Dr. P. Suganya
Assistant Professor
Sri Kaliswari College (Autonomous)

 Unstained living cells absorb practically no light. Poor
light absorption results in extremely small differences
in the intensity distribution in the image.
 This makes the cells barely, or not at all, visible in a
brightfield microscope.
 Phase-contrast microscopy is an optical microscopy
technique that converts phase shifts in the light passing
through a transparent specimen to brightness changes
in the image.
 It was first described in 1934 by Dutch physicist Frits
Zernike.
Definition

 When light passes through cells, small phase shifts
occur, which are invisible to the human eye. In a
phase-contrast microscope, these phase shifts are
converted into changes in amplitude, which can be
observed as differences in image contrast.
Working Principle


 Partially coherent illumination produced by the
tungsten-halogen lamp is directed through a collector
lens and focused on a specialized annulus
(labeled condenser annulus) positioned in the substage
condenser front focal plane.
 Wavefronts passing through the annulus illuminate the
specimen and either pass through undeviated or are
diffracted and retarded in phase by structures and
phase gradients present in the specimen.
 Undeviated and diffracted light collected by the
objective is segregated at the rear focal plane by a
phase plate and focused at the intermediate image
plane to form the final phase-contrast image observed
in the eyepieces.

Parts of Microscope

 Phase-contrast microscopy is basically a specially
designed light microscope with all the basic parts in
addition to which an annular phase plate and annular
diaphragm are fitted.
 The annular diaphragm
 It is situated below the condenser.
 It is made up of a circular disc having a circular annular
groove.
 The light rays are allowed to pass through the annular
groove.
 Through the annular groove of the annular diaphragm,
the light rays fall on the specimen or object to be studied.
 At the back focal plane of the objective develops an
image.
 The annular phase plate is placed at this back focal plane.

 The phase plate
 It is either a negative phase plate having a thick circular
area or a positive phase plate having a thin circular
groove.
 This thick or thin area in the phase plate is called the
conjugate area.
 The phase plate is a transparent disc.
 With the help of the annular diaphragm and the phase
plate, the phase contrast is obtained in this microscope.
 This is obtained by separating the direct rays from the
diffracted rays.
 The direct light rays pass through the annular groove
whereas the diffracted light rays pass through the
region outside the groove.
 Depending upon the different refractive indices of
different cell components, the object to be studied
shows a different degree of contrast in this microscope.


 to produce high-contrast images of transparent
specimens, such as
 living cells (usually in culture),
 microorganisms,
 thin tissue slices,
 lithographic patterns,
 fibers,
 latex dispersions,
 glass fragments, and
 subcellular particles (including nuclei and other
organelles).
 Applications of phase-contrast microscopy in biological
research are numerous.
Applications

 Living cells can be observed in their natural state without
previous fixation or labeling.
 It makes a highly transparent object more visible.
 No special preparation of fixation or staining etc. is needed to
study an object under a phase-contrast microscope which
saves a lot of time.
 Examining intracellular components of living cells at relatively
high resolution. eg: The dynamic motility of mitochondria,
mitotic chromosomes & vacuoles.
 It made it possible for biologists to study living cells and how
they proliferate through cell division.
 Phase-contrast optical components can be added to virtually
any brightfield microscope, provided the specialized phase
objectives conform to the tube length parameters, and the
condenser will accept an annular phase ring of the correct
size.
Advantages

 Phase-contrast condensers and objective lenses add
considerable cost to a microscope, and so phase
contrast is often not used in teaching labs except
perhaps in classes in the health professions.
 To use phase-contrast the light path must be aligned.
 Generally, more light is needed for phase contrast
than for corresponding bright-field viewing, since
the technique is based on the diminishment of the
brightness of most objects.
Limitations

 References
 https://en.wikipedia.org/wiki/Phase-
contrast_microscopy
 https://microbenotes.com/phase-contrast-
microscopy/


Phase contrast microscope

  • 1.
    Dr. P. Suganya AssistantProfessor Sri Kaliswari College (Autonomous)
  • 2.
      Unstained livingcells absorb practically no light. Poor light absorption results in extremely small differences in the intensity distribution in the image.  This makes the cells barely, or not at all, visible in a brightfield microscope.  Phase-contrast microscopy is an optical microscopy technique that converts phase shifts in the light passing through a transparent specimen to brightness changes in the image.  It was first described in 1934 by Dutch physicist Frits Zernike. Definition
  • 3.
      When lightpasses through cells, small phase shifts occur, which are invisible to the human eye. In a phase-contrast microscope, these phase shifts are converted into changes in amplitude, which can be observed as differences in image contrast. Working Principle
  • 4.
  • 5.
      Partially coherentillumination produced by the tungsten-halogen lamp is directed through a collector lens and focused on a specialized annulus (labeled condenser annulus) positioned in the substage condenser front focal plane.  Wavefronts passing through the annulus illuminate the specimen and either pass through undeviated or are diffracted and retarded in phase by structures and phase gradients present in the specimen.  Undeviated and diffracted light collected by the objective is segregated at the rear focal plane by a phase plate and focused at the intermediate image plane to form the final phase-contrast image observed in the eyepieces.
  • 6.
  • 7.
      Phase-contrast microscopyis basically a specially designed light microscope with all the basic parts in addition to which an annular phase plate and annular diaphragm are fitted.  The annular diaphragm  It is situated below the condenser.  It is made up of a circular disc having a circular annular groove.  The light rays are allowed to pass through the annular groove.  Through the annular groove of the annular diaphragm, the light rays fall on the specimen or object to be studied.  At the back focal plane of the objective develops an image.  The annular phase plate is placed at this back focal plane.
  • 8.
      The phaseplate  It is either a negative phase plate having a thick circular area or a positive phase plate having a thin circular groove.  This thick or thin area in the phase plate is called the conjugate area.  The phase plate is a transparent disc.  With the help of the annular diaphragm and the phase plate, the phase contrast is obtained in this microscope.  This is obtained by separating the direct rays from the diffracted rays.  The direct light rays pass through the annular groove whereas the diffracted light rays pass through the region outside the groove.  Depending upon the different refractive indices of different cell components, the object to be studied shows a different degree of contrast in this microscope.
  • 9.
  • 10.
      to producehigh-contrast images of transparent specimens, such as  living cells (usually in culture),  microorganisms,  thin tissue slices,  lithographic patterns,  fibers,  latex dispersions,  glass fragments, and  subcellular particles (including nuclei and other organelles).  Applications of phase-contrast microscopy in biological research are numerous. Applications
  • 11.
      Living cellscan be observed in their natural state without previous fixation or labeling.  It makes a highly transparent object more visible.  No special preparation of fixation or staining etc. is needed to study an object under a phase-contrast microscope which saves a lot of time.  Examining intracellular components of living cells at relatively high resolution. eg: The dynamic motility of mitochondria, mitotic chromosomes & vacuoles.  It made it possible for biologists to study living cells and how they proliferate through cell division.  Phase-contrast optical components can be added to virtually any brightfield microscope, provided the specialized phase objectives conform to the tube length parameters, and the condenser will accept an annular phase ring of the correct size. Advantages
  • 12.
      Phase-contrast condensersand objective lenses add considerable cost to a microscope, and so phase contrast is often not used in teaching labs except perhaps in classes in the health professions.  To use phase-contrast the light path must be aligned.  Generally, more light is needed for phase contrast than for corresponding bright-field viewing, since the technique is based on the diminishment of the brightness of most objects. Limitations
  • 13.
      References  https://en.wikipedia.org/wiki/Phase- contrast_microscopy https://microbenotes.com/phase-contrast- microscopy/
  • 14.