得改性CPC的合适配方,其可注射时间为12分钟,抗压强度为12MPa,终凝时间为40分钟。与无有机相的CPC相比,第7天后S-CT的释放速率会随着有机相比例的增加而增加。因此,获得了一种用于治疗骨质疏松性骨缺损的新型载S-CT生物活性可注射CPC,通过调节CO和CP的比例可轻松控制含S-CT的释放。