Direct Probing and Modeling of Adsorbed Layers of Surfactant/Lipid/Protein Mixtures at Air/Water Interfaces

空气/水界面表面活性剂/脂质/蛋白质混合物吸附层的直接探测和建模

• 批准号: 0457289
• 负责人: Elias Franses
• 金额: $ 16万
• 依托单位: Purdue University
• 依托单位国家: 美国
• 项目类别: Standard Grant
• 财政年份: 2005
• 资助国家: 美国
• 起止时间: 2005-02-01 至 2007-01-31
• 项目状态: 已结题
• 来源: https://www.nsf.gov/awardsearch/showAward?AWD_ID=0457289&HistoricalAwards=false
• 关键词: Direct; Probing; Modeling; Adsorbed; Layers

ABSTRACT - 0457289Purdue UniversityProject Summary The health related project examines how to measure, characterize, and control the extent and rate of adsorption of surfactants, lipids, and proteins at air/water interfaces by understanding the fundamental phenomena and mechanisms. Such adsorption determines the equilibrium and dynamic surface tension, which affects free surface flows involving bubbles, drops, and liquid jets. The dynamic surface tension at constant and pulsating area condition is measured and modeled. Unique features include: (i) direct probing of the interfacial layers of aqueous solutions or dispersions of surfactants, lipids, proteins, and their mixtures with quantitative ellipsometry and infrared spectroscopy; (ii) control of adsorption of insoluble lipids by controlling the method of lipid dispersion preparation; (iii) understanding of competitive adsorption of lipids and serum proteins (albumin or fibrinogen); (iv) models of micellar dissolution and diffusion, and their effect on adsorption dynamics; and (v) studies of rates and mechanisms by which lipids reach the surface where they produce very low dynamic surface tensions (less then 10 mN/m during surface compression); and (vi) studies of rates and mechanisms by which lipids can exclude or expel soluble proteins from the interfacial region. The surface layer composition of lipid/soluble protein dispersions is probed for the first time by quantitative IR spectroscopy and ellipsometry. Thermodynamic and interfacial mass transfer principles are applied for the first time for predicting and controlling how lipids can adsorb and expel proteins from the interface. This could be important for processes affected by foam stability and breakup, such as bioreactors, washing machines, and foam-based separations, and in lung surfactants design and formulations. The results are important in processes involving drop deformation and breakup, as in DNA and protein microarrays, inkjet printing processes, and the design and uses of agricultural pesticide sprays. Since albumin and fibrinogen serum proteins can leak to the alveoli and inhibit the function of lung surfactant, understanding the factors which affect their displacement could lead in biomedical engineering applications of treatment of lungs injured by the acute respiratory distress syndrome (ARDS). This may have direct and indirect implications in effectively treating or alleviating infant and adult respiratory diseases. Other societal impacts could be improved and leaner pesticide formulations, for reducing environmental pollution. This research will also lead to effective training of graduate and undergraduate students, who will be exposed to state-of-the-art experimentation and modeling. The results will be used in part in a graduate course and an undergraduate course. Developing and refining surface layer characterization will improve the infrastructure of research and education in interfacial, biomedical, biochemical, and mineral engineering. The P.I. is committed to diversity in recruiting graduate and undergraduate students for this project, and has worked with several members of underrepresented groups over the past five years. The results may lead to partnerships with medical researchers or professionals and with industrial and academic researchers dealing with surfactant, lipid, and protein applications.

摘要 - 0457289普渡大学项目摘要 该健康相关项目研究如何通过了解基本现象和机制来测量、表征和控制表面活性剂、脂质和蛋白质在空气/水界面的吸附程度和速率。这种吸附决定了平衡和动态表面张力，这会影响涉及气泡、液滴和液体射流的自由表面流动。对恒定和脉动面积条件下的动态表面张力进行了测量和建模。独特的功能包括：（i）通过定量椭圆光度法和红外光谱法直接探测表面活性剂、脂质、蛋白质及其混合物的水溶液或分散体的界面层； (ii)通过控制脂质分散体制备方法来控制不溶性脂质的吸附； (iii) 了解脂质和血清蛋白（白蛋白或纤维蛋白原）的竞争吸附； (iv) 胶束溶解和扩散模型及其对吸附动力学的影响； (v) 研究脂质到达表面的速率和机制，在表面产生非常低的动态表面张力（表面压缩期间小于 10 mN/m）； (vi) 研究脂质从界面区域排除或驱逐可溶性蛋白质的速率和机制。首次通过定量红外光谱和椭圆光度法探测脂质/可溶性蛋白质分散体的表面层组成。热力学和界面传质原理首次应用于预测和控制脂质如何从界面吸附和排出蛋白质。这对于受泡沫稳定性和分解影响的过程（例如生物反应器、洗衣机和基于泡沫的分离）以及肺表面活性剂的设计和配方来说可能很重要。这些结果对于涉及液滴变形和破碎的过程非常重要，例如 DNA 和蛋白质微阵列、喷墨打印过程以及农业杀虫剂喷雾剂的设计和使用。由于白蛋白和纤维蛋白原血清蛋白可以渗漏到肺泡并抑制肺表面活性物质的功能，因此了解影响其位移的因素可能会导致在治疗急性呼吸窘迫综合征（ARDS）所致肺部损伤的生物医学工程应用中。这可能对有效治疗或减轻婴儿和成人呼吸道疾病产生直接和间接的影响。其他社会影响可以通过改进和更精简的农药配方来减少环境污染。这项研究还将对研究生和本科生进行有效的培训，让他们接触最先进的实验和建模。结果将部分用于研究生课程和本科课程。开发和完善表面层表征将改善界面、生物医学、生物化学和矿物工程方面的研究和教育基础设施。 P.I.致力于为该项目招收研究生和本科生的多元化，并在过去五年中与代表性不足群体的多名成员合作。研究结果可能会导致与医学研究人员或专业人士以及与处理表面活性剂、脂质和蛋白质应用的工业和学术研究人员建立伙伴关系。