24. Medical physics A2
- Syllabus
- 9702–2028–2029
- Section
- 24
- Level
- A2

Apply a p.d. across a piezoelectric crystal and it changes shape. Reversing the p.d. reverses the deformation.
Mechanically compress, stretch or vibrate the crystal and charge separation produces an e.m.f. across it.
An alternating p.d. therefore drives alternating deformation; an incoming mechanical vibration produces an alternating electrical signal.
A steady p.d. gives a static deformation, not sustained ultrasound. Generation and detection are reverse conversions in the same material.
Generation: apply an alternating p.d. to the crystal. It repeatedly changes shape and drives pressure oscillations in the surrounding medium.
Choose the drive frequency equal to the crystal's natural frequency in the ultrasound range (>20 kHz). Resonance gives large-amplitude vibration and a stronger ultrasound pulse.
Detection: a returning ultrasound wave makes the crystal vibrate/change shape; the inverse piezoelectric effect produces an alternating e.m.f. that is amplified and processed.
The transducer does not emit and receive simultaneously in pulse-echo imaging: electronics switch from the drive pulse to listening for the much smaller echo signal.
The probe sends a short ultrasound pulse, then listens. At a boundary between tissues with different acoustic impedances, part of the pulse reflects and returns as an echo.
boundarydepthd=ct/2wheretisthetransmit−to−echotimeandcissoundspeedinthetissue.
For c=1540 m s⁻¹ and echo delay t=80 μs, d=(1540)(80×10⁻⁶)/2=6.16×10⁻² m=6.16 cm.
Echo timing locates boundaries; echo intensity gives information about impedance contrast and therefore boundary type. Repeating along many directions builds a cross-sectional image.
Coupling gel removes the air gap at skin, reducing the severe reflection that an air-tissue impedance mismatch would cause.
Divide by two because the pulse travels to the boundary and back. Pulses create listening intervals so the same probe can distinguish weak echoes from its transmitted signal.
Z=ρcρ=densityofthemedium;c=speedofsoundinthatmedium
With ρ in kg m⁻³ and c in m s⁻¹, Z has unit kg m⁻² s⁻¹.
For tissue with ρ=1060 kg m⁻³ and c=1540 m s⁻¹, Z=(1060)(1540)=1.63×10⁶ kg m⁻² s⁻¹.
It is the contrast between Z values on the two sides of a boundary—not either density alone—that determines the reflected intensity fraction.
Acoustic impedance is not electrical resistance. Use the sound speed and density for the same medium and keep prefix powers consistent.
R=IR/I0=((Z1−Z2)/(Z1+Z2))2
If Z₁=Z₂, R=0 and ideally no intensity reflects. If the impedances are very different, R approaches 1 and little intensity transmits.
For water Z₁=1.48×10⁶ and steel Z₂=40.4×10⁶ kg m⁻² s⁻¹, R=[(40.4−1.48)/(40.4+1.48)]²=0.864: about 86.4% reflects.
Attheboundary,neglectingabsorption:T=IT/I0=1−R
R is a dimensionless intensity fraction and the ratio is squared. Multiply by 100 only for a percentage; transmitted percentage is 100(1−R) when boundary absorption is neglected.
I=I0e(−μx)I/I0=e(−μx);μ=−ln(I/I0)/x
I₀ is intensity before a path length x, I is intensity after it, and μ is the linear attenuation coefficient. μ has reciprocal-length units matching x.
If I=0.62I₀ after x=2.1 cm, μ=−ln(0.62)/2.1=0.23 cm⁻¹.
The transmitted fraction is I/I₀; the fraction attenuated is 1−I/I₀. For μ=0.053 cm⁻¹ and x=9.3 cm, 39% is attenuated.
For an echo from depth d in one tissue, propagation covers approximately x=2d before adding boundary-reflection factors; each tissue layer contributes its own μx.
Keep x and μ in reciprocal units. Attenuation through matter and reflection at boundaries are separate losses and may both reduce the detected echo.
Electrons emitted by a heated cathode accelerate through a large p.d. V toward a metal target. Rapid deceleration and atomic interactions at the target produce X-ray photons.
maximumelectronkineticenergy=eVmaximumphotonenergy=hfmax=hc/λmin=eV
For V=58 kV, λmin=hc/eV=(6.63×10⁻³⁴)(3.00×10⁸)/[(1.60×10⁻¹⁹)(58×10³)]=2.14×10⁻¹¹ m=21.4 pm.
Most electron energy becomes thermal energy, so the target needs a high melting point and heat removal; tungsten is commonly suitable.
The minimum wavelength is the rare limit where one photon receives all eV. Increasing V decreases λmin; tube current mainly changes the number/intensity of X-rays, not this limit.
Send X-rays through the body and detect the transmitted beam. Different structures absorb/attenuate different fractions, so the detector records different transmitted intensities and forms an internal image.
Contrast is the difference in detector response or degree of blackening between image regions. Greater difference in transmitted intensity gives greater contrast.
Bone has a much larger attenuation coefficient than many soft tissues, so fewer X-rays reach the detector behind bone. Bone and soft tissue therefore give good contrast; tissues with similar μ give poor contrast.
On traditional film, more transmitted X-rays produce greater blackening; digital displays may map detector signal to brightness differently, but contrast still comes from signal differences.
Do not define contrast as brightness alone. It is a difference between regions produced by different attenuation/transmission through their material and thickness.
I=I0e(−μx)μ=−ln(I/I0)/x;x=−ln(I/I0)/μ
I/I₀ is the transmitted fraction. If 80% is absorbed, 20%=0.20 remains and belongs on the left of the exponential equation.
For muscle μ=0.22 cm⁻¹ and 80% absorption: 0.20=e^(−0.22x), so x=−ln(0.20)/0.22=7.3 cm.
Forsuccessivelayers:I/I0=e(−μ1x1)e(−μ2x2)…=e[−Σ(μixi)]
Equal thickness x through materials with μ=3.0 and 0.22 cm⁻¹ gives I/I₀=e^(−3.22x). If I/I₀=0.13, x=0.63 cm.
Add μx exponents, not transmitted fractions. Keep μ and x in reciprocal units and distinguish fraction transmitted from fraction absorbed=1−I/I₀.
Choose one thin body section. An X-ray source and detectors acquire many transmission projections through that same section from different angles.
A computer combines the angular attenuation data to reconstruct a two-dimensional map/image of that section.
Repeat the angular scan for successive sections along an axis, then combine/stack the reconstructed 2D section images to produce a three-dimensional representation.
manyanglesofonesection→onereconstructed2Dslicemanyadjacent2Dslices→one3Dvolume
Compared with one projection radiograph, CT separates overlapping structures and gives 3D localization, but multiple X-ray exposures generally increase ionising-radiation dose.
Different angles create one slice; different positions create different slices. A single rotating projection is not itself the final 3D image.
A tracer is a substance containing radioactive nuclei that is introduced into the body and absorbed by the tissue or biological process being studied.
Its emitted radiation can be detected from outside the body, so the spatial distribution of tracer reveals where that labelled substance is taken up or metabolically active.
A useful tracer behaves chemically like the substance of interest, gives detectable radiation and has a half-life long enough for the scan but short enough to limit unnecessary dose.
The tracer is not merely the radiation: it is the administered radioactive substance whose uptake carries biological information.
The PET tracer contains a radionuclide that undergoes β⁺ decay and emits a positron inside the tissue where the tracer has accumulated.
β+decay:ZAX→(AZ−1)Y++01e+νe
The positron is the antiparticle needed for the later electron-positron annihilation that produces detectable gamma photons.
PET does not inject a beam of free positrons and does not use β⁻ decay for this role: the administered tracer generates positrons by β⁺ decay in situ.
Annihilation occurs when a particle interacts with its antiparticle; their rest mass and any kinetic energy become energy of other particles, while total energy and total momentum are conserved.
electron+positron→gammaphoton+gammaphotone−+e+→γ+γ
If the electron-positron pair has negligible total momentum, one photon alone cannot leave zero final momentum. Two equal photons travelling in opposite directions give equal and opposite momenta.
Their combined rest energy 2mec² becomes photon energy (plus any initial kinetic energy). Matter has not vanished without accounting; its mass-energy has changed form.
Opposite directions follow from momentum conservation for an approximately stationary pair, not from energy conservation alone.
The electron and positron mass-energy becomes a pair of gamma-ray photons emitted in approximately opposite directions so that momentum is conserved.
Gamma photons are penetrating enough for many to leave the body and reach detectors around the patient; the scanner detects the paired event rather than the positron itself.
The two detected gamma photons are produced by later annihilation, not directly by β⁺ decay. The positron first travels and slows in tissue.
Etotal=2mec2foranapproximatelystationarye−e+pair
Momentum conservation gives two equal, opposite photons, so each photon receives half the total rest energy: Eγ=mec².
Eγ=(9.11×10⁻³¹)(3.00×10⁸)²=8.20×10⁻¹⁴ J.
Eγ=(8.20×10⁻¹⁴)/(1.60×10⁻¹⁹)=5.12×10⁵ eV=0.512 MeV (usually quoted as 0.511 MeV). Total photon energy is about 1.02 MeV.
Do not assign 2mec² to each photon. The two photons share the pair's total energy; initial kinetic energy is normally neglected in this syllabus calculation.
A ring of detectors records pairs of gamma photons that leave the body and arrive nearly simultaneously at opposite detectors. Coincidence identifies them as one annihilation event.
The two hit detectors define a line of response on which the annihilation occurred. A difference in arrival times places the event closer to the detector reached first.
fordetectorseparationalongtheline:displacementfrommidpoints=cΔt/2
Processing many event lines and timing differences reconstructs event locations. Regions with more events contain a greater concentration/uptake of tracer and are displayed more strongly.
The PET image is primarily a functional map of tracer concentration or metabolic activity, not simply a direct map of tissue density.
One photon detection does not locate an event. Localization depends on paired coincidence geometry, and arrival-time difference refines position along that line.