Biomedical subjects

H S Tung

Publications and source records attributed to H S Tung.

5 recordsLinked to original sources

PubMed2001

Application of capillary electrophoresis for organic acid analysis in herbal studies.

A capillary electrophoresis (CE) procedure has been developed for the separation of 25 inorganic and organic acid anions using a buffer system consisting of 15 mM tris(hydroxymethyl)aminomethane, 3 mM 1,2,4-benzenetricarboxylic acid, 1.5 mM tetraethylenepentaamine (TEPA) and 20% methanol with pH adjusted to 8.4. A good separation of organic acids extracted from a mixture of Chinese traditional medicine (TCM) containing three herbs, Flos chrysthemi, Spica prunellae, and Folium mori was obtained using the procedure developed with satisfactory working range (0.20-77 mg/g), low detection limit (90-190 microg/g), and good repeatability (relative standard deviation 4.47-6.99%, n = 4). A satisfactory extraction of organic acids was achieved within 20 min using 0.1 M NaOH. The addition of TEPA to provide a reduced electroosmotic flow (EOF) environment was shown to remove interfering organic compounds extracted from TCM. The applicability of using organic acids as markers for determining the mixing ratio of constituent herbs for a TCM mixture was investigated using a three-component mixture with a 1:1:1 mixing ratio. A satisfactory mixing ratio of 1.04:1.09:0.98 was obtained using the methodology developed based on organic acids as markers. The application of our method for determining more complicated TCM mixtures has been discussed.

Buffers↗

PubMed2000

Screening for Staphylococcus epidermidis markers discriminating between skin-flora strains and those responsible for infections of joint prostheses.

Fifty-four Staphylococcus epidermidis strains responsible for infections of joint prostheses and 23 strains isolated from skin flora were studied for markers of virulence, to discriminate invasive strains from normal flora. They were screened for binding to polystyrene and matrix proteins and for the presence of staphylococcal genes involved in adhesion. The ica operon involved in biofilm formation was the only marker discriminating between these 2 categories of strains.

Bacterial Adhesion↗

PubMed1999

Capillary electrophoresis for trace metal ion analysis in environmental studies.

A new buffer system consisting of 30 mM hydroxylamine hydrochloride, 0.1 mM 1,10-phenanthroline, 1% methanol and pH 3.7 was optimized for simultaneous determination of water and acid leachable metals from respirable, fine and coarse air particulate matters. A reducing environment was used to resolve metal ions with variable oxidation states. A suitable counteranion was employed to enable acidic pH to be used and methanol was added to improve the resolution of the electropherograms and to achieve simultaneous determination of several metal ions. Compared to existing capillary electrophoresis (CE) buffers, the buffer developed, based on direct UV detection of ion-pair with weak interaction, gives improved resolution and sharper, more stable and well-resolved peaks. It detects total irons and solves interfering problems due to the variable oxidation states of iron in environmental samples. Compared to existing mostly alkaline CE buffers for metal analysis, the acidic nature of the buffer system developed makes the pretreatment step simpler and reduces the risk of reagent contamination. Satisfactory working ranges (15-5500 ppb) and detection limits (0.5-3 ppb) were obtained for leachable Zn, Cu, Co, Fe and Cd. The NIST 1648 urban particulate matters were found to leach out 2.53-42.8% water-extractable and 2.76-71.7% acid-extractable Zn, Cu, Fe and Cd. High iron contents, and lower copper and zinc concentrations were found in respirable suspended particulates (RSP) sampled in Hong Kong.

Air Pollutants↗

PubMed1998

Virulence factors of Staphylococcus aureus strains causing infective endocarditis--a comparison with strains from skin infections.

The objective was to study potential bacterial virulence factors in S. aureus endocarditis. S. aureus strains isolated from patients with well-classified episodes of infective endocarditis (IE) (n=26) were compared with control S. aureus strains from consecutive patients with skin infections (n=30). The potential virulence factors studied were Staphylococcal enterotoxin A-D (SEA, SEB, SEC, SED) and toxic shock syndrome toxin-1 (TSST-1) production and binding capacity to the extracellular matrix proteins: fibronectin, collagen type I, collagen type II and bone sialoprotein (BSP). None of the potential virulence factors studied was more prevalent among the IE strains. BSP binding was more often found in the control group with skin infections. Endocarditis patients with previous damage of the heart valves were more often infected by strains not producing any enterotoxin. No correlation was found between the potential bacterial virulence factors studied and IE. Concerning the toxins known to act as superantigens (SEA-E and TSST-1), the tendencies in this and other studies indicate that a larger study group might identify them as pathogenic factors in a subgroup of staphylococcal endocarditis.

Adolescent↗

PubMed1997

Staphylococcus aureus causing osteomyelitis binds to a nonapeptide sequence in bone sialoprotein.

Bone sialoprotein is a glycoprotein of the bone and dentine extracellular matrix. This protein consists of 320 amino acids, of which 25% are glutamic and aspartic acid residues. Sialic acid, containing oligosaccharides and tyrosine sulphate residues, supplies additional polyanionic properties. Staphylococcal cells, isolated from patients suffering from infection of bone tissue, bind the bone-derived sialoprotein, an interaction which is specifically inhibited by the recombinant bone sialoprotein core protein. We have previously shown that the 150 N-terminal amino acid residues of bone sialoprotein are responsible for the binding to staphylococcal cells. By using recombinant deleted variants of bone sialoprotein and synthetic peptides, we have now localized the staphylococcal binding site to less than 10 residues within the N-terminal part of the protein.

Amino Acid Sequence↗