首页> 外文期刊>Journal of biomedical materials research, Part A >Fabrication and characterization of poly(D,L-lactide-co-glycolide)/ hydroxyapatite nanocomposite scaffolds for bone tissue regeneration
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Fabrication and characterization of poly(D,L-lactide-co-glycolide)/ hydroxyapatite nanocomposite scaffolds for bone tissue regeneration

机译:骨组织再生用聚(D,L-丙交酯-共-乙交酯)/羟基磷灰石纳米复合支架的制备与表征

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Conventional methods in fabrication of scaffolds based on polymer/bioceramic composites frequently make use of solution casting then particle leaching. The residues of common organic solvents can get trapped in this technique hence provide safety concerns on final scaffold. In this study, N-methyl pyrrolidone was used as an approved solvent for parenteral pharmaceutical products especially implants with acceptable toxicological profile. A combined freeze drying and solvent casting methods were adopted for complete removal of the solvent from final scaffold structure. Biodegradable scaffolds based on poly (D,L-lactide-co-glycolide) and different percentages of nano-hydroxyapatite (25, 35, and, 45% w/w) were characterized thoroughly regarding porosity, pore distribution as well as their bioactivity and biocompatibility. The results showed 70-80% porosity with a size distribution in the range of 50-200 lm for different conditions. Bioactivity of the scaffolds was directly dependent on the bioceramic content in the samples according to the results. Composites and neat samples showed the same cytocompatibility profile.
机译:基于聚合物/生物陶瓷复合材料的支架制造中的常规方法经常利用溶液浇铸,然后进行颗粒浸出。普通有机溶剂的残留物可能会在该技术中被捕集,因此在最终支架上会带来安全隐患。在这项研究中,N-甲基吡咯烷酮被用作肠胃外药品特别是具有可接受毒理学特征的植入物的认可溶剂。采用了组合的冷冻干燥和溶剂浇铸方法,以从最终的支架结构中完全除去溶剂。基于孔隙度,孔分布及其生物活性和生物相容性,对基于聚(D,L-丙交酯-乙交酯)和不同百分比的纳米羟基磷灰石(25%,35%和45%w / w)的可生物降解支架进行了全面表征。生物相容性。结果表明,在不同条件下,孔隙度为70-80%,尺寸分布在50-200 lm范围内。根据结果​​,支架的生物活性直接取决于样品中生物陶瓷的含量。复合材料和纯净样品显示出相同的细胞相容性。

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