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Enhanced angiogenesis by multiple release of platelet-rich plasma contents and basic fibroblast growth factor from gelatin hydrogels.

机译:通过从明胶水凝胶中多次释放富含血小板的血浆含量和碱性成纤维细胞生长因子来增强血管生成。

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摘要

The objective of this study is to evaluate the angiogenic effects induced by biodegradable gelatin hydrogel granules incorporating mixed platelet-rich plasma (PRP) growth factor mixture (PGFM) and bioactive basic fibroblast growth factor (bFGF). The PRP was prepared by a double-spinning technique for isolating animal bloods, followed by treatment with different concentrations of calcium chloride (CaCl(2)) solution. The CaCl(2) solution treatment activated the platelets of PRP, allowing the release of various growth factors, such as platelet-derived growth factor (PDGF)-BB, vascular endothelial growth factor (VEGF), transforming growth factor (TGF)-β(1), and epithelial growth factor (EGF). In the PRP treated with different CaCl(2) solutions, high amounts of representative platelet growth factor, PDGF-BB, VEGF, EGF, and TGF-β(1) were detected in the CaCl(2) concentrations of 1, 2, and 4wt.% compared with higher or lower ones. The PRP treated was impregnated into gelatin hydrogel granules freeze-dried at 37°C for 1h, and then the percentage of PGFM desorbed from the gelatin hydrogel granules was evaluated. The percentages of PDGF-BB, VEGF, EGF, and TGF-β(1) desorbed tended to decrease with decreasing CaCl(2) concentration. Taken together, the CaCl(2) concentration to activate PRP for PGFM release was fixed at 2wt.%. In vitro release tests demonstrated that the PGFM was released from the gelatin hydrogel granules with time. For the gelatin hydrogels incorporating PGFM and bFGF, the time profile of PDGF-BB or bFGF release was in good correspondence with that of gelatin hydrogel degradation. The gelatin hydrogel granules incorporating mixed PGFM and bFGF were prepared and intramuscularly injected to a mouse leg ischemia model to evaluate the angiogenic effects in terms of histological and laser Doppler perfusion imaging examinations. As controls, hydrogel granules incorporating bFGF, PGFM, and platelet-poor plasma were used for the angiogenic evaluation. The number of blood vessels newly formed and the percentage of anti-α-smooth muscle actin antibody-positive cells increased around ischemic sites injected with the gelatin hydrogel granules incorporating mixed PGFM and bFGF, in marked contrast to other control groups. The blood reperfusion level of ischemic tissues was enhanced by the hydrogel granules incorporating mixed PGFM and bFGF, whereas no enhancement was observed for other groups. It is concluded that the dual-release system of PGFM and bFGF from gelatin hydrogel granules shows promise as a method to enhance angiogenic effects.
机译:这项研究的目的是评估由可生物降解的明胶水凝胶颗粒与混合的富含血小板的血浆(PRP)生长因子混合物(PGFM)和生物活性碱性成纤维细胞生长因子(bFGF)混合产生的血管生成作用。 PRP是通过双重纺丝技术制备的,用于分离动物血液,然后用不同浓度的氯化钙(CaCl(2))溶液处理。 CaCl(2)溶液处理激活了PRP的血小板,从而释放了多种生长因子,例如血小板衍生的生长因子(PDGF)-BB,血管内皮生长因子(VEGF),转化生长因子(TGF)-β (1)和上皮生长因子(EGF)。在用不同的CaCl(2)解决方案处理的PRP中,在CaCl(2)的浓度为1,2和3中检测到大量的代表性血小板生长因子,PDGF-BB,VEGF,EGF和TGF-β(1)。 4wt。%与更高或更低的相比。将处理过的PRP浸入在37℃冷冻干燥1小时的明胶水凝胶颗粒中,然后评估从明胶水凝胶颗粒中解吸的PGFM的百分比。随着CaCl(2)浓度的降低,PDGF-BB,VEGF,EGF和TGF-β(1)的释放百分比倾向于降低。两者合计,以激活PFM释放PGFM的CaCl(2)浓度固定为2wt。%。体外释放试验表明,PGFM随时间从明胶水凝胶颗粒中释放出来。对于掺有PGFM和bFGF的明胶水凝胶,PDGF-BB或bFGF释放的时间曲线与明胶水凝胶降解的时间曲线非常吻合。制备掺有混合PGFM和bFGF的明胶水凝胶颗粒,并将其肌肉注射到小鼠腿部缺血模型中,以根据组织学和激光多普勒灌注成像检查评估血管生成作用。作为对照,将掺入bFGF,PGFM和贫血小板血浆的水凝胶颗粒用于血管生成评估。与其他对照组相比,在注入掺有PGFM和bFGF的明胶水凝胶颗粒的缺血部位周围,新形成的血管数量和抗α-平滑肌肌动蛋白抗体阳性细胞的百分比增加。掺入PGFM和bFGF的水凝胶颗粒可提高缺血组织的血液再灌注水平,而其他组则未见增强。结论是明胶水凝胶颗粒的PGFM和bFGF双重释放系统显示出有望作为增强血管生成作用的方法。

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