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首页> 外文期刊>BioMedical Engineering OnLine >Porous deproteinized bovine bone scaffold with three-dimensional localized drug delivery system using chitosan microspheres
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Porous deproteinized bovine bone scaffold with three-dimensional localized drug delivery system using chitosan microspheres

机译:使用壳聚糖微球的三维局部药物递送系统多孔牛脱蛋白牛骨支架

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Bone substation grafts, such as hydroxyapatite (HA) and tricalciumphosphate (TCP), have been extensively used in clinical applications, but evidence suggests that they offer poor osteoinductive properties compared to allografts and autografts. In order to increase bone growth with such grafts, Bone Morphogenetic Protein 2 (BMP-2) was incorporated into a three dimensional reservoir. The purpose of the present study was to develop a novel drug delivery system which is capable of controlled release of BMP-2. DBB were prepared from bovine cancellous bone harvested from fetal bovine femur or tibia and then sinting at 1000°C. BMP-2-loaded chitosan (CS) microspheres were fabricated by cross-linking. Then the treated DBB powders were blended with chitosan microspheres solution. Finally, the composites were lyophilized with a freeze dryer to obtain the DBB/CMs scaffolds. X-ray diffractor (XRD), scanning electron microscopy (SEM) and Fourier transform infrared (FT-IR) were used to characterize the sample. The quantification of the delivery profile of BMP-2 was determined using an enzyme-linked immunosorbent assay (ELISA) kit. The in vitro assays were to characterize the biocompatibility of this composite. In this study, BMP-2/Chitosan (CS) microspheres were successively loaded onto a deproteinized bovine bone (DBB) scaffold. The release profile of BMP-2 indicated an initial burst release followed by a more even sustained release. An in vitro bioactivity assay revealed that the encapsulated growth factor was biologically active. The cell culture assay suggest that the excellent biocompatibility of the DBB- BMP-2/CS. Therefore, this novel microsphere scaffold system can be effectively used in current tissue engineering applications.
机译:诸如羟基磷灰石(HA)和磷酸三钙(TCP)之类的骨置换移植物已广泛用于临床应用,但是有证据表明,与同种异体移植物和自体移植物相比,它们的骨诱导性能较差。为了利用这种移植物增加骨生长,将骨形态发生蛋白2(BMP-2)合并到三维储库中。本研究的目的是开发一种新型的药物递送系统,该系统能够控制BMP-2的释放。从胎牛股骨或胫骨中收集的牛松质骨制备DBB,然后在1000°C下犯罪。通过交联制备了载有BMP-2的壳聚糖(CS)微球。然后将处理过的DBB粉末与壳聚糖微球溶液混合。最后,将复合物用冷冻干燥机冻干以获得DBB / CMs支架。使用X射线衍射仪(XRD),扫描电子显微镜(SEM)和傅里叶变换红外(FT-IR)来表征样品。使用酶联免疫吸附测定(ELISA)试剂盒确定BMP-2的传递模式的量化。体外测定法旨在表征该复合物的生物相容性。在这项研究中,BMP-2 /壳聚糖(CS)微球相继加载到脱蛋白的牛骨(DBB)支架上。 BMP-2的释放曲线表明初始爆发释放,随后是更均匀的持续释放。体外生物活性测定表明,包封的生长因子具有生物活性。细胞培养测定表明,DBB-BMP-2 / CS具有优异的生物相容性。因此,这种新颖的微球支架系统可以有效地用于当前的组织工程应用中。

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