Quantitative biorelevant profiling of material microstructure within 3D porous scaffolds via multiphoton fluorescence microscopy

被引:14
作者
Liu, Er
Treiser, Matthew D.
Johnson, Patrick A.
Patel, Parth
Rege, Aarti
Kohn, Joachim
Moghe, Prabhas V. [1 ]
机构
[1] Rutgers State Univ, Dept Biomed Engn, Piscataway, NJ 08854 USA
[2] Rutgers State Univ, New Jersey Ctr Biomat, Piscataway, NJ 08854 USA
[3] Rutgers State Univ, Dept Chem & Biochem Engn, Piscataway, NJ 08854 USA
[4] Rutgers State Univ, Dept Chem & Chem Biol, Piscataway, NJ 08854 USA
关键词
biomaterials; porous scaffolds; biomedical imaging; two-photon microscopy; confocal microscopy;
D O I
10.1002/jbm.b.30732
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
This study presents a novel approach, based on fluorescence multiphoton microscopy (MPM), to image and quantitatively characterize the microstructure and cell-substrate interactions within microporous scaffold substrates fabricated from synthetic biodegradable polymers. Using fluorescently dyed scaffolds fabricated from poly(DTE carbonate)/poly(DTO carbonate) blends of varying porosity and complementary green fluorescent protein-engineered fibroblasts, we reconstructed the three-dimensional distribution of the microporous and macroporous regions in 3D scaffolds, as well as cellular morphological patterns. The porosity, pore size and distribution, strut size, pore interconnectivity, and orientation of both macroscale and microscale pores of 3D scaffolds were effectively quantified and validated using complementary imagings. Compared to other scaffold characterizing techniques such as confocal imaging and scanning electron microscopy (SEM), MPM enables the acquisition of images from scaffold thicknesses greater than a hundred microns with high signal-to-noise ratio, reduced bulk photobleaching, and the elimination of the need for deconvolution. In our study, the morphology and cytoskeletal organization of cells within the scaffold interior could be tracked with high resolution within the limits of penetration of MIPM. Thus, MIPM affords a promising integrated platform for imaging cell-material interactions within the interior of polymeric biomaterials. (C) 2007 Wiley Periodicals, Inc.
引用
收藏
页码:284 / 297
页数:14
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