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RADA 16-I肽的血液相容性评估。

Evaluation of the hemocompatibility of RADA 16-I peptide.

作者信息

Taghavi Laleh, Aramvash Asieh, Seyedkarimi Mansooreh Sadat, Malek Sabet Narges

机构信息

Department of Bioscience and Biotechnology, Malek-Ashtar University of Technology, Tehran, Iran.

出版信息

J Biomater Appl. 2018 Mar;32(8):1024-1031. doi: 10.1177/0885328217748861. Epub 2017 Dec 17.

Abstract

RADA 16-I is an ionic self-assembling peptide that can form macroscopic scaffolds through β-sheet structures which are used in favor of cell growth and tissue engineering. This peptide has also the ability to stop bleeding effectively and quickly (∼20 seconds) when applied directly to the injuries. This study is focused on coagulation process, platelet aggregation, C3 and C4 concentrations, CBC counting, hemolysis, and white blood cell morphology tests to analyze hemocompatibility of RADA 16-I at different concentrations - 0.1, 0.2, 0.3 and 0.5%. According to the results, RADA 16-I hydrogel decreased the number of blood cells, slightly increased clot formation time and platelet aggregation, and yielded negligible hemolysis and only small changes in C3 and C4 concentrations and white blood cell morphology. All by all, the in vitro tests of hemocompatibility showed no perturbation in the blood composition when the peptides were in contact with the blood. The observed rapid hemostasis might be a result of increasing local concentrations of molecules involved in the formation of clot near the peptide hydrogel, thereby making a barrier which ended up with complete hemostasis. In conclusion, our experiments strongly supported further development of biomaterials based on RADA 16-I peptide.

摘要

RADA 16-I是一种离子自组装肽,它可以通过有利于细胞生长和组织工程的β-折叠结构形成宏观支架。这种肽在直接应用于伤口时,还具有有效且快速(约20秒)止血的能力。本研究聚焦于凝血过程、血小板聚集、C3和C4浓度、全血细胞计数、溶血以及白细胞形态测试,以分析不同浓度(0.1%、0.2%、0.3%和0.5%)的RADA 16-I的血液相容性。根据结果,RADA 16-I水凝胶减少了血细胞数量,略微增加了凝血形成时间和血小板聚集,并产生了可忽略不计的溶血,且C3和C4浓度以及白细胞形态仅有微小变化。总体而言,血液相容性的体外测试表明,当肽与血液接触时,血液成分未受到干扰。观察到的快速止血可能是由于肽水凝胶附近参与凝血形成的分子局部浓度增加,从而形成了一个最终实现完全止血的屏障。总之,我们的实验有力地支持了基于RADA 16-I肽的生物材料的进一步开发。

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