Imaging properties in two-photon excitation microscopy and effects of refractive-index mismatch in thick specimens.

The detrimental effects of a refractive-index mismatch on the image formation in a two-photon microscope were investigated. Point-spread functions (PSF's) were recorded with an oil-immersion objective numerical aperture (NA) of 1.3 and a water-immersion objective NA of 1.2 in an aqueous sample at different depths. For the oil-immersion objective the enlargement of the PSF volume with increasing depth yields an axial and a lateral loss in resolution of approximately 380% and 160%, respectively, at a 90-microm depth in the sample. For the water-immersion objective no resolution decrease was found. Measurements on a thick aqueous biofilm sample shows the importance of matching the refractive index between immersion fluid and sample. With a good match, no loss in image resolution is observed.

[1]  Kjell Carlsson,et al.  The influence of specimen refractive index, detector signal integration, and non‐uniform scan speed on the imaging properties in confocal microscopy , 1991 .

[2]  Stefan W. Hell,et al.  Effect of the specimen refractive index on the imaging of a confocal fluorescence microscope employing high aperture oil immersion lenses , 1995 .

[3]  S. Hell,et al.  Aberrations in confocal fluorescence microscopy induced by mismatches in refractive index , 1993 .

[4]  P. Marsh,et al.  A modified chemostat system to study the ecology of oral biofilms. , 1996, The Journal of applied bacteriology.

[5]  W. Webb,et al.  Measurement of two-photon excitation cross sections of molecular fluorophores with data from 690 to 1050 nm , 1996 .

[6]  V. Centonze,et al.  Multiphoton excitation provides optical sections from deeper within scattering specimens than confocal imaging. , 1998, Biophysical journal.

[7]  Sytsma,et al.  Time‐gated fluorescence lifetime imaging and microvolume spectroscopy using two‐photon excitation , 1998 .

[8]  G. J. Brakenhoff,et al.  3‐D image formation in high‐aperture fluorescence confocal microscopy: a numerical analysis , 1990 .

[9]  T. Wilson,et al.  The axial response of confocal microscopes with high numerical aperture objective lenses , 1995 .

[10]  W. Denk,et al.  Two-photon laser scanning fluorescence microscopy. , 1990, Science.

[11]  H. M. Voort,et al.  Restoration of confocal images for quantitative image analysis , 1995 .

[12]  A. Entwistle The effects of total internal reflection on the spread function along the axis in confocal microscopy , 1995 .

[13]  Pekka Hänninen,et al.  Refractive‐index‐induced aberrations in two‐photon confocal fluorescence microscopy , 1994 .

[14]  Geert M. P. van Kempen,et al.  Avalanche photodiode detection with object scanning and image restoration provides 2–4 fold resolution increase in two‐photon fluorescence microscopy , 1996 .