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基于壳聚糖与聚乙二醇聚合物溶液和双相磷酸钙微球的可注射性骨替代物。

Injectable bone substitute based on chitosan with polyethylene glycol polymeric solution and biphasic calcium phosphate microspheres.

机构信息

Unidade Académica de Engenharia dos Materiais - CERTBIO, Universidade Federal de Campina Grande, Campina Grande, Paraíba, Brazil.

Programa de Pós-Graduação em Medicina Veterinária - PPGMV, Universidade Federal de Campina Grande, Campina Grande, Paraíba, Brazil.

出版信息

Carbohydr Polym. 2020 Oct 1;245:116575. doi: 10.1016/j.carbpol.2020.116575. Epub 2020 Jun 10.

Abstract

We described a method to produce an injectable bone substitute consisting of a solid and liquid phase, this solid was formed using the coacervation method consisting of a mixture of Hydroxyapatite (HAp) and beta-Tricalcium Phosphate (β-TCP) which the sodium alginate - precursor - was removed during sinterization. The biphasic calcium phosphate microspheres had varying size distributions depending on the flow rate and these microspheres were mixed with a polymeric solution, chitosan and polyethylene glycol, and depending on the ratio of these phases, the injectability results varied. Nonetheless, the force required for complete removal will not disrupt the accuracy of injection into the bone defect while the biomaterial exhibited no cytotoxicity with promising results from in vivo using tibia bone defect in rabbits at 30 and 60 days whereas bone repair was more intense and accentuated with the usage of the biomaterial, and was gradually absorbed during the evaluated periods.

摘要

我们描述了一种生产可注射骨替代物的方法,该替代物由固相和液相组成,该固相是通过凝聚方法形成的,该方法由羟基磷灰石 (HAp) 和 β-磷酸三钙 (β-TCP) 的混合物组成,其中海藻酸钠 - 前体 - 在烧结过程中被去除。双相磷酸钙微球的粒径分布因流速而异,这些微球与聚合物溶液壳聚糖和聚乙二醇混合,根据这些相的比例,可注射性结果有所不同。尽管如此,完全去除所需的力不会破坏将生物材料注入骨缺损的准确性,同时生物材料表现出无细胞毒性,在 30 和 60 天的兔子胫骨骨缺损的体内研究中结果有很大的希望,而骨修复在使用生物材料时更加强烈和明显,并且在评估期间逐渐被吸收。

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