Hall Barrientos Ivan Joseph, MacKenzie Graeme R, Wilson Clive G, Lamprou Dimitrios A, Coats Paul
Strathclyde Institute of Pharmacy and Biomedical Sciences (SIPBS), University of Strathclyde, Glasgow G4 0RE, UK.
School of Pharmacy, Queen's University Belfast, Belfast BT9 7BL, UK.
Materials (Basel). 2019 Jan 24;12(3):363. doi: 10.3390/ma12030363.
The evaluation of biological responses to polymeric scaffolds are important, given that the ideal scaffold should be biocompatible, biodegradable, promote cell adhesion and aid cell proliferation. The primary goal of this research was to measure the biological responses of cells against various polymeric and collagen electrospun scaffolds (polycaprolactone (PCL) and polylactic acid (PLA) polymers: PCL⁻drug, PCL⁻collagen⁻drug, PLA⁻drug and PLA⁻collagen⁻drug); cell proliferation was measured with a cell adhesion assay and cell viability using 5-bromo-2'-deoxyuridine (BrdU) and resazurin assays. The results demonstrated that there is a distinct lack of growth of cells against any irgasan (IRG) loaded scaffolds and far greater adhesion of cells against levofloxacin (LEVO) loaded scaffolds. Fourteen-day studies revealed a significant increase in cell growth after a 7-day period. The addition of collagen in the formulations did not promote greater cell adhesion. Cell viability studies revealed the levels of IRG used in scaffolds were toxic to cells, with the concentration used 475 times higher than the EC value for IRG. It was concluded that the negatively charged carboxylic acid group found in LEVO is attracting positively charged fibronectin, which in turn is attracting the cell to adhere to the adsorbed proteins on the surface of the scaffold. Overall, the biological studies examined in this paper are valuable as preliminary data for potential further studies into more complex aspects of cell behaviour with polymeric scaffolds.
鉴于理想的支架应具有生物相容性、可生物降解性、促进细胞黏附并有助于细胞增殖,因此评估对聚合物支架的生物学反应非常重要。本研究的主要目的是测量细胞对各种聚合物和胶原静电纺丝支架(聚己内酯(PCL)和聚乳酸(PLA)聚合物:PCL-药物、PCL-胶原-药物、PLA-药物和PLA-胶原-药物)的生物学反应;通过细胞黏附试验测量细胞增殖,并使用5-溴-2'-脱氧尿苷(BrdU)和刃天青试验测量细胞活力。结果表明,对任何载有氯己定(IRG)的支架,细胞生长明显缺乏,而对载有左氧氟沙星(LEVO)的支架,细胞黏附力要强得多。为期14天的研究显示,7天后细胞生长显著增加。配方中添加胶原蛋白并未促进更大的细胞黏附。细胞活力研究表明,支架中使用的IRG水平对细胞有毒,所用浓度比IRG的EC值高475倍。得出的结论是,LEVO中带负电荷的羧酸基团吸引带正电荷的纤连蛋白,而纤连蛋白又吸引细胞黏附到支架表面吸附的蛋白质上。总体而言,本文所进行的生物学研究作为潜在进一步研究聚合物支架更复杂细胞行为方面的初步数据具有重要价值。