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Production of Radionuclides

Topic 2-Production of Radionuclides & QA QC

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Page 1: Topic 2-Production of Radionuclides & QA QC

Production of Radionuclides

Page 2: Topic 2-Production of Radionuclides & QA QC

• All radionuclides commonly

administered to patients in nuclear

medicine are artificially produced

• Most are produced by cyclotrons,

nuclear reactors, or radionuclide

generators through bombardment or

fission

Page 3: Topic 2-Production of Radionuclides & QA QC

1. Cyclotrons

• Cyclotrons produce radionuclides by

bombarding stable nuclei with high-

energy charged particles

• Most cyclotron-produced radionuclides

are neutron poor and therefore decay by

positron emission or electron capture

Page 4: Topic 2-Production of Radionuclides & QA QC

>Specialized hospital-based cyclotrons have been developed to produce positron-emitting radionuclides for positron emission tomography (PET)

>Usually located near the PET imager

because of short half-lives of the

radionuclides produced

Page 5: Topic 2-Production of Radionuclides & QA QC

2. Nuclear Reactors

• Specialized nuclear reactors used

to produce clinically useful

radionuclides from fission products

or neutron activation of stable

target material

Page 6: Topic 2-Production of Radionuclides & QA QC

>Uranium-235 fission products can be chemically separated from other fission products.

>Concentration of these “carrier-free”

fission-produced radionuclides is very

high

Page 7: Topic 2-Production of Radionuclides & QA QC

Neutron Activation

• Neutrons produced by the fission of

uranium in a nuclear reactor can be

used to create radionuclides by

bombarding stable target material

placed in the reactor

Page 8: Topic 2-Production of Radionuclides & QA QC

>Process involves capture of neutrons by stable nuclei

>Almost all radionuclides produced

by neutron activation decay by

beta-minus particle emission

Page 9: Topic 2-Production of Radionuclides & QA QC
Page 10: Topic 2-Production of Radionuclides & QA QC

3. Radionuclide Generators

A generator is a self-contained system housing a parent/daughter mixture in equilibrium.

There must be a method of removing the daughter and leaving the parent behind to regenerate more daughter activity.

It is designed to produce the daughter for some purpose separate from the parent.

Page 11: Topic 2-Production of Radionuclides & QA QC

Generators produce certain short-lived radioisotopes on-site which cannot be shipped by commercial sources.

To be useful, the parent's half-life must be long compared to the travel time required to transport the generator to recipient.

The typical shelf-life of a Mo/Tc generator is 2 weeks, as is the expiration date.

Page 12: Topic 2-Production of Radionuclides & QA QC

the process of removing the daughter

from the generator is referred to as

elution;

the solution used to remove the

daughter is called the eluent;

and the solution collected from the generator containing the daughter radioisotope is called the eluate.

Page 13: Topic 2-Production of Radionuclides & QA QC

• Technetium-99m has been the

most important radionuclide used in

nuclear medicine

• Short half-life (6 hours) makes it

impractical to store even a weekly

supply

Page 14: Topic 2-Production of Radionuclides & QA QC

• Supply problem overcome by obtaining parent Mo-99, which has a longer half-life (67 hours) and continually produces Tc-99m

• A system for holding the parent in such a way that the daughter can be easily separated for clinical use is called a radionuclide generator

Page 15: Topic 2-Production of Radionuclides & QA QC

1. Generator output must be sterile and pyrogen-free.

2. The chemical properties of the daughter must be different than those of the parent to permit separation of daughter from parent.

Page 16: Topic 2-Production of Radionuclides & QA QC

3. Generator should be eluted with 0.9% saline solution and should involve no violent chemical reactions.

4.Daughter isotope for diagnostic studies should be short-lived gamma-emitting nuclides.

Page 17: Topic 2-Production of Radionuclides & QA QC

5. Inexpensive, effective shielding of

generator, minimizing radiation dose to

those using it.

This is easy to accomplish since lead is very dense and therefore a good attenuator of radiation.

Page 18: Topic 2-Production of Radionuclides & QA QC
Page 19: Topic 2-Production of Radionuclides & QA QC

DRY column generator

The saline supply is in a 30-ml bottle/vial for elution

Because saline used never exceeds 20ml, up to 10ml of air follow the saline through the fluid path, effectively drying the column

Page 20: Topic 2-Production of Radionuclides & QA QC

WET column generator

The saline supply is a 500ml bottle and is an integral part of the generator

Once elution is completed, the fluid path is filled with a saline for the life of the generator and the alumina column is always saturated with 0.9% NaCl solution

Page 21: Topic 2-Production of Radionuclides & QA QC

Equilibrium

is a condition established in a parent/daughter mixture when both parent and daughter are radioactive and when the daughter’s half-life is shorter than that of the parent.

if the daughter’s half-life exceeds that of the parent, equilibrium will never be reached.

Page 22: Topic 2-Production of Radionuclides & QA QC

Transient Equilibrium

-is a condition reached when the half-life of the parent is approximately 10 times greater than the half-life of the daughter.

Page 23: Topic 2-Production of Radionuclides & QA QC

Secular Equilibrium

-if the half-life of the parent is very much longer than that of the daughter (e.g., more than 100 longer).

Page 24: Topic 2-Production of Radionuclides & QA QC

99Mo/99mTc GENERATOR: PRINCIPLES OF OPERATION

1. Prior to shipping the generator to the

Nuclear Medicine Department, 99Mo

sodium molybdate is immobilized on a

column of alumina (Al2O3; aluminum

oxide).

Page 25: Topic 2-Production of Radionuclides & QA QC

2. 0.9% saline solution (the eluent) is

passed through the column and Na

pertechnetate, the daughter of 99Mo

decay, is eluted from the column with

high efficiency due to its almost total

lack of affinity for alumina.

Page 26: Topic 2-Production of Radionuclides & QA QC

3. The pertechnetate is collected in a

shielded, evacuated sterile vial and

must undergo quality control testing,

then must be calibrated prior to use. It

is referred to as the eluate.

Page 27: Topic 2-Production of Radionuclides & QA QC

99Mo/99mTc GENERATOR

is considered to be the workhorse of all generators and is ideal with no significant limitations

used in almost 80% of nuclear scan performed

Page 28: Topic 2-Production of Radionuclides & QA QC
Page 29: Topic 2-Production of Radionuclides & QA QC

Commonly Transported Radioisotopes

*Americium-241= Diagnose thyroid disorders, smoke detectors.

*Cesium-137= Cancer treatment.

*Iodine-125,131= Diagnosis & treatment liver, kidney,heart, lung and brain.

*Technetium-99m=Bone and brain imaging; thyroid and liver studies; localization of brain tumors.

Page 30: Topic 2-Production of Radionuclides & QA QC
Page 31: Topic 2-Production of Radionuclides & QA QC

6. Low radiation dose

7. Safe

8. Convenient

9. Cost-effective

Page 32: Topic 2-Production of Radionuclides & QA QC

QC program is especially important in

two main areas:

Instrumentation

Radiopharmaceutical preparation

Page 33: Topic 2-Production of Radionuclides & QA QC

Instrumentation:

Well counters

Dose calibrators

Thyroid probes

Gamma camera

Page 34: Topic 2-Production of Radionuclides & QA QC

QC for Gamma Camera

Spatial resolution Weekly

Uniformity Daily (before first patient)

Image linearity Weekly

Energy resolution Annually

Count rate response Annually

Sensitivity Annually

Collimator integrity Annually or when suspicious of damage

Formatter performance Annually

Whole-body accessory Annually

Window setting For each patient

Page 35: Topic 2-Production of Radionuclides & QA QC

Radiopharmacy

Generator and radionuclide purity

Radiochemical labeling

Sterility

Page 36: Topic 2-Production of Radionuclides & QA QC

Operation and routine QA

• Energy discrimination windows

must be adjusted to center them on

the photopeak or photopeaks of the

desired radionuclide

Page 37: Topic 2-Production of Radionuclides & QA QC

Operation and routine QA (cont.)

• Uniformity of the camera should be assessed daily and after each repair

• May be made intrinsically by using a Tc-99m point source

Page 38: Topic 2-Production of Radionuclides & QA QC

• Images must contain enough counts that quantum mottle does not mask uniformity defects

• Uniformity test will reveal most

malfunctions of a scintillation

camera

Page 39: Topic 2-Production of Radionuclides & QA QC

Other QA

• Spatial resolution and spatial

linearity should be assessed at

least weekly

• Efficiency of each camera head

should be measured periodically

Page 40: Topic 2-Production of Radionuclides & QA QC

• Complete evaluation at least annually

– Include multienergy spatial registration and count-rate performance

Page 41: Topic 2-Production of Radionuclides & QA QC

Peaking

Counting Rate

Field Uniformity

Spatial Resolution

Spatial Linearity

Sensitivity

QC for Gamma Camera

Page 42: Topic 2-Production of Radionuclides & QA QC

Gamma Camera Quality Control

QC Procedure Frequency

Peaking Daily & before each new radionuclide used

Counting rate limits Daily

Field uniformity Daily, after repair

Spatial resolution Weekly, after repair

Spatial linearity Weekly, after repair

Sensitivity Quarterly

Page 43: Topic 2-Production of Radionuclides & QA QC

• Energy discrimination windows

must be adjusted to center them

on the photopeak or photopeaks

of the desired radionuclide.

QC Procedures for Gamma Camera

Peaking

Page 44: Topic 2-Production of Radionuclides & QA QC

• “Peaking” may be done manually

by adjusting the energy window

settings while viewing the spectrum

or automatically by the camera

• Should be peaked before first use

each day and before imaging a

different radionuclide

Page 45: Topic 2-Production of Radionuclides & QA QC

• Small source used to

peak camera; radiation

emitted by the patient

would have a large scatter

component.

Page 46: Topic 2-Production of Radionuclides & QA QC

• Sensitivity of a gamma camera generally decreases with increased amounts of activity.

• During the high activity the detector is “paralyzed” & cannot count.

• Dead Time is the system’s inability to count

QC Procedures for Gamma Camera

Counting Rate Limits

Page 47: Topic 2-Production of Radionuclides & QA QC

Field Uniformity

• Refers to the gamma camera’s ability to detect a uniform source of radiation

• Uniformity depends on the uniform response of the NaI crystal & the PMTs.

QC Procedures for Gamma Camera

Page 48: Topic 2-Production of Radionuclides & QA QC

Intrinsic Uniformity Flood

A. Field Uniformity Flood B. Non-uniform Flood

Page 49: Topic 2-Production of Radionuclides & QA QC

Intrinsic Uniformity Flood

A, B, C. Damage PMT D. Cracked Crystal

Page 50: Topic 2-Production of Radionuclides & QA QC

• Uniformity can be:

intrinsically (w/o collimator)

extrinsically (w/ collimator)

• May be made intrinsically by using a Tc-99m point source

• Edge packing – is the phenomenon that can show up as a bright rim activity around the perimeter of the flood.

Page 51: Topic 2-Production of Radionuclides & QA QC

Extrinsic uniformity

• Two common radionuclide sources used:

• acrylic plastic (Plexiglas) container filled w/ H2O 1-10mCi Tc-99m

• solid-sealed 10 mCi cobalt-57 sheet

• Extrinsic can be evaluate/assess the defects of the collimator

Page 52: Topic 2-Production of Radionuclides & QA QC

Extrinsic Uniformity Flood

Damaged Collimator

Page 53: Topic 2-Production of Radionuclides & QA QC

• Images must contain enough counts that quantum mottle does not mask uniformity defects

• Uniformity test will reveal most

malfunctions of a scintillation camera

Page 54: Topic 2-Production of Radionuclides & QA QC

• Spatial resolution – gamma camera’s ability to reproduce small details of a radioactive distribution.

• Required to be performed a minimum of once a week on every imaging system

• Spatial Linearity – gamma camera’s ability to produce a linear image w/ straight lines corresponding to the same straight lines of the bar pattern.

Page 55: Topic 2-Production of Radionuclides & QA QC

• Performed to determine the gamma camera detector’s ability to detect the ionizing event that occur in the NaI crystal.

• Events recorded as counts per minute are calculated and expressed as cpm per microcurie of acitivity present

• Performed biannualy

Sensitivity

Page 56: Topic 2-Production of Radionuclides & QA QC

• NRC requires that all photo-emitting sealed sources containing 100 µCi or more be tested for leakage biannualy.

• USNRC stated that any sealed sources with more than 0.005 µCi of removable activity per test must immediately be removed, properly stored, and reported to the NRC.

• NRC requires that all sealed sources be inventoried and surveyed quarterly for radiation exposure.

Sealed Radioactive Source

Page 57: Topic 2-Production of Radionuclides & QA QC

• Two common generators used:

• Molybdenum-99

• Technetium-99m

• QC is essential on the Technetium eluent each time generator is eluted, to ensure that the eluent does not contain any contaminants or impurities including radionuclide impurity of Mo-99, molybdate, chemical impurity of Al+3, alumina, or radiochemical impurity of hydrolyzed reduced technetium(HR-Tc).

Radionuclide Generator

Page 58: Topic 2-Production of Radionuclides & QA QC

Radiation Protection

The basis for all radiation protection

activities is the supposition that radiation

is harmful and that the smaller the

radiation doses we receive, the smaller

are the risks.

Page 59: Topic 2-Production of Radionuclides & QA QC

Justification- no practice involving exposures to radiation should be adopted unless it produces sufficient benefit

Optimization- individual doses, number of people exposed and occurrence of exposures should be kept ALARA

Individual dose and risk limits- the exposure of individuals from the combination of all relevant practices is subject to dose limits

Page 60: Topic 2-Production of Radionuclides & QA QC

Cardinal Principles

Shielding: If you have a thick shield between yourself and the radioactive material, more of the radiation will be absorbed by the thick shield, and you will be exposed to less rays.

Page 61: Topic 2-Production of Radionuclides & QA QC

Time: Minimizing the time spent with the radioactive source will also reduce radiation risks.

Page 62: Topic 2-Production of Radionuclides & QA QC

Distance:

The farther you are from the radioactive source,the lower your exposure. Thus reducing the probable risks.