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Chih-Hsin Tsai

Publications and source records attributed to Chih-Hsin Tsai.

5 recordsLinked to original sources

A new approach for the detection of a nonfluorescent compound by CE-resonance Raman spectroscopy based on the sweeping-MEKC mode.

A CE-resonance Raman spectroscopy (CE-RRS) method based on MEKC and sweeping-MEKC modes is described. A nonfluorescent compound, malachite green (MG), and a doubled Nd:YAG laser (532 nm, 300 mW) were selected as model compound and light source, respectively. In order to carry out a quantitative analysis of MG, a monochromator (effective bandwidth, 0.4 nm) was used to collect the specific Raman line at 1616 cm(-1) (N-phi and C-C stretch, corresponding to 582 nm when the wavelength of the exciting source was 532 nm). As a result, the LOD for MG was 10 ppm, based on the MEKC/RRS mode. This could be improved to 5 ppb when the sweeping-MEKC/RRS mode was applied. Furthermore, with the addition of nano-size silver colloids to the CE buffer the detection limits can be further improved, but the data obtained with surface-enhanced resonance Raman spectroscopy (SERRS) are less useful for quantitative purposes.

Chromatography, Micellar Electrokinetic Capillary↗

Sample-stacking techniques in non-aqueous capillary electrophoresis.

In sample-stacking techniques, the detection limit cannot be improved by simply increasing the length of the sample solution, because the individual electrophoretic parameters must be optimized. In an attempt to increase the amount of sample injected, as well as to focus them onto a small zone, two novel methods are proposed. One of these employs an "ultra-high conductivity zone", which was inserted between the sample zone and background solution to build an unequal conductivity gradient. The other employs a "low temperature bath". A portion of the capillary (near the junction between the sample solution and the background solution) was immersed in a low temperature bath, which served as a "pseudo-high-conductivity zone" due to the fact that conductivity would increases when the temperature is decreased. As a result, a large volume of sample injection can be achieved. Using 3,4-methylenedioxymethamphetamine as a model compound, the detection limit was determined to be 1.6 x 10(-6) M (S/N = 3) by means of normal non-aqueous capillary electrophoresis (NACE). This could be improved to 3.0 x 10(-8) M, 4.8 x 10(-9) M and 5.0 x 10(-9) M, respectively, when the normal stacking, ultra-high conductivity zone NACE-stacking and the low-temperature zone NACE-stacking methods were applied.

Electrophoresis, Capillary↗

Stacking and low-temperature technique in nonaqueous capillary electrophoresis for the analysis of 3,4-methylenedioxymethamphetamine.

Low-temperature and ambient-temperature nonaqueous stacking techniques in capillary electrophoresis (CE) are described for the first time. A low-temperature bath was used to control the temperature from ambient to subzero degrees, by which a novel hyphenated method, low-temperature bath-nonaqueous capillary electrophoresis stacking (LTB-NACE stacking) is demonstrated. 3,4-Methylenedioxymethamphetamine (3,4-MDMA) was determined at a concentration of 4.7 x 10(-6) M (at a 92.1% confidence level) by normal nonaqueous capillary zone electrophoresis (NACZE) and this was improved to 2.6 x 10(-8) M and 5.0 x 10(-9) M, respectively, when the NACZE stacking and LTB-NACZE stacking techniques were applied. The content of 3,4-MDMA in an illicit drug and a suspect urine sample was readily detected. Upon application of the LTB to the separation of isomers the resolution (R) for the separation of 2,3-/3,4-MDMA was improved from 0.6 (LTB, 22 degrees C) to 1.6 (LTB, -55 degrees C) and for (+)3,4-MDMA/(-)3,4-MDMA, from 0.4 (LTB, 25 degrees C) to 1.0 (LTB, -10 degrees C).

3,4-Methylenedioxyamphetamine↗

Functional MR images and scientific inference: reproducibility maps.

Historically, reproducibility has been the sine qua non of experimental findings that are considered to be scientifically useful. Typically, findings from functional magnetic resonance imaging (fMRI) studies are assessed with statistical parametric maps (SPMs) using a p value threshold. However, a smaller p value does not imply that the observed result will be reproducible. In this study, we suggest interpreting SPMs in conjunction with reproducibility evidence. Reproducibility is defined as the extent to which the active status of a voxel remains the same across replicates conducted under the same conditions. We propose a methodology for assessing reproducibility in functional MR images without conducting separate experiments. Our procedures include the empirical Bayes method for estimating effects due to experimental stimuli, the threshold optimization procedure for assigning voxels to the active status, and the construction of reproducibility maps. In an empirical example, we implemented the proposed methodology to construct reproducibility maps based on data from the study by Ishai et al. (2000). The original experiments involved 12 human subjects and investigated brain regions most responsive to visual presentation of 3 categories of objects: faces, houses, and chairs. The brain regions identified included occipital, temporal, and fusiform gyri. Using our reproducibility analysis, we found that subjects in one of the experiments exercised at least 2 mechanisms in responding to visual objects when performing alternately matching and passive tasks. One gave activation maps closer to those reported in Ishai et al., and the other had related regions in the precuneus and posterior cingulate. The patterns of activated regions are reproducible for at least 4 out of 6 subjects involved in the experiment. Empirical application of the proposed methodology suggests that human brains exhibit different strategies to accomplish experimental tasks when responding to stimuli. It is important to correlate activations to subjects' behavior such as reaction time and response accuracy. Also, the latency between the stimulus presentation and the peak of the hemodynamic response function varies considerably among individual subjects according to types of stimuli and experimental tasks. These variations per se also deserve scientific inquiries. We conclude by discussing research directions relevant to reproducibility evidence in fMRI.

Brain↗

Violet light emitting diode-induced fluorescence detection combined with on-line sample concentration techniques for use in capillary electrophoresis.

The first application of a violet light-emitting diode (LED) for fluorescence detection in capillary electrophoresis (CE) is described. The utility of violet LED (peak emission wavelength at 410 nm, approximately 2 mW) for fluorescence detection is demonstrated by examining reserpine and dopamine-labeled NDA (naphthalene-2,3-dicarboxaldehyde), respectively. The detection limit for reserpine was determined to be 2.5 x 10(-6) M by normal micellar electrokinetic capillary chromatography (MEKC) and this was improved to 2.0 x 10(-9) M and 2.0 x 10(-10) M when sweeping-MEKC and cation-selective exhaustive injection (CSEI)-sweep-MEKC techniques were applied, respectively. In addition, the detection limit of NDA-labeled dopamine was determined to be 6.3 x 10(-6) M by means of normal MEKC and this was improved to 3.0 x 10(-8) M when the sweeping-MEKC mode was applied.

Buffers↗