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Biomedical subjects

P K Wong

Publications and source records attributed to P K Wong.

At least 19 recordsLinked to original sources
PubMed2007

Disinfection of Legionella pneumophila by photocatalytic oxidation.

Photocatalytic oxidation (PCO) was proven to be efficacious in the inactivation of Legionella pneumophila serogroup 1 Strains 977, 1009, 1014 and ATCC 33153. The local (Strains 997, 1009 and 1014) and ATCC (Strain 33153) strains showed sensitivity differences towards PCO. The inactivation mechanisms of PCO were investigated by transmission and scanning electron microscopy by which PCO was found to disintegrate the cells eventually. Before the disintegration, there was lipid peroxidation of outer and cytoplasmic membrane causing holes formation and leading to the entry of OH into the cells to oxidize the intracellular components. Fatty acid profile analysis found that the amount of saturated, 16-carbon branched-chain fatty acid, which is predominant in Legionella, decreased in the surviving populations from PCO. A relationship between the amount of this fatty acid and the PCO sensitivity of the tested strains was also observed. Mineralization of cells by PCO was proven by total organic carbon analysis.

Antigens, Bacterial↗
PubMed2006

Short-term dynamic change of gill copper in common carp, Cyprinus carpio, evaluated by a sequential extraction.

Dynamic changes in Cu speciation and its binding to fish gills were investigated by exposing common carp (Cyprinus carpio) to a 1 mg/1 Cu solution for 7 hours. Cu speciation in the bulk solution and fish gill microenvironment was calculated using general chemical equilibrium modeling. A sequential extraction procedure using distilled water, magnesium dichloride (1.0 mol/1), and acetic acid (10%) was used to characterize the Cu associated with the fish gills. Cu residual in the gill tissue was measured after the sequential extraction. Changes in total Cu concentration, pH, and dissolved organic carbon (Doc) in the bulk solution were recorded during the experimental period and calculated for the fish gill microenvironment. Cu-hydroxide species and Cu2 were dominant Cu species in both bulk solution and the fish gill microenvironment, whereas increased Cu-mucus was found in the fish gill microenvironment. DOC in the exposure medium, assumed to arise from mucus release, also increased and complexed Cu in solution. Forty-three percent of the Cu associated with the gills was readily water extractable, with an additional 22% exchangeable with Mg2+ or protons. Only 35% of the Cu accumulated within the gill tissues. The binding of Cu to the fish gills reached apparent equilibrium after 3 hours of exposure. Furthermore, the amount of water-extractable Cu within the gills showed significant correlation to the concentration of Cu predicted to be complexed with calculated free mucus in the gill microenvironment.

Animals↗
PubMed2006

An approach to assess ecological risk for polycyclic aromatic hydrocarbons (PAHs) in surface water from Tianjin.

Three approaches were applied and compared to evaluate additive toxic effects of eight PAHs to aquatic organisms in rivers in the Tianjin area. Although the toxicity of the studied PAH compounds did not significantly increase the risk to aquatic organisms, the results of all three approaches indicated that the additive effect of the eight PAHs was significantly stronger than any individual compound acting alone, which indicated the applicability of the approaches. Further, of the compounds studied, anthracene was the major contributor to the overall toxic effect of the mixture. The calculated geometric means of the hazard quotient for the additive effect varied from 0.00055 to 0.00062, compared to the hazard quotient of individual PAHs which ranged from 5.1 x 10-6 to 0.00053. The hazard quotient distribution geometric mean was 0.00058, with 95% of the quotient between 6.6 x 10-5 and 0.051. Overlapping areas varied from 0.00015 to 0.02 for individual PAHs and was 0.03 for additive toxicity.

Animals↗
PubMed2005

Toxicity identification evaluation (TIE) of pore water of contaminated marine sediments collected from Hong Kong waters.

Marine sediment can function both as a source and as a sink of marine chemical contaminants. The toxicity of contaminated marine sediment can be assessed by toxic evaluation of its pore water, the inter-particle water of sediment, because toxicants in the pore water may be bioavailable to marine organisms. In this study, the toxicity identification evaluation (TIE) was performed to identify the major toxicants in the pore water of marine sediment collected in Hong Kong waters. In Phase 1 TIE, the suspected toxicants were characterized as anions or organic compounds that are either oxidizable or filterable in alkaline medium. In Phase 2 TIE, the suspected toxicants were identified as sulfide (S(2-)) based on the reduction of toxicity due to lowering of sulfide concentrations by experimental manipulations. The mass balance and spiking analyses in Phase 3 confirmed that S(2-) was one of the major toxicants and that some non-toxic unknown compounds measured by LC-MS, which was removed by C18 solid phase extraction, enhanced the toxicity of S(2-) in the pore water samples.

Chromatography, Liquid↗
PubMed2005

Determination of dichloroacetic acid and trichloroacetic acid in drinking water by acidic methanol esterification and headspace gas chromatography.

A simple and rapid headspace method for gas chromatographic determination of dichloroacetic acid (DCAA) and trichloroacetic acid (TCAA) in drinking water was developed. Acidic methanol esterification followed by a headspace technique using a capillary column gas chromatograph (GC) equipped with an electron capture detector (ECD) was applied to determine the levels of DCAA and TCAA in drinking water. The major advantages of this method are the use of acidic methanol as the derivatization agent instead of the hazardous diazomethane, and esterification is carried out in water instead of organic solvent. DCAA and TCAA methyl esters produced in the reaction were determined directly by a headspace GC/ECD method. The linear correlation coefficients at concentrations ranging from 0 to 60 microg/L were 0.992 and 0.996 for DCAA and TCAA, respectively. The relative standard deviations (RSD, %) for the determination of DCAA and TCAA in drinking water were 15 and 21.3%, respectively (n=3). The detection limits of this method were 3 and 0.5 microg/L for DCAA and TCAA, respectively, and the recovery was 68-103.2% for DCAA and TCAA.

Chromatography, Gas↗
PubMed2005

Human exposure and health risk of alpha-, beta-, gamma- and delta-hexachlorocyclohexane (HCHs) in Tianjin, China.

The dynamic exposures to HCHs of individuals born between the years 1913 and 1993 in Tianjin have been simulated by connecting a fugacity model (IV) with a multimedia exposure model. Ingestion is the most important pathway for human beings to take up HCHs, and concentrations in the human body correlate with body weight changes. Accumulations of HCHs were derived assuming that the degradation in human body behaved linearly. The health risk of exposure to HCHs was measured using cancer risk and loss of life expectancy (LLE), and LLE was modified from its original definition to incorporate a dynamic calculation that takes variances in exposure into account. Monte-Carlo simulations were run to analyze the uncertainties of the model.

Age Factors↗
PubMed2005

Contamination of rivers in Tianjin, China by polycyclic aromatic hydrocarbons.

Tianjin urban/industrial complex is highly polluted by some persistent organic pollutants. In this study, the levels of 16 priority polycyclic aromatic hydrocarbons (PAHs) were tested in sediment, water, and suspended particulate matter (SPM) samples in 10 rivers in Tianjin. The total concentration of 16 PAHs varied from 0.787 to 1943 microg/g dry weight in sediment, from 45.81 to 1272 ng/L in water, and from 0.938 to 64.2 microg/g dry weight in SPM. The levels of PAHs in these media are high in comparison with values reported from other river and marine systems. Variability of total concentrations of PAHs in sediment, water, and SPM from nine different rivers is consistent with each other. No obvious trends of total PAHs concentration variations were found between upstream and downstream sediment, water, and SPM samples for most rivers, which indicate local inputs and disturbances along these rivers. The spatial distributions of three-phase PAHs are very similar to each other, and they are also similar to those found in topsoil. However, their chemical profiles are significantly different from that of topsoil. The change of profiles is consistent with the different aqueous transport capability of 16 PAHs. Low molecular weight PAHs predomination suggests a relatively recent local source and coal combustion source of PAHs in the study area.

China↗
PubMed2004

Optimization of photocatalytic oxidation of 2,2',3,3'-tetrachlorobiphenyl.

Polychlorinated biphenyls (PCBs) are wide spread environmental pollutants. This research focused the optimum physico-chemical conditions under which photocatalytic oxidation (PCO) can be used to degrade 2,2',3,3'-tetrachlorobiphenyl (tetra-CB). Among the optimal physico-chemical conditions studied were UV intensity, hydrogen peroxide (H2O2) and titanium dioxide (TiO2) concentrations, initial pH, and possible reaction intermediates were also determined. The results indicate that the optimal physico-chemical conditions necessary for the degradation of tetra-CB by PCO were UV intensity at 3.16 mW/cm2, 30 mM of H2O2 and 100 mg/l of TiO2. In contrast to the results of PCO studies on other organic compounds, the optimum pH for PCO degradation of tetra-CB was 5.5. The removal efficiency was also higher under acidic conditions than alkaline conditions. Although degradation intermediates such as 1,3-bis(1,1-dimethylethyl)benzene, 2,4-bis(1,1-dimethylethyl)phenol, and 3,5-di-tert-butyl-4-hydroxybenzaldehyde were identified at an early stage in the reaction process, they were not completely degraded even after 7h of PCO reaction.

Catalysis↗
PubMed2004

Treatment of atrazine by integrating photocatalytic and biological processes.

This research examines the degradation of atrazine by photocatalytic oxidation (PCO) under different experimental conditions. Deisopropylatrazine, deethylatrazine and deethyldeisopropylatrazine were formed as major intermediates based on gas chromatography-mass spectrometry. The reaction mixture was found to be toxic towards two bioassays, i.e. the Microtox and amphipods survival tests even when atrazine was completely degraded by PCO within 2 h under optimized conditions. The results indicate that adding H2O2 could significantly enhance the degradation of atrazine by PCO. Ammeline, ammelide and cyanuric acid (CA) became the major intermediates/products as detected by high performance liquid chromatography from 6th to the 40th h of PCO treatment. After 72 h PCO treatment, only CA was detectable in the reaction mixture. Further degradation of CA was carried out by a newly isolated CA-degrading bacterium, Sphingomonas capsulata. The photochemical pretreatment integrated with microbial degradation lead to the complete degradation and detoxification of atrazine.

Animals↗
PubMed2003

Application of a toxicity identification evaluation for a sample of effluent discharged from a dyeing factory in Hong Kong.

A first toxicity identification evaluation (TIE) was conducted in three phases using the Microtox test to identify the major toxicant(s) in effluent discharged from a dyeing plant in Hong Kong. In Phase I toxicity characterization indicated that anions were likely to be the major toxicants for the entire effluent. In Phase II concentrations of sulfite and other anions in the original and the anion exchange resin-treated effluent samples were determined by ion chromatography. Anions, which were found in the effluent at comparatively high concentrations and were suspected of being responsible for the toxicity to luminescent bacteria, were selected for further study in Phase III. Investigation in Phase III using the spiking and mass balance approaches confirmed that the sulfite ion was the major toxicant in the effluent.

Chromatography, Ion Exchange↗
PubMed2003

Role of cell surface components on Cu2+ adsorption by Pseudomonas putida 5-x isolated from electroplating effluent.

A gram-negative bacterium Pseudomonas putida 5-x with high Cu2+ accumulating capability was isolated from electroplating effluent in Kwun Tong, Hong Kong. The pretreated cells without superficial layer-capsule, isolated cell envelopes and the separated peptidoglycan layer materials were obtained from fresh P. putida 5-x cells, their Cu2+ adsorption capacities and properties were compared with that of the fresh cells. Pretreatment by 0.1 mol L(-1) HCl enhanced Cu2+ adsorption capacity due to the degradation of cell superficial layer-capsule of P. putida 5-x cells. Isolated cell envelopes possessed five times more Cu2+ adsorption capacity than that of fresh intact cell. The Cu2+ adsorption of separated peptidoglycan layer materials indicated that the peptidoglycan layer only played 10-15% part of the Cu2+ adsorption capacity, and implied other cell surface components such as outer membrane or inner membrane might play an important role in such high Cu2+ binding of the cell envelopes. The adsorption process of fresh cells, pretreated cells and cell envelopes of P. putida 5-x could be described with Freundlich isotherm, while the adsorption of Cu2+ by separated peptidoglycan layer materials was better described with Langmuir isotherm.

Adsorption↗
PubMed2003

Correlation relationships between physico-chemical properties and gas chromatographic retention index of polychlorinated-dibenzofurans.

Correlation relationships between physico-chemical properties including vapor pressures (P), water solubilities (S), Henry's law constants (H(c)), n-octanol-water partition coefficients (K(ow)), sediment-water partition coefficient (K(pw)) and biotic lipid-water partition coefficient (K(bw), bioconcentration factor) of polychlorinated-dibenzofurans (PCDFs) and their gas chromatographic retention indices (GC-RIs) were established. A model equation between GC-RIs (= RI) and these physico-chemical properties (K) of PCDFs was in a form of log K = aRI2 + bRI + c with correlation coefficients (R2) greater than 0.94, except H(c). These equations were derived from six experimental data (five experimental data for log K(bw)) in each physico-chemical properties of PCDFs reported previously. The values of log P, log S, log H(c), log K(ow), log K(pw) and log K(bw) of PCDFs predicted by these equations based on their GC-RIs in the present study derviated from those calculated by the solubility parameters for fate analysis method in a previous study by 0.49, 0.32, 0.11, 0.34, 0.14 and 0.22 log units, respectively.

Benzofurans↗
PubMed2003

Microbial enhancement of Cu2+ removal capacity of Eichhornia crassipes (Mart.).

Bacteria resistant to Cu2+, Ni2+ or Zn2+ were isolated from the rhizosphere of water hyacinth (Eichhornia crassipes (Mart.)) and their metal ion removal capacities (RCs) were determined. The Ni2+ and Zn2+ RCs of the respective metal ion-resistant bacteria were less than 4.1 mg g(-1), while one of the Cu2+-resistant bacteria (Strain CU-1) showed a significant high Cu2+ RC of 10.6 mg g(-1). The effect of inoculating water hyacinth with Strain CU-1 on its Cu2+ RC was further studied. Water hyacinths were treated with an antibiotic, oxytetracycline (OTC), to remove most rhizospheric bacteria of plant roots. Inoculation of Strain CU-1 increased the Cu2+ RC of the plant root by 1.91 (OTC-treated) and 1.56 (OTC-untreated) folds respectively when compared with the control. Results also showed that Strain CU-1 colonized onto the plant root and led to the increase of Cu2+ RC of the roots of water hyacinth.

Bacteria↗
PubMed2003

Ni2+ removal and recovery from electroplating effluent by Pseudomonas putida 5-x cell biomass.

Ni2+ and Cu2+ are the major heavy metal ions in electroplating wastewater of Hong Kong. In the present study, Pseudomonas putida 5-x cell biomass was used to remove Ni2+ from electroplating effluent. Ni2+ adsorption capacity of P. putida 5-x cell biomass cultured in sulphate-limiting medium was found to be minimum in early logarithmic growth phase, and maximum of 28.1 mg g(-1) in late stationary growth phase. Pretreated cells by 0.1 mol L(-1) HCl could greatly enhance the Ni2+ adsorption capacity of cell biomass from 28.1 to 36.7 mg g(-1) and had no significant effect on biomass loss. The adsorption process of P. putida 5-x fresh cells and pretreated cell all could be expressed with Freundlich isotherm. TEM analyses indicated that acidic pretreatment degraded the superficial layer-capsule outside of the fresh cell to improve the adsorption capacity of cell to Ni2+. The Ni2+ bound by P. putida 5-x cell biomass could be efficiently recovered using 0.1 mol L(-1) HCl, and the cell biomass could be reused at least five cycles for Ni2+ removal and recovery with 93% above removal efficiency and 98% above recovery rate. Owing to the Cu2+ presented in electroplating wastewater inhibiting Ni2+ adsorption process by P. putida 5-x cell biomass, two-stage biosorption processes should be designed to remove and recover Cu2+ and Ni2+ sequentially from electroplating effluent.

Adsorption↗
PubMed2003

Development of seaweed biomass as a biosorbent for metal ions .

Three seaweed species collected from Hong Kong waters were screened for their adsorption abilities for Cu2+, Ni2+ and Zn2+ and Ulva lactuca having the highest metal ion removal capacity (RC) was chosen for further study. Effects of algal biomass and medium pH on the metal ions RC of Ulva lactuca were determined and optimized. Under the optimal conditions of the corresponding metal ions, the algal Cu2+, Ni2+ and Zn2+ RCs were 65.54, 21.00 and 49.54 mg/g, respectively. The presence of other cations and anions affected the metal ions adsorption by the seaweed. The effect was dependent on the between the target metal ions and other cations/anions. The kinetic study revealed that the adsorption of Cu2+, Ni2+ and Zn2+ by Ulva lactuca fitted the Langmuir isotherm. Comparing with 0.1 M HCl, citric acid, thiourea, EDTA and HNO3, 0.1 M H2SO4 efficiently recovered close to 100% adsorbed metal ions from Ulva lactuca. In three successive adsorption-desorption cycles, reduction in metal ion RCs was found in the second and third cycles, but almost all adsorbed metal ion could be recovered.

Adsorption↗
PubMed2002

Mathematical relationships between vapor pressure, water solubility, Henry's law constant, n-octanol/water partition coefficent and gas chromatographic retention index of polychlorinated-dibenzo-dioxins.

Mathematical relationships between vapor pressures (P), water solubilities (S), Henry's law constants (Hc). noctanol/water partition coefficients (Kow) and gas chromatograph retention indices (GC-RIs) of polychlorinated-dibenzo-dioxins (PCDDs) were established. A model equation was established between GC-RIs (= RI) and other physico-chemical parameters (K) of PCDDs in the form of log K = aRI2 + bRI + c with correlation coefficients (R2) greater than 0.97, except Hc. These equations were derived from 56 experimental data of PCDDs reported previously. The values of P, S, Hc and Kow of PCDDs predicted by these equations based on their GC-RIs in the present study deviated from those calculated by the SOFA method in a previous study by only 0.19, 0.13, 0.18 and 0.096 log units, respectively.

Chromatography, Gas↗