Biomedical subjects

Cheng-Chih Hsu

Publications and source records attributed to Cheng-Chih Hsu.

4 recordsLinked to original sources

PubMed2016

Sharing and community curation of mass spectrometry data with Global Natural Products Social Molecular Networking.

The potential of the diverse chemistries present in natural products (NP) for biotechnology and medicine remains untapped because NP databases are not searchable with raw data and the NP community has no way to share data other than in published papers. Although mass spectrometry (MS) techniques are well-suited to high-throughput characterization of NP, there is a pressing need for an infrastructure to enable sharing and curation of data. We present Global Natural Products Social Molecular Networking (GNPS; http://gnps.ucsd.edu), an open-access knowledge base for community-wide organization and sharing of raw, processed or identified tandem mass (MS/MS) spectrometry data. In GNPS, crowdsourced curation of freely available community-wide reference MS libraries will underpin improved annotations. Data-driven social-networking should facilitate identification of spectra and foster collaborations. We also introduce the concept of 'living data' through continuous reanalysis of deposited data.

Biological Products↗

PubMed2005

Interplay between intra- and interligand charge transfer with variation of the axial N-heterocyclic ligand in osmium(II) pyridylpyrazolate complexes: extensive color tuning by phosphorescent solvatochromism.

The rational design and syntheses of a new series of Os(II) complexes with formula [Os(fppz)(2)(CO)(L)] (1: L=4-dimethylaminopyridine; 2: L = pyridine; 3: L = 4,4'-bipyridine; 4: L = pyridazine; 5: L = 4-cyanopyridine), bearing two (2-pyridyl)pyrazolate ligands (fppz) together with one carbonyl and one N-heterocyclic ligand at the axial positions are reported. Single-crystal X-ray diffraction studies of, for example, 2 reveal a distorted octahedral geometry in which both fppz ligands reside in the equatorial plane with a trans configuration and adopt a bent arrangement at the metal center with a dihedral angle of approximately 23 degrees , while the carbonyl and pyridine ligands are located at the axial positions. Variation of the axial N-heterocyclic ligand leads to remarkable changes in the photophysical properties as the energy gap and hence the phosphorescence peak wavelength can be tuned. For complexes 1 and 2 the solvent-polarity-independent phosphorescence originates from a combination of intraligand (3)pi-pi* ((3)ILCT) and metal-to-ligand charge transfer transitions ((3)MLCT). In sharp contrast, as supported by cyclic voltammetry measurements and theoretical calculations, complexes 3--5 exhibit mainly ligand-to-ligand charge transfer (LLCT) transitions, resulting in a large dipolar change. The phosphorescence of complexes 3--5 thus exhibits a strong dependence on the polarity of the solvent, being shifted for example, from 560 (in C(6)H(12)) to 665 nm (in CH(3)CN) and from 603 (in C(6)H(12)) to 710 nm (in CH(3)CN) for complexes 3 and 5, respectively. The results clearly demonstrate that a simple, straightforward derivatization of the axial N-heterocyclic ligand drastically alters the excitation properties per se from intraligand charge transfer (ILCT) to LLCT transitions. The latter exhibit remarkable LLCT phosphorescence solvatochromism so that a broad range of color tunability can be achieved.

Journal Article↗

PubMed2003

Interferometric optical sensor for measuring glucose concentration.

With a specially designed probe, the phase difference between s andp polarization of light reflected under surface-plasmon resonance is measured by use of a common-path heterodyne interferometer. For specific ratios of phase difference to glucose concentration, the glucose concentration can be estimated as a function of the measured phase data. A prototype was set up to demonstrate the feasibility of this sensor, which was experimentally tested in the range 40-500 mg/dl with a small quantity of solution and had a measurement resolution of 1.41 mg/dl at 25 degrees C.

Feasibility Studies↗

PubMed2002

Method for determining the optical axis and (n(e), n(o)) of a birefringent crystal.

There is a phase difference between s and p polarizations when a circularly polarized heterodyne light beam is reflected from a birefringent crystal. It can be measured accurately with a common-path heterodyne interferometric technique. We have derived an equation that describes the relationship between the phase differences and n(e), n(o), and alpha. Two groups of solutions for (n(e), n(o)) can be obtained from this equation by the phase measurements performed at three incident angles under moderate conditions. Each group consists of three pairs of solutions for (ne), n(o)). Finally, by justifying with physical conditions, we obtained the correct solution for (n(e), n(o)). Azimuth angle alpha of the birefringent crystal optical axis can also be determined. And the feasibility of this method is demonstrated.

Journal Article↗