ArticleIEEE transactions on ultrasonics, ferroelectrics, and frequency control2012
Multi-layer phase analysis: quantifying the elastic properties of soft tissues and live cells with ultra-high-frequency scanning acoustic microscopy.
Article in IEEE transactions on ultrasonics, ferroelectrics, and frequency control, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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7 citing papers in PubMed.
- Biomechanical changes after repeated collagen cross-linking on human corneas assessed in vitro using scanning acoustic microscopy.Investigative ophthalmology & visual science · 2014Trial
- Frequency-modulated atomic force microscopy localises viscoelastic remodelling in the ageing sheep aorta.Journal of the mechanical behavior of biomedical materials · 2016Article
- A pilot study of scanning acoustic microscopy as a tool for measuring arterial stiffness in aortic biopsies.Artery research · 2016Article
- Localized micro- and nano-scale remodelling in the diabetic aorta.Acta biomaterialia · 2014Article
- Combining AFM and acoustic probes to reveal changes in the elastic stiffness tensor of living cells.Biophysical journal · 2014Article
- Growth differentiation factor 6 and transforming growth factor-beta differentially mediate mesenchymal stem cell differentiation, composition, and micromechanical properties of nucleus pulposus constructs.Arthritis research & therapy · 2014Article
- Biomechanical properties of human corneas following low- and high-intensity collagen cross-linking determined with scanning acoustic microscopy.Investigative ophthalmology & visual science · 2013Article
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9 authors.
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Abstract
Scanning acoustic microscopy is potentially a powerful tool for characterizing the elastic properties of soft biological tissues and cells. In this paper, we present a method, multi-layer phase analysis (MLPA), which can be used to extract local speed of sound values, for both thin tissue sections mounted on glass slides and cultured cells grown on cell culture plastic, with a resolution close to 1 μm. The method exploits the phase information that is preserved in the interference between the acoustic wave reflected from the substrate surface and internal reflections from the acoustic lens. In practice, a stack of acoustic images are captured beginning with the acoustic focal point 4 μm above the substrate surface and moving down in 0.1-μm increments. Scanning parameters, such as acoustic wave frequency and gate position, were adjusted to obtain optimal phase and lateral resolution. The data were processed offline to extract the phase information with the contribution of any inclination in the substrate removed before the calculation of sound speed. Here, we apply this approach to both skin sections and fibroblast cells, and compare our data with the V(f) (voltage versus frequency) method that has previously been used for characterization of soft tissues and cells. Compared with the V(f) method, the MPLA method not only reduces signal noise but can be implemented without making a priori assumptions with regards to tissue or cell parameters.
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