相差和微分干涉显微镜

Unstained living cells are transparent because they lack contrast with their surroundings. Most cellular components have refractive indices similar to the surrounding medium, so light passes through without significant scattering. This makes it nearly impossible to distinguish cell structures using conventional imaging biological samples with optical microscopy techniques without staining or specialized contrast methods.

Phase-contrast microscopy exploits interference between direct light and light diffracted by cellular components. An annular stop produces a hollow cone of light, while a phase plate in the objective shifts diffracted light by approximately half a wavelength. When waves are out-of-phase, they undergo destructive interference, causing structures that refract light to appear dark against a bright background.

The extent of light diffraction depends directly on the refractive indices of cell components. Structures with greater differences in refractive index from their surroundings diffract more light and appear darker in the final image. This allows phase-contrast microscopy to visualize specific organelles in eukaryotic cells and endospores in prokaryotic cells without staining.

Halo artifacts are bright or dark rings that appear around cell structures in phase-contrast images due to sharp changes in refractive indices at boundaries. Differential interference contrast (DIC) microscopy avoids these artifacts by using polarized light to modulate waves passing through the sample. DIC generates contrast based on the rate of change of refractive indices, producing cleaner, three-dimensional images.

DIC microscopy creates two polarized light beams that travel through the specimen or specimen-free space before recombination. The specimen causes differences in interference patterns between these beams, generating high-contrast images with an apparent three-dimensional effect. Unlike phase-contrast, DIC contrast depends on steep changes in refractive indices across the specimen rather than diffraction alone.

DIC microscopy excels at visualizing thick, unstained specimens such as brain slices, eggs, and embryos. The technique's ability to generate high-contrast images with three-dimensional appearance makes it particularly useful for distinguishing internal structures within live specimens. DIC is especially valuable when studying complex tissues that would be difficult to section or stain.

Phase-contrast microscopy creates high-contrast, high-resolution images without requiring chemical stains that can damage or kill living cells. By altering wavelengths of light rays passing through the specimen using an annular stop and phase plate, it preserves cell viability while enabling clear visualization of organelles and cellular structures in real time.