Desai N P, Hubbell J A
Department of Chemical Engineering, University of Texas, Austin 78712-1062.
Biomaterials. 1992;13(8):505-10. doi: 10.1016/0142-9612(92)90101-s.
Polyethylene terephthalate films surface modified with polyethylene oxide of mol wt 18,500 g/mol (18.5 k) by a previously described technique, were implanted in the peritoneal cavity of mice, along with their respective untreated controls, for periods of 1-28 d. The implants were retrieved and examined for tissue reactivity and cellular adherence. The control polyethylene terephthalate surfaces showed an initial inflammatory reaction followed by an extensive fibrotic response with a mean thickness of 60 microns at 28 d. By contrast, polyethylene oxide-modified polyethylene terephthalate showed only a mild inflammatory response and no fibrotic encapsulation throughout the implantation period: at 28 d a cellular monolayer was observed. Apparently either the polyethylene oxide-modified surface was stimulating less inflammation, which was in turn stimulating less fibroblastic overgrowth, or the cellular adhesion to the polyethylene oxide-modified surface was too weak to support cellular multilayers.
采用先前描述的技术,用分子量为18500 g/mol(18.5 k)的聚环氧乙烷对聚对苯二甲酸乙二酯薄膜进行表面改性,将其与各自未处理的对照物一起植入小鼠腹腔,持续1 - 28天。取出植入物,检查其组织反应性和细胞黏附情况。对照聚对苯二甲酸乙二酯表面显示出初始炎症反应,随后是广泛的纤维化反应,在28天时平均厚度为60微米。相比之下,聚环氧乙烷改性的聚对苯二甲酸乙二酯在整个植入期仅表现出轻微的炎症反应,且无纤维化包囊形成:在28天时观察到细胞单层。显然,要么是聚环氧乙烷改性表面引发的炎症较少,进而刺激的成纤维细胞过度生长较少,要么是细胞对聚环氧乙烷改性表面的黏附力太弱,无法支持细胞多层生长。