Diffusion measured by fluorescence recovery after photobleaching based on multiphoton excitation laser scanning microscopy

作者：Schnell Edrun Andrea; Eikenes Live; Tufto Ingunn; Erikson Arne; Juthajan Aphirak; Lindgren Mikael; Davies Catharina de Lange^*

来源：Journal of Biomedical Optics, 2008, 13(6): 064037.

DOI：10.1117/1.3042274

• fluorescence recovery after photobleaching
• interstitial diffusion
• mobile fraction
• multicellular spheroids
• tumor tissue

Fluorescence recovery after photobleaching (FRAP) is a widely used method to measure diffusion. The technique is normally based on one-photon excitation, which limits diffusion to two dimensions due to extended photobleaching in the axial direction. Multiphoton excitation, on the other hand, creates a well-defined focal volume. In the present work, FRAP based on a scanning laser beam and two-photon excitation is used to measure diffusion of macromolecules in solution and gels, as well as in the extracellular matrix in multicellular spheroids and tumor tissue in dorsal chambers. The bleaching profile is determined experimentally in immobilized gels, and for small scanning areas (approximately twice the lateral radius of the laser beam) a Gaussian bleaching distribution is found. In addition, the bleaching profile is determined theoretically based on the convolution of the Gaussian point spread function and a circular scanning area. The diffusion coefficient is determined by fitting a mathematical model based on a Gaussian laser beam profile to the experimental recovery curve. The diffusion coefficient decreases with increasing complexity of the sample matrix and increasing the amount of collagen in the gels. The potential of using two-photon laser scanning microscopes for noninvasive diffusion measurements in tissue is demonstrated.

• 出版日期2008-12