24. Medical physics A2

Syllabus
9702–2028–2029
Section
24
Level
A2

24.1 Production and use of ultrasound

Syllabus
9702–2028–2029
Topic
24.1
Level
A2

A piezoelectric crystal converts energy in both directions

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.

A piezoelectric transducer alternates between ultrasound transmitter and receiver

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.

Pulse-echo ultrasound maps boundary depth and tissue contrast

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.boundary depth d=ct/2 where t is the transmit-to-echo time and c is sound speed in the tissue.

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.

Specific acoustic impedance is density × sound speed

Z=ρcρ=densityofthemedium;c=speedofsoundinthatmediumZ=ρc ρ = density of the medium; c = speed of sound in that medium

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.

Acoustic-impedance mismatch sets the reflected intensity fraction

R=IR/I0=((Z1−Z2)/(Z1+Z2))2R=I_R/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−RAt the boundary, neglecting absorption: T=I_T/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.

Ultrasound intensity attenuates exponentially with distance in matter

I=I0e(−μx)I/I0=e(−μx);μ=−ln(I/I0)/xI=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.

24.2 Production and use of X-rays

Syllabus
9702–2028–2029
Topic
24.2
Level
A2

Electron bombardment of a metal target produces X-rays with a minimum wavelength

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=eVmaximum electron kinetic energy=eV maximum photon energy=hf_max=hc/λ_min=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.

X-ray contrast comes from differences in transmitted intensity

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.

Calculate X-ray attenuation through one or several material layers

I=I0e(−μx)μ=−ln(I/I0)/x;x=−ln(I/I0)/μI=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)]For successive layers: 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.

CT builds a 3D volume from many-angle X-ray projections of many sections

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→one3Dvolumemany angles of one section → one reconstructed 2D slice many adjacent 2D slices → one 3D volume

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.

24.3 PET scanning

Syllabus
9702–2028–2029
Topic
24.3
Level
A2

A radioactive tracer follows the tissue process being studied

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.

PET uses a beta-plus-emitting tracer to create positrons inside the body

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+νeβ⁺ decay: ᴬ_ZX → ᴬ_(Z−1)Y + ⁰_+1e + ν_e

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.

Particle-antiparticle annihilation conserves mass-energy and momentum

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+γelectron + positron → gamma photon + gamma photon e⁻ + 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.

A PET positron annihilates with a tissue electron to produce two opposite gamma photons

  1. The β⁺ tracer decays in tissue and emits a positron. 2. The positron loses kinetic energy over a short distance. 3. It meets a tissue electron and the pair annihilates.

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.

Each PET annihilation photon carries about 0.511 MeV

Etotal=2mec2foranapproximatelystationarye−e+pairE_total=2m_ec² for an approximately stationary e⁻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.

Coincident gamma arrival times locate PET events and map tracer concentration

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/2for detector separation along the line: displacement from midpoint s=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.