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Articles 31 - 38 of 38
Full-Text Articles in Analytical Chemistry
Rapid Determination Of Serum Melatonin By Esi–Ms–Ms With Direct Sample Injection, Shuming Yang, Xiaohui Zheng, Yan Xu, Xiang Zhou
Rapid Determination Of Serum Melatonin By Esi–Ms–Ms With Direct Sample Injection, Shuming Yang, Xiaohui Zheng, Yan Xu, Xiang Zhou
Chemistry Faculty Publications
This paper describes a rapid, simple and sensitive analytical method for the quantitative determination of melatonin in human serum by ESI–MS–MS with direct serum sample injection and on-line extraction. The method uses N-acetyltryptamine as the internal standard. It has high specificity and sensitivity for serum melatonin analysis. The internal calibration curve shows a wide linear range from 0.500 to 200 ng/ml with a correlation coefficient, R2>0.999. The limit of quantitation is 0.500 ng/ml and the limit of detection is 0.100 ng/ml with 10-μl sample injection. The recoveries of serum melatonin at three levels are approximately 70%. The intra-assay precision …
Simultaneous Determination Of Enantiomers Of Structurally Related Anticholinergic Analogs In Human Serum By Liquid Chromatography–Electrospray Ionization Mass Spectrometry With On-Line Sample Cleanup, Vladimı́R Čápka, Yan Xu
Simultaneous Determination Of Enantiomers Of Structurally Related Anticholinergic Analogs In Human Serum By Liquid Chromatography–Electrospray Ionization Mass Spectrometry With On-Line Sample Cleanup, Vladimı́R Čápka, Yan Xu
Chemistry Faculty Publications
Trihexyphenidyl, biperiden and procyclidine are anticholinergic drugs produced as racemates for the treatment of Parkinson’s disease. This paper describes a simple and sensitive LC–MS method for the simultaneous determination of these compounds in human serum. An on-line sample clean-up procedure was used, where serum samples were directly injected into a “restricted-access media” pre-column. After the exclusion of the serum proteins, the drug molecules were eluted to a β-cyclodextrin analytical column for chiral separation. The quantitation was done by electrospray ionization MS using diphenidol as an internal standard. The method developed has limits of detection of 1 ng/ml, at least two-orders-of-magnitude …
Determination Of Lysophosphatidic Acids By Capillary Electrophoresis With Indirect Ultraviolet Detection, Yi Lung Chen, Yan Xu
Determination Of Lysophosphatidic Acids By Capillary Electrophoresis With Indirect Ultraviolet Detection, Yi Lung Chen, Yan Xu
Chemistry Faculty Publications
Lysophosphatidic acid (LPA) is the simplest form of lysophospholipid. Molecular species of LPA have been identified as the potent components in the ovarian cancer activation factor. The elevated plasma LPAs may be used as potential biomarkers for the early detection of ovarian cancer. This paper is the first report on the quantitative analysis of molecular species of LPA using capillary electrophoresis. In this work, the separation of LPAs was achieved within 14 min in an adenosine monophosphate-borate–methanol–water solution, and the measurement was accomplished by indirect UV detection. With LPA (D) as internal standard, the method had linear calibration ranges for …
Stereoselective Determination Oftrihexyphenidyl In Human Serum By Lc–Esi–Ms, Vladimı́R Čápka, Yan Xu, Yong Hong Chen
Stereoselective Determination Oftrihexyphenidyl In Human Serum By Lc–Esi–Ms, Vladimı́R Čápka, Yan Xu, Yong Hong Chen
Chemistry Faculty Publications
The antiparkinsonian drug trihexyphenidyl (THP) is currently manufactured and administered as a racemate. However, stereochemistry can play significant role in the drug’s pharmacokinetics, biotransformation, metabolism, interaction with cellular and tissue components and overall effect on human body. It is necessary to consider such a drug as a mixture of two compounds (drug enantiomers), with their own effect on the human body. The present paper describes a simple and sensitive LC–MS method for the stereoselective determination of THP in human serum. In this study, the sample was prepared by a solid-phase extraction (SPE) procedure. The enantiomer separation was done using native …
Enhancing The Performance Of Membrane Introduction Mass Spectrometry By Organic Carrier And Liquid Chromatographic Separation, Shi Ouyang, Yong Hong Chen, Yan Xu
Enhancing The Performance Of Membrane Introduction Mass Spectrometry By Organic Carrier And Liquid Chromatographic Separation, Shi Ouyang, Yong Hong Chen, Yan Xu
Chemistry Faculty Publications
A method of membrane introduction mass spectrometry with liquid chromatographic separation (LC/MIMS) for the analysis of volatile organic compounds (VOCs) in water has been developed. The method not only inherited all the advantages of membrane introduction mass spectrometry by flow-injection analysis (FIA/MIMS), but also expanded the application of MIMS to the determination of compounds with identical quantitation ions. Because the quantitation by LC/MIMS is based on two-dimensional identification (retention time (tr) and mass-to-charge ratio ()), it provides a tangible approach to the analysis of VOCs in complex aqueous samples. In this work, a C18 column and a mobile phase (methanol/water) …
Indirect Ultraviolet Detection Of Biologically Relevant Organic Acids By Capillary Electrophoresis, Hong Chen, Yan Xu, Frederick Van Lente, Michael P.C. Ip
Indirect Ultraviolet Detection Of Biologically Relevant Organic Acids By Capillary Electrophoresis, Hong Chen, Yan Xu, Frederick Van Lente, Michael P.C. Ip
Chemistry Faculty Publications
Indirect UV detection of fourteen short-chain organic acids (e.g., oxalic acid, citric acid, malonic acid, tartaric acid, methylmalonic acid, α-ketoglutaric acid, succinic acid, ethylmalonic acid, methylsuccinic acid, glutaric acid, apidic acid, methylglutaric acid, lactic acid and pyruvic acid) by capillary electrophoresis is described. The method used phthalate as the UV-absorbing additive in carbonate buffer and the non-absorbing analytes were detected indirectly at 230 nm. The influences of buffer pH, ionic strenght, concentration of phthalate and organic modifier on indirect signal response and migration behavior of the organic acids were investigated. Comparisons of reproducibility on migration time, limit of detection and …
Electrochemical Enzyme Immunoassay Using Sequential Saturation Technique In A 20-Μl Capillary: Digoxin As A Model Analyte, Noriaki Kaneki, Yan Xu, Anu Kumari, H. Brian Halsall, William R. Heineman, Peter T. Kissinger
Electrochemical Enzyme Immunoassay Using Sequential Saturation Technique In A 20-Μl Capillary: Digoxin As A Model Analyte, Noriaki Kaneki, Yan Xu, Anu Kumari, H. Brian Halsall, William R. Heineman, Peter T. Kissinger
Chemistry Faculty Publications
Capillary enzyme immunoassay with flow-injection analysis for digoxin using the sequential saturation technique has been developed. Glass capillary tubes (10 cm × 0.53 mm i.d.) with immobilized digoxin antibody were used as the immunoassay reactor. The product of enzymatic reaction. 4-aminophenol, was detected amperometrically. The digoxin and the labeled digoxin binding reaction with the immobilized digoxin antibody were completed in 2 and 10 min, respectively. Digoxin was determined in a 20-μl sample with a detection limit of 10 pg ml−1 (200 fg or 260 attomoles) and a 3 orders of magnitude range.
Solid-Phase Electrochemical Enzyme Immunoassay With Attomole Detection Limit By Flow Injection Analysis, Yan Xu, H. Brian Halsall, William R. Heineman
Solid-Phase Electrochemical Enzyme Immunoassay With Attomole Detection Limit By Flow Injection Analysis, Yan Xu, H. Brian Halsall, William R. Heineman
Chemistry Faculty Publications
A sandwich electrochemical enzyme immunoassay with flow injection analysis for the model antigen mouse IgG has been developed with alkaline phosphatase as the enzyme label. The enzyme substrate, 4-aminophenyl phosphate and its enzymatic reaction product, 4-aminophenol have been studied by cyclic and hydrodynamic voltammetry. The determination of 4-aminophenol by flow injection analysis with electrochemical detection (FIAEC) has a linear range of 5.0 × 10−8 to 1.0 × 10−5 M, a detection limit of 2.4 × 10−8 M, and a sample throughput of 72 samples/h. The detection limit is set by a background capacitance response, which depends on the ionic strength …