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BEVEL
cutting facet, found on the tapered edge of all knives.
BEVEL ANGLE
the angle formed between the cutting edge
27 to 32 Degrees
BEVEL ANGLE
KNIFE BACK
maintains the bevel angle
CUTTING ANGLE
optimal angle of 15 degrees.
CUTTING ANGLE
Less distortion and maximum penetration
CLEARANCE ANGLE
0-15 Degrees
CLEARANCE ANGLE
Angle formed between the surface of the block and the cutting edge of the knife
HONING
HARD Knife Sharpening
HONING
Removes gross nicks on the knife edge (Coarse honing)
Removes blemishes.
HONING
Grinding the cutting edge of the knife on a stone
BELGIUM YELLOW
manual sharpening. Best honing result
ARKANSAS
more polishing effect compared to Belgium Yellow
FINE CARBORUNDUM
much coarser than others. Used for badly nicked knives.
LUBRICANTS FOR HONING
Soapy water, mineral oil, Clove oil, Xylene or Liquid Paraffin
HONING MOVEMENT
EDGE FIRST
HONING MOVEMENT
HEEL TO TOE DIRECTION
20-30 strokes
HONING- NUMBER OF STROKES
10-20 strokes
HONING- In Minot or Plane Wedge Knife
STROPPING
removes the burr of the knife formed during honing
STROPPING
Polishing and sharpening of the cutting edge
Paddle strop
is made of a fine horse leather.
STROPPING MOVEMENT
EDGE LAST
STROPPING MOVEMENT
TOE TO HEEL DIRECTION
knife is turned around at the end of each stroke
STROPPING – In Minot or Plane Wedge Knife
the concave surface is stropped
STROPPING – For Plane Concave Knives
Frozen Sections
for rapid diagnosis during surgery, research enzyme histochemistry, lipids and carbohydrates studies
Frozen Sections
For immunofluorescent and immunocytochemical staining.
Frozen Sections
For special silver staining particularly in neuropathology
COLD KNIFE METHOD
Use of conventional freezing microtome with Carbon Dioxide
3-5 mm
COLD KNIFE METHOD- Tissue block thickness is
Dew Line
point where the tissues may be cut at 10 um.
-40 Celsius to -60 Celsius
TEMPERATURES FOR OPTIMUM OPERATION (KNIFE)
-5 Celsius to -10 Celsius
TEMPERATURES FOR OPTIMUM OPERATION (TISSUE)
0 Celsius to -10 Celsius
TEMPERATURES FOR OPTIMUM OPERATION (ENVIRONMENT)
CRYOSTAT METHOD
Near – 20 Celsius (Microtome Knife, Specimen and the Atmosphere)
-18 to -20 Celsius
CRYOSTAT METHOD- Optimum working temperature is
Common freezing agents
Liquid Nitrogen, Isopentane cooled by
Liquid Nitrogen, Carbon Dioxide Gas and Aerosol Sprays
LIQUID NITROGEN
Histochemistry, Intra-operative diagnosis, most rapid.
LIQUID NITROGEN
Main disadvantage is soft tissues is liable to crack due to rapid expansion. (Ice crystallization inside the tissue)
ISOPENTANE
Liquid at room temperature
ISOPENTANE
Tissue is frozen, affixed on a cork disc, aluminum foil or cryostat chuck
AEROSOL SPRAY
For small tissues except the muscle
AEROSOL SPRAY
Fluorinated Hydrocarbons (Cryokwik) – rapid freezing of any tissues
CARBON DIOXIDE GAS
At – 50 Celsius
-5 TO -15 Celsius
Brain, lymph nodes, liver, spleen, uterine curetting and soft cellular tumor
-15 TO -25 Celsius
Non-fatty breast tissue, ovary, prostate, tongue and GI tract
-35 Celsius
Fatty Breast and omental tissue