Strategies for quantitation of endogenous adenine nucleotides in human plasma using novel ion-pair hydrophilic interaction chromatography coupled with tandem mass spectrometry

•A novel and highly sensitive IP–HILIC–MS/MS method was reported for the quantitation of nucleotides.•The lower limit of quantitation (LLOQ) of 2.00ng/mL obtained for ATP.•This novel chromatographic mechanism is first reported and named as IP–HILIC–MS/MS. We present here a novel and highly sensitive...

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Veröffentlicht in:Journal of Chromatography A 2014-01, Vol.1325, p.129-136
Hauptverfasser: Zhang, Guodong, Walker, Annie D., Lin, Zhaosheng, Han, Xiaogang, Blatnik, Matthew, Steenwyk, Rick C., Groeber, Elizabeth A.
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container_end_page 136
container_issue
container_start_page 129
container_title Journal of Chromatography A
container_volume 1325
creator Zhang, Guodong
Walker, Annie D.
Lin, Zhaosheng
Han, Xiaogang
Blatnik, Matthew
Steenwyk, Rick C.
Groeber, Elizabeth A.
description •A novel and highly sensitive IP–HILIC–MS/MS method was reported for the quantitation of nucleotides.•The lower limit of quantitation (LLOQ) of 2.00ng/mL obtained for ATP.•This novel chromatographic mechanism is first reported and named as IP–HILIC–MS/MS. We present here a novel and highly sensitive ion-pair hydrophilic interaction chromatography–tandem mass spectrometry (IP–HILIC–MS/MS) method for quantitation of highly polar acid metabolites like adenine nucleotides. A mobile phase based on diethylamine (DEA) and hexafluoro-2-isopropanol (HFIP) and an aminopropyl (NH2) column were applied for a novel chromatographic separation for the determination of AMP, ADP and ATP in biological matrices. This novel IP–HILIC mechanism could be hypothesized by the ion-pairing reagent (DEA) in the mobile phase forming neutral and hydrophilic complexes with the analytes of polar organic acids. The IP–HILIC–MS/MS assay for adenine nucleotides was successfully validated with satisfactory linearity, sensitivity, accuracy, reproducibility and matrix effects. The lower limit of quantitation (LLOQ) at 2.00ng/mL obtained for ATP showed a least 10-fold higher sensitivity than previous LC–MS/MS assays except nano-LC–MS/MS assay. In summary, this novel IP–HILIC–MS/MS assay provides a sensitive method for nucleotides bioanalysis and shows great potential to determine a number of organic acids in biological matrices.
doi_str_mv 10.1016/j.chroma.2013.12.017
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We present here a novel and highly sensitive ion-pair hydrophilic interaction chromatography–tandem mass spectrometry (IP–HILIC–MS/MS) method for quantitation of highly polar acid metabolites like adenine nucleotides. A mobile phase based on diethylamine (DEA) and hexafluoro-2-isopropanol (HFIP) and an aminopropyl (NH2) column were applied for a novel chromatographic separation for the determination of AMP, ADP and ATP in biological matrices. This novel IP–HILIC mechanism could be hypothesized by the ion-pairing reagent (DEA) in the mobile phase forming neutral and hydrophilic complexes with the analytes of polar organic acids. The IP–HILIC–MS/MS assay for adenine nucleotides was successfully validated with satisfactory linearity, sensitivity, accuracy, reproducibility and matrix effects. The lower limit of quantitation (LLOQ) at 2.00ng/mL obtained for ATP showed a least 10-fold higher sensitivity than previous LC–MS/MS assays except nano-LC–MS/MS assay. 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subjects Adenine Nucleotides - blood
ADP
AMP
ATP
Biological and medical sciences
Chromatography, High Pressure Liquid - instrumentation
Chromatography, High Pressure Liquid - methods
Humans
Hydrophobic and Hydrophilic Interactions
Investigative techniques, diagnostic techniques (general aspects)
Ions - chemistry
IP–HILIC–MS/MS
Medical sciences
Miscellaneous. Technology
Nucleotides
Organic Acids
Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques
Reproducibility of Results
Tandem Mass Spectrometry - instrumentation
Tandem Mass Spectrometry - methods
title Strategies for quantitation of endogenous adenine nucleotides in human plasma using novel ion-pair hydrophilic interaction chromatography coupled with tandem mass spectrometry
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