Image-inspired 3D multiphoton excited fabrication of extracellular matrix structures by modulated raster scanning

被引:25
作者
Ajeti, Visar [1 ,2 ]
Lien, Chi-Hsiang [1 ]
Chen, Shean-Jen [3 ]
Su, Ping-Jung [1 ,2 ]
Squirrell, Jayne M. [2 ]
Molinarolo, Katharine H. [2 ]
Lyons, Gary E. [2 ,4 ]
Eliceiri, Kevin W. [1 ,2 ]
Ogle, Brenda M. [1 ,2 ]
Campagnola, Paul J. [1 ,2 ]
机构
[1] Univ Wisconsin, Dept Biomed Engn, Madison, WI 53706 USA
[2] Lab Opt & Computat Instrumentat, Madison, WI USA
[3] Natl Cheng Kung Univ, Dept Engn Sci, Tainan 701, Taiwan
[4] Dept Cell & Regenerat Biol, Madison, WI USA
基金
美国国家科学基金会;
关键词
CROSS-LINKING; MICROFABRICATION; PROTEINS; PHOTOCHEMISTRY; LITHOGRAPHY; MICRO; MICROENVIRONMENT; MIGRATION; HYDROGELS; EFFICIENT;
D O I
10.1364/OE.21.025346
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Multiphoton excited photochemistry is a powerful 3D fabrication tool that produces sub-micron feature sizes. Here we exploit the freeform nature of the process to create models of the extracellular matrix (ECM) of several tissues, where the design blueprint is derived directly from high resolution optical microscopy images (e.g. fluorescence and Second Harmonic Generation). To achieve this goal, we implemented a new form of instrument control, termed modulated raster scanning, where rapid laser shuttering (10 MHz) is used to directly map the greyscale image data to the resulting protein concentration in the fabricated scaffold. Fidelity in terms of area coverage and relative concentration relative to the image data is similar to 95%. We compare the results to an STL approach, and find the new scheme provides significantly improved performance. We suggest the method will enable a variety of cell-matrix studies in cancer biology and also provide insight into generating scaffolds for tissue engineering. (C) 2013 Optical Society of America
引用
收藏
页码:25346 / 25355
页数:10
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