Department of Biomedical Engineering, Virginia Commonwealth University, Richmond, Virginia 23284-3067, USA.
J Biomed Mater Res A. 2010 Mar 15;92(4):1321-8. doi: 10.1002/jbm.a.32458.
The purpose of this study was to quantify the acute expression of tissue factor (TF) by monocytes on interaction with electrospun bioresorbable constructs. A minimal expression of TF will demonstrate the potential for scaffolds to be used as a vascular graft without enhanced risk of failure from acute thrombotic occlusion. Polydioxanone (PDO) (60, 80, 120, and 160 mg/mL) and polycaprolactone (PCL) (80, 10, and 160 mg/mL) dissolved in 1,1,1,3,3,3 hexafluoro-2-propanol (HFP) were electrospun to form fibrous scaffolds. Circular discs (10 mm diameter) of each scaffold were disinfected and seeded with human monocytes (50,000 cells/well). The discs were statically cultured under standard conditions (37 degrees C and 5% CO2), and removed after 24 h for TF analysis with an In-Cell Western assay. Fiber diameter was calculated through ImageTool analysis of scanning electron micrographs. Acute monocyte interaction with scaffolds of PCL (120 mg/mL) resulted in the lowest amount of TF expressed (4 ng/disc), whereas scaffolds of 160 mg/mL PDO elicited the highest amount of TF expressed (51 ng/disc). TF levels expressed on all scaffolds were comparable with the amount expressed on e-PTFE (20 ng/disc). Preliminary data for TF expression on scaffolds of silk (70 mg/mL and 150 mg/mL) and silk:PCL (100 mg/mL, v/v) blends (50:50 and 70:30) resulted in values of TF expression ranging from 0 to 24 ng. Results from this study reveal electrospun grafts composed of PDO and PCL provide no greater risk of failure from an acute thrombotic occlusion due to TF expression when compared with that of the standard e-PTFE graft.
这项研究的目的是量化单核细胞与静电纺生物可吸收构建物相互作用时组织因子 (TF) 的急性表达。TF 的最小表达将证明支架有可能被用作血管移植物,而不会因急性血栓闭塞而增加失败的风险。聚二氧杂环已酮 (PDO)(60、80、120 和 160 mg/mL)和聚己内酯 (PCL)(80、10 和 160 mg/mL)溶解在 1,1,1,3,3,3 六氟-2-丙醇 (HFP) 中被静电纺丝形成纤维状支架。每个支架的圆形圆盘(直径 10 毫米)被消毒并接种人单核细胞(50,000 个细胞/孔)。圆盘在标准条件(37°C 和 5%CO2)下静态培养,并在 24 小时后取出,通过 In-Cell Western 测定法分析 TF。通过对扫描电子显微镜图像的 ImageTool 分析计算纤维直径。与 PCL(120 mg/mL)支架的急性单核细胞相互作用导致表达的 TF 量最低(4 ng/盘),而 160 mg/mL PDO 支架表达的 TF 量最高(51 ng/盘)。所有支架上表达的 TF 水平与 e-PTFE(20 ng/盘)表达的量相当。丝(70 mg/mL 和 150 mg/mL)和丝:PCL(100 mg/mL,v/v)混合物(50:50 和 70:30)支架上 TF 表达的初步数据导致 TF 表达值范围为 0 至 24 ng。这项研究的结果表明,与标准 e-PTFE 移植物相比,由 PDO 和 PCL 组成的静电纺丝移植物由于 TF 表达而导致急性血栓闭塞失败的风险没有增加。