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1
Chapter 8 Measurement of Absorbed Dose
The most direct measurement of radiation dose in a medium is to measure the heat generated in the medium due to the radiation. But the temperature increase in the medium is generally very small, making this type of measurement very difficult.
2
Commonly used dosimeters
• Ionization chambers.
• cylindrical: photons, high-energy electrons (>10 MeV)
• parallel plate (plane parallel): low energy electrons (<10 MeV)
• Diodes.
• Thermo luminescent dosimeters (chips, powders).
• Film, radiochromic film.
3
Ionization Chamber
An ion chamber is a volume of air (cavity), usually surrounded by a layer of material (chamber wall) just thick enough to provide electron equilibrium. The electrons generated in the wall enter the cavity, causing ionization. The ions produced in the air cavity are collected and read out through an electrometer.An ion chamber may be sealed (used in machines as monitor chamber) or unsealed (used for routine calibrations).There are 2 major designs of unsealed ion chambers, cylindrical and parallel-plate.
wall
air cavity
electrodeelectrode
air cavity wall
4
8.1 Radiation Absorbed Dose
Exposure: applicable only to photon beams, in air, E < 3 MeVAbsorbed dose is defined for all types of radiation (charged,
uncharged particles); all materials; and all energies.Dose is defined as the mean energy imparted by ionizing radiation to a given material per unit mass.
dm
ddose
Old unit: 1 rad = 100 ergs/g = 10-2 J/kg New unit: 1 Gy = 1 J/kg = 100 rad, or 1 cGy = 1 rad
5
8.2-A Relationship Between KERMA, Exposure, and Absorbed Dose (KERMA)
KERMA (K) (kinetic energy released in the medium) is defined as dEtr/dm, where dEtr is the sum of the kinetic energies of all the charged particles liberated by the neutral particles (photons) in a material of mass dm.
trK
K = Kcol + Krad
Kcol is the part of the energy loss due to collision with the atoms, resulting in ionization and excitation.
Krad is the part of energy loss in producing bremsstrahlung photons.
)1()1(
g
gggK enentrtr
6
Energy Transfer and Energy Absorption
The transfer of energies from a photon beam to the medium is a two-step process: (1) The photon interacts with the atom, causing one or more electrons ejected from the atom. All or part of the photon energy is transferred to the electron(s). (2) the kinetic energy the ejected electron(s) is absorbed by the medium through ionization and excitation (excluding the bremsstrahlung photons produced by these electrons).
hv’
hv
e-
hv’’
ray
7
Energy Transfer Coefficients
Energy transfer coefficient: (cm-1)
is the average energy transferred into the kinetic energy of the charged particles per interaction, hv is the original photon energy.
tr is the fraction of energy transferred per unit pathlength traversed by the photon.
Mass Energy transfer coefficient: tr/ (cm2/g)
h
Etrtr
trE
8
KERMAKERMA (Kinetic Energy Released in the Medium). It occurs at a point. K = <dEtr>/dm, where <dEtr> is the average kinetic energy transferred from photons to electrons in a volume element whose mass is dm.
hv’
hv
e-
photo-electron
hv
K L
dEtr= hv- hv’hv- Bk dEtr hv
Compton scattering Photo-electric effect
9
trEK
is the photon fluence (# photons /cm2),
is the linear attenuation coefficient: number of collisions per unit pathlength (cm), per incident photon (# collisions/photon/cm).
is the number of collisions per unit volume (# collisions /cm3).
Etr is the average kinetic energy transferred to the electron(s) per collision, (MeV/collision).
Etr is the amount of kinetic energy transferred per unit volume (MeV/cm3).
Etr is the amount of kinetic energy transferred per unit mass (MeV/g or J/kg or Gy).
10
trtr
tr hEK
trtr/hthe fractional energy transferred per unit pathlength (/cm).
= h, energy fluence (MeV/cm2).
tris the energy transferred per unit volume (MeV/cm3).
tris the energy transferred per unit mass (MeV/g or J/kg or Gy)
11
For a spectrum of photon energies, the KERMA is defined as:
dEEEE
EK tr
E)(
)()(
max
0
Example: A beam of 10 MeV photons with fluence of 1014/m2 is incident on a small block of carbon. Calculate the Kerma:
Given () = 0.00196 m2/kg and Etr = 7.30 MeV
K = 1014 (/m2) x 0.00196 (m2/kg) x 7.30 MeV
= 1.43x1012 (MeV/kg)
= 1.43x1012 (MeV/kg) x 1.602x10-13 (J/MeV)
= 0.229 J/kg = 0.229 Gy
12
DOSE
Energy is transferred to electron(s) at the point of collision, but not all of it is retained in the medium; some of it radiated away as bremsstrahlung. The absorbed dose is the energy actually deposited in the medium along the electron track.
KERMA (at a point) and energy deposition (over a distance) do not take place at the same location.
hv’
hv0
e-
hv’’
Kc (collision kerma)
r (radiative kerma)
cr
13
Energy Absorption Coefficient
Energy absorption coefficient: en = tr (1-g) (cm-1)
‘g’ is the fraction of the energy of secondary charged particles that is lost to bremsstrahlung in the material.
Thus, en represents the fractional energy absorbed locally in the material.
Mass Energy absorption coefficient: en/ (cm2/g)
In soft tissues (low Z materials), g 0. Thus, en tr .
Sometimes ab is used instead of en.
14
The absorbed dose is defined as D = <dEab>/dm.
<dEab> is the mean energy imparted by the electrons to a mass dm of the medium.
The absorbed dose is also defined at a point, including all electron tracks coming in and going out of a small volume dV (containing mass dm) at that point.
The unit for the dose is Gray: 1 Gray = 1 J/kg1 Gy = 100 cGy = 100 rad (old unit, has been phased out).
dV
dm
15
hv1
hv0
e-hv2
’’
Vm
K = T / m = (hv0 -hv1) / m
D = (T-T’-hv2) / m
Example: Kerma and Dose as a result of a Compton scattering
T = initial kinetic energy of the electron
T’ = kinetic energy of the electron when crossing the boundary of volume V
17
hv0
e- hv=0.511 MeV
Vm
K = (T1+T2) / m = (hv0-1.022 MeV) / m
D = (T1+T2) / m
Example: Kerma and Dose involving pair production and annihilation
e+
hv=0.511 MeV
18
8.2-B Relationship Between KERMA and Exposure
eW
KX aircol
eW
Xair
enair
e
W is the amount of energy required to produce 1 ion pair in air, 33.97 eV/ion-pair, or 33.97 J/C.
Exposure defined as ionization produced in air, applicable to photons up to 3 MeV only.
19
Exposure is defined (only for photons in air) as: X = dQ/dm, where
dQ is the total charge of the ions of either sign produced in air when all of the electrons liberated by photons in a volume element of air having a mass dm are completely stopped in air.
The unit of exposure is the roentgen (R), defined as the exposure to produce 1 esu of charge in 1 cm3 of air under STP.
1 R = 1 esu / 1 cm3 of air under STP = 3.3310-10 C / 0.001293 g of air = 2.5810-4 C / kg of air
hv’
hv0
e-
hv’’
X
dQ = charges produced along the track
air
dm
20
eWair is the mean energy expended in air to produce one ion
pair, ~34 eV/ion-pair, or 34 J/C.
34/,
airceW
airc KKX air
eairW
airEen
RmRm
J
RmJ
RmJ
kgJR
kgJ
kgm
airmJ
photonsJh
X
X en
2
2
22
2
2
1313
/00876.01
1096.110602.1
14.3
14.300279.0
00876.0
00279.0)(
Example: calculate the energy fluence and photon fluence per R for h = 1 MeV. Given enair = 0.0279 m2/kg.
1 R = 2.5810-4 C/kg of air = 2.5810-4 C/kg of air (34 J/C)
= 0.00876 J/kg of air
21
depth
Ker
ma
or d
ose
Relationship between Kerma and Dose(no attenuation of the photon beam)
trEK
Electron track
dose
kerma
Buildup region
equilibrium region
dose
22
depth
Ker
ma
or d
ose
Relationship between Kerma and Dose(with attenuation of the photon beam)
trEK
dose
Buildup region
transient equilibrium region
kerma
dose
Electron track
700800
9001000
23
8.2-C Relationship Between KERMA and Absorbed Dose
<1>1
KERMADose
depth
Abs
orbe
d do
se a
nd K
erm
a
= D/Kcol = 1
Under (transient) electron equilibrium conditions, depends on the beam energy, not material. For Co-60, =1.005
Buildup region
(Transient) equilibrium
region
enD
cep
24
8.3 Calculation of Absorbed Dose from Exposure (A- absorbed dose to air)
Under conditions of electron equilibrium:
e
WXKD air
colair
Dair(J/kg) = X(R) • 2.5810-4 (C/kg/R) • 33.97 (J/C)
Dair(cGy) = 0.876 (cGy/R) • X(R)
1 roentgen (R) of exposure produces 2.58×10-4 coulombs of charges per Kg of air.
roentgen-to-rad conversion factor for air
25
8.3 Calculation of Absorbed Dose from Exposure (B- absorbed dose to any medium)
medenmedmedD Under conditions of charged particle equilibrium:
airmed
airen
meden
airenair
medenmed
air
med AwhereAD
D
,
AXf
AX
Ae
WXD
med
airen
meden
airen
medenairmed
876.0
fmed (f-factor) is the roentgen-to-rad conversion factor (dose-to-air to dose-to-medium conversion). It is a function of the material composition and photon energy.
26
8.3 Calculation of Absorbed Dose from Exposure (C- dose calibration with ion chamber in air)
air air
P P
For megavoltage beams, build-up cap is needed to provide electron equilibrium
M X=M•Nx
M is the corrected reading
Nx is the exposure calibration factor for the given chamber for the same beam
quality
air
P
Dfs= ftissue• X•Aeq
Equilibrium mass of tissue
ftissue is the f-factor (exposure-to-dose
conversion factor) for tissue Aeq =Ψtissue/Ψair
27
8.3 Calculation of Absorbed Dose from Exposure (D- dose measurement from exposure with ion chamber in a medium)
P PP
chamber with build-up cap
M X=M•Nx Dmed= fmed• X•Am
medium
Air cavity
ΨbΨc Ψm
Am =Ψm/Ψc
m
med
air
enxmed A
e
WNMD
28
8.4 The Bragg-Gray Cavity Theory (how to convert dose-to-cavity-air to dose-to-medium)
0
0
00
0
0
00 )(
)()(
)()()( E
E
EE
dEE
dEESE
dEEdEESED
(# e-/cm2)
S(energy loss/cm)
S (energy loss/cm3)
is the electron fluence at the point of measurement,
is the mass collision stopping power averaged
over the electron energy spectrum
S
E0 is the maximum electron energy
S
D
29
8.4 The Bragg-Gray Cavity Theory (how to convert dose-to-cavity-air to dose-to-medium)
med
g
gmed
g
med
g
med S
e
WJDor
S
S
D
D
med
med
SD
medium
×
cavity removed, assuming not affected
e
WJ
SD g
g
g
medium
gas
×
Jg is charge produced per unit mass of air
30
Bragg-Gray Conditions
1. The cavity is so small that it does not perturb the electron fluence, i.e. Φ is not changed
2. Absorbed dose (energy) deposited in the cavity is entirely due to electrons crossing it, i.e., no electrons produced nor lost in the cavity.
Φ
A B
Electron fluence Φ is continuous and unchanged across the boundary between A and B, since nothing is produced nor lost at the interface
Φ
A B
The condition remains true if a slab of ‘vacuum’ is sandwiched between A and B, since no interaction takes place inside the vacuum.
vacu
um Φ
A B
air
The situation is no longer true for a slab of ‘air’- low energy electrons are stopped in and high energy -rays produced in and escaped from the slab
31
8.4 The Bragg-Gray Cavity Theory (A- Stopping power, the Spencer-Attix formulation)
med
g
gmed
L
e
WJD
0
0
)(
)()(
E
E
dEE
dEEL
EL
To exclude low-energy electrons (E<) that enter and then stop in the cavity
is the electron energy required to cross the cavity, typically ~10 kev)
L is the restricted mass collision stopping power with as the cutoff energy
To exclude high-energy -rays (E>) that are produced and then escape from the cavity
32
8.4 The Bragg-Gray Cavity Theory (B-chamber volume)
If chamber volume V is known, then Jg can be obtained from:
V
QJ g
where Q is the charge produced, is the density of (cavity) air
But V cannot be accurately measured directly.
However, it can be indirectly determined from the chamber exposure calibration factor Nx.
33
air
P
mass of wall material
wall
aircav
wall
airairchamwall
LDD
8.4 The Bragg-Gray Cavity Theory (B-chamber volume)
Electron fluence ratio
Bragg-Gray theory
wall
aircav
wall
airairchamwall
LDD
transient electron equilibrium exists
air
P
chamber with wall & buildup cap
e
WJD air
aircham
Jair= charge produced per unit mass in air in chamber volume
air
P
air
wallcham
air
wall
enwallair DD
34
8.4 The Bragg-Gray Cavity Theory (B-chamber volume)
Combining the equations for Dcham-air, Dwall, and Dair, we have:
air
wallchamwall
aircav
air
wall
en
wall
air
airair
L
e
WJD
Dair can also be measured with a chamber with an exposure calibration factor NX:
airionxionair e
WkANPMD
chamber reading corrected for recombination
chamber exposure calibration factor corrected for recombination
exposure (R)2.58x10-4 C/kg/R
33.97 J/C
Converts from kerma to dose
35
wall
wall
air
en
air
wall
wallionxionair AL
kANPMJ
8.4 The Bragg-Gray Cavity Theory (B-chamber volume)
Combining the two previous equations for Dair, we have:
wall
airchamair
wallcav
wall
air
en
air
wall
wallionxionair
LkANPMJ
Awall = change of photon energy fluence due to the wall and buildup cap
A
wall
cap
air
en
air
cap
wall
air
en
air
wall
wallionxionair
ALL
kANPMJ
1
wall and buildup cap made of different materials, is the fraction of electrons generated in wall
36
8.4 The Bragg-Gray Cavity Theory (B-chamber volume)
Jair is the charge produced per unit mass of air in the chamber:
cair
ionair V
PMJ
where air = density of air,
Vc = chamber volume
wallwallionxairc AAANk
V
1
Combining the two equations above, we have the relationship between Vc and Nx:
wallwallionxionair AAkANPMJ From the previous slide:
37
8.4 The Bragg-Gray Cavity Theory (C- effective point of measurement)
Effective point of measurement
For parallel plate chambers, the effective point of measurement is at the inner face of the front plate
Effective point of measurement
For cylindrical chambers, the effective point of measurement is displaced 0.85r from the center
0.85r
38
8.4 The Bragg-Gray Cavity Theory (C- effective point of measurement)
d
ds
2/
0
2/
0
cos2
cos2
dsx
dsxxxeff
xr
2x
cosrx Xeff = 8r/3= 0.85r
Area perpendicular to electron fluence
Number of electrons entering the circle through ds
Tracklength of each electron entering through ds amount of ionization produced
Total amount of ionization produced due to electrons entering through ds
41
Ngas = Dair / Q
where Dair is the dose to the chamber cavity air, Q is the charge produced in the cavity, or
Ngas = Dair / (M P‧ ion)
where M is the collected charge (or meter reading), corrected for recombination loss Pion.
8.5 Calibration of Megavoltage Beams: TG-21 Protocol (A. Cavity-Gas Calibration Factor)
The cavity-gas calibration factor Ngas, is defined as the absorbed dose to the cavity gas per unit charge produced in the cavity. It has a unit of Gy/C.
Co-60
M
chamber with wall & buildup cap
CGy
mVVm
Q
DN
ccair
eW
eW
airgas /
)(
379.2813
Ngas is unique to each ionization chamber, determined entirely by its cavity volume.
3197.1
97.33
mkg
CJeW
air
42
8.5 Calibration of Megavoltage Beams: TG-21 Protocol (A. Cavity-Gas Calibration Factor)
Conversion from Nx to Ngas:
andPM
eWJ
PM
DN
ion
air
ion
airgas ,
wall
cap
air
en
air
cap
wall
air
en
air
wall
wallionxionair
ALL
kANPMJ
1
wall
cap
air
en
air
cap
wall
air
en
air
wall
wallionxgas
ALL
eWkANN
1
43
8.5 Calibration of Megavoltage Beams: TG-21 Protocol (B. Chamber as a Bragg-Gray Cavity) Conversion from Dose-to-air to Dose-to-medium
Dair
gasionair NPMD
Dwall
repl
wall
air
airwall PL
DD
Dmed
x
wall
med
wall
wallmed PL
DD
replwall
med
air
airmed PPL
DD
medium wall
44
Dair Dmed
x
Thin-wall approximation
Dair
med
ium
wall
air
LairairD
med
LmedmedD
airL
air
medL
med
air
med
DD
Thick-wall approximation
Dair Dwall
x wall
air
wall
airL
DD
cavair
wall
medmedmed
CPE
medenD
wallwallwall
CPE
wallenD
med
wall
med
wallchambwall
med en
D
D
med
air
L
med
aircavmedair
45
Dair(med)Dmed
medium
wall
Dair(wall)
x
From the previous slide: Thin-wall
approximation:
Thick-wall approximation: med
wall
med
wallchambwall
aircav
wall
airL
airmedenDD
med
aircav
med
airL
airmed DD
(1-)
1
1
)()1()(
wall
med
wall
medchambmed
wallcav
med
wallL
med
aircav
med
airL
gasion
med
air
medcav
air
medL
wall
med
wall
medchambair
wallcav
air
wallL
medair
airairair
en
en
NPMD
DD
medDwallDD
replPairD
wallP/1
= fraction of electrons generated in ‘wall’.
1- = fraction of electrons generated in ‘medium’.
46
Alternative approach to Prepl
Dair
replwall
med
air
airmed PPL
DPD
)(
medium cavity air
xd
Dmed(P)
Dair Dmed(P’)wall
med
air
airmed PL
DPD
)'(
mediumeffective point of measurement x
dηr
)(
)(
)'(
)()(
rdD
dD
PD
PDdPrepl
47
For electron beams:
Dair z
z
E
medaircav
med
airairmed
E
repl
med
airairmed
LDD
orPL
DD
medium cavity air
xz
Dmed
Pwall is assumed to be 1.
zat energy electron mean theis where zE
dose-depth ionization-depth therefore
dependentdepth not are thusandenergy electron beams,photon For
ratios'power stopping' apply the
dose,-depth toionization-depth from converting when therefore,
dependentdepth are thusandenergy electron beams,electron For
:Note
medair
medair
medair
L
L
L
48
For electron beams:
• Calibration made at dmax. (gradient correction = 1)
• For depth-dose measurement:
– Apply stopping power ratios correction
– For parallel-plate chambers, Prepl = 1
– For cylindrical chambers, the gradient correction part of Prepl is handled by shifting the effective point of measurement towards the surface by 0.5r.
Prepl has two parts: Prepl = Pfl ‧ Pgr
1. Fluence correction (Pfl): accounts for in-scattering effect and obliquity effect.
2. Gradient correction (Pgr): accounts for displacement in the effective point of measurement.
49
Conversion from dose-to-water to dose-to-muscle
For photon beams:
muscle
water
enwatermuscle DD
For electron beams:
muscle
water
watermuscleS
DD
99.0
muscle
water
muscle
water
en S
50
The TG-51 protocol (Med Phys 26, 1847-70, 1999)
The TG-51 protocol is based on ‘absorbed dose to water’ calibration (also in a Co-60 beam).
The chamber calibration factor is denoted .
The calibrated chamber can be used in any beam modality (photon or electron beams) and any energy, in water.
The formalism is simpler than the TG-21, but it is applicable in water only.
CowDN
60
,
51
• Ion chamber and electrometer
– calibration traceable to standard laboratory
• waterproofing for ion chamber ( if needed) <1mm PMMA
• water phantom (at least 30x30x30 cm3)
• lead foil for photons 10MV and above
– 1 mm 20%
• system to measure air pressure and water temperature
Equipment Needed
52
Obtain an Absorbed-dose to Water Calibration Factor CowDN
60
,
M (corrected)
rdgorC
Gy
M
DN Co
wD
60
,
60Co sourced m
ax
D
Dose to water per unit charge (reading)
53
Quality Conversion Factor
Ideally, for a given chamber individual calibration factor should be obtained for each beam quality used in the clinic. So that:
This is impractical, as the standard laboratory may not have the particular beam quality Q available, thus a quality conversion factor kQ is introduced to convert the calibration factor for Co-60 to that for the beam quality Q.
QwDN ,
QwD
Qw NMD ,
CowDQ
QwD NkN
60
,,
54
General Formalism
In a Co-60 beam:
CowDQ
Qw NkMD
60
,
In any other photon beam:(only cylindrical chamber allowed at present)
)(6060
, correctedisMNMD CowD
Cow
In any electron beam:(both cylindrical and parallel-plate chambers allowed)
CowDecalR
Qgr
Qw NkkPMD
60
50 ,'
55
Charge measurement
rawpolelecion MPPPPM TP
raw
-rawraw
pol 2
-
M
MMP
P
TPTP
33.101
222.273
2.273
Polarity correction
Press/temperature
Electrometer correction Pelec
L
HLraw
Hraw
L
H
Hion
VV
M
M
VV
VP
-
-1)( Ion recombination correction
56
kQ values for cylindrical chambers in photon beams
NRC-CNRCNRC-CNRC
57
Point of Measurement and Effective Point of Measurement
point of measurement
Effective point of measurement
cylindrical parallel plate
rcav
r
Photon: r = 0.6 rcav
electron: r = 0.5 rcav
58
Percent Depth-Dose (ionization) for photon beams
Depth in water (cm)5 10 15 20
20
40
60
80
100
% d
epth
-dos
e (i
oniz
atio
n)
III
Parallel-plate chamber: measured curve II.
Cylindrical chamber: measured curve I, needs to be shifted by 0.6 rcav to get curve II.
Curve II is the percent dose (percent ionization) curve, including contaminated electrons.
Percent depth dose to be measured at SSD = 100 cm for a 1010 cm2 field size.
%dd(10)
59
Beam Quality Specification (photons)
For this protocol, the photon beam quality is specified by %dd(10)x, the percent depth-dose at 10 cm depth in water due to the photon component only, that is, excluding contaminated electrons.
For low energy photons (<10 MV with %dd(10) < 75%) %dd(10)x = %dd(10) (contaminated electron is negligible)
For high energy photons (>10 MV with 75%<%dd(10)<89%) %dd(10)x 1.267%dd(10) – 20.0
A more accurate method requires the use of a 1-mm thick lead foil placed about 50 cm from the surface.
%dd(10)x = [0.8905+0.00150%dd(10)pb] %dd(10)pb
[foil at 50 cm, %dd(10)pb>73%]
60
Percent depth dose measured at SSD = 100 cm for a 1010 cm2 field size with a 1mm Pb filter placed at ~50 cm from the surface.
Depth in water (cm)5 10 15 20
20
40
60
80
100
(% d
d)P
b
III
%dd(10)Pb
1mm Pb filter
~50 cm
Curve II is the (%dd)Pb curve, with the contaminated electrons in the original beam removed, but generates its own contaminated electrons.%dd(10)x = [0.8905+0.00150%dd(10)pb] %dd(10)pb
61
Reference conditions for Photon Beams
photon source
SSD setup SAD setup
1010 cm2
100
cm
10 c
m
10 c
m
1010 cm2
water water
62
Photon Beam Dosimetry
CowDQ
Qw NkMD
60
,
where
M is the fully corrected (temperature, pressure, polarity, recombination) chamber reading,
kQ is the quality conversion factor,
is the absorbed dose to water chamber calibration factorCowDN
60
,
63
Reference conditions for Electron Beams
Depth: dref = 0.6 R50 - 0.1 cm
where R50 is the depth in water at which the dose is 50% of the maximum dose. dref is approx. at dmax
field size: (why different field sizes for different energies?)
> 10x10 cm2 on surface R50<8.5 cm
> 20x20 cm2 on surface R50>8.5 cm
SSD: as used in clinic between 90 cm and 110 cm (typically 100 cm)
SSD setupd re
f
water
Electron source
SS
D
CowDecalR
Qgr
Qw NkkPMD
60
50 ,'
64
Percent Depth-ionization for electron beams
Depth in water (cm)2 4 6 8
20
40
60
80
100
% d
epth
-ion
izat
ion I
II
Parallel-plate chamber: measured curve II.
Cylindrical chamber: measured curve I, needs to be shifted by 0.5 rcav to get curve II.
Curve II is the percent ionization curve.
Percent depth ionization to be measured at SSD = 100 cm for field size 1010 cm2 (or 2020 cm2 for E>20 MeV).
I50
R50 = 1.029I50 – 0.06 (cm) for 2I50 10
cmR50 = 1.059I50 – 0.37 (cm)
for I50 > 10 cm
66
Electron Beam Dosimetry ( )
depends on user’s beam must be measured in clinic.
Cylindrical chamber:
parallel plate chamber:
0.1QgrP
QgrP
)(
)5.0(
refraw
cavrefrawQgr dM
rdMP
Same as shifting the point of
measurement upstream by 0.5rcav.
QgrP
67
Electron Beam Dosimetry (Kecal )
Kecal is the photon-to-electron conversion factor, for an arbitrary electron beam quality Qecal, taken as R50 = 7.5 cm.
The values of Kecal are available in the TG-51 protocol.
chamber Attix Capintec PTB Exradin Holt Markus NACP
kecal 0.883 0.921 0.901 0.888 0.900 0.905 0.888
Parallel-plate chambers:
chamberExradin
A12NE2571 NE2581 PR-06 N23331 N30004 …
kecal 0.906 0.903 0.885 0.900 0.896 0.905 …
cylindrical chambers:
ecalQCo
wDwD NN ,,
60
68
Electron Beam Dosimetry ( )'
50Rk
'
50Rk is the electron quality conversion factor converting from Qecal to Q.
'
50Rk for a number of cylindrical and parallel-plate chambers are available in Figs. 5-8 in the TG-51 protocol. It can also be calculated from the following expressions:
Cylindrical:67.3' 50
500710.09905.0)( R
R ecylk
Parallel-plate:214.0
50' )(145.02239.1)(
50RppkR
69
k’R50 for Cylindrical Chambers
NRC-CNRCNRC-CNRC
70
k’R50 for Parallel Plate Chambers
NRC-CNRCNRC-CNRC
71
Electron Beam Dosimetry
CowDecalR
Qgr
Qw NkkPMD
60
50 ,'
where
M is the fully corrected chamber reading,
is the correction factor that accounts for the ionization gradient at the point of measurement (for cylindrical chamber only)
is the electron quality conversion factor.
kecal is the photon to electron conversion factor, fixed for a given chamber model
is the absorbed dose to water chamber calibration factorCowDN
60
,
QgrP
'
50Rk
72
Summary - photons
• get a traceable
• measure %dd(10)Pb with lead foil (shift depth if necessary)
• deduce %dd(10)x for open beam from %dd(10)Pb
• measure Mraw at 10 cm depth in water (no depth shift !!!)
• M = PionPTPPelecPpol Mraw
• lookup kQ for your chamber
Co
wDN60
,
Co
wDQQw NkMD
60
,
73
Summary - electrons
• get a traceable
• measure I50 to give R50 (shift depth if necessary)
• deduce dref = 0.6 R50 -0.1 cm (approx. at dmax)
• measure Mraw at dref (no depth shift !!!)
• M = PionPTPPelecPpol Mraw
• lookup kecal for your chamber
• determine (fig, formula)
• establish (Mraw 2 depths)
Co
wDN60
,
'
50RkQ
grPCo
wDRQ
grQw NkkPMD
60
50 ,ecal'
74
8.8 Exposure from Radioactive Sources
Exposure rate from a radioactive source can be determined from the photon energy fluence and the relevant mass energy absorption coefficients for air, assuming charged particle equilibrium:
airair
en
air
en
airair
W
eX
therefore
e
WXD
,
75
N
iii Ef
12
10
)1(4
3600107.3 source Ci-1 from 1mat fluence/h energy
where fi is the number of photons of energy Ei emitted per decay.
airiair
enN
iii W
eEf
,1
2
10
)1(4
3600107.3
X source Ci-1 from 1mat exposure/h
photon fluence
JRkgJeW air-13101.602MeV 1 ),/(00876.0 ngsubstituti
iair
enN
iii EfhR
,1
93.81 )/(X
76
)/()(93.81 )(
:constant rate exposure thedefine
2
,1
112
2
kgmMeVEfCihRm
XA
l
iair
enN
iii
The exposure rate constant is a property of the radioactive isotope.
Example: calculate the exposure rate constant for 60Co:
fi
Ei(MeV)
1 1.17 0.00270
1 1.33 0.00261
)/( 2, kgmiairen
11229.1
)00261.033.100270.017.1(8.193
CihRm
Exposure rate (R/min) from 5,000-Ci 60Co source at 80cm:
min/168
60/80
100500029.1/
22
R
lAX
77
8.9 Other Methods of Measuring Absorbed Dose
A. Calorimetry
B. Chemical Dosimetry
C. Solid State Methods
D. Silicon Diodes
E. Radiographic Film
78
8.9 (A-calorimetry & B-chemical dosimetry)
Calorimetry is based on the principle that the energy absorbed in a medium from radiation eventually appears as heat energy, resulting in a small rise in temperature, which can be measured with a thermistor. The temperature increase in water produced by 1 Gy is 2.3910-4°C
Chemical dosimetry is based on the principle that energy absorbed from radiation may cause chemical change. Most developed system is the ferrous sulfate (Fricke dosimetry). The absorbed dose D, can be determined by the measured chemical change M, and the G-value (# of molecules produced per 100 eV of absorbed dose) of the chemical.
These methods are used in national standards laboratories.
79
8.9-C Solid State Methods (TLD)
When certain crystal is irradiated, a small fraction of the absorbed energy is stored in the crystal. Some of this energy can be recovered later as visible light when the crystal is heated. This phenomenon is called thermoluminescence (TL).
The emitted light is amplified by the photomultiplier tube.
valence band
conduction band
ener
gy
irradiation
electron trap
heatingionizing
radiat
ion
TL photon
80
8.9-C Solid State Methods (TLD)
When a previously exposed sample of TLD is heated, the light output as a function of time is called a ‘glow curve’. The area under the glow curve can be used to measure dose.
81
The most commonly used TLD material is lithium fluoride (LiF). Prior to use, the LiF is annealed for 1 hour at 400° C, followed by 24 hours at 80° C (pre-irradiation annealing).
In radiation therapy, TLD is primarily used for in vivo measurement (if placed on skin, proper build-up is needed, e.g. bolus). TLD is available in different forms (powder, chips, rods) and sizes.
For megavoltage dosimetry, TLD can provide accuracy of ±3%.
8.9-C Solid State Methods (TLD)
83
Diode is a solid state semi-conductor device which generates a current when exposed to radiation.
Small size, instantaneous response, ruggedness, and high sensitivity, but is energy, directional, and temperature dependent, also suffers from radiation damage.
Primarily used for relative dose measurement (dose distribution)
It can also be used for in-vivo dosimetry (does not require 300 V high voltage).
Absolute dose measurement (machine output calibration) is done with a chamber.
8.9-D Silicon Diodes
84
8.9-D Silicon Diodes (theory)
Silicon diode p-type (receptor)
+
++
+
++
-
-
-
--
-
--
n-type (donor)
A silicon (14Si) doped with impurities to make p-type (electron receptor, e.g. 5B) and n-type (electron donor, e.g. 15P).
--
-
--
--
--
+
++
+
++
++
At equilibrium, a built-in potential is established in the depletion zone.
+
++
+
++
-
-
-
--
-
--
depletion zone
(built-in potential)+ V –
Silicon diode p-type (receptor)
n-type (donor)
Carriers near the interface diffuse across the boundary and recombine with the opposite carrier, forming a depletion zone
-
-+
+
+
- +-
The ion pairs produced along the electron track are attracted towards to +/- sides of the depletion zone, generating a current that can be measured.
85
8.9-D Silicon Diodes
• no bias voltage applied.
• diodes are more sensitive than ion chambers –
• (W/e)Si ~ 3.5 eV [In contrast, (W/e)air ~ 34 eV ]
• Si ~ 1800 air
• energy dependency for photons (due to Z=14 for Si), but not for electrons (therefore can be used for electron relative depth-dose measurement).
• angular dependency.
• temperature dependency, but independent of pressure.
• radiation damage – needs periodic calibration.
• used for patient dose monitoring and when small detector size is needed.
86
8.9-E Radiographic Film
Film base, cellulose acetate or polyester resin, ~0.1 mm.
Emulsion containing silver bromide crystals
Radiation or visible light
When the film is exposed to ionizing radiation, chemical change takes place in the crystals to form the latent image. When the film is developed, the affected crystals reduced to small grains of metallic silver, and the film is fixed. The unaffected granules are removed by the fixing solution. The metallic silver remains on the film, causing darkness. The degree of blackening depends on the dose.
87
net o
ptic
al d
ensi
ty
3.0
2.0
1.0
The degree of blackening is measured by optical density, defined as: OD = log10 (I0/It), where I0, It are incident and transmitted light intensities, respectively.
In dosimetry, the background fog (OD of unexposed processed film) should be subtracted to obtain the net optical density, whose relationship with dose is called H-D curve, or sensitometric curve.
Dose (cGy)
5 10 15Each box of films may have different characteristics, prior to use, H-D curve should be obtained for samples from the box.
8.9-E Radiographic Film
xv-2
(for illustration only)
RPM-2
50 100 150
RPM-2
xv-2
88
• Advantages:
High spatial resolution ( < 1 mm)
Ideal for 1D or 2D relative dose distribution measurement. (beam profiles, isodose distributions), accurate to within ~ 3%.
Inexpensive for personnel dosimetry (film badge, accurate to within 10%)
• Disadvantages:
Requires careful calibration prior to use.
Over responds to low energy photons (due to increased photo-electric events in silver bromide), not suitable for absolute dose measurement.
8.9-E Radiographic Film
89
Comparison of Calculation and Measurement
Film Calc.
90
• large dynamic range (10-2-106 Gy): suitable for brachy source dose distribution measurement.• no dark room processing required: the radiochromic film is insensitive to visible light, the emulsion changes color when exposed to radiation without any processing.
• tissue equivalent (zeff 6.0 to 6.5)• less energy dependency compared to conventional film• film response dependent on room temperature. Acceptable range of room temperatures 20-30° C.• sensitive to ultraviolet light (do not expose to fluorescent light)• more expensive, requires special densitometer (laser scanner at specific wavelength 610-670 nm)
Radiochromic film