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Development and biocompatibility of the injectable collagen/nano-hydroxyapatite scaffolds as in situ forming hydrogel for the hard tissue engineering application

机译:可注射胶原/纳米 - 羟基磷灰石支架的开发和生物相容性在原位形成水凝胶中的硬组织工程应用

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Injectable hydrogels attract more attention to hard tissue engineering for the fulfilment of the defects with irregular shapes. Therefore, the researchers investigated the biocompatibility and immune response to the injectable PCL-PEG-PCL-Col/nHA hydrogels in a mouse model. The histological examination was done via H&E. The activation of the immune cells was evaluated by using antibodies against the CD68, CD4, and CD8 markers. The expression of CCL-2, BCL-2, IL-10, and CD31 genes was measured. Moreover, serum levels of the ALT, ALP, AST, and Urea were detected. The results of the chemical analysis showed that the collagen and Nano-hydroxyapatite were successfully integrated into the PCL-PEG-PCL hydrogels. The histological examination revealed a delayed biodegradation rate after the addition of the collagen and Nano-hydroxyapatite. No prominent pro-inflammatory response was found at the site of the injection. There are no significant differences in the levels of the CD68 and CD8/CD4 lymphocyte ratio among groups ( p ?.05). The expression of the CD31, IL-10 was significantly increased in the PCL-PEG-PCL-Col/nHA hydrogel ( p ?.05). These in?vivo results demonstrated that the injectable PCL-PEG-PCL-Col/nHA hydrogels are biocompatible and suitable for further research in hard tissue regeneration.
机译:可注射水凝胶吸引更多地关注硬组织工程,以满足具有不规则形状的缺陷。因此,研究人员在小鼠模型中研究了对可注射的PCL-PEG-PCL-COL / NHA水凝胶的生物相容性和免疫应答。通过H&E进行组织学检查。通过使用针对CD68,CD4和CD8标记物的抗体来评价免疫细胞的激活。测定CCL-2,Bcl-2,IL-10和CD31基因的表达。此外,检测到ALT,ALP,AST和尿素的血清水平。化学分析的结果表明,胶原和纳米 - 羟基磷灰石成功集成到PCL-PEG-PCL水凝胶中。组织学检查显示添加胶原和纳米羟基磷灰石后的延迟的生物降解速率。在注射部位发现没有突出的促炎反应。 CD68和CD8 / CD4淋巴细胞比在群体中没有显着差异(P>Δ05)。在PCL-PEG-PCL-COL / NHA水凝胶中显着增加CD31,IL-10的表达(P?.05)。这些在α体内结果表明,可注射的PCL-PEG-PCL-COL / NHA水凝胶是生物相容性的,适用于在硬组织再生中进一步研究。

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