Biomedical subjects

Chi-Ming Chan

Publications and source records attributed to Chi-Ming Chan.

6 recordsLinked to original sources

PubMed2006

Concentric-ringed structures in polymer thin films.

Novel polymer crystalline structures containing micrometer-sized concentric rings (or bands) were observed in thin poly(bisphenol A hexane ether) (BA-C6) films. The origin of the banded structures was found to be different from that of traditional banded spherulites in polymer systems. Analyses based on optical microscopy (OM) and atomic force microscopy (AFM) revealed that the banded structures contained alternating ridge and valley bands of polymer crystals in the flat-on orientation. No lamellar twisting was observed within the concentric-ringed structures, which were developed as a result of the formation of a depletion zone during crystallization. The formation of a depletion zone was determined to be caused by the specific volume decrement between the crystal and the melt and by the diffusion of polymer chains to the fold surfaces of the flat-on lamellae. The height of the ridges and the interband widths could be adjusted by controlling the diffusion rate. Time-of-flight secondary ion mass spectrometry ion images showed higher concentrations of low-molecular-weight polymer chains on the surfaces of the ridges than in the valleys.

Benzhydryl Compounds↗

PubMed2006

Posterior pole retinal thickness measurements by the retinal thickness analyzer in healthy Chinese subjects.

PURPOSE: To assess retinal thickness at the posterior pole in healthy Chinese subjects with the retinal thickness analyzer (RTA). METHODS: Retinal thicknesses at the posterior pole and fovea were measured by the RTA in 331 eyes of 178 healthy Chinese subjects. Retinal thicknesses as a function of sex, age, refractive errors, and axial length were also evaluated. RESULTS: The average thickness of the foveal area +/- SD was 158.6 +/- 24.8 microm, the average thickness of the perifoveal region (600-2,500 microm from fovea) +/- SD was 174 +/- 25.2 microm, and the average thickness of the posterior pole region (600-6,000 microm from fovea) +/- SD was 171.9 +/- 25.3 microm. There was no significant difference in retinal thicknesses of the foveal, perifoveal, and posterior pole regions in either right or left eyes or as a function of different spherical equivalents. Moreover, there was no significant difference of foveal thickness between males and females. Greater retinal thicknesses of the foveal, perifoveal, and posterior pole regions were associated with age of older than 40 years and axial length of < 24 mm, and greater perifoveal and posterior pole thicknesses were found for females. Furthermore, there were no significant correlations between age, refractive errors, and axial lengths with retinal thicknesses. CONCLUSION: Retinal thicknesses of the posterior pole region differed by age, axial length, and sex, but there was no effect of laterality or different spherical equivalents. The RTA is a fast and noninvasive technology to assess retinal conditions with thickening or thinning in the fovea and posterior pole.

Adult↗

PubMed2005

Morphology-driven surface segregation in a blend of poly(epsilon-caprolactone) and poly(vinyl chloride).

A blend of poly(epsilon-caprolactone) (PCL) and poly(vinyl chloride) (PVC) with 90 wt % PCL was prepared. Two films of this blend, which were grown at 35 and 45 degrees C, showed the absence and presence of banded spherulites, respectively. A detailed examination conducted with time-of-flight secondary ion mass spectrometry (ToF-SIMS) found that the surface composition of the film grown at 45 degrees C was related to its structure, which was shown to contain ridges and valleys. Phase images obtained using atomic force microscopy (AFM) indicated that the ridges and valleys consisted of edge-on and flat-on lamellae, respectively. ToF-SIMS imaging revealed that PVC and PCL were located mainly on the surface of the valleys and ridges, respectively. This morphology-driven surface segregation was caused by the difference in the surface energy between the flat-on and edge-on lamellae.

Microscopy, Atomic Force↗

PubMed2004

Real-time observation of lamellar branching induced by an AFM tip and the stability of induced nuclei.

Branching of edge-on lamellae of poly(bisphenol A octane ether) (BA-C8) was studied at room temperature (21 +/- 1 degrees C) using real-time tapping mode atomic force microscopy (AFM). Lamellar branches were shown to develop from induced nuclei that had originated from lamellar defects, namely protruding cilia and loose loops, of parent lamellae. Induced nuclei appeared and also disappeared-a phenomenon observed first time by AFM. Induced nuclei are one of the possible origins for the branching of lamellae. Branching of edge-on lamellae can be induced by an AFM tip though the adjustment of the set-point amplitude ratio (r(sp)). Using an r(sp) smaller than 0.65, defects could be created on the lamellar surface, which gave rise to lamellar branches.

Benzhydryl Compounds↗

PubMed2004

Combined X-ray photoelectron spectroscopy and time-of-flight secondary ion MS surface quantitative analysis of polymer blends with varying mixing thermodynamics.

Time-of-flight secondary ion mass spectrometry (TOF-SIMS) was used to quantitatively correlate to the surface chemical composition determined from XPS in poly(styrene-co-p-hexafluorohydroxyisopropyl-alpha-methyl styrene)/poly(4-vinyl pyridine) (PS(OH)/PVPy) blends or complexes when the p-(hexafluoro-2-hydroxyisopropyl)-alpha-methylstyrene (HFMS) contents in PS(OH) copolymers were gradually increased. It was found that different mixing thermodynamics, such as immiscibility, miscibility, and complexation, have little effect on the quantitative analysis of PS(OH) copolymers in the blends or complexes using TOF-SIMS. In the positive spectra, either the normalized intensities or relative peak intensities can be used to quantitatively analyze the surface HFMS, PS(OH), or PVPy concentration when peaks at m/z = 257, 271, 285, and 373 are used for HFMS, peaks at m/z = 91, 103, 105, 115 for styrene, and peaks at m/z = 132, 195, 209 for PVPy. In the negative spectra, the normalized intensities of peaks characteristic of PVPy seem to be not affected by hydrogen bonding formation and can be used in quantitative analysis, whereas peaks characteristic of HFMS, such as a peak at m/z = 283, cannot be used in quantitative analysis due to enhancement of its secondary ion yield resulting from hydrogen bond formation.

Journal Article↗

PubMed2003

Supramolecular assembly of poly(phenylene vinylene) with crown ether substituents to form nanoribbons.

Poly(para-phenylene vinylene) with crown ether substituents (C-PPV) could form nanoribbons through supramolecular assembly with K(+) in dilute chloroform solution. The length of the nanoribbons increased with an increase in the standing time of the C-PPV/K(+) solution. Experimental evidence to support the interaction between K(+) and crown ether substituents was provided, and the growth mechanism of C-PPV/K(+) nanorods to nanoribbons was proposed. The influence of the length of the nanoribbons on the photophysics of C-PPV was also investigated.

Journal Article↗