The document describes the structure and processing of radiographic film. It discusses the components of film, including the base, emulsion, and silver halide crystals. It explains the formation of latent images when x-rays strike the film. The stages of film processing are outlined, including development, fixing, washing and drying. Both manual and automated processing techniques are covered. Factors that can affect film processing like temperature are also mentioned.
Photolithography, also called optical lithography or UV lithography, is a process used in microfabrication to pattern parts on a thin film or the bulk of a substrate (also called a wafer). It uses light to transfer a geometric pattern from a photomask (also called an optical mask) to a photosensitive (that is, light-sensitive) chemical photoresist on the substrate. A series of chemical treatments then either etches the exposure pattern into the material or enables deposition of a new material in the desired pattern upon the material underneath the photoresist. In complex integrated circuits, a CMOS wafer may go through the photolithographic cycle as many as 50 times.
Photolithography shares some fundamental principles with photography in that the pattern in the photoresist etching is created by exposing it to light, either directly (without using a mask) or with a projected image using a photomask. This procedure is comparable to a high precision version of the method used to make printed circuit boards. Subsequent stages in the process have more in common with etching than with lithographic printing. This method can create extremely small patterns, down to a few tens of nanometers in size. It provides precise control of the shape and size of the objects it creates and can create patterns over an entire surface cost-effectively. Its main disadvantages are that it requires a flat substrate to start with, it is not very effective at creating shapes that are not flat, and it can require extremely clean operating conditions. Photolithography is the standard method of printed circuit board (PCB) and microprocessor fabrication. Directed self-assembly is being evaluated as an alternative to photolithography
Photolithography, also called optical lithography or UV lithography, is a process used in microfabrication to pattern parts on a thin film or the bulk of a substrate (also called a wafer). It uses light to transfer a geometric pattern from a photomask (also called an optical mask) to a photosensitive (that is, light-sensitive) chemical photoresist on the substrate. A series of chemical treatments then either etches the exposure pattern into the material or enables deposition of a new material in the desired pattern upon the material underneath the photoresist. In complex integrated circuits, a CMOS wafer may go through the photolithographic cycle as many as 50 times.
Photolithography shares some fundamental principles with photography in that the pattern in the photoresist etching is created by exposing it to light, either directly (without using a mask) or with a projected image using a photomask. This procedure is comparable to a high precision version of the method used to make printed circuit boards. Subsequent stages in the process have more in common with etching than with lithographic printing. This method can create extremely small patterns, down to a few tens of nanometers in size. It provides precise control of the shape and size of the objects it creates and can create patterns over an entire surface cost-effectively. Its main disadvantages are that it requires a flat substrate to start with, it is not very effective at creating shapes that are not flat, and it can require extremely clean operating conditions. Photolithography is the standard method of printed circuit board (PCB) and microprocessor fabrication. Directed self-assembly is being evaluated as an alternative to photolithography
- Video recording of this lecture in English language: https://youtu.be/lK81BzxMqdo
- Video recording of this lecture in Arabic language: https://youtu.be/Ve4P0COk9OI
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
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- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Ve...kevinkariuki227
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
Report Back from SGO 2024: What’s the Latest in Cervical Cancer?bkling
Are you curious about what’s new in cervical cancer research or unsure what the findings mean? Join Dr. Emily Ko, a gynecologic oncologist at Penn Medicine, to learn about the latest updates from the Society of Gynecologic Oncology (SGO) 2024 Annual Meeting on Women’s Cancer. Dr. Ko will discuss what the research presented at the conference means for you and answer your questions about the new developments.
Couples presenting to the infertility clinic- Do they really have infertility...Sujoy Dasgupta
Dr Sujoy Dasgupta presented the study on "Couples presenting to the infertility clinic- Do they really have infertility? – The unexplored stories of non-consummation" in the 13th Congress of the Asia Pacific Initiative on Reproduction (ASPIRE 2024) at Manila on 24 May, 2024.
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Prix Galien International 2024 Forum ProgramLevi Shapiro
June 20, 2024, Prix Galien International and Jerusalem Ethics Forum in ROME. Detailed agenda including panels:
- ADVANCES IN CARDIOLOGY: A NEW PARADIGM IS COMING
- WOMEN’S HEALTH: FERTILITY PRESERVATION
- WHAT’S NEW IN THE TREATMENT OF INFECTIOUS,
ONCOLOGICAL AND INFLAMMATORY SKIN DISEASES?
- ARTIFICIAL INTELLIGENCE AND ETHICS
- GENE THERAPY
- BEYOND BORDERS: GLOBAL INITIATIVES FOR DEMOCRATIZING LIFE SCIENCE TECHNOLOGIES AND PROMOTING ACCESS TO HEALTHCARE
- ETHICAL CHALLENGES IN LIFE SCIENCES
- Prix Galien International Awards Ceremony
Title: Sense of Taste
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the structure and function of taste buds.
Describe the relationship between the taste threshold and taste index of common substances.
Explain the chemical basis and signal transduction of taste perception for each type of primary taste sensation.
Recognize different abnormalities of taste perception and their causes.
Key Topics:
Significance of Taste Sensation:
Differentiation between pleasant and harmful food
Influence on behavior
Selection of food based on metabolic needs
Receptors of Taste:
Taste buds on the tongue
Influence of sense of smell, texture of food, and pain stimulation (e.g., by pepper)
Primary and Secondary Taste Sensations:
Primary taste sensations: Sweet, Sour, Salty, Bitter, Umami
Chemical basis and signal transduction mechanisms for each taste
Taste Threshold and Index:
Taste threshold values for Sweet (sucrose), Salty (NaCl), Sour (HCl), and Bitter (Quinine)
Taste index relationship: Inversely proportional to taste threshold
Taste Blindness:
Inability to taste certain substances, particularly thiourea compounds
Example: Phenylthiocarbamide
Structure and Function of Taste Buds:
Composition: Epithelial cells, Sustentacular/Supporting cells, Taste cells, Basal cells
Features: Taste pores, Taste hairs/microvilli, and Taste nerve fibers
Location of Taste Buds:
Found in papillae of the tongue (Fungiform, Circumvallate, Foliate)
Also present on the palate, tonsillar pillars, epiglottis, and proximal esophagus
Mechanism of Taste Stimulation:
Interaction of taste substances with receptors on microvilli
Signal transduction pathways for Umami, Sweet, Bitter, Sour, and Salty tastes
Taste Sensitivity and Adaptation:
Decrease in sensitivity with age
Rapid adaptation of taste sensation
Role of Saliva in Taste:
Dissolution of tastants to reach receptors
Washing away the stimulus
Taste Preferences and Aversions:
Mechanisms behind taste preference and aversion
Influence of receptors and neural pathways
Impact of Sensory Nerve Damage:
Degeneration of taste buds if the sensory nerve fiber is cut
Abnormalities of Taste Detection:
Conditions: Ageusia, Hypogeusia, Dysgeusia (parageusia)
Causes: Nerve damage, neurological disorders, infections, poor oral hygiene, adverse drug effects, deficiencies, aging, tobacco use, altered neurotransmitter levels
Neurotransmitters and Taste Threshold:
Effects of serotonin (5-HT) and norepinephrine (NE) on taste sensitivity
Supertasters:
25% of the population with heightened sensitivity to taste, especially bitterness
Increased number of fungiform papillae
Ozempic: Preoperative Management of Patients on GLP-1 Receptor Agonists Saeid Safari
Preoperative Management of Patients on GLP-1 Receptor Agonists like Ozempic and Semiglutide
ASA GUIDELINE
NYSORA Guideline
2 Case Reports of Gastric Ultrasound
Anti ulcer drugs and their Advance pharmacology ||
Anti-ulcer drugs are medications used to prevent and treat ulcers in the stomach and upper part of the small intestine (duodenal ulcers). These ulcers are often caused by an imbalance between stomach acid and the mucosal lining, which protects the stomach lining.
||Scope: Overview of various classes of anti-ulcer drugs, their mechanisms of action, indications, side effects, and clinical considerations.
The prostate is an exocrine gland of the male mammalian reproductive system
It is a walnut-sized gland that forms part of the male reproductive system and is located in front of the rectum and just below the urinary bladder
Function is to store and secrete a clear, slightly alkaline fluid that constitutes 10-30% of the volume of the seminal fluid that along with the spermatozoa, constitutes semen
A healthy human prostate measures (4cm-vertical, by 3cm-horizontal, 2cm ant-post ).
It surrounds the urethra just below the urinary bladder. It has anterior, median, posterior and two lateral lobes
It’s work is regulated by androgens which are responsible for male sex characteristics
Generalised disease of the prostate due to hormonal derangement which leads to non malignant enlargement of the gland (increase in the number of epithelial cells and stromal tissue)to cause compression of the urethra leading to symptoms (LUTS
Tom Selleck Health: A Comprehensive Look at the Iconic Actor’s Wellness Journeygreendigital
Tom Selleck, an enduring figure in Hollywood. has captivated audiences for decades with his rugged charm, iconic moustache. and memorable roles in television and film. From his breakout role as Thomas Magnum in Magnum P.I. to his current portrayal of Frank Reagan in Blue Bloods. Selleck's career has spanned over 50 years. But beyond his professional achievements. fans have often been curious about Tom Selleck Health. especially as he has aged in the public eye.
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Introduction
Many have been interested in Tom Selleck health. not only because of his enduring presence on screen but also because of the challenges. and lifestyle choices he has faced and made over the years. This article delves into the various aspects of Tom Selleck health. exploring his fitness regimen, diet, mental health. and the challenges he has encountered as he ages. We'll look at how he maintains his well-being. the health issues he has faced, and his approach to ageing .
Early Life and Career
Childhood and Athletic Beginnings
Tom Selleck was born on January 29, 1945, in Detroit, Michigan, and grew up in Sherman Oaks, California. From an early age, he was involved in sports, particularly basketball. which played a significant role in his physical development. His athletic pursuits continued into college. where he attended the University of Southern California (USC) on a basketball scholarship. This early involvement in sports laid a strong foundation for his physical health and disciplined lifestyle.
Transition to Acting
Selleck's transition from an athlete to an actor came with its physical demands. His first significant role in "Magnum P.I." required him to perform various stunts and maintain a fit appearance. This role, which he played from 1980 to 1988. necessitated a rigorous fitness routine to meet the show's demands. setting the stage for his long-term commitment to health and wellness.
Fitness Regimen
Workout Routine
Tom Selleck health and fitness regimen has evolved. adapting to his changing roles and age. During his "Magnum, P.I." days. Selleck's workouts were intense and focused on building and maintaining muscle mass. His routine included weightlifting, cardiovascular exercises. and specific training for the stunts he performed on the show.
Selleck adjusted his fitness routine as he aged to suit his body's needs. Today, his workouts focus on maintaining flexibility, strength, and cardiovascular health. He incorporates low-impact exercises such as swimming, walking, and light weightlifting. This balanced approach helps him stay fit without putting undue strain on his joints and muscles.
Importance of Flexibility and Mobility
In recent years, Selleck has emphasized the importance of flexibility and mobility in his fitness regimen. Understanding the natural decline in muscle mass and joint flexibility with age. he includes stretching and yoga in his routine. These practices help prevent injuries, improve posture, and maintain mobilit
Tom Selleck Health: A Comprehensive Look at the Iconic Actor’s Wellness Journey
DESCRIBE THE RADIOGRAPHIC FILM AND FILM PROCESSING.pptx
1. DESCRIBE THE RADIOGRAPHIC
FILM AND FILM PROCESSING
NDANSAW JOSEPH NDIFELAYE
DEPARTMENT OF RADIOLOGY
AMINU KANO TEACHING HOSPITAL, KANO
05-05-2022
5/2/2023 1
2. OUTLINE:
• Introduction
• Structure of a film
• Classification of X-ray films
• Latent image formation
• Conventional Film processing – manual, automatic.
• Factors affecting conventional film processing
• Artifacts
• Film storage
• Digital film processing.
• Summary
• Conclusion
5/2/2023 2
3. Introduction
• When an X-ray beam reaches the patient, it has no useful medical
information.
• After interaction with the tissues, it has all information that can be
revealed by that particular radiographic examination.
• This information cannot be used unless its transformed in a form that
can be viewed with the eye.
• The photographic film is the material used to decode the information
carried by the attenuated X-ray beam.
5/2/2023 3
4. Introduction cont
• Radiographic film acquires an image and must be processed before it
is visible.
• The method of transfer of this information might involve a magnetic
tape or disc, a fluoroscopic screen or xenography.
5/2/2023 4
5. Film Structure
• X – ray film is a photographic film consisting of a photographically
active or radiation sensitive emulsion.
• The emulsion is coated on one or both sides of the base.
• The emulsion is attached to the base by a thin layer of adhesive.
• The delicate emulsion is protected from mechanical damage by layers
known as supercoatings.
5/2/2023 5
7. Film Structure cont – Film Base
• It provides support to the fragile photographic emulsion.
• It must not produce visible pattern or absorb too much light when the
radiographic film is viewed.
• It flexibility, thickness and strength must allow for ease of processing.
• It must have dimensional stability.
5/2/2023 7
8. Film Structure cont – film base
• Glass plates
• Cellulose nitrate
• Cellulose triacetate
• Polyester: DMT and ethylene glycol.
• Blue tint added to X-ray base or emulsion.
• Polyester are thinner than triacetate.
5/2/2023 8
9. Film Structure cont- emulsion
• Contains gelatin and silver halide
• The exact composition of the various emulsions is a closely guarded
industrial secret.
• Most conventional X-ray film is made for use with intensifying screens
and has emulsion coated on both sides of the base.
• Emulsion thickness varies with film type but not usually thicker than
0.5mm.
5/2/2023 9
10. Film Structure cont – emulsion - gelatin
• Made from mostly cattle bone.
• It keeps silver halide grains well dispersed and prevent clumping of
grains.
• Can be penetrated by processing solution rapidly without destroying
its strength.
• Its readily available in large quantity and uniform quality.
5/2/2023 10
11. Film Structure cont – emulsion – silver halide
• It’s the light sensitive material in the emulsion.
• It consist of 90-95% AgBr and 5-10% AgI.
• The presence of AgI produces an emulsion of much higher sensitivity
than pure AgBr emulsion.
• The silver iodobromide crystals are precipitated under particular
concentration and temperature.
• The silver iodobromide is not a perfect crystal.
5/2/2023 11
12. Film Structure cont – emulsion – silver halide
• Chemical sensitization of a crystal is by addition of allylthiourea to
emulsion which react with the halide to produce silver sulfide.
• Silver sulfide referred to as the sensitive speck.
• The sensitive speck traps electrons to begin the formation of the
latent image.
5/2/2023 12
13. Film structure cont - Layers
• Base: cellulose triacetate or polyester for support.
• Substratum: adhesive layer containing gelatin and solvent that bind
emulsion and base.
• Emulsion: silver halide and gelatin with some hardening agents in
main layer where latent images are formed.
• Protective layer: gelatin protects emulsion from damage.
• Total thickness of the film is about 0.25mm.
5/2/2023 13
14. • TYPES OF X-RAY FILM
• Screen type films Direct exposure type Structure Others
• Conventional dental procedures single emulsion
• Orthochromatic double emulsion
5/2/2023 14
15. Type of film – single and double emulsion
• Single Emulsion Film e.g. Mammography
• It has the advantage of better image quality/contrast
• Double Emulsion Film e.g. conventional Film
• Its has an advantage of higher efficiency with relative poor contrast
• Laser Films: CT, MRI
• Duplication films
• Subtraction films
• Fluoroscopic spot filming
5/2/2023 15
16. Type of film - Screen film
• Some films needs to be used in combination with screens.
• Screens uses various types of phosphor layer that emit light photon of
different colors.
• It is important to note that the color of light emitted (wavelength) by
a screen must match the light sensitivity of the film used (spectral
matching).
• Conventional films: sensitive to ultraviolet and blue lights.
• Orthochromatic films: sensitive to ultraviolet, blue and green lights.
5/2/2023 16
19. Concept of latent image formation
When x-ray photons or light strike the grains of the sensitive silver
halide in the emulsion, some of the Br- ion electrons are liberated
which are then capture by the Ag+ ions to be converted to metallic
silver at the region of the sensitivity speck.
5/2/2023 19
20. Concept of latent image formation
• This single atom of silver then acts as electron trap for a second
electron.
• The negative charge causes a second silver ion to migrate to the trap
to form another silver atom and the process continues.
• The negative bromide lost is taken by the gelatin of the emulsion.
• The small clumps of silver can be seen with electron microscope.
• The clumps of silver are termed latent image centers.
• This needs processing to become visible image.
5/2/2023 20
21. Film processing
• Film processing is a series of chemical processes that converts the
latent image into a visible image
• Processing of conventional radiograph can either be; Manual or
Automatic film processing
• Both share the same principle but differ in the temperature and
concentration of chemicals used
• Automatic film processing use roller transport or track system .
5/2/2023 21
25. Development
• A chemical process that amplifies the latent image to form a visible
image
• The basic reaction is reduction (addition of an electron) of the silver
ion to black metallic silver by the developing agent.
• This causes the crystals to become visible black specks in the
emulsion.
• Development is generally an all-or-none phenomenon because an
entire grain is developed once the process begins.
5/2/2023 25
26. Development cont
• Development is usually initiated at the site of the latent image.
• The silver in a grain that does not contain a latent image can also be
reduced by the developer but at a much slower rate.
• Development should be discontinued when the difference between
exposed developed grains and unexposed undeveloped grains is at a
maximum .
5/2/2023 26
28. Developing agents
• They are reducing agents which supply electrons to the silver
ions in the exposed silver halide grains converting them to atoms
of metallic silver.
• The chemical agents used are hydroquinone, phenidone and
metol.
• Hydroquinone is used mainly in combination with metol or
phenidone.
• This leads to synergy.
5/2/2023 28
29. Developing Agents cont.
• They reduce silver ions to metallic silver causing oxidation and
inactivation of developing agent and the liberation of hydrogen ions.
• The silver thus formed is deposited at the latent image site.
• It gradually enlarge this initially microscopic black spot into a single
visible black speck of silver in the emulsion.
5/2/2023 29
30. Developing Agent cont
• Activator (Sodium carbonate) – provide alkaline medium, softens and
swells the emulsion so that the reducers can reach the exposed
crystal
• Restrainer (Potassium bromide) – moderates the development by
making them become more selective therefore reduce fogging.
• Preservative (Sodium sulfite) – Helps to protect the reducing agents
from oxidation by atmospheric oxygen
• Hardener (Glutaraldehyde) - retards the swelling of the emulsion.
5/2/2023 30
31. Developing agents cont
Properties of an ideal developer
Must be selective and distinguish between exposed and unexposed
grains.
Sufficiently high activity.
As resistant as possible to the presence of bromine ions.
No single reducing agent satisfies all these requirements so
combinations are used.
5/2/2023 31
32. Developer Replenishment
• During use, developer solution is consumed but acquire hydrogen
ions and bromide.
• Replenishment must compensate for these agents by being free from
bromide, by containing alkali agents and buffers and restoring
preservative and developing agent.
• Each time a film is processed, a small portion of the developing
solution is removed and replaced with a replenishment solution.
5/2/2023 32
33. Developer Replenishment cont
• Almost all conventional radiographs are now processed with
automatic film processor with automatic developer replenishment.
• Traditional replenishment was developed for high volume operations
were many films are processed in a day.
• Many automatic processors operate in small installations making
oxidation of the developer more important than the consequences of
the development process.
• Replenishment is either for high volume of low volume.
5/2/2023 33
34. Developer Replenishment – high volume
• During use, developer solution is consumed but acquire hydrogen
ions and bromide.
• Replenishment must compensate for these agents by being free from
bromide, by containing alkali agents and buffers and restoring
preservative and developing agent.
• Lifetime of a tank of developer will last about 2-3months in a busy
department.
• Replenishment rate is 60ml of developer for each 14x17 inch film
processed.
5/2/2023 34
35. Developer Replenishment – low volume
• Many automatic processors operate in small installations making
oxidation of the developer more important than the consequences of
the development process.
• Here, pH increases, no bromide produced and replenishment is
infrequent.
• Standard replenisher has high pH with no bromide.
• Decrease bromide concentration has adverse effect on the film
sensitometry.
5/2/2023 35
36. Developer Replenishment – low volume
• A developer with low pH and higher sulfite concentration retard
oxidation
• High buffering capacity to minimize pH effect of oxidation.
• Replenisher has low pH than developer and contains bromide.
• Replenisher rate is usually higher, 90ml per 14x17 inch film to
increase developer turnover rate.
5/2/2023 36
37. Rinsing
• Rinsing or Stop bath: The film is next rinsed to remove the developer
solution before proceding to the fixing solution
• Rinsing time – 30secs.
5/2/2023 37
38. Fixing
• Only part of the silver halide in the emulsion is reduced to silver
during development.
• The remaining silver impairs both the immediate and permanence
usefulness of the developed radiograph.
• The fixing solution must remove silver halide without damaging the
image formed by the metallic silver.
• Ag+ x Br- = constant
5/2/2023 38
39. Fixing
• The fixing agents used are cyanides and thiosulfates.
• The thiosulfates in the form of sodium and ammonium salts are
commonly used.
• The ammonium thiosulfate is more active and is used in fixer supplied
in liquid form.
• Fixing solution also contains a chromium or aluminum compound.
• It also contains an acid, stabilizers and a buffer to maintain the acidic
pH level.
• Fixing time: 15mins.
5/2/2023 39
40. Washing
• The film is washed with water to remove all the fixing-bath chemicals
• Retained thiosulfate in the emulsion will react with silver image to
form brown silver sulfide.
• The amount of thiosulfate retained determines the useful lifetime of
processed film
• The less the amount of retained thiosulfate the longer the life span
• Duration: 20mins.
5/2/2023 40
41. Drying
• The film is finally dried for viewing
• It is passed through a chamber in which hot air is circulating
• Duration: 30mins.
5/2/2023 41
42. Summary of events in processing a Radiograph
Step Purpose Manual Automatic
Development Production of manifest image from the latent image 5 min 22s
Rinsing to remove the developer solution before proceeding to the fixing
solution.
30s -
Fixing Arrest the chemical activity of the residual developer,removes
remaining silver halides and hardening of gelatin.
15 min 22s
Washing Removal of Excess/residual chemicals. 20 mins 20s
Drying Removal of water and preparation of Radiograph for viewing 30mins 26s
>1Hour 90s
5/2/2023 42
43. Darkroom procedure
• A light tight room in the vicinity of a radiography cubicle.
• Two sources of light, white light(ceiling) for regular illuminations for
mixing solutions &cleaning the room.
• Safelight which contains 10-15watts bulb with special filters. located
4feets from the work surface.
• Safe handling time – should be 30 – 40 seconds.
• Development temperature – usually 20oC(manual) 33-
33.8’C(automatic)
• Development time – 3 – 10 minutes.
5/2/2023 43
46. Manual Processing Cont.
• Tension clip hanger
• Stationary clips first
• Movable clips second
• Stretch film
• Channel hanger
• Hold with one hand and slide the film into the channel with the other
47. Manual Processing Cont.
• Developing
• Agitate film while in developer to remove air bubbles from film surface
• 5 minutes
• While processing, refill the cassette
• Carfeul to have dry hands when reloaded
• Water spots can cause an artifact
48. Manual Processing Cont.
• Rinse
• Tilt film so chemical carryover goes into the rinse bath
• This places more of the exhausted developer into rinse
• Agitated in rinse for 30 seconds
• Fix
• Agitate film for about 15 seconds to remove air bubbles from film
surface
• Fix twice the time of developing example 10 minutes
• Can view in normal room light after 1 minute but need to place back
into fixer
49. Manual Processing Cont.
• Wash for 20-30 minutes
• Drying
• Dust free environment
• Don’t allow films to touch
• Cut off sharp points on corners where tension clip hangers put holes in
corners
• Store in envelope
50. Automatic Processing
• Highly standardized
• Produces dry film in short period
• Costly machine
• Pays for itself in a short period of time
51. Automatic Processing Cont.
• Same routine as manual processing
• Higher temps and special chemicals
• Film transported through the machine with rollers at controlled
speed
• Rinse between developer and fixer eliminated
• Carryover removed by compression of rollers on film
52. Automatic Processing Cont.
• Chemicals in peak condition because they are replenished on regular basis
• Tubs under processor
• Maintain temp and mix chemicals
• Maintenance
• Solution level check
• Replenishment rate check
• Temp check
• Roller operation check
• Rinsing and wiping of rollers and racks
• Regular cleaning of tanks
53. Factors Affecting Film Processing
• The thermostat is set to maintain the developer
temperature in the range between 33°C and 33.8°C in
90-second automatic processors.
• Developer temperatures below this range result in
slower chemical reactions and an underdeveloped
film with decreased density and low contrast.
• Temperatures above this range result in rapid
chemical reactions, overdeveloped film, increased
image density, and a high-contrast, narrow-latitude
image.
5/2/2023 53
54. Artifacts
• It can be described as an undesirable optical density on radiograph
• They are produced due to fault in exposure, processing, handling or
storage of films.
5/2/2023 54
62. Conventional film storage and handling
• Fresh film should be stored in a cool, dry place with a temperature
<70°C and with 40-60% relative humidity.
• Storage under heat conditions above 70°C will increase the fog and
decrease the image contrast.
• Storage under conditions of low humidity, less than about 40%, will
increase static artifacts.
• Film must be shielded from radiation exposure, heat and chemical
fumes.
• The stocks should be rotated, on the first in/first out principle (FIFO)
the oldest should be used first.
5/2/2023 62
63. Digital film processing
• It replaces the traditional film/screen systems with special detectors.
• They are either cassette based or cassette-less.
• Regardless of the system, the process of image acquisition is basically
the same.
• After the primary x-ray radiation beam passes through the patient,
the exit radiation is detected, and signal data are processed, displayed
and stored.
5/2/2023 63
66. Analog-To-Digital Converter
• All direct digital systems initially convert the analog signal from the
detector to a digital signal using ADC.
• The digital data are available for processing, display and storage.
• Imaging detectors produce continuously varying signals called analog
signals, these signals make up the latent image.
• Digital systems represent the signal by a series of discrete values
which makes up the intensity of the pixels.
5/2/2023 66
67. Sources of digital images
• 1.Directly from MR, CT
• 2. Digitized fluoroscopic images
• 3. Computed radiographic plates
• 4. Direct Digital Radiography
• 5. Digitized conventional film images
5/2/2023 67
68. Computed Radiography
• CR is a “cassette-based” system that uses a special solid-state
detector plate instead of a film inside a cassette.
• The exterior dimensions and appearance of the CR cassette are the
same as those of a conventional film cassette.
• The CR cassette is placed in the Bucky tray or for portable
examinations and exposed in the same manner as a conventional film
cassette.
5/2/2023 68
69. Computed Radiography
• Most CR systems are set up to have the same response as a 200-
speed film per screen system, although this can be changed.
• The resolution of CR systems depends on the pixel size but is not as
good as that of conventional film/screen systems.
• The contrast resolution of CR is superior to that of conventional
film/screen systems.
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70. Computed Radiography
• The CR cassette contains a solid-state plate called a photostimulable
storage phosphor imaging plate (PSP) that responds to radiation by
trapping energy in the locations where the x-rays strike.
• The CR detector plate is made of a thin, plastic material and is
extremely fragile.
• CR plates and cassettes can be reused many thousands of times, but
will break if dropped.
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72. Layers of Imaging plate
● Protective layer: This is a very thin, tough, clear plastic that protects
the phosphor layer from handling trauma.
● Phosphor layer: This is the active layer. This is the layer of
photostimulable phosphor that traps electrons during exposure. It is
typically made of barium fluorohalide phosphors.
● Conductive layer: This layer grounds the plate to reduce static
electricity problems and to absorb light to increase sharpness
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73. Layers of Imaging plate
● Support layer: This is a semi-rigid material that provides the imaging
sheet with strength and is a base for coating the other layers.
● Light shield layer: This prevents light from erasing data on the
imaging plate or striking through the backing layer.
● Backing layer: This is a soft polymer that protects the back of the
cassette.
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75. Computed Radiography
• The radiation dose from a CR exposure is usually set to correspond to
a comparable film/screen exposure.
• The incident x-ray beam interacts with the photostimulable
phosphors that are in the active layer of the imaging plate.
• The interaction stimulates the electrons in the phosphors allowing
the electrons to enter the conductive layer, where they are trapped in
an area of the phosphor known as the phosphor center.
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76. Computed Radiography
• This is the latent image that will create the digital image for the
computer to record and display.
• The trapped signal will remain for hours or days; however,
deterioration of the signal begins almost immediately.
• So it is vitally important to process the imaging plate immediately
after exposure
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78. Reading the image plate
• After the exposure, the CR cassette is placed in the processing reader
to produce a visible image.
• The processing reader opens the CR cassette and removes and scans
the detector plate with a laser beam or solid state laser diodes.
• As the plate is fed through the processing reader, a laser beam scans
the plate with red light in a raster pattern and gives energy to the
trapped electrons.
• The red laser light is emitted using 2 eV, which is needed to energize
the trapped electrons.
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79. Reading the image plate
• The trapped electrons are now able to leave the active layer where
they emit blue light photons as they return to a lower energy state.
• As the laser beam scans, the imaging plate lines of light intensity
information will be detected by a photomultiplier tube.
• The photomultiplier tube converts the visible light into an electronic
signal which is in analog form.
• The analog signal must be converted to a digital signal for the
computer to apply algorithmic formulas to the information
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80. Reading the image plate
• When the laser beam scans the plate each line of the imaging plate
correlates to one pixel dimension.
• The analog signal emitted for each pixel has an infinite range of values
which the ADC must convert into discrete values which can be stored
as digital code.
• This digital code will determine the gray scale for each individual
pixel.
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81. Reading the image plate
• All the pixel densities will be combined to represent the many
density values in the image which affects the density and contrast of
the image.
• Once the conversion is complete, the light intensity and the position
of the laser beam are stored as digital data for each pixel.
• At this point, the manifest image is now visible on the computer
monitor.
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82. Reading the image plate
• After the entire plate has been scanned, a high-intensity light source
releases any remaining trapped energy to prepare the plate for reuse.
• The cassette is then closed and returned to the ready bin for reuse.
• The entire processing cycle requires about 60 seconds (s).
• It is never necessary to open the CR cassette or to handle the
detector plate.
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83. Advantages of CR
• It utilizing your existing equipment.
• The images are stored on computer with a back-up system in place.
• One are able to transmit images to remote sites.
• The radiologist has quick access to previous CR images for
comparison.
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85. Direct Radiography
• DR is yet another way to record the x-ray exposure after it has passed
through the patient.
• DR is used to describe images which are recorded on an electronically
readable device that is hard-wired directly to the computer
processing system.
• The detectors and sensors of a DR system are contained inside a rigid
protective housing.
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86. Direct Radiography
• DR uses an array of small solid state detectors to convert incident x-
ray photons to directly form the digital image.
• The major advantage of the DR system is that no handling of a
cassette is required as this is a “cassette-less” system
• The image data are transferred directly to the computer for
processing.
• There are two forms of DR systems: one uses a linear array of
detectors, which sweeps across the area to be imaged, the other has
an array of detectors formed into a matrix.
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87. Direct Radiography
• The linear array records the position of the array and the signal from
each detector to form the image.
• In the matrix system, each detector provides data for one pixel.
• The linear array requires fewer detectors but a longer time to form
each image. This increases the tube heat load and the possibility of
patient motion artifacts.
• A matrix array system requires many more detectors than a linear
array system to achieve the same spatial resolution.
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88. Direct Radiography
• Digital radiography is similar to CR because it is filmless and the image
is stored on the computer.
• The image is displayed for the technologist to check prior to the next
exposure. The images are then sent to a storage system.
• This storage system allows for long term storage or the image can be
printed out on a laser printer to film.
• It has the same benefit as CR.
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89. Direct Radiography
• When using CR or digital radiography imaging, both images are placed
on computer.
• Once transferred, the images can be transferred electronically to
“Picture Archiving and Communication System” (PACS).
• The images can then be sent to the radiologist and ordering physician.
• The images are then archived
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90. Film Digitization
• Any image recorded using a conventional film/screen cassette can be
converted into a digital image by a film digitizer.
• A film digitizer measures the light transmitted at each location on the
film.
• It converts the light intensity to a digital value, and records the
location and intensity values as an image pixel
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91. Film Digitization
• The film is introduced into the feed tray and transported through the
digitizer while the image is scanned for digitization.
• After digitization, the image can be processed, displayed, or
transmitted just like any other digital image.
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92. Film/Printer Combination
• Hard copies are produced on multiformat cameras or laser printers.
• A multiformat camera takes a picture of the display screen.
• A laser printer scans a laser beam across a sheet of film to expose the
image.
• The intensity of the laser beam, and hence the density of the image,
is controlled by the digital data.
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93. Film/Printer Combination
• The laser printer can also produce multiple images on the same film.
• Both the laser printer and the multiformat camera are connected to
an automatic film processor.
• Their images are ready for immediate interpretation after the film is
printed.
• The digital image data are stored in a computer and can be retrieved
whenever required to produce additional hard copies or replace lost
films.
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94. Summary
• X-ray film is a photographic film coated with emulsion on both sides
of the film base.
• Impurities in the silver halide crystal structure increase the light
sensitivity of the film emulsion.
• Exposure causes the grains in the emulsion to develop an invisible
latent image.
• The developing process magnifies the latent image to produce a
visible pattern of black metallic silver.
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95. Summary
• A digital image is formed by a matrix of numbers called pixels.
• Each pixel specifies a unique location and contains information about
the image intensity at that location.
• Digital imaging systems include CR, DR, MR, CT, and fluoroscopic
units.
• Detectors used in digital imaging include fluoroscopic image
intensifiers and scintillation crystals.
• Images on film can be digitized and then processed and transmitted in
PACS.
• An ADC changes analog signals into digital signals.
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96. Conclusion
• If a film is not processed properly, the whole effort made in the X-ray
room or in the ward to obtain a good radiograph will be lost.
• It is essential to pay similar attention to film processing as we do in
the X-ray room or in the ward when taking X-rays.
• Most centers use digital imaging modalities.
• The use of manual/automatic image processing is rapidly being
replaced by digital radiography.
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