Noninvasive In Vivo Measurement of Pb with a Portable XRF Device

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Noninvasive In Vivo Measurement of Pb with a Portable XRF Device Linda Nie, Assistant Professor School of Health Sciences Purdue University

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Noninvasive In Vivo Measurement of Pb with a Portable XRF Device. Linda Nie, Assistant Professor School of Health Sciences Purdue University. Outline. Why portable x-ray fluorescence technology Approach Results and discussion More work in progress Acknowledgements. Why Portable XRF?. - PowerPoint PPT Presentation

Transcript of Noninvasive In Vivo Measurement of Pb with a Portable XRF Device

Page 1: Noninvasive  In Vivo  Measurement of  Pb  with a Portable XRF Device

Noninvasive In Vivo Measurement of Pb with a Portable XRF

DeviceLinda Nie, Assistant Professor

School of Health SciencesPurdue University

Page 2: Noninvasive  In Vivo  Measurement of  Pb  with a Portable XRF Device

Why portable x-ray fluorescence technology

Approach Results and discussion More work in progress Acknowledgements

Outline

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Portable Multi-metals Fast More sensitive in some cases

Accessible, suitable for large population human studies

Why Portable XRF?

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Soft tissue attenuationIt is difficult to detect signals

through tissue over 5 mm Soft tissue attenuation correction

◦Spectrum to determine the soft tissue thickness

Bone surface/volumn? (mfp in bone: 0.5 mm vs. 25 mm)

Bone Pb Quantification with Portable XRF- Disadvantage

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Schematic plot

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Overall: develop a portable XRF technology to quantify multiple metals in bone and skin

Hardware designselection of tube target, filter combination, and geometry design; selection of parameters

Methodology and algorithm development Consider in vivo situation Radiation risk assessment

Objectives

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Monte Carlo simulations (MCNP) X-ray tube voltage, current, filter combinations;

x-ray tube target, geometry design etc.

Calculate minimum detection limit (MDL)

Approach - Hardware

2 bnMDL ct

( )m

t b

C ppmc

n n

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Approach – calibration

2-A(2)( ) = A(1) exp(- ) (4) exp( (5) )A(3)xy x A A x

222

1 ( )i ii

X y y x

Once the hardware design is determined ……

Method #1: peak fitting and traditional cal.

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Method #2: background subtraction

Calibration – Cont.

21 1 1( ) = K bkg A c B c C

22 2 2(100 ) = K ppm A c B c C

21 1 1( ) = ( ) ( )K net K total A c B c C

= ( ) 100 / (100 )Concentration K net K ppm

K ( ) ( )2 concentrationlive time =

( )

total K bkg

K net

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Soft Tissue Thickness Determination

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MC simulation

Experiments

Dosimetry

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Phantom, goat bone, and cadaver bone experiments◦ICP-MS, KXRF

Human studies

Validation of the Technology

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Lucite Thickness (mm)

Detection Limit (ppm)

0 2.31 4.12.04 7.13.08 11.84.08 18.64.92 25.9

Detection limit

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Phantom Concentration

(ppm)

Portable XRF (ppm) KXRF (ppm) ICPMS (ppm)

0mm Lucite 1mm Lucite 2.72mm Lucite

0 -1.05±1.73 0.72±2.30 0.62±7.26 -.068±1.96 0.63±0.20

10 11.3±1.83 12.8±3.07 9.81±7.09 8.97±1.81 11.2±0.71

20 17.2±1.90 17.3±3.15 20.2±7.16 19.6±1.91 16.7±1.89

30 31.3±2.09 29.3±3.30 26.6±7.34 30.6±1.84 36.0±0.89

50 45.4±2.24 45.0±3.49 40.0±7.59 51.8±1.77 72.5±11.7

100 99.9±2.72 96.0±3.96 100±8.16 106±2.16 127±16.0

Bone lead concentration of phantoms using portable XRF, conventional XRF, and ICPMS

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Goat Bone # Portable XRF (ppm) KXRF (ppm)0mm Lucite 1mm Lucite 2mm Lucite

1 19.7±1.95 15.4±3.05 22.2±5.31 23.5±1.649 2.73±2.23 0.84±2.72 6.33±5.30 4.5±1.4012 29.9±2.00 32.3±3.17 30.5±5.32 31.5±1.7513 13.6±1.79 15.6±2.91 19.1±5.06 12.3±1.49

Comparison of portable XRF and KXRF bone lead measurements for goat bones

(adjusted for Compton peak counts)

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LXRF vs. KXRF for goat bones

0 5 10 15 20 25 30 35-5

0

5

10

15

20

25

30

35

40

KXRFBare LXRF2mm LXRF

Concentration From KXRF (ppm)

Mea

sure

d Co

ncen

trat

ion

from

por

tabl

e XR

F (p

pm)

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Bone KXRF LXRF (0mm) ICPMS ICPMS ICPMS

7202 21.37 1.51E+01

6895 13.17 1.03E+01

6900 22.63 1.30E+01 1.16E+01 9.87E+00 1.13E+01

6918 18.78 1.16E+01

7002 16.56 9.93E+00

7031 20.33 1.10E+01

7131 20.59 1.41E+01 1.23E+01 1.81E+01 1.40E+01

7142 15.72 7.39E+00 9.73E+00 8.03E+00 5.74E+00

7162 18.30 8.45E+00 8.47E+00 8.45E+00 6.82E+00

7168 6.90 3.04E+00 2.28E+00 1.50E+00 2.88E+00

Cadaver bone results

Overestimate backgroundSolution: a. ‘real’ bone phantoms; b. adjustment using MC simulation results;Surface bone? Pb distribution in bone.

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Validation: KXRF vs. Portable XRF

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Radiation Risk Skin dose of ~13 mSv and total body

effective dose of 1.5µSv compared with

Exposure limit of 500 mSv per year to extremities for occupational workers (no limit set for general public) and a typical whole body effective dose of 100 µSv for chest x-ray

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System optimization – customized device Standardize the calibration process (true

bone equivalent phantoms, or MC simulations to adjust for differences)

Validation of the technology with a large human population

Apply the technology for metal epi and metal toxicology study

Bone Sr measurement

More work in progress

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X-ray tube output simulation

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In vivo simulation

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Steven Sanchez, Graduate Student, School of Health Sciences, Purdue University

Aaron Specht, Graduate Student, School of Health Sciences, Purdue University

Dr. Lee Grodzins, ThermoFisher Niton

Dr. Marc Weisskopf, HSPH

Acknowledgement

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Thank you!Questions??

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Cadaver Bone Spectrum

Portable XRF Cadaver Measurement,Pb concentration ~20ppm

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0 0.5 1 1.5 2 2.5 3 3.5 4 4.5 50

500

1000

1500

2000

2500

3000

Goat BonePlaster

Lucite thickness (mm)

Com

pton

pea

k co

unrs

(/s)

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Pilot studies – Methodology and Feasibility

ThermoFisher Niton: XL3t-GOLDD

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1. 100 lbs vs. 3 lbs2. 30 mins vs. 2 min3. Multi-metals

Bone Pb Measurement Quantification with Portable XRF - Advantages