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Bacterial cellulose membrane functionalized with hydroxiapatite and anti-bone morphogenetic protein 2: A promising material for bone regeneration

机译:用羟基磷灰石和抗骨形态发生蛋白功能化的细菌纤维素膜2:一种有希望的骨再生材料

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摘要

Bone tissue engineering seeks to adequately restore functions related to physical and biological properties, aiming at a repair process similar to natural bone. The use of compatible biopolymers, such as bacterial cellulose (BC), as well as having interesting mechanical characteristics, presents a slow in vivo degradation rate, and the ability to be chemically modified. To promote better bioactivity towards BC, we synthesized an innovative BC membrane associated to hydroxyapatite (HA) and anti-bone morphogenetic protein antibody (anti-BMP-2) (BC-HA-anti-BMP-2). We present the physical-chemical, biological and toxicological characterization of BC-HA-anti-BMP-2. Presence of BC and HA components in the membranes was confirmed by SEM-EDS and FTIR assays. No toxic potential was found in MC3T3-E1 cells by cytotoxicity assays (XTT Assay and Clonogenic Survival), genotoxicity (Comet Assay) and mutagenicity (Cytokinesis-blocked micronucleus Test). The in vitro release kinetics of anti-BMP-2 antibodies detected gradually reducing antibody levels, reducing approximately 70% in 7 days and 90% in 14 days. BC-HA-anti-BMP-2 increased SPP1, BGLAP, VEGF, ALPL, RUNX2 and TNFRSF11B expression, genes involved in bone repair and also increased mineralization nodules and phosphatase alcalin (ALP) activity levels. In conclusion, we developed BC-HA-anti-BMP-2 as an innovative and promising biomaterial with interesting physical-chemical and biological properties which may be a good alternative to treatment with commercial BMP-2 protein.
机译:骨组织工程学试图充分恢复与物理和生物学特性有关的功能,其目标是类似于天然骨的修复过程。使用相容的生物聚合物,例如细菌纤维素(BC),以及具有令人感兴趣的机械特性,会导致体内降解速度缓慢,并具有化学修饰的能力。为了促进对BC更好的生物活性,我们合成了与羟基磷灰石(HA)和抗骨形态发生蛋白抗体(anti-BMP-2)(BC-HA-anti-BMP-2)相关的创新BC膜。我们介绍了BC-HA-抗BMP-2的物理化学,生物学和毒理学表征。通过SEM-EDS和FTIR分析证实了膜中BC和HA成分的存在。通过细胞毒性测定(XTT测定和克隆形成存活),基因毒性(彗星测定)和诱变性(细胞分裂阻滞微核试验),在MC3T3-E1细胞中未发现潜在毒性。检测到抗BMP-2抗体的体外释放动力学逐渐降低了抗体水平,在7天内降低了约70%,在14天内降低了90%。 BC-HA-anti-BMP-2增加了SPP1,BGLAP,VEGF,ALPL,RUNX2和TNFRSF11B的表达,参与骨骼修复的基因,还增加了矿化结节和磷酸酶alcalin(ALP)的活性。总而言之,我们开发了BC-HA-anti-BMP-2,它是一种具有创新意义的有前途的生物材料,具有有趣的物理化学和生物学特性,可能是商业BMP-2蛋白治疗的良好选择。

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