Fourth ASA/ASJ Joint Meeting, Honoloulu, Hawaii


Biomedical Application of Acoustic Microscopy

Yoshifumi Saijo - saijo@idac.tohoku.ac.jp
Department of Medical Engineering and Cardiology
Institute of Development, Aging and Cancer
Tohoku University
Sendai 980-8575 Japan

Hidehiko Sasaki
Naohiro Hozumi
Kazuto Kobayashi
Hiroaki Okawai
Motonao Tanaka
Floyd Dunn

Popular version of paper 3pBB3
Presented Thursday afternoon, Nov. 30, 2006
Fourth Joint ASA/ASJ Meeting, Honolulu, Hawaii

Brief History of Acoustic Microscopy

Optics has been the main observational mode in the microscopic world for many years. However, its domain is restricted to largely transparent media. Sokolov in the former Soviet Union, first proposed the concept of an ultrasonic microscope in order to visualize opaque media in 1949. He pointed out that the wavelength of 3-GHz ultrasound in water is the same as the wavelength of green light in air. At that time, however, the technologies to produce 3-GHz ultrasound did not exist. In 1959, Dunn and Fry at University of Illinois developed an ultrasonic absorption microscope method with 12-MHz ultrasound. During the 1970s, high frequency techniques were developed for the microwave technology for radar and for satellite communications. In 1973, Quate and Lemons at Stanford University developed a scanning acoustic microscope (SAM), now used in the biomedical field because of its high resolution and high quality imaging.

Principles and Objectives of Classical Acoustic Microscopy

The acoustic focusing element comprises a ZnO piezoelectric transducer with a sapphire lens. The ultrasonic frequency is variable over the range of 100 to 210 MHz and the beam width at the focal volume ranges from 5 mm (at 210 MHz) to 10 mm (at 100 MHz). The attenuation and sound speed of the material can be derived from the intensity and phase of the reflected signal, respectively. The attenuation depends on the molecular weight of the material. Sound speed has close correlation to the density and elastic bulk modulus. Thus, acoustic properties can be applied to assess the mechanical or physical properties of biological materials.

We have been developing SAM for medicine and biology since 1985. The objectives of the SAM study in medicine and biology are following. First, SAM can be applied for intra-operative pathological examinations since it does not require special staining techniques. Second, ultrasonic data obtained with the high frequency SAM can be used for assessing reflectability or texture in clinical echographic imaging. Third, the biomechanics tissues are measured by acoustic parameters because the sound speed has close correlation to the elastic bulk modulus.

Each pixel in the acoustic microscope image shows the quantitative value of the acoustic parameters. The values are shown by the color bar scale. The arrows in the following images indicate 500 mm.

Examples of Classical Acoustical Microscopy Images

1) Myocardial Infarction [1]

 

2) Atherosclerosis [2-4]

3) Brain

4) Cells [5]

Sound Speed Microscopy [6,7]

In 2002, we proposed a new concept acoustic microscope using a single pulsed ultrasound instead of burst waves in the conventional acoustic microscopy. The pulse response is analyzed in the frequency domain and the thickness, attenuation and speed of sound are measured at all the sampling points. Thanks for the development of computer and digital technology, the size of the instruments can be reduced to set on a desktop.

Examples of Sound Speed Microscopy Images

1) Atherosclerosis

2) Cardiomyopathy

3) Breast Cancer

Acoustic Impedance Microscopy

As the specimens for classical acoustic microscopy and sound speed microscopy need to be flat and thin, the application was limited to the excised sample or cultured cells. In 2005, we proposed another new concept acoustic microscopy to observe the surface of the specimen without slicing. The system enables the in vivo high resolution imaging and can be applied for intra-operative examination

References

  1. Saijo Y, Tanaka M, Okawai H, Sasaki H, Nitta S, Dunn F. Ultrasonic tissue characterization of infarcted myocardium by scanning acoustic microscopy. Ultrasound Med Biol Vol 23, No 1; 77-85, 1997.
  2. Saijo Y, Ohashi T, Sasaki H, Sato M, Jorgensen CS, Nitta S. Application of scanning acoustic microscopy for assessing stress distribution in atherosclerotic plaque. Ann Biomed Eng, Vol 29, 1048-53, 2001.
  3. Saijo Y, Miyakawa T, Sasaki H, Tanaka M, Nitta S. Acoustic properties of aortic aneurysm obtained with scanning acoustic microscopy. Ultrasonics, Vol. 42, No. 1-9, 695-698, 2004.
  4. Saijo Y, Jorgensen CS, Falk E. Ultrasonic tissue characterization of collagen in lipid-rich plaques in apoE-deficient mice. Atherosclerosis Vol 158, No.2; 289-295, 2001.
  5. Saijo Y, Sasaki H, Sato M, Nitta S, Tanaka M. Visualization of human umbilical vein endothelial cells by acoustic microscopy. Ultrasonics Vol 38, No 1-8; 396-399, 2000.
  6. Hozumi N, Yamashita R, Lee CK, Nagao M, Kobayashi K, Saijo Y, Tanaka M, Tanaka N, Ohtsuki S. Time–frequency analysis for pulse driven ultrasonic microscopy for biological tissue characterization. Ultrasonics, Vol. 42, No. 1-9, 717-722, 2004.
  7. Saijo Y, Sasaki H, Hozumi N, Kobayashi K, Tanaka M, Yambe T. Sound speed scanning acoustic microscopy for biomedical applications. Technol Health Care. Vol. 13, No. 4: 261-7, 2005.
  8. Hozumi N, Kimura A, Terauchi S, Nagao M, Yoshida S, Kobayashi K, Saijo Y. Acoustic Impedance Micro-imaging for Biological Tissue Using a Focused Acoustic Pulse with a Frequency Range up to 100 MHz. Proc 2005 IEEE International Ultrasonics Symposium, 170-173, 2005.

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