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Collaborative Research in Nanostructure Control via Surfactant Mixing and Polymerization

Collaborative Research in Nanostructure Control via Surfactant Mixing and Polymerization
通过表面活性剂混合和聚合控制纳米结构的合作研究
批准号:
0436124
负责人:
Joseph Zasadzinski
金额:
$16.05万
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
项目状态:
已结题
起止时间:
2005-02-01 至 2008-01-31

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University of Delaware/ University of California Santa BarbaraABSTRACT - 0436195/0436124Project SummaryMuch of nanotechnology is devoted to creating two-dimensional structures on surfaces. However,learning the composition-structure-function relationships for biomimetic self-assembly will lead to nanoscale, three-dimensional vesicle structures for specific tasks including drug delivery, catalysis, specific recognition, among others. This proposal addresses the science and engineering needed to advance the self-assembly of functional nano-containers of polymers and surfactants, based on our group's expertise with the combining the physics and chemistry of nanostructures with the self-assembly and specific recognition processes of biology. The basic theme is centered on the self-assembly of oppositely charged surfactants and/or hydrotropes into unilamellar vesicles that can be fixed by polymerization to yield stable, hollow capsules that can be further functionalized. Specific aims are:1. Study the formation and polymerization of vesicles formed from polymerizable surfactants andorganic and inorganic monomers to best retain the size, shape and polydispersity of templating vesicles;2. Modify and control vesicle properties adding block co-polymers to adjust the spontaneous curvature (size), bending elasticity (polydispersity) and the steric interactions between vesicles (stability). In particular, near equimolar mixtures of polymerizable anionic and cationic surfactants with copolymers that likely create monodisperse vesicle systems will be formulated;3. Examine the novel properties of vesicles formed in mixtures of surfactant and hydrotropes (which are weakly surface-active, amphiphilic, and highly water-soluble organic salts), and to probe microstructural changes therein caused by changes in pH or light exposure.Project 1 will involve synthesis and formulation carried out primarily at U. Delaware by Kaler'sgroup and microscopy characterization at UCSB by Zasadzinski's group. The formulations needed for project 2 will be done at UCSB and characterization will be carried out using light scattering and electron microscopy by Zasadzinski's group, and neutron spin-echo and neutron scattering by Kaler's group. Project 3 will be initiated at U. Delaware by Kaler's group and characterized by microscopy done in Zasadzinski's group. The reduction in time from 3 to 2 years will cause us to not be able to get as far in the project; however, all of the specific aims will be examined and the most promising routes identified.Intellectual Merit: The self-assembly of oppositely charged surfactants and hydrotropes opens newareas of biomimetic structures for exploration, and will likely put the process of vesicle formation under thermodynamic control. Exploiting thermodynamic control means being able to determine the size, polydispersity, stability, etc. of vesicles by simple manipulation of simple, inexpensive detergents. Chemical reactions (i.e., polymerization) to fix such structures open new ways to form nanoscale materials that retain the nanostructure of the template. The proposed work expands and links these two areas, and will provide both novel experimental observations and further theoretical understanding.Technical Impact: Surfactant formulations, particularly surfactant mixtures, are widely used inmany industrial processes. The ability to control surfactant microstructure by mixing surfactants or adding hydrotropes could provide new organic templates for novel organic and inorganic materials such as polymer latices and molecular sieves. Manufacturing polymerized vesicles cheaply could open the way to high-volume usages in printing or agricultural applications. Work with spontaneous vesicles made of biological surfactants will lead to useful pharmaceutical applications. Controlling the aggregation and fusion of vesicles is of crucial importance to drug delivery schemes, as is minimization of the free surfactant concentration.Broader Impact: The scientific aspects of this proposed work will enable discovery of newnanoscale surfactant architectures through the development of and understanding of their thermodynamic and mechanical properties, including the nature of their equilibrium state. Study of these mixtures has already led to fruitful reexamination of many of the fundamental dogmas of self-assembly. Study of both organic and inorganic polymerizations can open ways to make new materials that could have application beyond those discussed above. Undergraduate and graduate students involved in this work will be exposed to a range of characterization tools and appropriate analytical methods, and thereby be prepared for either academic or industrial work in this area. K-12 students will be exposed to concepts relevant to this work, including surfactant and polymer properties and elements of nanotechnology.Statement of Effect of Time Reduction:We have proposed three specific aims:1. Study the formation and polymerization of vesicles formed from polymerizable surfactantsand organic and inorganic monomers to best retain the size, shape and polydispersity oftemplating vesicles;2. Modify and control vesicle properties adding block co-polymers to adjust the spontaneouscurvature (size), bending elasticity (polydispersity) and the steric interactions between vesicles(stability). In particular, near equimolar mixtures of polymerizable anionic and cationicsurfactants with copolymers that likely create monodisperse vesicle systems will be formulated;3. Examine the novel properties of vesicles formed in mixtures of surfactant and hydrotropes(which are weakly surface-active, amphiphilic, and highly water-soluble organic salts), and toprobe microstructural changes therein caused by changes in pH or light exposure.Project 1 will involve synthesis and formulation carried out primarily at U. Delaware by Kaler'sgroup and microscopy characterization at UCSB by Zasadzinski's group. The formulationsneeded for project 2 will be done at UCSB and characterization will be carried out using lightscattering and electron microscopy by Zasadzinski's group, and neutron spin-echo and neutronscattering by Kaler's group. Project 3 will be initiated at U. Delaware by Kaler's group andcharacterized by microscopy done in Zasadzinski's group. The reduction in time from 3 to 2years will cause us to not be able to get as far in the project; however, all of the specific aims willbe examined at some level and the most promising routes identified for subsequent proposals.
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Effects of Curvature on Monolayer Morphology and Dynamics
  • 批准号:
    1706378
  • 项目类别:
    Standard Grant
  • 资助金额:
    $37.0万
  • 财政年份:
    2017
  • 负责人:
    Joseph Zasadzinski
  • 依托单位:
Acquisition of a High Vacuum Freeze-Fracture System for Microstructural Characterization of Complex Fluids and Biomaterials
ENGINEERING RESEARCH EQUIPMENT: A Combined Fluorescence Optical Microscope/Non-Contact Atomic Force Microscope for Monolayer and Multilayer Studies
Engineering Research Equipment: A Modified STM/AFM for Complex Fluid Investigations
国内基金
海外基金
Research on Quantum Field Theory without a Lagrangian Description
  • 批准号:
    24ZR1403900
  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2024
  • 负责人:
    SATOSHI NAWATA
  • 依托单位:
Cell Research
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