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Spatial Distribution of Copper and Iron in Cardiac Tissue Grant Allen

Spatial Distribution of Copper and Iron in Cardiac Tissue

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Page 1: Spatial Distribution of Copper and Iron in Cardiac Tissue

Spatial Distribution

of Copper and Iron in

Cardiac Tissue

Grant Allen

Page 2: Spatial Distribution of Copper and Iron in Cardiac Tissue

Seminar Outline

Electron Probe Microanalysis

Nuclear Microscopy

Acknowledgements

Secondary Ion Mass Spectrometry

Conclusion

Introduction

Page 3: Spatial Distribution of Copper and Iron in Cardiac Tissue

Introduction

Investigate the spatial distribution of Cu and Fe in cardiac tissue

Analytical techniques:

Cardiac tissue that exhibits marked histological damage may

possess elevated levels of Cu and Fe

Electron probe x-ray microanalysis (EPMA)

Secondary ion mass spectrometry (SIMS)

Nuclear microscopy (NM)

Correlate topographical features with chemical composition

UHV techniques influence method of sample preparation

Page 4: Spatial Distribution of Copper and Iron in Cardiac Tissue

Electron Probe Microanalysis

Image courtesy of the Microscopy and Microanalysis Facility at the Department of Materials Engineering – Monash University

Detection limit in the region of 100 ppm

Primary ion beam: 5-20 kV electrons

Lateral resolution of 1 µm

Quantitative

Cryochamber

Specimen maintained at 80 K

Page 5: Spatial Distribution of Copper and Iron in Cardiac Tissue

Electron Probe Microanalysis

Energy /keV

Page 6: Spatial Distribution of Copper and Iron in Cardiac Tissue

Nuclear Microscopy

Rutherford Backscattering Spectroscopy (RBS) - normalisation

Scanning Transmission Ion Microscopy (STIM) - structural information

Particle Induced X-ray Emission (PIXE) - elemental analysis

Secondary electrons – complementary topographical information

Incident beam: 1.0-3.0 MeV H+ or He+

Lateral resolution of between 0.1 and 10 µm

Detection limit: ppb to ppm

Quantitative

UHV chamber

Specimen section freeze dried

Page 7: Spatial Distribution of Copper and Iron in Cardiac Tissue

Secondary Ion Mass Spectrometry

Image courtesy of the Bristol University CVD Diamond Group

Detection limit: ppb to ppm

Primary ion beam: 1-30 KeV 133Cs+

Non-quantitative analysis of biological specimens

Lateral resolution of 1 µm is possible

UHV chamber

Specimen section freeze dried

Page 8: Spatial Distribution of Copper and Iron in Cardiac Tissue

Secondary Ion Mass Spectrometry

Page 9: Spatial Distribution of Copper and Iron in Cardiac Tissue

Conclusion

Nuclear microscopy: provided the specimen is prepared in an

appropriate manner, determination of the spatial distribution of

metals in biological tissue is possible

Secondary ion mass spectrometry: non-quantitative

Electron probe x-ray microanalysis: insufficient sensitivity

Page 10: Spatial Distribution of Copper and Iron in Cardiac Tissue

Prof. Garth Cooper (Protemix)

Acknowledgements

Dr Anthony Phillips (Protemix)

Catherine Hobbis (School of Engineering - EPMA)

Dr Marcus Gustafsson (Department of Chemistry - SIMS)

Dr V. John Kennedy (Institute of Geological and Nuclear

Sciences - NM)

Dr Ritchie Sims (Department of Geology - EPMA)