Biomedical subjects

Gui-bin Jiang

Publications and source records attributed to Gui-bin Jiang.

15 recordsLinked to original sources

PubMed2006

Equilibrium sampling of freely dissolved alkylphenols into a thin film of 1-octanol supported on a hollow fiber membrane.

A new negligible depletion extraction procedure was proposed for equilibrium sampling of 4-tert-octylphenol (OP) and 4-nonylphenol (NP) into a thin film of 1-octanol supported on a hollow fiber membrane. This thin liquid film extraction technique was directed at the determination of (1) freely dissolved concentrations, (2) distribution coefficients to 1-octanol (D(ow)), and (3) binding to dissolved organic matter (DDOC). The sampling device was prepared by dipping pieces of polypropylene microporous hollow fiber membrane (10-mm length, 30-microm wall thickness, 240-microm inner diameter) into 1-octanol for a few seconds to impregnate the pores of the hollow fiber wall. After stirring in 100 mL of sample solution for 24 h, the sampling device was harvested and desorbed with 30 microL of methanol, of which 20 microL was injected for HPLC analysis. With the measured D(ow) of a chemical and its equilibrium concentration in the 1-octanol sampling phase (C(octanol)), the freely dissolved concentration (Cfree) was calibrated based on Cfree = C(octanol)/D(ow). Measured log Dow values of OP (4.32 +/- 0.06) and NP (4.79 +/- 0.02) were independent of the chemical concentration, only minimally affected by the environmentally relevant pH, buffering capacity, and salinity of samples, and agreed well with reported values. Log DDOC values of OP (4.89 +/- 0.43) and NP (5.14 +/- 0.37), determined in Aldrich humic acid solution, agreed with reported partition coefficients to organic carbon (log Koc) for particles in river water and effluent wastewater. Short equilibration times and high enrichment factors were obtained for both analytes due to the high surface to volume ratio of the new sampler. The technique was successfully applied to determine Cfree of OP and NP in real water samples and to study their association with humic acids and bovine albumin.

Journal Article↗

PubMed2006

Evaluating the impacts of some environmentally relevant factors on the availability of bisphenol A with negligible-depletion SPME.

The effect of some environmentally relevant factors including salinity, pH, and humic acids on the availability of bisphenol A (BPA) was evaluated by using the negligible-depletion solid-phase microextraction (nd-SPME) biomimetic method. With the variation of salinity (0-500 mM NaCl) and pH (5.0-8.5) of aqueous solutions, the partition coefficients of BPA between the nd-SPME fiber and the aqueous solution varied in the range of logD=3.55-3.86, which indicates that the salinity and pH can influence the availability of BPA. By using Acros humic acid as model dissolved organic matter (DOM), it was also demonstrated that the environmental factors such as salinity and pH could affect the partitioning of BPA between DOM and aqueous solutions. The determined partition coefficients of BPA between dissolved organic carbon (DOC) and aqueous solutions were in the range of logD(DOC)=4.03-5.60 for Acros humic acid solutions with 1-50 mg l(-1) DOC. The influence of salinity and pH on logD(DOC) was more significant at low concentration (0-5 mg l(-1)) of DOC.

Benzhydryl Compounds↗

PubMed2006

[Study on the contamination status of butyltins in Taihu Lake].

Butyltins in surface water, sediments and biota samples from Taihu Lake were determined. The results show that butyltins content in most of the surface water samples is under the limit of the detection; five out of ten sediment samples are measured detectable butyltins. Monobutyltin (MBT) was the main species with the concentrations ranging from below the detection limits to 0.95 ng/g; while all biota samples were detected relatively higher butyltin concentrations with a range of 27.05 - 181.23 ng/g due to the obvious bioaccumulation. Tributyltin (TBT) was the main composition that occupied almost 70% of the total butyltins. The antifouling paints applied on the aquatic cultural box and boats was the possible main source of butyltin compounds in Taihu Lake.

China↗

PubMed2006

Gridded inventories of historical usage for selected organochlorine pesticides in Heilongjiang River Basin, China.

The use of technical HCH (1, 2, 3, 4, 5, 6-hexachlorocyclohexane), DDT (dichlorodiphenyltrichloroethane) and lindane in Heilongjiang River Basin (HRB) of China was studied. Between 1952 and 1984 the total usage in the HRB was 108900 t for technical HCH, and 4900 t for DDT, respectively, and the use of DDT due to dicofol application in the HRB was 220 t from 1984 to 2003. The usage of lindane in HRB was 109 t from 1991 to 2000. The results show that the highest technical HCH use (41800 t) in HRB was on maize, accounting for 38.3% of the total usage on all crops, followed by the use on wheat (28000 t, 25.7%) and on soybean (26600 t, 24.4%). The highest DDT use (2300 t) was on soybean, accounting for 46.8% of the total usage on all crops, followed by the use on maize (1500 t, 31.3%) and on sorghum (600 t, 13.2%). The major use of lindane was mainly on wheat. Gridded usage inventories of these three OCPs (organochlorine pesticides), in HRB with a 1/6 degrees latitude by 1/4 degrees longitude resolution have been created by using different gridded cropland as surrogates. Some soil samples have also been collected in HRB. Data of usage and soil concentrations of sigma HCH in HRB match quite well to those in Shanghai region, and much higher soil concentration of sigma DDT in Shanghai region could be due to much heavier dicofol use in this region.

Agriculture↗

PubMed2005

Butyltin accumulation in the marine clam Mya arenaria: an evaluation of its suitability for monitoring butyltin pollution.

The use of Mya arenaria as a new sensitive biomonitor of butyltins pollution in the oceanic system was investigated. Field survey indicated that much higher levels of butyltin compounds were found in M. arenaria compared with the other species investigated. Using Mytilus edulis as a control organism, a 28 days exposure of tributyltin chloride (TBT) to M. arenaria for accumulation and subsequent 28 days breeding in clean seawater for elimination were conducted under laboratory conditions in order to confirm its high accumulation ability and characterize its kinetic behavior to TBT. Bioconcentration factor (BCF) of M. arenaria ranged from 15,538 to 91,800 after 28 days exposure. The rapid uptake and low rate to eliminate TBT of M. arenaria displayed first-order kinetics. M. arenaria shows potential as a new bioindicator to monitor TBT pollution in marine environment.

Animals↗

PubMed2005

Ionic liquid for high temperature headspace liquid-phase microextraction of chlorinated anilines in environmental water samples.

Based on the non-volatility of room temperature ionic liquids (IL), 1-butyl-3-methylimidazolium hexafluorophosphate ([C4MIM][PF6]) IL was employed as an advantageous extraction solvent for high temperature headspace liquid-phase microextraction (LPME) of chloroanilines in environmental water samples. At high temperature of 90 degrees C, 4-chloroaniline, 2-chloroaniline, 3,4-dichloroaniline, and 2,4-dichloroaniline were extracted into a 10 microl drop of [C4MIM][PF6] suspended on the needle of a high-performance liquid chromatography (HPLC) microsyringe held at the headspace of the samples. Then, the IL was injected directly into the HPLC system for determination. Parameters related to LPME were optimized, and high selectivity and low detection limits of the four chlorinated anilines were obtained because the extraction was performed at high temperature in headspace mode and the very high affinity between IL and chlorinated anilines. The proposed procedure was applied for the analysis of the real samples including tap water, river water and wastewater samples from a petrochemical plant and a printworks, and only 3,4-dichloroaniline was detected in the printworks wastewater at 88.2 microg l(-1) level. The recoveries for the four chlorinated anilines in the four samples were all in the range of 81.9-99.6% at 25 microg l(-1) spiked level.

Aniline Compounds↗

PubMed2005

The levels and distribution of organochlorine pesticides (OCPs) in sediments from the Haihe River, China.

The levels and distribution patterns of the selected organochlorine pesticides (OCPs=p,p'-DDT, o,p'-DDT, p,p'-DDE, p,p'-DDD, alpha-, beta-, gamma- and delta-HCH) in surficial sediments from the Haihe River and Dagu Drainage River of Tianjin were investigated by means of gas chromatography coupled with micro-electronic capture detector (GC-microECD). Concentrations of OCPs in the sediments from the Haihe River ranged from 1.88 to 18.76ng g(-1) (mean 7.33ng g(-1)) for sum HCH, 0.32-80.18ng g(-1) (mean 15.94ng g(-1)) for sum DDT. Compared with the Haihe River, the Dagu Drainage River was much more contaminated by HCHs and DDTs, wherein sum HCH ranged from 33.24 to 141.03ng g(-1) (mean 87.74ng g(-1)) and sum DDT ranged from 3.60 to 83.49ng g(-1) with a mean value of 35.52ng g(-1). The concentration distribution of sum DDT and sum HCH was different indicated their different contamination sources. Composition analyses indicated that a recent usage or discharge of HCH and DDT into the Dagu Drainage River.

China↗

PubMed2005

Disposable ionic liquid coating for headspace solid-phase microextraction of benzene, toluene, ethylbenzene, and xylenes in paints followed by gas chromatography-flame ionization detection.

Solid-phase microextraction (SPME) with a disposable ionic liquid (IL) coating was developed for headspace extraction of benzene, toluene, ethylbenzene, and xylenes (BTEX) in paints. The SPME fiber was coated with IL prior to every extraction, then the analytes were extracted and desorbed on the injection port of gas chromatography, and finally the IL coating on the fiber was washed out with solvents. The coating and washing out of IL from the fiber can be finished in a few minutes. This disposable IL-coated fiber was applied to determine BTEX in water-soluble paints with results in good agreement with that obtained by using commercially available SPME fibers. For all the four studied paints samples, the benzene contents were under the detection limits, but relatively high contents of toluene, ethylbenzene and xylenes (56-271 microg g(-1)) were detected with spiked recoveries in the range of 70-114%. Compared to the widely used commercially available SPME fibers, this proposed disposable IL-coated fiber has much lower cost per determination, comparable reproducibility (RSD < 11%), and no carryover between each determination. Considering that IL possess good extractability for various organic compounds and metals ions, and that task-specific IL can be designed and synthesized for selective extraction of target analytes, this disposable IL coating SPME might has great potential in sample preparation.

Benzene↗

PubMed2005

Occurrence and distribution of organochlorine pesticides (HCH and DDT) in sediments collected from East China Sea.

Sediments used in this study were collected from different depths of eight sites in East China Sea in November 2002. The levels and distribution patterns of the selected organochlorine pesticides (OCPs=p,p'-DDT, o,p'-DDT, p,p'-DDE, p,p'-DDD, alpha-, beta-, gamma- and delta-HCH) in samples were investigated by the technique of sonication extraction followed by the analysis of gas chromatography (GC) coupled with a micro-electron capture detector (muECD). The concentrations of SigmaHCH and SigmaDDT in the surface sediments were in the range of <0.05-1.45 ng/g (mean 0.76 ng/g), <0.06-6.04 ng/g (mean 3.05 ng/g) based on dry weight (dw), respectively. In the vertical distributions, the SigmaHCH and SigmaDDT were in the range of <0.05-2.52 ng/g, <0.06-10.94 ng/g dw, respectively. Residues of OCPs varied significantly with different sampling sites. SigmaDDT in the surface sediments was correlated well with total organic carbon (TOC) content (r2=0.71), while SigmaHCH showed no obvious correlation. The distribution showed that the sediments from the vicinity estuary or near shore had higher TOC contents, and higher OCPs concentrations. The contamination record indicated an extensive use of OCPs in the catchments from Yangtze River in the past might greatly affect the OCP residues.

China↗

PubMed2005

A novel fiber coating for solid phase microextraction and its application for the extraction of n-alkane from aqueous sample.

Base on the previous work in laboratory, a novel polyaniline doped with polydimethylsiloxane coating was developed on a stainless steel wire for solid phase microextraction(SPME) by electroplating method. This electroplating method not only has advantages of ease preparation and simple equipments required, but also increases the lifetime of the SPME fiber. The composite fiber (polyaniline/ polydimethylsiloxane(PANI/PDMS)) was evaluated by analyzing n-tridecane, n-tetradecane and n-pentadecane in aqueous sample. The new fiber coating showed comprehensive abilities to extract alkanes compounds. The relative standard deviations were found to be 6.8%-10.33%.

Alkanes↗

PubMed2004

Ionic liquid-based liquid-phase microextraction, a new sample enrichment procedure for liquid chromatography.

Room temperature ionic liquids (RTILs) were used as extraction solvent in liquid-phase microextraction (LPME) coupled with liquid chromatography. Using 1-hexyl-3-methylimidazolium hexafluorophosphate ([C6MIM][PF6]) as extraction solvent, some parameters related to LPME of 4-nonylphenol (4-NP) and 4-tert-octylphenol (4-t-OP) were optimized. Although [C6MIM][PF6] can suspend a much larger volume of drop on the needle of the microsyringe than the conventional solvents such as 1-octanol and carbon tetrachloride, the method sensitivity was analyte dependent because of the different partition coefficients and the relatively large viscosity of [C6MIM][PF6]. The proposed procedure has a detection limit and enrichment factor of 0.3 microg l(-1) and 163 for 4-NP, and 0.7 microg l(-1) and 130 for 4-t-OP, respectively. Aqueous samples including tap water, river water, and effluent from sewage treatment plant were analyzed by the proposed method and the recoveries at 10 microg l(-1) spiked level were in the range of 90-113%.

Chromatography, High Pressure Liquid↗

PubMed2004

Determination of methyl tert-butyl ether (MTBE) in Chinese fuels by gas chromatography/mass spectrometry and gas chromatography/flame ionization detector.

A method was developed to determine the concentration of methyl tert-butyl ether(MTBE) in gasoline, diesel and heating oil by gas chromatography(GC) with mass spectrometry(GC-MS) or flame ionization detection (FID). The diluted gasoline was directly injected into the GC, and the complete separation of MTBE from co-eluting hydrocarbons was not required. GC/MS or GC/FID method can be used to analyze MTBE in different concentration range and have good consistency.

Carcinogens↗

PubMed2003

Use of ionic liquids for liquid-phase microextraction of polycyclic aromatic hydrocarbons.

This paper demonstrates, for the first time, that ionic liquids (IL) such as 1-octyl-3-methylimidazolium hexafluorophosphate ([C(8)MIM][PF(6)]) are excellent extraction solvents in liquid-phase microextraction (LPME). The unique properties of nonvolatility and adequate viscosity allow IL to be conveniently adopted as extraction solvents in both direct-immersion and headspace LPME. Model compounds, polycyclic aromatic hydrocarbons (PAHs), are conveniently and rapidly enriched in a 3-microL drop of [C(8)MIM][PF(6)] suspended on the tip of a microsyringe followed by liquid chromatographic determination. Compared to 1-octanol, a larger volume drop of [C(8)MIM][PF(6)] can be formed and survive for a longer extraction time; therefore, a much higher enrichment factor for PAHs can be reached. For low-volatility PAHs, direct-immersion LPME provides higher enrichment factors than that of headspace LPME. However, the enrichment factor obtained by headspace LPME was almost 3-fold of that by direct-immersion LPME in a 30-min extraction of the most volatile PAH, naphthalene. For 30-min direction-immersion LPME of EPA priority PAHs, the enrichment factor, correlation coefficient (R(2)), and reproducibility (RSD, n = 5) were in the range of 42-166, 0.9169-0.9976, and 2.8-12%, respectively. Considering that IL can be easily prepared from relatively inexpensive materials and tuned by combination of different anions and cations for task-specific extraction of analytes from various solvent media, this proposed method should have great potentiality in sample preparation. Furthermore, the nonvolatility of IL makes it potentially useful for headspace LPME of volatile analytes.

Journal Article↗

PubMed2003

Trace analysis of sulfonylurea herbicides in water by on-line continuous flow liquid membrane extraction--C18 precolumn liquid chromatography with ultraviolet absorbance detection.

An on-line system that consists of continuous-flow liquid membrane extraction (CFLME), C18 precolumn, and liquid chromatography with UV detection was applied to trace analysis of sulfonylurea herbicides in water. During preconcentration by CFLME, five target compounds, including metsulfuron methyl, bensulfuron methyl, tribenuron methyl, sulfometuron methyl, and ethametsulfuron, were enriched in 960 microl of 0.5 mol l(-1) Na2CO3-NaHCO3 (pH 10.8) buffer used as acceptor. This acceptor was on-line neutralized and transported to the C18 precolumn where the analytes were absorbed and focused. Then the focused analytes were injected onto a C18 analytical column for separation and detection at 240 nm. The proposed method was applied to determine sulfonylurea herbicides in water, river, and reservoir water with detection limits of 10-50 ng l(-1) when enriching a 120-ml sample. Throughput is typically one sample per hour.

Chromatography, Liquid↗

PubMed2002

Organotin pollution in China.

A preliminary investigation of the occurrence of butyltin compounds was made in various environmental samples including water, sediment, sea products, and other commodities from China. Detection was carried out by the method of hydrogenation coupled with SPME or Grignard derivatization, followed by GC-FPD analysis. The results showed the universal existence of butyltin compounds in a wide range of tested samples, which was a potential danger for human health. Urgent control or management of organotin compounds is necessary to prevent the underlying hazard caused by this kind of pollutant.

Animals↗