Biomedical Chromatography · 2015 · 11 citations · 15 references
Life SciencesBiochemistryCellular MetabolismChromatographic AnalysisMetabolismBioanalytical Method ValidationCarbohydrate MetabolismChromatographyLiquid ChromatographyMetabolite ExtractionChromatographic Separation Of SugarsGluconeogenesisGlucose ConcentrationGlucose QuantificationHepatic GluconeogenesisInternal Standard AnalysisLower Limit Of QuantificationLower Limit Of Quantitation
A new pre-column derivative high-performance liquid chromatography (HPLC) method for determination of d-glucose with 3-O-methyl-d-glucose (3-OMG) as the internal standard was developed and validated in order to study the gluconeogenesis in HepG2 cells. Samples were derivatized with 1-phenyl-3-methy-5-pyrazolone at 70°C for 50 min. Glucose and 3-OMG were extracted by liquid-liquid extraction and separated on a YMC-Triart C18 column, with a gradient mobile phase composed of acetonitrile and 20 mm ammonium acetate solution containing 0.09% tri-ethylamine at a flow rate of 1.0 mL/min. The eluate were detected using a UV detector at 250 nm. The assay was linear over the range 0.39-25 μm (R(2) = 0.9997, n = 5) and the lower limit of quantitation was 0.39 μm (0.070 mg/mL). Intra- and inter-day precision and accuracy were <15% and within ±3%, respectively. After validation, the HPLC method was applied to investigate the gluconeogenesis in Dulbecco's modified Eagle medium (DMEM) cultured HepG2 cells. Glucose concentration was determined to be about 1-2.5 μm in this gluconeogenesis assay. In conclusion, this method has been shown to determine small amounts of glucose in DMEM successfully, with lower limit of quantitation and better sensitivity when compared with common commercial glucose assay kits.
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Hydrogen Sulfide Impairs Glucose Utilization and Increases Gluconeogenesis in Hepatocytes
Ling Zhang, Guangdong Yang, Ashley Untereiner et al. · Endocrinology · 2012 · 94 citations · Full text
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