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Featured researches published by Zhilong Gong.


Talanta | 2002

Arsenic speciation analysis

Zhilong Gong; Xiufen Lu; Mingsheng Ma; Corinna Watt; X. Chris Le

Nearly two dozen arsenic species are present in the environmental and biological systems. Differences in their toxicity, biochemical and environmental behaviors require the determination of these individual arsenic species. Considerable analytical progresses have been made toward arsenic speciation analysis over the last decade. Hyphenated techniques involving a highly efficient separation and a highly sensitive detection have become the techniques of choice. Methods based on high-performance liquid chromatography separation with inductively coupled plasma mass spectrometry, hydride generation atomic spectrometry, and electrospray mass spectrometry detection have been shown most useful for arsenic speciation in environmental and biological matrices. These hyphenated techniques have resulted in the determination of new arsenic species, contributing to a better understanding of arsenic metabolism and biogeochemical cycling. Methods for extracting arsenic species from solid samples and for stabilizing arsenic species in solutions are required for obtaining reliable arsenic speciation information.


Fifth International Conference on Arsenic Exposure and Health Effects, San Diego, California, USA, 14-18 July, 2002. | 2003

Trivalent arsenic species: Analysis, stability, and interaction with a protein

Guifeng Jiang; Xiufen Lu; Zhilong Gong; William R. Cullen; X. Chris Le

Publisher Summary Biomethylation is the major metabolic process for inorganic arsenic (As). The methylation process involves stepwise two-electron reduction of As, followed by oxidative addition of a methyl group. Methyltransferases are responsible for methyl transfer, and S-adenosyl-methionine (SAM) is the methyl donor. Trimethylarsine oxide (TMAOV) and trimethylarsine (TMAIII) are the end products formed by some microorganisms. Dimethylarsinic acid (DMAV) is the usual end product detected in humans, although dimethylarsinous acid (DMAIII) has recently been detected in human urine. An important issue regarding the speciation of monomethylarsonous acid (MMAIII) and dimethylarsinous acid (DMAIII) is the stability and preservation of these species. It has been reported that MMAIII and DMAIII are less stable than the other As species, suggesting that new strategies for sample handling are needed for the analysis of these trivalent As species.


Archive | 2003

Trivalent arsenic species

Guifeng Jiang; Xiufen Lu; Zhilong Gong; William R. Cullen; X. Chris Le

Publisher Summary Biomethylation is the major metabolic process for inorganic arsenic (As). The methylation process involves stepwise two-electron reduction of As, followed by oxidative addition of a methyl group. Methyltransferases are responsible for methyl transfer, and S-adenosyl-methionine (SAM) is the methyl donor. Trimethylarsine oxide (TMAOV) and trimethylarsine (TMAIII) are the end products formed by some microorganisms. Dimethylarsinic acid (DMAV) is the usual end product detected in humans, although dimethylarsinous acid (DMAIII) has recently been detected in human urine. An important issue regarding the speciation of monomethylarsonous acid (MMAIII) and dimethylarsinous acid (DMAIII) is the stability and preservation of these species. It has been reported that MMAIII and DMAIII are less stable than the other As species, suggesting that new strategies for sample handling are needed for the analysis of these trivalent As species.


Arsenic Exposure and Health Effects V#R##N#Proceedings of the Fifth International Conference on Arsenic Exposure and Health Effects, July 14–18, 2002, San Diego, California | 2003

Chapter 4 – Trivalent arsenic species: Analysis, stability, and interaction with a protein

Guifeng Jiang; Xiufen Lu; Zhilong Gong; William R. Cullen; X. Chris Le

Publisher Summary Biomethylation is the major metabolic process for inorganic arsenic (As). The methylation process involves stepwise two-electron reduction of As, followed by oxidative addition of a methyl group. Methyltransferases are responsible for methyl transfer, and S-adenosyl-methionine (SAM) is the methyl donor. Trimethylarsine oxide (TMAOV) and trimethylarsine (TMAIII) are the end products formed by some microorganisms. Dimethylarsinic acid (DMAV) is the usual end product detected in humans, although dimethylarsinous acid (DMAIII) has recently been detected in human urine. An important issue regarding the speciation of monomethylarsonous acid (MMAIII) and dimethylarsinous acid (DMAIII) is the stability and preservation of these species. It has been reported that MMAIII and DMAIII are less stable than the other As species, suggesting that new strategies for sample handling are needed for the analysis of these trivalent As species.


Journal of Analytical Atomic Spectrometry | 2001

Unstable trivalent arsenic metabolites, monomethylarsonous acid and dimethylarsinous acid

Zhilong Gong; Xiufen Lu; William R. Cullen; X. Chris Le


Chemical Research in Toxicology | 2003

Interaction of trivalent arsenicals with metallothionein.

Guifeng Jiang; Zhilong Gong; Xing-Fang Li; and William R. Cullen; X. Chris Le


Chemical Research in Toxicology | 2004

Arsenic speciation in urine from acute promyelocytic leukemia patients undergoing arsenic trioxide treatment.

Zhongwen Wang; Jin Zhou; Xiufen Lu; Zhilong Gong; X. Chris Le


Clinical Chemistry | 2004

Reverse Transcription-Multiplex PCR Assay for Simultaneous Detection of Escherichia coli O157:H7, Vibrio cholerae O1, and Salmonella Typhi

Nicole Morin; Zhilong Gong; Xing-Fang Li


Analytica Chimica Acta | 2006

Speciation analysis of arsenic in groundwater from Inner Mongolia with an emphasis on acid-leachable particulate arsenic

Zhilong Gong; Xiufen Lu; Corinna Watt; Bei Wen; Bin He; Judy L. Mumford; Zhixiong Ning; Yajuan Xia; X. Chris Le


Chemical Research in Toxicology | 2002

Determination of arsenic metabolic complex excreted in human urine after administration of sodium 2,3-dimercapto-1-propane sulfonate.

Zhilong Gong; Guifeng Jiang; William R. Cullen; H. Vasken Aposhian; X. Chris Le

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Xiufen Lu

University of Alberta

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William R. Cullen

University of British Columbia

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Bei Wen

University of Alberta

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Bin He

University of Alberta

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Hai Zhang

University of Alberta

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