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BY: Dr Bhavya
MODERATORS: Dr Kishan
Dr Hemalatha
AUTOMATION IN HISTOPATHOLOGY
TABLE OF CONTENTS
 INTRODUCTION
 ADVANTAGES OF AUTOMATION
 WHAT ISTISSUE PROCESSING?
 AUTOMATION –
GROSSING
TISSUE PROCESSING
EMBEDDING
MICROTOMY
H & E STAINING AND COVERSLIP
POST H&ETECHNIQUES
SLIDE DIGITIZATION
INTRODUCTION
 Providing high quality and efficiency is needed for the
laboratory including histopathology section.
 One of the ways to achieve this is by automation.
 AUTOMATION is the technique of operating or
controlling a process by highly automated means.
 The word automation is used to describe the maximum
use of instruments to perform laboratory work with
minimum involvement of laboratory personale.
ADVANTAGES OF AUTOMATION
 Rapid than manual methods and turn around time
is minimum by automation.
 Less man power required than manual processing.
 Clean , healthy and safer laboratory environment.
 High quality results.
 Reduces exposure to hazardous chemicals.
WHAT IS TISSUE PROCESSING ?
(i) FIXATION – This is the process of preserving or fixing tissues by
passing them through chemicals called fixatives. The fixatives
will help protect the tissue from decay and autolysis. Routine
fixative of use is 10% formalin.
(ii) DEHYDRATION – This is the process of removing water
molecules from the tissue by passing the tissue through
ascending grades of alcohol. E.g methanol, acetone, 70-100%
alcohol.
(iii) CLEARING – This is the process of removing alcohol from the
tissue by passing it through chemicals that will remove the
alcohol molecules. These agents are called clearing agents.
Xylene is mostly used for clearing.
(iv) INFILTRATION – This is the process of filling intracellular
spaces left in the tissue by paraffin wax. This will help confer a
bit of rigidity to the processed tissue.
(v) EMBEDDING- This last step is manually done. This has to do
with immersing the processed tissue into a mould containing
liquid paraffin wax. This is for external support so that the tissue
won’t crumble during microtomy
SLIDE PRESENTATION ON AUTOMATION IN HISTOPATHOLOGY
SLIDE PRESENTATION ON AUTOMATION IN HISTOPATHOLOGY
BARCODING
 Automation in reception of tissue sample.
 Tissue arrives at the pathology laboratory.
 Barcode scanner accesses the specimen
and barcode cassette generated.
 A barcode scanner can be utilized to read
the code and transfer the information
between source and the laboratory
information system.
GROSSING
 Laser based devices are used to measure thickness of
specimens.
 It raises processing quality by making sure that the
thickness of specimens meets chosen protocols (3-4mm).
 Special grossing tools are available making it easy to
produce sections of uniform thickness on a consistent basis.
 The tools set includes a board with an adjustable depth
tissue well and a guide for the knife or surgical blade.
 The tissue wells provide an area for the placement of
the tissue and knife guide keeps the cutting blade
level.
AUTOMATED TISSUE PROCESSING
 A tissue processor is a device that prepares tissue
samples for sectioning and microscopic examination
in the diagnostic laboratory.
 The ATP machine plays a big role in the preparation
of the tissue by passing them through various
chemicals; a major process called TISSUE
PROCESSING.
TYPES OF TISSUE PROCESSORS
 CAROUSEL TYPE
 STATIONARY CHAMBER PROCESSOR
 VACCUM TISSUE PROCESSOR
 MICROWAVE PROCESSORS
Automated carousel type
 In the instrument, tissue samples were placed in a
basket which revolved from one reagent-containing
dish to the next and remained in each for an
established set period of time.
 Current automated carousel-type tissue processors,
such as those manufactured by Leica and Thermo
Shandon.
Stationary-Chamber Processor.
 In this type of instrument, the tissue samples are placed
in a retort into which the reagents are pumped in and
drained out following a time schedule.
 Stationary-retort processors are made by a number of
companies, including Leica, Sakura Finetek, Thermo
Shandon, and Vision BioSystems.
The elements used for processing in carousel or
stationary-chamber processors are
 Solvents: Formalin
Alcohol
Xylene and
Paraffin
 Physical agents : Vacuum,
Convective heat
Agitation
OPEN TYPE LINEAR TYPE
Electromechanical
mechanism for station to
station transfer with transfer
arm
Microcomputer control
Programmable 24 hrs clock Fume hood facility
Variable delay time Capacity: 110 casettes
2L Capacity glass beakers 10 reagent container areas
2 wax baths
AUTOMATED TISSUE
PROCESSOR LEICA TP
1020
AUTOMATED VACCUM
TISSUE PROCESSOR
PARTS OF THE ATPM – using TP 1050 Leica
model
ATPM – processing time schedule
 Processing schedule varies and it depends oh the following:
(i) Nature and size of tissue
(ii) Urgency
Beaker I – fixative (formalin) 1-2 hours
Beaker II – fixative 1 hour
Beaker III – fixative. 30- 45 minutes
Beaker IV – 70% alcohol. 30 minutes
Beaker V – 90% alcohol. 30 minutes
Beaker VI – Absolute alcohol. 1 hour
Beaker VII – Absolute alcohol. 1 hour
Beaker VIII – Methanol 30 minutes
Beaker IX – Xylene. 1-2 hours
Beaker X – Xylene 45 minutes – 1 hour
Wax bath I (done at 45°c) 2 hours
Wax bath II. 2 hours
 Most machines consists of ten beakers and two wax
baths thermostatically controlled to 56 C±3 C.
⁰ ⁰
 Beakers are filled with appropriate fluids and the wax
baths are filled with wax .the main switch is switched
on in order to keep the wax in a molten state.
 The tissue present perforated tissue basket is moved
through the different processing fluids according to
the time adjustment made on the machine.
Advantages of vaccum tissue processor
 Tissue cassettes are loaded into static chamber and
tissue remain in retort chamber through out the
process.
 Static single reaction chamber helps in keeping the
potentially hazardous solvents in special cabinet
separate from reaction chamber .
 Facilitates to process tissues with application of heat
vaccum at all stages of processing .
 Using vaccum and pressure, reagents and melted
paraffin wax moves into and out of the retort chamber.
 Each step is customized by controlling time,
temperature or pressure/ vaccum.
 Turnaround time is short .
 No evaporation of reagents.
DISADVANTAGES
 Because of the time required by these automated
instruments (8 hrs or longer), most processing is
carried out overnight, small biopsies can be done in
approximately 2.5 hrs on the regular processor.
 Laboratory problems:
1. The need to monitor the instruments
2. The safety concerns for instruments operating
unattended overnight.
3. The requirement for batch processing, which
interrupts the work flow.
MICROWAVE PROCESSORS
 Shortening the procedure is greatly facilitated by
replacing convective heat with microwave heating.
 Remove the need for hazardous chemicals such as
xylene.
Currently available microwave based tissue processors:
1. Energy beam science
2. Milestone
3. Sakura fineteck
4. Tissue tek express120.
Tissue-Tek ® Xpress® x120
Efficiency
•Continuous efficient workflow/ Loading every 20
minutes.
•Fewer human errors and rework , Reduced cost
•Reagent volume reduction of more than 80%
Speed
•Standardized 1-hour processing/ Loading every 20 mins
•Throughput of 120 cassettes/ hour leading to 960 cassettes in
an 8-hour shift
•Reduced patient waiting time
Quality
•Excellent morphology and sharp nuclear details due to
gentle microwave technology
•Standardized reproducible results: QC ready to use reagent
kits
•Formalin- and xylene free processing
SLIDE PRESENTATION ON AUTOMATION IN HISTOPATHOLOGY
Leica PELORIS
 The Leica PELORIS is a dual retort
processor capable of traditional or
xylene -free processing.
 Xylene -free protocols use two sets of
dehydrants : industrial denatured
alcohol (IDA) and isopropyl alcohol (IPA)
rather than separate dehydration and
clearing steps.
 This allows the use of higher
temperature paraffin wax impregnation
steps leading to faster processing.
MICROWAVE PROCESSORS
ADVANTAGES DISADVANTAGES
 Environment friendly
reagents: ethanol,
isopropanol, mixtures of
alcohol and paraffin.
 Reduce the number and
volume of reagents:
 No need of concentration of
solutions and no need of
clearing agent.
 Morphology antigenicity of
specimen is preserved.
 Improved turn around time.
 Size of tissue sample is
critical.(2mm)
 Expensive
 Required careful calibration
and monitoring.
 Solutions are manually
manipulated and
temperatures must be
maintained(70-85c)
AUTOMATION IN EMBEDDING
 The paraffin-impregnated samples taken from the tissue
processor must be suspended in molten paraffin and then cooled
to form a hard paraffin block for microtomy.
 This step, called embedding, is tedious and cumbersome
because the tissue must be removed from the cassettes, visually
oriented and placed in a mold, bathed with melted paraffin, and
transferred to a cold plate.
 Special care is necessary to ensure that the tissue is
appropriately oriented for sectioning, particularly for small
biopsies, and that pressure is applied on the sample to flatten
the surface and prevent air bubbles from collecting in the block.
 Two examples of automated embedding equipment are the
Sakura Finetek Tissue-Tek® AutoTEC® and Milestone’s
SYNERGY system
 Central to this unique instrument is the development of a
sectionable paraform cassette, which is used instead of the
regular plastic cassettes.
 The Paraform cassettes’ plastic mesh is the same density as the
solid paraffin so the resulting block can be sectioned using
routine microtomy techniques.
 The system is capable of embedding up to 120 cassettes per
hour with continuous loading of 4 magazines
Tissue-
Tek®
Paraform®
Cassettes,
are capable of locking in and
preserving the orientation of
very tiny or difficult to orient
tissues from grossing
through to imaging, helping
to further extend the range of
tissues suitable for
automated embedding.
Tissue-Tek®
Paraform®
biopsy
gels.
Tissue-Tek® AutoTEC®
MICROTOMY
 In this step, very thin sections of tissue are cut with
long, flat blades from a paraffin block, floated on a
water bath, and then transferred to a glass slide.
 there is not a single functional, fully-automated
microtome available to assist in standardizing this
highly-technical and variation-rich task of producing
thin tissue sections.
TYPES OF MICROTOMES
ROTARY MICROTOME
 Most commonly used
 Rotation of hand wheel by 360degree
cause the movement of the specimen
vertically past the cutting surface
 Ability to cut thin 2-3 micrometer sections.
 Can easily cut all types of hard, fragile, fatty tissues.
 ideal instrument for cutting serial sections
 Large block of tissues may be cut.
 Cutting angle and knife angle can be adjusted.
 They align and trim the
tissue blocks with
optimal precision.
 They reduce the risk of
losing tissue.
 Blocks are ready for
sectioning in only 10
seconds.
 This enables
laboratories to work
faster, better and more
efficiently.
Leica RM2255 Fully
Automated Rotary
Microtome
SLEDGE MICROTOME
 The specimen is held stationary and knife slides or
moves across the top of the specimen during
sectioning.
 Cutting sections of very large blocks of tissue and
hard tissues.
 Knife holding clamps are adjustable.
SLIDING MICROTOME FREEZING MICROTOME
AUTOMATED MICROTOME KNIFE
SHARPNERS
 They perform the actual honing
process automatically.
 They consists of a plate on which
knife held by arm rests at an
angle so that the cutting facet is in
contact with the plate.
 The plate moves in an oscillatory
and rotatory fashion which
produces sharpening of knife
edge.
STAINING AND COVERSLIP
 Alongside tissue processing, H & E stain is another
major component of histology which is automated in a
majority of labs.
 Linear style stainer.
 X-Y stainer design.
Linear style stainer
 The slide progress along a conveyer individually or with in a
rack being submerged in various solvents and dye pots.
 Time in each container is constant.
Disadvantages:
 Constant use of the same reagent pots can lead to variation in
staining as the day progresses and frequent reagent changes or
monitoring may be required.
 These systems are not fully enclosed.
 Issue arising from evaporation , humidity and increase user
contact with the chemicals
X-Y STAINER DESIGN
 This is usually enclosed and can attach to ovens and cover
slipper.
 These machines feature a robotic arm which moves the racks
along, following a predesigned protocol.
 Protocols can be designed by dictating the sequence of
reagents, and the time in each can be modified independently,
allowing multiple stains to be performed in single unit.
.
 User contact can be minimized as the rack can be loaded into
an empty input area.
 Disadvantage : they can cause batching of work and delay.
LINEAR STYLE STAINER X-Y STAINER
AUTOMATED COVERSLIPPERS
 Leica’s ST5020/CV5030
 Sakura’s Prisma and
 Ventana’s Symphony accept glass slides mounted
with blank sections and return H&E slides ready for
microscopic evaluation.
 The two widely used histochemical stainers are
 The dako artisan link system
 Ventana benchmarkSS
Leica ST5020-CV5030
 The Leica ST5020 reagent management system
(RMS) allows your lab to minimize reagent
changes and maintenance time by maximizing
reagent life.
.
Dako’s Artisan Link
First instrument to provide true walk-away automation for complex special stains.A slide
barcode reader standardizes and increases the speed of slide processing, reduces errors and
improves your laboratory productivity.The software allowsArtisan Link to be operated
either as a stand-alone or in a networked configuration system using a LAN System
(DakoLink) or a Laboratory Information System (LIS) providing 24/7 access to stainer
processing status.
A COMPARISON OF TWO COMMERCIALLY AVAILABLE AUTOMATED
TINCTORIAL STAINING PLATFORMS TO MANUAL STAINING
Manual Bench Mark SS Artisan
Slide capacity Limited by space, time
and reproducibility
1-20 1-48
Reagent
capacity
Limited by space and
safety
25 50
Unmanned runs No Yes Requires advance
deparaffinization of
section
Overnight runs No Yes Yes, but reduces life span
of reagents recommended
to be Refrigerated
Reduces contact
with harmful
components
No Yes Yes
Post-H&E Techniques
 Post-H&E techniques performed on histologic material fall into
the 2 general categories of “tissue-homogenate-based” and
“slide-based” procedures.
 The post-H&E slide-based methods include histochemistry,
immunohistochemistry and in situ hybridization.
 Automated histochemical stainers improve workflow in the
histology laboratory by reducing the turnaround time for special
stains. Some of the current systems available include Artisan
(Dako), Autostainer RSt (Vision BioSystems), and NexES
SS (Ventana).
The following is a list of automated
immunohistochemical systems marketed in the
United States:
 Nemesis 7200 (Biocare Medical),
 i6000 (BioGenex),
 Autostainer Plus and
 Eridan (Dako), Autostainer 720 (LabVision),
 Bench-Mark XT and BenchMark LT (Ventana), and
BondMax (VisionBioSystems).
Semi automatic autostainers Fully automated Autostainers
 They have facility to
stain the slides after
antigen retreival.
 Deparaffinization and
antigen retrieval steps
are done outside the
equipment.
 They execute complete
processing of
slides ,drying to counter
staining and continous
batch processing.
 Automation is also
provide with centralized
slide programming by
connecting equipment
to computer.
MOLECULAR TECHNIQUES
 Insitu hybridization and other molecular tests are increasingly
used techniques, where specific nucleic acids are targeted
with formalin fixed tissue sections.
 Individual gain or loss of gene expression can be veiwed with
both temporal and spatial information,and the targets can
either be RNA or DNA.
 THE BIOGenex Xmatrix Infinity is a staining system which can
can provide either IHC,ISH,IF.
 This system fully automates the run from dewax to final
coverslip, producing upto 100 slides per day.
Slide digitization
 Once a slide has been produced and stained, automated slide
scanners can scan it and produce high resolution images.
 most software and hardware can be used to scan at multiple
levels, allowing ‘z-stacking’ of images to duplicate the effect of
focusing up and down through the tissue.
 Omnyx flatbed scanner with a ‘load-and-go’ operation which
enables continuous scanning (overnight if required) to produce
images in a timely manner
REFERENCES
 Automation of the Histology Laboratory Azorides R.
Morales, MD, Mehdi Nassiri, MD
 Bancroft’s THEORY and PRACTICE of
HISTOLOGICAL TECHNIQUES 8th
edition.
 Histopathology Techniques and its Management,
Ramdas Naik MD.
 Internet
THANK YOU

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SLIDE PRESENTATION ON AUTOMATION IN HISTOPATHOLOGY

  • 1. BY: Dr Bhavya MODERATORS: Dr Kishan Dr Hemalatha AUTOMATION IN HISTOPATHOLOGY
  • 2. TABLE OF CONTENTS  INTRODUCTION  ADVANTAGES OF AUTOMATION  WHAT ISTISSUE PROCESSING?  AUTOMATION – GROSSING TISSUE PROCESSING EMBEDDING MICROTOMY H & E STAINING AND COVERSLIP POST H&ETECHNIQUES SLIDE DIGITIZATION
  • 3. INTRODUCTION  Providing high quality and efficiency is needed for the laboratory including histopathology section.  One of the ways to achieve this is by automation.  AUTOMATION is the technique of operating or controlling a process by highly automated means.  The word automation is used to describe the maximum use of instruments to perform laboratory work with minimum involvement of laboratory personale.
  • 4. ADVANTAGES OF AUTOMATION  Rapid than manual methods and turn around time is minimum by automation.  Less man power required than manual processing.  Clean , healthy and safer laboratory environment.  High quality results.  Reduces exposure to hazardous chemicals.
  • 5. WHAT IS TISSUE PROCESSING ? (i) FIXATION – This is the process of preserving or fixing tissues by passing them through chemicals called fixatives. The fixatives will help protect the tissue from decay and autolysis. Routine fixative of use is 10% formalin. (ii) DEHYDRATION – This is the process of removing water molecules from the tissue by passing the tissue through ascending grades of alcohol. E.g methanol, acetone, 70-100% alcohol. (iii) CLEARING – This is the process of removing alcohol from the tissue by passing it through chemicals that will remove the alcohol molecules. These agents are called clearing agents. Xylene is mostly used for clearing.
  • 6. (iv) INFILTRATION – This is the process of filling intracellular spaces left in the tissue by paraffin wax. This will help confer a bit of rigidity to the processed tissue. (v) EMBEDDING- This last step is manually done. This has to do with immersing the processed tissue into a mould containing liquid paraffin wax. This is for external support so that the tissue won’t crumble during microtomy
  • 9. BARCODING  Automation in reception of tissue sample.  Tissue arrives at the pathology laboratory.  Barcode scanner accesses the specimen and barcode cassette generated.  A barcode scanner can be utilized to read the code and transfer the information between source and the laboratory information system.
  • 10. GROSSING  Laser based devices are used to measure thickness of specimens.  It raises processing quality by making sure that the thickness of specimens meets chosen protocols (3-4mm).  Special grossing tools are available making it easy to produce sections of uniform thickness on a consistent basis.  The tools set includes a board with an adjustable depth tissue well and a guide for the knife or surgical blade.
  • 11.  The tissue wells provide an area for the placement of the tissue and knife guide keeps the cutting blade level.
  • 12. AUTOMATED TISSUE PROCESSING  A tissue processor is a device that prepares tissue samples for sectioning and microscopic examination in the diagnostic laboratory.  The ATP machine plays a big role in the preparation of the tissue by passing them through various chemicals; a major process called TISSUE PROCESSING.
  • 13. TYPES OF TISSUE PROCESSORS  CAROUSEL TYPE  STATIONARY CHAMBER PROCESSOR  VACCUM TISSUE PROCESSOR  MICROWAVE PROCESSORS
  • 14. Automated carousel type  In the instrument, tissue samples were placed in a basket which revolved from one reagent-containing dish to the next and remained in each for an established set period of time.  Current automated carousel-type tissue processors, such as those manufactured by Leica and Thermo Shandon.
  • 15. Stationary-Chamber Processor.  In this type of instrument, the tissue samples are placed in a retort into which the reagents are pumped in and drained out following a time schedule.  Stationary-retort processors are made by a number of companies, including Leica, Sakura Finetek, Thermo Shandon, and Vision BioSystems.
  • 16. The elements used for processing in carousel or stationary-chamber processors are  Solvents: Formalin Alcohol Xylene and Paraffin  Physical agents : Vacuum, Convective heat Agitation
  • 17. OPEN TYPE LINEAR TYPE Electromechanical mechanism for station to station transfer with transfer arm Microcomputer control Programmable 24 hrs clock Fume hood facility Variable delay time Capacity: 110 casettes 2L Capacity glass beakers 10 reagent container areas 2 wax baths
  • 18. AUTOMATED TISSUE PROCESSOR LEICA TP 1020 AUTOMATED VACCUM TISSUE PROCESSOR
  • 19. PARTS OF THE ATPM – using TP 1050 Leica model
  • 20. ATPM – processing time schedule  Processing schedule varies and it depends oh the following: (i) Nature and size of tissue (ii) Urgency Beaker I – fixative (formalin) 1-2 hours Beaker II – fixative 1 hour Beaker III – fixative. 30- 45 minutes Beaker IV – 70% alcohol. 30 minutes Beaker V – 90% alcohol. 30 minutes Beaker VI – Absolute alcohol. 1 hour Beaker VII – Absolute alcohol. 1 hour Beaker VIII – Methanol 30 minutes Beaker IX – Xylene. 1-2 hours Beaker X – Xylene 45 minutes – 1 hour Wax bath I (done at 45°c) 2 hours Wax bath II. 2 hours
  • 21.  Most machines consists of ten beakers and two wax baths thermostatically controlled to 56 C±3 C. ⁰ ⁰  Beakers are filled with appropriate fluids and the wax baths are filled with wax .the main switch is switched on in order to keep the wax in a molten state.  The tissue present perforated tissue basket is moved through the different processing fluids according to the time adjustment made on the machine.
  • 22. Advantages of vaccum tissue processor  Tissue cassettes are loaded into static chamber and tissue remain in retort chamber through out the process.  Static single reaction chamber helps in keeping the potentially hazardous solvents in special cabinet separate from reaction chamber .  Facilitates to process tissues with application of heat vaccum at all stages of processing .
  • 23.  Using vaccum and pressure, reagents and melted paraffin wax moves into and out of the retort chamber.  Each step is customized by controlling time, temperature or pressure/ vaccum.  Turnaround time is short .  No evaporation of reagents.
  • 24. DISADVANTAGES  Because of the time required by these automated instruments (8 hrs or longer), most processing is carried out overnight, small biopsies can be done in approximately 2.5 hrs on the regular processor.  Laboratory problems: 1. The need to monitor the instruments 2. The safety concerns for instruments operating unattended overnight. 3. The requirement for batch processing, which interrupts the work flow.
  • 25. MICROWAVE PROCESSORS  Shortening the procedure is greatly facilitated by replacing convective heat with microwave heating.  Remove the need for hazardous chemicals such as xylene. Currently available microwave based tissue processors: 1. Energy beam science 2. Milestone 3. Sakura fineteck 4. Tissue tek express120.
  • 26. Tissue-Tek ® Xpress® x120 Efficiency •Continuous efficient workflow/ Loading every 20 minutes. •Fewer human errors and rework , Reduced cost •Reagent volume reduction of more than 80% Speed •Standardized 1-hour processing/ Loading every 20 mins •Throughput of 120 cassettes/ hour leading to 960 cassettes in an 8-hour shift •Reduced patient waiting time Quality •Excellent morphology and sharp nuclear details due to gentle microwave technology •Standardized reproducible results: QC ready to use reagent kits •Formalin- and xylene free processing
  • 28. Leica PELORIS  The Leica PELORIS is a dual retort processor capable of traditional or xylene -free processing.  Xylene -free protocols use two sets of dehydrants : industrial denatured alcohol (IDA) and isopropyl alcohol (IPA) rather than separate dehydration and clearing steps.  This allows the use of higher temperature paraffin wax impregnation steps leading to faster processing.
  • 29. MICROWAVE PROCESSORS ADVANTAGES DISADVANTAGES  Environment friendly reagents: ethanol, isopropanol, mixtures of alcohol and paraffin.  Reduce the number and volume of reagents:  No need of concentration of solutions and no need of clearing agent.  Morphology antigenicity of specimen is preserved.  Improved turn around time.  Size of tissue sample is critical.(2mm)  Expensive  Required careful calibration and monitoring.  Solutions are manually manipulated and temperatures must be maintained(70-85c)
  • 30. AUTOMATION IN EMBEDDING  The paraffin-impregnated samples taken from the tissue processor must be suspended in molten paraffin and then cooled to form a hard paraffin block for microtomy.  This step, called embedding, is tedious and cumbersome because the tissue must be removed from the cassettes, visually oriented and placed in a mold, bathed with melted paraffin, and transferred to a cold plate.  Special care is necessary to ensure that the tissue is appropriately oriented for sectioning, particularly for small biopsies, and that pressure is applied on the sample to flatten the surface and prevent air bubbles from collecting in the block.
  • 31.  Two examples of automated embedding equipment are the Sakura Finetek Tissue-Tek® AutoTEC® and Milestone’s SYNERGY system  Central to this unique instrument is the development of a sectionable paraform cassette, which is used instead of the regular plastic cassettes.  The Paraform cassettes’ plastic mesh is the same density as the solid paraffin so the resulting block can be sectioned using routine microtomy techniques.  The system is capable of embedding up to 120 cassettes per hour with continuous loading of 4 magazines
  • 32. Tissue- Tek® Paraform® Cassettes, are capable of locking in and preserving the orientation of very tiny or difficult to orient tissues from grossing through to imaging, helping to further extend the range of tissues suitable for automated embedding. Tissue-Tek® Paraform® biopsy gels.
  • 34. MICROTOMY  In this step, very thin sections of tissue are cut with long, flat blades from a paraffin block, floated on a water bath, and then transferred to a glass slide.  there is not a single functional, fully-automated microtome available to assist in standardizing this highly-technical and variation-rich task of producing thin tissue sections.
  • 35. TYPES OF MICROTOMES ROTARY MICROTOME  Most commonly used  Rotation of hand wheel by 360degree cause the movement of the specimen vertically past the cutting surface  Ability to cut thin 2-3 micrometer sections.  Can easily cut all types of hard, fragile, fatty tissues.  ideal instrument for cutting serial sections  Large block of tissues may be cut.  Cutting angle and knife angle can be adjusted.
  • 36.  They align and trim the tissue blocks with optimal precision.  They reduce the risk of losing tissue.  Blocks are ready for sectioning in only 10 seconds.  This enables laboratories to work faster, better and more efficiently. Leica RM2255 Fully Automated Rotary Microtome
  • 37. SLEDGE MICROTOME  The specimen is held stationary and knife slides or moves across the top of the specimen during sectioning.  Cutting sections of very large blocks of tissue and hard tissues.  Knife holding clamps are adjustable.
  • 39. AUTOMATED MICROTOME KNIFE SHARPNERS  They perform the actual honing process automatically.  They consists of a plate on which knife held by arm rests at an angle so that the cutting facet is in contact with the plate.  The plate moves in an oscillatory and rotatory fashion which produces sharpening of knife edge.
  • 40. STAINING AND COVERSLIP  Alongside tissue processing, H & E stain is another major component of histology which is automated in a majority of labs.  Linear style stainer.  X-Y stainer design.
  • 41. Linear style stainer  The slide progress along a conveyer individually or with in a rack being submerged in various solvents and dye pots.  Time in each container is constant. Disadvantages:  Constant use of the same reagent pots can lead to variation in staining as the day progresses and frequent reagent changes or monitoring may be required.  These systems are not fully enclosed.  Issue arising from evaporation , humidity and increase user contact with the chemicals
  • 42. X-Y STAINER DESIGN  This is usually enclosed and can attach to ovens and cover slipper.  These machines feature a robotic arm which moves the racks along, following a predesigned protocol.  Protocols can be designed by dictating the sequence of reagents, and the time in each can be modified independently, allowing multiple stains to be performed in single unit. .  User contact can be minimized as the rack can be loaded into an empty input area.  Disadvantage : they can cause batching of work and delay.
  • 43. LINEAR STYLE STAINER X-Y STAINER
  • 44. AUTOMATED COVERSLIPPERS  Leica’s ST5020/CV5030  Sakura’s Prisma and  Ventana’s Symphony accept glass slides mounted with blank sections and return H&E slides ready for microscopic evaluation.  The two widely used histochemical stainers are  The dako artisan link system  Ventana benchmarkSS
  • 45. Leica ST5020-CV5030  The Leica ST5020 reagent management system (RMS) allows your lab to minimize reagent changes and maintenance time by maximizing reagent life. .
  • 46. Dako’s Artisan Link First instrument to provide true walk-away automation for complex special stains.A slide barcode reader standardizes and increases the speed of slide processing, reduces errors and improves your laboratory productivity.The software allowsArtisan Link to be operated either as a stand-alone or in a networked configuration system using a LAN System (DakoLink) or a Laboratory Information System (LIS) providing 24/7 access to stainer processing status.
  • 47. A COMPARISON OF TWO COMMERCIALLY AVAILABLE AUTOMATED TINCTORIAL STAINING PLATFORMS TO MANUAL STAINING Manual Bench Mark SS Artisan Slide capacity Limited by space, time and reproducibility 1-20 1-48 Reagent capacity Limited by space and safety 25 50 Unmanned runs No Yes Requires advance deparaffinization of section Overnight runs No Yes Yes, but reduces life span of reagents recommended to be Refrigerated Reduces contact with harmful components No Yes Yes
  • 48. Post-H&E Techniques  Post-H&E techniques performed on histologic material fall into the 2 general categories of “tissue-homogenate-based” and “slide-based” procedures.  The post-H&E slide-based methods include histochemistry, immunohistochemistry and in situ hybridization.  Automated histochemical stainers improve workflow in the histology laboratory by reducing the turnaround time for special stains. Some of the current systems available include Artisan (Dako), Autostainer RSt (Vision BioSystems), and NexES SS (Ventana).
  • 49. The following is a list of automated immunohistochemical systems marketed in the United States:  Nemesis 7200 (Biocare Medical),  i6000 (BioGenex),  Autostainer Plus and  Eridan (Dako), Autostainer 720 (LabVision),  Bench-Mark XT and BenchMark LT (Ventana), and BondMax (VisionBioSystems).
  • 50. Semi automatic autostainers Fully automated Autostainers  They have facility to stain the slides after antigen retreival.  Deparaffinization and antigen retrieval steps are done outside the equipment.  They execute complete processing of slides ,drying to counter staining and continous batch processing.  Automation is also provide with centralized slide programming by connecting equipment to computer.
  • 51. MOLECULAR TECHNIQUES  Insitu hybridization and other molecular tests are increasingly used techniques, where specific nucleic acids are targeted with formalin fixed tissue sections.  Individual gain or loss of gene expression can be veiwed with both temporal and spatial information,and the targets can either be RNA or DNA.  THE BIOGenex Xmatrix Infinity is a staining system which can can provide either IHC,ISH,IF.  This system fully automates the run from dewax to final coverslip, producing upto 100 slides per day.
  • 52. Slide digitization  Once a slide has been produced and stained, automated slide scanners can scan it and produce high resolution images.  most software and hardware can be used to scan at multiple levels, allowing ‘z-stacking’ of images to duplicate the effect of focusing up and down through the tissue.  Omnyx flatbed scanner with a ‘load-and-go’ operation which enables continuous scanning (overnight if required) to produce images in a timely manner
  • 53. REFERENCES  Automation of the Histology Laboratory Azorides R. Morales, MD, Mehdi Nassiri, MD  Bancroft’s THEORY and PRACTICE of HISTOLOGICAL TECHNIQUES 8th edition.  Histopathology Techniques and its Management, Ramdas Naik MD.  Internet