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UNS: Collaborative Research: Describing Macromolecular Transport through Chemically-Tuned Nanoporous Membranes via Theory, Computation, and Experiment

UNS: Collaborative Research: Describing Macromolecular Transport through Chemically-Tuned Nanoporous Membranes via Theory, Computation, and Experiment
UNS:合作研究:通过理论、计算和实验描述通过化学调节的纳米多孔膜的大分子运输
批准号:
1511835
负责人:
Bryan Boudouris
金额:
$16.47万
依托单位:
依托单位国家:
美国
项目类别:
Standard Grant
财政年份:
2015
资助国家:
美国
项目状态:
已结题
起止时间:
2015-07-01 至 2018-06-30

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中文摘要
翻译
合作提案#1511835/#1511862 Boudouris,Bryan/Phillip,William膜在许多分离过程中至关重要,在这些分离过程中,需要的产品与不需要的物种分离。特别是,许多新兴的药物治疗需要在活性长链生物大分子离开生物制药反应器时进行纯化。这些生物大分子最近已被批准用于治疗各种危及生命的疾病,包括癌症和自身免疫性疾病。然而,大规模生产和提纯这些重要材料的高昂成本,往往会转移到患者身上,阻碍了它们在临床实践中的广泛应用。这项提案将评估这些重要的治疗剂等大分子是如何通过膜材料运输的。通过将实验结果与理论预测和计算模拟相结合,将形成一个关于如何通过小孔进行传输的完整图景。这开启了产生更具成本效益的纯化系统的可能性,这可以降低患者治疗的成本,并打开一种经济的方法来治疗一些毁灭性的疾病。大分子物种的运输在一系列具有重要技术意义的膜分离应用(例如,治疗性蛋白质的分离)中是至关重要的。然而,溶解的高分子链如何在没有外部刺激(如外加电场)的情况下,在热力学平衡下穿过孔径等于或小于链的流体力学直径的膜的确切机制还不完全清楚。因此,迫切需要确定孔大小、孔化学和溶液环境如何影响大分子在结构良好的膜中的界面传输。在这里,实验技术、热力学理论和计算模型的结合被用来将纳米尺度的现象与宏观层面的物理观测联系起来。这一愿景将导致对通过小孔的化学选择性大分子传输的分子到膜层面的理解;这种理解将通过先进的材料表征方法将连续介质传输属性与分子模型联系起来,将使PI能够在一些当前和新兴的分离平台中为化学选择性膜的合理设计开发设计原则。在尺寸和化学选择性膜领域产生结构-性质-性能关系将导致改进膜设计。反过来,这将有助于降低生产成本,提高生产普通消费品和更高价值产品(例如,治疗性药品)所需的许多工艺的能效。因此,这项工作的成功完成有可能对当前的制造工艺产生积极的影响。此外,普渡大学和圣母大学之间的合作将使两所大学的学生能够在合作机构开展工作。通过这种方式,学生将拥有更多样化的教育体验。除了研究生,本科生和高中生将对这个项目进行研究。特别是,这名高中生将成为美国化学学会种子项目的一部分。因此,这项工作有能力推进基础膜科学,并影响具有不同社会经济和教育背景的独特的跨学科科学家和工程师群体。
英文摘要
Collaborative Proposals#1511835 / #1511862Boudouris, Bryan / Phillip, WilliamMembranes are crucial in a number of separation processes where desired products are isolated from undesired species. In particular, many emerging pharmaceutical treatments require the purification of active long-chain biomacromolecules as they leave the biopharmaceutical reactor. These biomacromolecules recently have been approved for the treatment of a variety of life-threatening diseases, including cancer and autoimmune diseases. However, the high cost of large-scale production and purification of these important materials, which is often transferred to the patient, has prevented their widespread implementation in clinical practice. This proposal will evaluate how macromolecules such as these important therapeutic agents are transported through membrane materials. By combining experimental results with theoretical predictions and computational simulations, a complete picture of how transport occurs through small pores will be developed. This opens the potential of generating more cost-effective purification systems, which could lessen the costs of patient treatment and open an economical means by which to treat a number of devastating diseases.The transport of macromolecular species is of fundamental import in a range of technologically-important membrane separations applications (e.g., the separation of therapeutic proteins). However, the exact mechanism of how a dissolved polymer chain traverses a membrane with pore sizes comparable to or smaller than the hydrodynamic diameter of the chain at thermodynamic equilibrium and without external stimuli (e.g., applied electric fields) is not understood fully. As such, a critical need exists to establish how pore size, pore chemistry, and the solution environment affect the interfacial transport of macromolecules across well-structured membranes. Here, a combination of experimental techniques, thermodynamic theory, and computational modeling is utilized in order to tie nanoscale phenomena to physical observables at the macroscopic level. The vision will result in a molecule-to-membrane level understanding of chemically-selective macromolecular transport through small pores; this understanding, which will be developed by connecting continuum transport properties to molecular models through advanced materials characterization methodologies, will enable the PIs to develop the design principles for the rational engineering of chemically-selective membranes in a number of current and emerging separations platforms.Generating structure-property-performance relationships in the realm of size and chemically-selective membranes will lead to improved membrane design. This, in turn, will help decrease production costs and increase the energy efficiency of many processes required for the production of common consumer goods and more high-value products (e.g., therapeutic pharmaceuticals). As such, successful completion of this work has the potential to impact current manufacturing processes in a positive manner. Furthermore, the collaboration between Purdue University and the University of Notre Dame will allow students from both institutions to perform work at the partner institution. In this way, the students will have a more diverse educational experience. In addition to graduate students, undergraduate and high school students will perform research on this project. In particular, the high school student will be part of the American Chemical Society's Project SEED program. Therefore, this work has the ability to advance fundamental membrane science and to impact a unique group of interdisciplinary scientists and engineers with diverse socioeconomic and educational backgrounds.
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Impact of Radical Polymer Architecture on Spin Transport
  • 批准号:
    2321618
  • 项目类别:
    Standard Grant
  • 资助金额:
    $54.0万
  • 财政年份:
    2023
  • 负责人:
    Bryan Boudouris
  • 依托单位:
Intergovernmental Mobility Assignment
  • 批准号:
    2053097
  • 项目类别:
    Intergovernmental Personnel Award
  • 资助金额:
    $22.61万
  • 财政年份:
    2020
  • 负责人:
    Bryan Boudouris
  • 依托单位:
Tailoring Transport in Transparent and Conducting Non-conjugated Polymers for Next-Generation Materials in Organic Photovoltaic Devices
  • 批准号:
    1336731
  • 项目类别:
    Continuing Grant
  • 资助金额:
    $25.0万
  • 财政年份:
    2013
  • 负责人:
    Bryan Boudouris
  • 依托单位:
海外基金