School of Chemical, Biological and Environmental Engineering, Oregon State University, Corvallis, OR 97331, USA.
J Colloid Interface Sci. 2011 Jun 1;358(1):14-24. doi: 10.1016/j.jcis.2011.03.014. Epub 2011 Mar 10.
Stable, pendant polyethylene oxide (PEO) layers were formed on medical-grade Pellethane® and Tygon® polyurethane surfaces, by adsorption and gamma-irradiation of PEO-polybutadiene-PEO triblock surfactants. Coated and uncoated polyurethanes were challenged individually or sequentially with nisin (a small polypeptide with antimicrobial activity) and/or fibrinogen, and then analyzed with time-of-flight secondary ion mass spectrometry (TOF-SIMS). Data reduction by robust principal components analysis (PCA) allowed detection of outliers, and distinguished adsorbed nisin and fibrinogen. Fibrinogen-contacted surfaces, with or without nisin, were very similar on uncoated polymer surfaces, consistent with nearly complete displacement or coverage of previously-adsorbed nisin by fibrinogen. In contrast, nisin-loaded PEO layers remained essentially unchanged upon challenge with fibrinogen, suggesting that the adsorbed nisin is stabilized within the pendant PEO layer, while the peptide-loaded PEO layer retains its ability to repel large proteins. Coatings of PEO loaded with therapeutic polypeptides on medical polymers have the potential to be used to produce anti-fouling and biofunctional surfaces for implantable or blood-contacting devices.
在医用级聚醚嵌段酰胺(Pellethane®)和热塑性聚酯弹性体(Tygon®)聚氨酯表面上,通过吸附和γ辐照聚氧化乙烯-聚丁二烯-聚氧化乙烯三嵌段表面活性剂,形成稳定的悬挂聚氧化乙烯(PEO)层。单独或依次用乳链菌肽(一种具有抗菌活性的小多肽)和/或纤维蛋白原对涂覆和未涂覆的聚氨酯进行挑战,然后用飞行时间二次离子质谱(TOF-SIMS)进行分析。通过稳健的主成分分析(PCA)进行数据简化,能够检测到异常值,并区分吸附的乳链菌肽和纤维蛋白原。在未涂覆的聚合物表面上,与乳链菌肽接触的纤维蛋白原表面(有或没有乳链菌肽)非常相似,这与纤维蛋白原几乎完全取代或覆盖先前吸附的乳链菌肽一致。相比之下,当用纤维蛋白原挑战时,负载乳链菌肽的 PEO 层基本保持不变,这表明吸附的乳链菌肽在悬挂的 PEO 层内稳定,而负载肽的 PEO 层保持排斥大蛋白的能力。在医用聚合物上负载治疗性多肽的 PEO 涂层具有用于生产抗污和生物功能表面的潜力,可用于植入物或与血液接触的设备。