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首页> 外文期刊>Colloids and Surfaces, B. Biointerfaces >Modification of lipid transport through a microporous PTFE membrane wall grafted with poly(ethylene glycol)
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Modification of lipid transport through a microporous PTFE membrane wall grafted with poly(ethylene glycol)

机译:用聚(乙二醇)接枝的微孔PTFE膜壁改性脂质传输

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摘要

Lipid interaction with ePTFE arterial prostheses has been identified in previous studies as being one of the causes leading to graft failure. Our research group has previously proposed a mathematical model of the lipid uptake mechanism in Teflon Prostheses as two first-order reactions based on in vitro experiments. The present study sought to determine whether surface modification with methoxy poly(ethylene glycol) (MPEG) derivatives of various molecular weights modified the kinetics of lipid transport through microporous PTFE membranes. PTFE films and ePTFE tubular microporous membranes were functionalized with amine groups using an ammonia radio frequency glow discharge plasma. MPEGs were conjugated as succinimidyl activated esters on the aminated-PTFE surfaces. In order to maximize the surface coverage by MPEGs, the conjugation reactions were performed under conditions near the cloud point. XPS and contact angle analyses confirmed the ability to covalently graft activated MPEGs to amino-functionalized PTFE surfaces of the films and microporous membranes. Lipid adsorption onto PTFE films monitored by ATR-FTIR spectroscopy demonstrated that the surface coverage by each MPEG resulted in a significant decrease in lipid adsorption regardless of the MPEG molecular weight (M_w). ATR-FTIR spectroscopy and FTIR microscopy were used to characterize lipid adsorption onto the PTFE microporous membrane surface and lipid absorption across the microporous structure, respectively. The surface modification by the MPEG, regardless of its M_w, resulted in both decrease of lipid adsorption onto the surface of the modified membrane and delayed lipid uptake kinetics. It was concluded that MPEG anchored to the surface of a PTFE microporous membrane may modify mass transport through the ePTFE porous structure.
机译:在以前的研究中已经确定了与EPTFE动脉假体的脂质相互作用是导致移植失败的原因之一。我们的研究组先前已经提出了Teflon Prestheses中的脂质摄取机制的数学模型,作为基于体外实验的两次一阶反应。本研究试图确定各种分子量的甲氧基聚(乙二醇)(MPEG)衍生物的表面改性是否通过微孔PTFE膜修饰了脂质传输的动力学。使用氨射频辉光放电等离子体,用胺基团官能化PTFE薄膜和ePTFE管状微孔膜。 MPEG在酰胺-PTFE表面上以琥珀酰亚胺激活酯缀合。为了通过MPEG最大化表面覆盖,在浊点附近的条件下进行缀合反应。 XPS和接触角分析证实了将共价接枝活化的MPEG的能力与膜和微孔膜的氨基官能化的PTFE表面。通过ATR-FTIR光谱监测的PTFE膜上的脂质吸附表明,无论MPEG分子量(M_W)如何,每个MPEG的表面覆盖导致脂质吸附的显着降低。 ATR-FTIR光谱和FTIR显微镜分别用于在PTFE微孔膜表面和微孔结构上的脂质吸收来表征脂质吸附。由MPEG的表面改性无论其m_W如何导致脂质吸附的降低到改性膜的表面和延迟脂质摄取动力学。得出结论,将MPEG固定在PTFE微孔膜的表面上可通过EPTFE多孔结构改变质量传输。

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