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Tissue Eng Part C Methods ; 17(4): 495-504, 2011 Apr.
Article in English | MEDLINE | ID: mdl-21303258

ABSTRACT

A multimodal diagnostic system that integrates time-resolved fluorescence spectroscopy, fluorescence lifetime imaging microscopy, and ultrasound backscatter microscopy is evaluated here as a potential tool for assessing changes in engineered tissue composition and microstructure nondestructively and noninvasively. The development of techniques capable of monitoring the quality of engineered tissue, determined by extracellular matrix (ECM) content, before implantation would alleviate the need for destructive assays over multiple time points and advance the widespread development and clinical application of engineered tissues. Using a prototype system combining time-resolved fluorescence spectroscopy, FLIM, and UBM, we measured changes in ECM content occurring during chondrogenic differentiation of equine adipose stem cells on 3D biodegradable matrices. The optical and ultrasound results were validated against those acquired via conventional techniques, including collagen II immunohistochemistry, picrosirius red staining, and measurement of construct stiffness. Current results confirm the ability of this multimodal approach to follow the progression of tissue maturation along the chondrogenic lineage by monitoring ECM production (namely, collagen type II) and by detecting resulting changes in mechanical properties of tissue constructs. Although this study was directed toward monitoring chondrogenic tissue maturation, these data demonstrate the feasibility of this approach for multiple applications toward engineering other tissues, including bone and vascular grafts.


Subject(s)
Bioengineering/methods , Cartilage/physiology , Imaging, Three-Dimensional/methods , Tissue Engineering/methods , Tissue Scaffolds/chemistry , Ultrasonics/methods , Adipose Tissue/cytology , Animals , Collagen/metabolism , DNA/metabolism , Elastic Modulus , Glycosaminoglycans/metabolism , Horses , Linear Models , Mechanical Phenomena , Spectrometry, Fluorescence , Staining and Labeling , Stem Cells/cytology , Stem Cells/metabolism , Time Factors
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