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1.
Dent Mater ; 28(4): 385-91, 2012 Apr.
Article in English | MEDLINE | ID: mdl-22209572

ABSTRACT

OBJECTIVES: We had previously discovered that the flexural and tensile strengths of human dentin were 2-2.4 times greater after being heated to 140°C, and deduced that the generation of higher-density structures and therefore dehydration probably promoted the increased strength. Our test hypotheses were that intertubular dentin, which constitutes a major part of organic components, was selectively affected by heating, and such changes could happen without critical damages to the basic structure of dentin type I collagen. METHODS: Micro-mechanical changes of human dentin by heating at 140°C were investigated by nano-indentation. Chemical changes in dentin collagen after heating were also investigated by X-ray diffraction study, a microscopic Fourier transform infrared (micro-FTIR) and a laser Raman spectroscopic analyses, and a cross-linking analysis by high-performance liquid chromatography. RESULTS: The results of nano-indentation showed that the micro-hardness of intertubular dentin increased after heating at 140°C to 1.8 times more than unheated dentin; on the other hand, peritubular dentin was unchanged. Results of X-ray diffraction showed that the lateral packing of collagen molecules shrank from 13.6±0.3 to 10.6±0.1Å after heating, but the shrinkage reversed to the original after rehydration for seven days. After heating, no substantial chemical changes in the collagen molecules were detected in tests by micro-FTIR or Raman analyses, or by cross-linking analysis. SIGNIFICANCE: These results suggest that intertubular dentin, which contains most of the type I collagen, was selectively affected by heating at 140°C without critical damage to its collagen.


Subject(s)
Collagen Type I/chemistry , Dentin/chemistry , Chromatography, High Pressure Liquid , Cross-Linking Reagents , Crystallography, X-Ray , Dental Stress Analysis , Desiccation , Elastic Modulus , Hardness , Hot Temperature , Humans , Microscopy, Atomic Force , Molecular Structure , Spectroscopy, Fourier Transform Infrared , Spectrum Analysis, Raman
2.
Appl Opt ; 44(24): 5131-9, 2005 Aug 20.
Article in English | MEDLINE | ID: mdl-16121800

ABSTRACT

We demonstrate two methods for the characterization of deformable membrane mirrors and the training of adaptive optics systems that employ these mirrors. Neither method employs a wave-front sensor. In one case, aberrations produced by a wave-front generator are corrected by the deformable mirror by use of a rapidly converging iterative algorithm based on orthogonal deformation modes of the mirror. In the other case, a simple interferometer is used with fringe analysis and phase-unwrapping algorithms. We discuss how the choice of singular values can be used to control the pseudoinversion of the control matrix.

3.
J Biomed Opt ; 10(2): 024010, 2005.
Article in English | MEDLINE | ID: mdl-15910084

ABSTRACT

We develop a compact scanning head for use in laser confocal fluorescence microscopy for in situ fluorescence imaging of organs. The head, cylindrical in shape, has 3.5 mm diameter and 30 mm length, and is thus small enough to operate in a living rat heart. The lateral and axial resolutions, defined as full widths at half maximum (FWHM) of a point spread function (PSF), measures 1.0 and 5.0 microm, respectively, for 488-nm excitation and 1.0 and 5.4 microm, respectively, for 543-nm excitation. The chromatic aberration between 488- and 543-nm laser beams is well suppressed. We perform Ca2+ imaging in cardiomyocytes through the right ventricular chamber of a perfused rat heart in line-scan mode with 2.9-ms time resolution. We also carried out two-color imaging of a fixed mouse heart and liver with subcellular resolution. The compact head of the microscope equipped with a line-scan imaging mode and two-color imaging mode is useful for in situ imaging in living organs with subcellular resolution and can advantageously be applied to in vivo research.


Subject(s)
Calcium/metabolism , Liver/ultrastructure , Microscopy, Confocal/methods , Microscopy, Fluorescence , Myocytes, Cardiac/metabolism , Myocytes, Cardiac/ultrastructure , Animals , Color , Heart , Heart Ventricles , In Vitro Techniques , Male , Perfusion , Rats , Rats, Wistar
4.
Opt Lett ; 28(6): 465-7, 2003 Mar 15.
Article in English | MEDLINE | ID: mdl-12659281

ABSTRACT

The axial position of a laser-trapped particle has been controlled by modification of the wave front by means of a membrane deformable mirror. The mirror gives wave-front modulation in terms of Zernike polynomials. By modulation of the Zernike defocus term we can modulate the particle position under conditions of laser trapping. A polystyrene particle of 1-microm diameter was moved along the optical axis direction for a distance of 2370 nm in minimum steps of 55.4 nm. We also demonstrated particle oscillation along the optical axis by changing the focal position in a sinusoidal manner. From the frequency dependency of the amplitude of particle oscillation we determined the spring constant as 91.7 nN/m.

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