Hemocompatibility And Cytotoxicity Of Small-Diameter Bioabsorbable Tissue-Engineered Vascular Grafts Depending On Anti-Thrombogenic And Antimicrobial Coating

IF 0.2 Q4 MEDICINE, GENERAL & INTERNAL Russian Open Medical Journal Pub Date : 2021-12-30 DOI:10.15275/rusomj.2021.0423
Eugenia O. Krivkina, E. Velikanova, E. A. Senokosova, M. Khanova, T. V. Glushkova, L. Antonova, L. Barbarash
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Abstract

Anti-thrombogenic and antimicrobial coatings of polymer grafts constitute a promising approach to preventing infection and thrombosis of vascular grafts. The objective was to study the hemocompatibility and cytotoxicity of PHBV/PCL grafts with iloprost and amphiphilic coating. Material and Methods — Polymer matrices were manufactured by electrospinning a mixture of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) and poly(ε-caprolactone) (PCL) polymers. Several matrices were modified by complexation between polyvinylpyrrolidone (PVP) and cationic amphiphile and/or iloprost. The amphiphile was covalently cross-linked to the surface of other PHBV/PCL matrices. Unmodified PHBV/PCL matrices were used as the control group. Hemocompatibility and cytotoxicity of scaffolds before and after the modification were evaluated. Results — The hemocompatibility assessment revealed that hemolysis degree did not exceed normal values in all types of matrices. The PHBV/PCL/PVP matrices had increased platelet aggregation on the surface of the grafts. Subsequent addition of iloprost and amphiphile resulted in a sevenfold reduction of platelet aggregation. In PHBV/PCL/PVP matrices, the degree of platelet adhesion increased without changing the platelet deformation index values. Iloprost and amphiphilic coating of PHBV/PCL/PVP matrices diminished the number of adhered platelets and platelet deformation index by 1.5 times. The amphiphile, covalently cross-linked to PHBV/PCL matrices, caused a negative effect on the platelet adhesion, aggregation, and deformation index values. Evaluation of cytotoxicity of PHBV/PCL/PVP matrices, coated with iloprost and/or cationic amphiphile, demonstrated a slight decline in the rates of cell growth and proliferation after three days. Moreover, after three days, cell deaths and a sharp drop in the cell index values were noted in PHBV/PCL matrices with covalently cross-linked amphiphile. Conclusion — Iloprost and amphiphilic coating of PHBV/PCL grafts has increased their hemocompatibility. Also, there were no signs of cytotoxicity while using the complexation technique. However, covalently cross-linked amphiphile caused an increase in the cytotoxicity of matrices, which may have been indicative of the negative effect observed in this type of surface modification.
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基于抗血栓形成和抗菌涂层的小直径生物可吸收组织工程血管移植物的血液相容性和细胞毒性
聚合物移植物的抗血栓和抗菌涂层是预防血管移植物感染和血栓形成的一种很有前途的方法。目的研究伊洛前列素和两亲性涂层对PHBV/PCL移植物的血液相容性和细胞毒性。材料和方法——通过静电纺丝聚(3-羟基丁酸酯-共-3-羟基戊酸酯)(PHBV)和聚(ε-己内酯)(PCL)聚合物的混合物来制备聚合物基质。通过聚乙烯吡咯烷酮(PVP)与阳离子两亲物和/或伊洛前列素的络合作用对几种基质进行了改性。将该两亲物共价交联到其他PHBV/PCL基质的表面。使用未修饰的PHBV/PCL基质作为对照组。评价了改性前后支架的血液相容性和细胞毒性。结果——血液相容性评估显示,所有类型基质的溶血程度均未超过正常值。PHBV/PCL/PVP基质增加了移植物表面的血小板聚集。随后加入伊洛前列素和两亲试剂,导致血小板聚集减少7倍。在PHBV/PCL/PVP基质中,血小板粘附程度增加,而不改变血小板变形指数值。Iloprost和PHBV/PCL/PVP基质的两亲性涂层使粘附的血小板数量和血小板变形指数减少了1.5倍。与PHBV/PCL基质共价交联的两亲物对血小板粘附、聚集和变形指数值产生负面影响。用伊洛前列素和/或阳离子两亲物包被的PHBV/PCL/PVP基质的细胞毒性评估显示,三天后细胞生长和增殖速率略有下降。此外,三天后,在具有共价交联两亲物的PHBV/PCL基质中观察到细胞死亡和细胞指数值的急剧下降。结论:Iloprost和PHBV/PCL移植物的两亲性涂层提高了其血液相容性。此外,在使用络合技术时没有细胞毒性的迹象。然而,共价交联的两亲物导致基质的细胞毒性增加,这可能表明在这种类型的表面修饰中观察到的负面影响。
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来源期刊
Russian Open Medical Journal
Russian Open Medical Journal MEDICINE, GENERAL & INTERNAL-
CiteScore
0.90
自引率
0.00%
发文量
39
期刊介绍: Russian Open Medical Journal (RusOMJ) (ISSN 2304-3415) is an international peer reviewed open access e-journal. The website is updated quarterly with the RusOMJ’s latest original research, clinical studies, case reports, reviews, news, and comment articles. This Journal devoted to all field of medicine. All the RusOMJ’s articles are published in full on www.romj.org with open access and no limits on word counts. Our mission is to lead the debate on health and to engage, inform, and stimulate doctors, researchers, and other health professionals in ways that will improve outcomes for patients. The RusOMJ team is based mainly in Saratov (Russia), although we also have editors elsewhere in Russian and in other countries.
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