首页> 美国卫生研究院文献>The Saudi Dental Journal >Growth factor release and enhanced encapsulated periodontal stem cells viability by freeze-dried platelet concentrate loaded thermo-sensitive hydrogel for periodontal regeneration
【2h】

Growth factor release and enhanced encapsulated periodontal stem cells viability by freeze-dried platelet concentrate loaded thermo-sensitive hydrogel for periodontal regeneration

机译:冻干血小板浓缩液负载的热敏水凝胶释放生长因子并增强封装的牙周干细胞活力从而促进牙周再生

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Periodontium regeneration is a highly challenging process as it requires the regeneration of three different tissues simultaneously. The aim of this study was to develop a composite material that can be easily applied and can sufficiently deliver essential growth factors and progenitor cells for periodontal tissue regeneration.Freeze-dried platelet concentrate (FDPC) was prepared and incorporated in a thermo-sensitive chitosan/β-glycerol phosphate (β-GP) hydrogel at concentrations of 5, 10, or 15 mg/ml. The viscosity of the hydrogels was investigated as the temperature rises from 25 °C to 37 °C and the release kinetics of transforming growth factor (TGF-β1), platelet-derived growth factor (PDGF-BB) and insulin-like growth factor (IGF-1) were investigated at four time points (1 h, 1 day, 1 week, 2 weeks). Periodontal ligament stem cells (PDLSCs) were isolated from human third molars and encapsulated in the different hydrogel groups. Their viability was investigated after 7 days in culture in comparison to standard culture conditions and non FDPC-loaded hydrogel.Results showed that loading FDPC in the hydrogel lowered the initial viscosity in comparison to the unloaded control group and did not affect the sol-gel transition in any group. All FDPC-loaded hydrogel groups exhibited sustained release of TGF-β1 and PDGF-BB for two weeks with significant difference between the different concentrations. The loading of 10 and 15 mg/ml of FDPC in the hydrogel increased the PDLSCs viability significantly compared to the unloaded hydrogel and was comparable to the standard culture conditions.Accordingly, it may be concluded that loading FDPC in a chitosan/β-GP hydrogel can offer enhanced injectability, a sustained release of growth factors and increased viability of encapsulated stem cells which can be beneficial in periodontium tissue regeneration.
机译:牙周膜再生是一个极富挑战性的过程,因为它需要同时再生三个不同的组织。这项研究的目的是开发一种复合材料,该复合材料易于使用,并且可以为牙周组织再生提供足够的必需生长因子和祖细胞。制备了冻干血小板浓缩物(FDPC)并将其掺入热敏壳聚糖/浓度为5、10或15μmg/ ml的β-甘油磷酸酯(β-GP)水凝胶。研究了温度从25°C升至37°C时水凝胶的粘度以及转化生长因子(TGF-β1),血小板衍生生长因子(PDGF-BB)和胰岛素样生长因子(TGF-β1)的释放动力学在四个时间点(1小时,1天,1周,2周)对IGF-1进行了研究。从人的第三磨牙中分离出牙周膜干细胞(PDLSC),并封装在不同的水凝胶组中。与标准培养条件和未装载FDPC的水凝胶相比,在培养7天后对其活力进行了研究。结果表明,将FDPC装载在水凝胶中比未装载的对照组降低了初始粘度,并且不影响溶胶-凝胶转变在任何组中。所有加载了FDPC的水凝胶组均表现出TGF-β1和PDGF-BB的持续释放两个星期,不同浓度之间存在显着差异。与未加载的水凝胶相比,在水凝胶中加载10和15μmg/ ml的FDPC可以显着提高PDLSCs的活力,并且与标准培养条件相当。因此,可以得出结论,在壳聚糖/β-GP水凝胶中加载FDPC。可以提供增强的注射性,生长因子的持续释放和封装的干细胞活力的增加,这可能对牙周组织的再生有益。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号