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通过体外和体内方法对两种商用骨异种移植物进行生物相容性评估。

Biocompatibility Assessment of Two Commercial Bone Xenografts by In Vitro and In Vivo Methods.

作者信息

Valencia-Llano Carlos Humberto, López-Tenorio Diego, Grande-Tovar Carlos David

机构信息

Grupo Biomateriales Dentales, Escuela de Odontología, Universidad del Valle, Calle 4B # 36-00, Cali 76001, Colombia.

Grupo de Investigación de Fotoquímica y Fotobiología, Universidad del Atlántico, Carrera 30 Número 8-49, Puerto Colombia 081008, Colombia.

出版信息

Polymers (Basel). 2022 Jun 30;14(13):2672. doi: 10.3390/polym14132672.

Abstract

Bone substitutes based on xenografts have been used for a long time in bone regeneration thanks to their inductive capacity for bone tissue regeneration. Some bone-based scaffolds have been modified by adding collagen and other proteins to improve their regenerative capacity and prevent migration and aggregation, especially particles. However, rejection of this graft has been reported due to protein residues caused by poor material preparation. We compared the in vitro and in vivo biological response of two commercial xenografts (InterOss, F1 and InterOss Collagen, F2) and a commercial porcine collagen membrane (InterCollagen Guide, F3) as a rapid degradation control. Fourier Transform Infrared Spectroscopy (FT-IR) analysis evidenced the presence of hydroxyl, orthophosphate, and carbonate groups of the xenografts and amide groups of collagen. Thermogravimetric analysis (TGA) of the xenografts demonstrated their thermal stability and the presence of a few amounts of organic material. The study by differential scanning calorimetry showed the presence of endothermic peaks typical of the dehydration of the xenografts (F1 and F2) and for the collagen membrane (F3), the beginning of structural three-dimensional protein changes. Subsequently, in vitro biocompatibility tests were carried out for the materials with and MTT cell viability with HeLa cells, demonstrating the high biocompatibility of the materials. Finally, in vivo biocompatibility was studied by implanting xenografts in biomodels (Wistar rats) at different periods (30, 60, and 90 days). The F1 xenograft (InterOss) remained remarkably stable throughout the experiment (90 days). F2 (InterOss Collagen) presented a separation of its apatite and collagen components at 60 days and advanced resorption at 90 days of implantation. Finally, the collagen membrane (F3) presented faster resorption since, at 90 days, only some tiny fragments of the material were evident. All the in vivo and in vitro test results demonstrated the biocompatibility of the xenografts, demonstrating the potential of these materials for tissue engineering.

摘要

基于异种移植物的骨替代物因其对骨组织再生的诱导能力,已在骨再生领域使用了很长时间。一些基于骨的支架已通过添加胶原蛋白和其他蛋白质进行了改良,以提高其再生能力,并防止迁移和聚集,尤其是颗粒的迁移和聚集。然而,由于材料制备不佳导致的蛋白质残留,已有关于这种移植物排斥反应的报道。我们比较了两种商业异种移植物(InterOss,F1和InterOss Collagen,F2)以及一种商业猪胶原蛋白膜(InterCollagen Guide,F3)作为快速降解对照的体外和体内生物学反应。傅里叶变换红外光谱(FT-IR)分析证明了异种移植物中羟基、正磷酸盐和碳酸盐基团以及胶原蛋白酰胺基团的存在。异种移植物的热重分析(TGA)表明了它们的热稳定性以及少量有机材料的存在。差示扫描量热法研究显示,异种移植物(F1和F2)脱水的典型吸热峰存在,而对于胶原蛋白膜(F3),则出现了结构三维蛋白质变化的开始。随后对材料进行了体外生物相容性测试,并对HeLa细胞进行了MTT细胞活力测试,证明了材料具有高生物相容性。最后,通过在不同时期(30、60和90天)将异种移植物植入生物模型(Wistar大鼠)中来研究体内生物相容性。F1异种移植物(InterOss)在整个实验(90天)中保持非常稳定。F2(InterOss Collagen)在植入60天时其磷灰石和胶原蛋白成分出现分离,在植入90天时出现进一步吸收。最后,胶原蛋白膜(F3)吸收更快,因为在90天时,仅能看到材料的一些微小碎片。所有体内和体外测试结果均证明了异种移植物的生物相容性,表明了这些材料在组织工程中的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4360/9268806/0d7497d59dae/polymers-14-02672-g001.jpg

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