Surface viscometry of an evaporating droplet containing a protein (collagen) as a function of time and depth

There is a need for tissue engineers to recreate extracellular matrix that mimics the highly organized extracellular structures as seen in vivo. In a previous study in the extracellular matrix engineering research laboratory (EMERL), a micromechanical system was used to create such structures by dra...

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Online Access:http://hdl.handle.net/2047/D20195404
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spelling ndltd-NEU--neu-rx917b86j2021-05-28T05:22:20ZSurface viscometry of an evaporating droplet containing a protein (collagen) as a function of time and depthThere is a need for tissue engineers to recreate extracellular matrix that mimics the highly organized extracellular structures as seen in vivo. In a previous study in the extracellular matrix engineering research laboratory (EMERL), a micromechanical system was used to create such structures by drawing fibers from a droplet of neutralized collagen monomers at room temperature. For further investigation in the formation of highly aligned and continuous fibers, the laboratory is interested in developing a more effective experimental procedure. Therefore, to supply the proper concentration of collagen monomers for a collagen fiber printing device, a good estimate of the collagen concentration in the droplet surface is required. The goal of this study was to measure the concentration variation as a function of thickness in the dense layer on the droplet's top surface when a fiber can be created.http://hdl.handle.net/2047/D20195404
collection NDLTD
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description There is a need for tissue engineers to recreate extracellular matrix that mimics the highly organized extracellular structures as seen in vivo. In a previous study in the extracellular matrix engineering research laboratory (EMERL), a micromechanical system was used to create such structures by drawing fibers from a droplet of neutralized collagen monomers at room temperature. For further investigation in the formation of highly aligned and continuous fibers, the laboratory is interested in developing a more effective experimental procedure. Therefore, to supply the proper concentration of collagen monomers for a collagen fiber printing device, a good estimate of the collagen concentration in the droplet surface is required. The goal of this study was to measure the concentration variation as a function of thickness in the dense layer on the droplet's top surface when a fiber can be created.
title Surface viscometry of an evaporating droplet containing a protein (collagen) as a function of time and depth
spellingShingle Surface viscometry of an evaporating droplet containing a protein (collagen) as a function of time and depth
title_short Surface viscometry of an evaporating droplet containing a protein (collagen) as a function of time and depth
title_full Surface viscometry of an evaporating droplet containing a protein (collagen) as a function of time and depth
title_fullStr Surface viscometry of an evaporating droplet containing a protein (collagen) as a function of time and depth
title_full_unstemmed Surface viscometry of an evaporating droplet containing a protein (collagen) as a function of time and depth
title_sort surface viscometry of an evaporating droplet containing a protein (collagen) as a function of time and depth
publishDate
url http://hdl.handle.net/2047/D20195404
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