PubMed HealthSearch

Biomedical subjects

S F Gibson

Publications and source records attributed to S F Gibson.

2 recordsLinked to original sources

Experimental test of an analytical model of aberration in an oil-immersion objective lens used in three-dimensional light microscopy.

Oil-immersion microscope objective lenses have been designed and optimized for the study of thin, two-dimensional object sections that are mounted immediately below the coverslip in a medium that is index matched to the immersion oil. It has been demonstrated both experimentally and through geometrical- and physical-optics theory that, when the microscope is not used with the correct coverslip or immersion oil, when the detector is not located at the optimal plane in image space, or when the object does not satisfy specific conditions, aberration will degrade both the contrast and the resolution of the image. In biology the most severe aberration is introduced when an oil-immersion objective lens is used to study thick specimens, such as living cells and tissues, whose refractive indices are significantly different from that of the immersion oil. We present a model of the three-dimensional imaging properties of a fluorescence light microscope subject to such aberration and compare the imaging properties predicted by the model with those measured experimentally. The model can be used to understand and compensate for aberration introduced to a microscope system under nondesign optical conditions so that both confocal laser scanning microscopy and optical serial sectioning microscopy can be optimized.

Mathematics

Diffraction by a circular aperture as a model for three-dimensional optical microscopy.

Existing formulations of the three-dimensional (3-D) diffraction pattern of spherical waves that is produced by a circular aperture are reviewed in the context of 3-D serial-sectioning microscopy. A new formulation for off-axis focal points is introduced that has the desirable properties of increased accuracy for larger field angles, invariance to shifts of the focal point about spheres of constant radius when the detection point is on the sphere for both intensity and amplitude fields, and invariance to shifts in three transformed coordinates for intensity fields. Finally, calculated intensity fields for both on-axis and off-axis focal points are included to illustrate the proposal that the classical 3-D diffraction patterns that have been used as analytical models in 3-D serial-sectioning fluorescence microscopy may not be accurate enough for this application.

Algorithms