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Colloidosomes: Nanoparticle-Assembled Microcapsules with Selective Permeability

Colloidosomes: Nanoparticle-Assembled Microcapsules with Selective Permeability
胶体体:具有选择性渗透性的纳米颗粒组装微胶囊
批准号:
230456922
负责人:
Privatdozent Dr. Michael Maas
金额:
$0.0万
依托单位国家:
德国
项目类别:
Research Grants
财政年份:
2012
资助国家:
德国
项目状态:
已结题
起止时间:
2011-12-31 至 2017-12-31

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中文摘要
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英文摘要
The goal of this research project is the preparation of stable colloidosomes with selective permeability for the controlled release of molecules. Colloidosomes are microcapsules that consist of a shell of nanoparticles. The advantages of colloidosomes over other microcapsules (e.g. based on polymers) are their easily tunable porosity and the promising potential to fabricate colloidosomes from many different types of nanoparticles.The colloidosomes that are prepared in this project are to be loaded with different molecules that are examples for different classes of active agents (e.g. standard proteins, antibodies, small molecules). Furthermore, the release of these molecules from the colloidosomes will be studied. Accordingly, the project is comprised of three parts:The first part of the project focuses on the preparation of the colloidosomes. Colloidosome preparation is based on specific interactions between nanoparticles and lipids during the formation of thin films at the interfaces of emulsion droplets. Interfacial shear rheology will be predominately used to characterize the interactions between nanoparticles and lipids in the respective thin films. Through a better grasp of the formation of multicomponent films in emulsions and on planar interfaces we want to produce stable microcapsules without the help of further additives like polymers. On the basis of these insights, it is possible to derive design rules for the preparation of stable colloidosomes from a library of nanoparticles and lipids.In the second part of the project, molecules are loaded into the colloidosomes. Molecule loading and colloidosome preparation can proceed simultaneously. Since the molecules are present during capsule formation, the influence of the molecules on thin film formation, emulsion stability and all other aspects of colloidosome preparation needs to be studied. Again, interfacial shear rheology is the most important characterization method in this part of the project. As could be demonstrated in our preliminary research, loading of the colloidosomes cannot be understood separately from capsule formation and has to be studied as a whole.In the third part of the project, the release of the molecules from the colloidosomes will be studied. The release rate is an important feature of the colloidosomes. It is based on the interactions between the different components (nanoparticles, lipids, molecules) and the pore size. New insights from the release studies can be directly evaluated in light of the design-rules that have been established in the preceding parts of the project.
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DOI: 10.1021/cm401610a
发表时间: 2013-09-10
期刊: CHEMISTRY OF MATERIALS
影响因子: 8.6
作者: [Bollhorst, Tobias, Grieb, Tim, Rezwan, Kurosch]
通讯作者: Rezwan, Kurosch
Self-assembly of nanoparticle thin films at the liquid-liquid interface
  • 批准号:
    144407670
  • 项目类别:
    Research Fellowships
  • 资助金额:
    $0.0万
  • 财政年份:
    2010
  • 负责人:
    Privatdozent Dr. Michael Maas
  • 依托单位:
海外基金