RNI Flashcards

1
Q

What are radionuclides, and how do they differ from radioisotopes?

A
  • Radionuclides are radioactive elements with unstable nuclei that release radiation through nuclear decay.
  • the correct term in nuclear medicine is radionuclides because:
  • Radionuclides encompass all radioactive atoms, whether they are isotopes of the same element or not.
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2
Q

What are the key characteristics of radionuclides?

A
  • Unstable Nucleus: An imbalance of protons and neutrons causes instability.

-Radioactive Decay: Emit alpha (α), beta (β), or gamma (γ) radiation to become stable.

-Energy Emission: The emitted radiation can be detected and used for imaging or therapy.

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3
Q

How are radionuclides named and identified using standard notation?

A

Element Name: Specifies the chemical element (e.g., Technetium, Iodine).
Mass Number: The sum of protons and neutrons in the nucleus.
For example, Technetium-99m (99mTc) is a radionuclide where 99 is the mass number, and “m” indicates a metastable state.

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4
Q

What is radioactive decay, and how does it work?

A

Radioactive Decay: A natural process where an unstable nucleus releases energy to become stable.

How it works:
1 -The unstable nucleus has an imbalance of protons and neutrons.
2- It emits particles (alpha or beta) or energy (gamma rays) to achieve stability.
3- This transformation may result in a new element or isotope (daughter nuclide).

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5
Q

Explain the differences between alpha, beta and gamma decay?

A

Alpha decay:
- Emits an alpha particle (2 protons + 2 neutrons, like a helium nucleus).
- Results in a decrease in the atomic number by 2 and the mass number by 4.

Beta decay:
-A neutron transforms into a proton and emits a beta particle (electron or positron).
-Increases or decreases the atomic number by 1 but keeps the mass number unchanged.

Gamma decay:
Releases gamma rays (high-energy electromagnetic radiation) without changing atomic or mass numbers.

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6
Q

What are the parent nuclide and daughter nuclide in radioactive decay?

A

Parent nuclide: The original unstable nucleus before decay.
Daughter nuclide: The resulting nucleus after decay, which may or may not be stable.

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7
Q

Radionuclides are produced through three primary methods, what are they?

A

1- Cyclotron:
Accelerates charged particles (e.g., protons, deuterons) to bombard stable materials.
Produces radionuclides like 18F and 11C for PET imaging.

2- Nuclear Reactor:
Uses fission reactions or neutron activation to produce radionuclides.
Produces commonly used radionuclides like 99Mo and 131I.

3- Radionuclide Generator:
Contains a long-lived parent radionuclide that decays into a short-lived daughter radionuclide.
Example: 99Mo/99mTc generator for SPECT imaging.

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8
Q

What factors influence the choice of radionuclides for diagnostic and therapeutic applications?

A

1 -Type of Application:
Diagnostic: Requires radionuclides with short half-lives to minimize radiation exposure while providing clear images (e.g., 99mTc, 18F).
Therapeutic: Uses radionuclides with longer half-lives for sustained radiation targeting specific tissues (e.g., 131I for thyroid cancer).

2- Imaging Modality:
- Gamma emitters for SPECT (e.g., 99mTc).
- Positron emitters for PET (e.g., 18F).

3- Half-Life Matching:
The radionuclide’s half-life should align with:
- The biological process being imaged.
- The duration of therapeutic efficacy.

4 - Energy Level:
Gamma rays must have energies suitable for clear imaging without excessive radiation dose.

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9
Q

How does half-life affect the suitability of a radionuclide for imaging or therapy?

A
  • Short Half-Life:
    Suitable for rapid imaging of biological processes.
    Example: 15O (2 minutes) for brain perfusion.
  • Intermediate Half-Life:
    Ideal for diagnostic imaging, balancing imaging time and radiation exposure.
    Example: 99mTc (6 hours).
  • Long Half-Life:
    Suitable for therapeutic applications, providing sustained radiation to target tissues.
    Example: 131I (8 days).
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10
Q

How are radionuclides attached to biological molecules for imaging and therapy?

A

1- Labelling Process:
- The radionuclide is chemically bonded to a biologically active molecule (e.g., peptides, antibodies).
- This molecule targets specific tissues or processes in the body (e.g., glucose metabolism, cancer cells).

2- Controlled Conditions:
- Solvents, temperature, and purification methods are carefully managed to ensure the radiopharmaceutical is safe and effective.

Examples:
18F is attached to glucose molecules (FDG) for PET scans to track metabolism.

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11
Q

What is a radiopharmaceutical, and how is it administered?

A

Radiopharmaceutical: A compound consisting of a radionuclide bonded to a biologically active molecule, used for diagnostic imaging or therapy.

Common Administration Methods:
1- Intravenous (IV): Most common, ensuring rapid delivery to target tissues.
2 -Oral: Example: Iodine-131 capsules for thyroid therapy.
3 - Inhalation: Example: 99mTc aerosols for lung ventilation studies.

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12
Q

What are the differences between diagnostic and therapeutic radiopharmaceuticals?

A

Diagnostic Radiopharmaceuticals:
- Use radionuclides with short half-lives.
- Emit gamma or positron radiation for imaging (e.g., 99mTc, 18F).

Therapeutic Radiopharmaceuticals:
- Use radionuclides with longer half-lives.
- Emit alpha or beta particles to deliver localized radiation to diseased tissues.

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13
Q

How are radiopharmaceuticals purified?

A

Purification:
- Removes unwanted by-products and impurities from the chemical reaction.
- Ensures only the desired radiopharmaceutical is present.

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14
Q

How are radiopharmaceuticals sterilized after production?

A

1- Micromembrane Filtration: Removes microorganisms using a 0.22 µm filter before transferring the product into a sterile vial.

2- Autoclaving: Uses steam under pressure to eliminate bacteria and ensure sterility.

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15
Q

Why is automation important in the synthesis of radiopharmaceuticals?

A

1- Safety: Reduces radiation exposure to staff.

2- Consistency: Produces high-quality radiopharmaceuticals with fewer errors.

3- Efficiency: Allows for faster production, essential for short-lived radionuclides.

Synthesis Modules:
Automated systems that mix, label, and purify radiopharmaceuticals under sterile conditions.

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16
Q

What is PET-CT, and how does it combine functional and anatomical imaging?

A

PET-CT:
- Combines Positron Emission Tomography (PET) for functional imaging (e.g., metabolism, blood flow) with Computed Tomography (CT) for anatomical localization.
- PET provides data on cellular processes,
- while CT maps the location within the body.

17
Q

How does SPECT differ from PET in terms of radiotracers and detectors?

A

Radiotracers:
- PET uses positron emitters (e.g., 18F) that produce annihilation photons.
- SPECT uses gamma emitters (e.g., 99mTc) for direct photon emission.

Detectors:
-PET uses coincidence detection with a ring of detectors.
- SPECT uses rotating gamma cameras with collimators.

18
Q

What is attenuation in PET imaging, and how is it corrected?

A

Attenuation:
- The reduction in gamma photon intensity as they pass through tissues.
- Leads to inaccuracies in image localization and quantification.

Correction Methods:
1 - CT Attenuation Correction: Uses CT data to estimate and adjust for photon loss, enhancing accuracy.

19
Q

What is time-of-flight (TOF) technology in PET, and how does it enhance spatial resolution?

A

TOF Technology:
- Measures the time difference between the detection of two annihilation photons to pinpoint the annihilation site.

Advantages:
1- Enhances spatial resolution by reducing uncertainty in photon localization.
2- Reduces noise in images.
3- Speeds up scan times, especially for small lesions.

20
Q

What are the key components of a gamma camera, and what is their function?

A

1 -Collimator:
- Filters gamma rays based on their direction.
- Ensures only rays traveling in the correct path reach the detector.

2- Scintillation Crystal:
- Converts gamma rays into visible light.

3- Photomultiplier Tubes (PMTs):
- Amplify light signals from the scintillation crystal.
- Convert light into electrical signals for processing.

4- Computer System:
- Processes electrical signals to create images.
- Enhances image resolution and quantifies data.

21
Q

How do PET detectors work, and what materials are commonly used for scintillation crystals?

A

PET Detector Workflow:
1- Gamma photons produced by annihilation events are detected.
2- Scintillation Crystals convert gamma photons into visible light.
3- Photodetectors (e.g., PMTs or SiPMs) convert light into electrical signals.
4- Coincidence detection reconstructs images from the paired photons.

22
Q

Explain the role of calibration tools like phantoms and dose calibrators in nuclear medicine imaging.

A

Phantoms:
- Test the performance of imaging systems.

Types:
- Uniformity phantoms: Ensure even detector response.
- Resolution phantoms: Evaluate image sharpness.

Dose Calibrators:
- Measure the activity of radiopharmaceuticals before administration.
- Ensure patients receive the correct dose, balancing diagnostic quality and safety.

23
Q

What are hybrid SPECT/CT system advantages?

A

Advantages:
1- Shorter scan times with reduced radiation dose.
2- Enhanced image quality with improved contrast and resolution.
3- Precise anatomical localization of functional abnormalities.
4- Useful for oncology (tumour detection), cardiology (myocardial perfusion), and neurology (brain perfusion).

24
Q

How are dynamic imaging and static imaging used in nuclear medicine?

A

Dynamic Imaging:
- Records tracer distribution over time to assess processes like blood flow or organ function.

Static Imaging:
Captures a snapshot after the tracer has localized in the body.
Example: Bone scans for detecting metastases.

25
Q

What safety measures are taken to minimize radiation exposure in nuclear medicine?

A
  • ALARA Principle: Keep radiation exposure “As Low As Reasonably Achievable.”

Key Measures:
- Shielding: Use lead aprons, barriers, and syringe shields.
- Distance: Maximize distance from radiation sources.
- Time: Minimize time spent near radioactive materials.
- Radiation Monitoring: Use personal dosimeters for staff to track exposure.
- Proper Handling: Follow protocols for radiopharmaceutical preparation and administration.

26
Q

What are the daily quality control procedures for gamma cameras?

A

Daily Quality Control Procedures:

1- Uniformity Checks:
Ensure even response of detectors across the field of view.
Use uniformity phantoms to verify consistency.

2- Energy Window Calibration:
Confirm proper energy discrimination of gamma photons.

3- Spatial Resolution Checks:
Evaluate the camera’s ability to distinguish small structures using resolution phantoms.

4-Sensitivity Tests:
Measure the gamma camera’s efficiency in detecting radiation.

27
Q

Why is individual dosimetry important, and how is it determined?

A

Importance:
1- Ensures patient safety by tailoring the dose to individual physiology.
2- Balances effective imaging or treatment with minimal radiation exposure.

Determination:
1- Organ Uptake: Assessed using pre-treatment imaging or calculations.
2- Biological Half-Life: Measured to estimate retention and clearance.
3- Dosimetry Models: Use mathematical formulas or software to estimate absorbed doses.