Literature DB >> 15894637

Determining diffusion coefficients in inhomogeneous tissues using fluorescence recovery after photobleaching.

Y H Sniekers1, C C van Donkelaar.   

Abstract

Diffusion plays an important role in the transport of nutrients and signaling molecules in cartilaginous tissues. Diffusion coefficients can be measured by fluorescence recovery after photobleaching (FRAP). Available methods to analyze FRAP data, however, assume homogeneity in the environment of the bleached area and neglect geometrical restrictions to diffusion. Hence, diffusion coefficients in inhomogeneous materials, such as most biological tissues, cannot be assessed accurately. In this study, a new method for analyzing data from FRAP measurements has been developed, which is applicable to inhomogeneous tissues. It is based on a fitting procedure of the intensity recovery after photobleaching with a two-dimensional finite element analysis, which includes Fick's law for diffusion. The finite element analysis can account for distinctive diffusivity in predefined zones, which allows determining diffusion coefficients in inhomogeneous samples. The method is validated theoretically and experimentally in both homogeneous and inhomogeneous tissues and subsequently applied to the proliferation zone of the growth plate. Finally, the importance of accounting for inhomogeneities, for appropriate assessment of diffusivity in inhomogeneous tissues, is illustrated.

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Year:  2005        PMID: 15894637      PMCID: PMC1366614          DOI: 10.1529/biophysj.104.053652

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  16 in total

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Authors:  D A Berk; F Yuan; M Leunig; R K Jain
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  16 in total

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4.  Characterization of Cell Boundary and Confocal Effects Improves Quantitative FRAP Analysis.

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Review 8.  Single-cell imaging of mechanotransduction in endothelial cells.

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9.  Characterization of anisotropic diffusion tensor of solute in tissue by video-FRAP imaging technique.

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10.  Photothermal bleaching in time-lapse photoacoustic microscopy.

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