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Purpose:
To develop and evaluate a quantitative high performance liquid chromatography UV and tandem mass spectrometric method (HPLC-UV-MS/MS) for simultaneous determination of nutritional nucleotides and nucleosides in infant formula.
Methods:
Infant formula samples were centrifugated after acid protein precipitation and filtered before analysis. Separation was achieved on an Acclaim C30 reversed phase column using an Ultimate RSLC UHPLC system. UV and selected reaction monitoring (SRM) were used in series to provide the flexibility for routine and trace quantitation purposes.
Results:
Total chromatographic resolution for ten nucleotides and nucleosides was achieved within 12 minutes. Linearity was achieved from 20 to 4000 ppb with coefficient of determination (r2) greater than 0.999 for each analyte. Precision was evaluated at 50 ppb and 2000 ppb and was achieved within 5% RSD and accuracy within the range from 90.3% (guanosine 5т-phosphate
GMP
2000ppb) to 112% (GMP
50 ppb). Powdered and liquid infant formula samples were successfully analyzed using this method.
Nucleosides (adenosine, cytosine, guanosine, inosine, uridine) and their monophosphate nucleotides (AMP, CMP, GMP, IMP and UMP respectively) are the building blocks of nucleic acids, and are fully involved in essential cell functions such as energy production, transfer and storage, cellular signaling, as well as enzymatic activities.
Purpose:
To develop and evaluate a quantitative high performance liquid chromatography UV and tandem mass spectrometric method (HPLC-UV-MS/MS) for simultaneous determination of nutritional nucleotides and nucleosides in infant formula.
Methods:
Infant formula samples were centrifugated after acid protein precipitation and filtered before analysis. Separation was achieved on an Acclaim C30 reversed phase column using an Ultimate RSLC UHPLC system. UV and selected reaction monitoring (SRM) were used in series to provide the flexibility for routine and trace quantitation purposes.
Results:
Total chromatographic resolution for ten nucleotides and nucleosides was achieved within 12 minutes. Linearity was achieved from 20 to 4000 ppb with coefficient of determination (r2) greater than 0.999 for each analyte. Precision was evaluated at 50 ppb and 2000 ppb and was achieved within 5% RSD and accuracy within the range from 90.3% (guanosine 5т-phosphate, GMP, 2000ppb) to 112% (GMP, 50 ppb). Powdered and liquid infant formula samples were successfully analyzed using this method.
"Purpose:
To develop and evaluate a quantitative high performance liquid chromatography UV and tandem mass spectrometric method (HPLC-UV-MS/MS) for simultaneous determination of nutritional nucleotides and nucleosides in infant formula.
Methods:
Infant formula samples were centrifugated after acid protein precipitation and filtered before analysis. Separation was achieved on an Acclaim C30 reversed phase column using an Ultimate RSLC UHPLC system. UV and selected reaction monitoring (SRM) were used in series to provide the flexibility for routine and trace quantitation purposes.
Results:
Total chromatographic resolution for ten nucleotides and nucleosides was achieved within 12 minutes. Linearity was achieved from 20 to 4000 ppb with coefficient of determination (r2) greater than 0.999 for each analyte. Precision was evaluated at 50 ppb and 2000 ppb and was achieved within 5% RSD and accuracy within the range from 90.3% (guanosine 5т-phosphate, GMP, 2000ppb) to 112% (GMP, 50 ppb). Powdered and liquid infant formula samples were successfully analyzed using this method."; null; Purpose:; To develop and evaluate a quantitative high performance liquid chromatography UV and tandem mass spectrometric method (HPLC-UV-MS/MS) for simultaneous determination of nutritional nucleotides and nucleosides in infant formula.; Methods:; Infant formula samples were centrifugated after acid protein precipitation and filtered before analysis. Separation was achieved on an Acclaim C30 reversed phase column using an Ultimate RSLC UHPLC system. UV and selected reaction monitoring (SRM) were used in series to provide the flexibility for routine and trace quantitation purposes.; Results:; Total chromatographic resolution for ten nucleotides and nucleosides was achieved within 12 minutes. Linearity was achieved from 20 to 4000 ppb with coefficient of determination (r2) greater than 0.999 for each analyte. Precision was evaluated at 50 ppb and 2000 ppb and was achieved within 5% RSD and accuracy within the range from 90.3% (guanosine 5т-phosphate; GMP; 2000ppb) to 112% (GMP; 50 ppb). Powdered and liquid infant formula samples were successfully analyzed using this method.
Nucleosides (adenosine, cytosine, guanosine, inosine, uridine) and their monophosphate nucleotides (AMP, CMP, GMP, IMP and UMP respectively) are the building blocks of nucleic acids, and are fully involved in essential cell functions such as energy production, transfer and storage, cellular signaling, as well as enzymatic activities.
2014-02-11T17:22:04-05:00
Leo Jinyuan Wang, Bill Schnute, Thermo Fisher Scientific, Sunnyvale, CA, USA
Simultaneous Quantification of Nutritional Nucleotides and Nucleosides in Infant Formula Using HPLC-UV-MS/MS
2012-10-18T09:49:55-04:00
2012-03-09T13:51:12-05:00
2012-10-18T09:49:55-04:00
Acrobat PDFMaker 9.1 for PowerPoint
2014-02-11T17:22:01-05:00
9baa1bbf58fb497a14b82c09d6642b5373d1fabd
Adobe PDF Library 9.0
Leo Jinyuan Wang, Bill Schnute, Thermo Fisher Scientific, Sunnyvale, CA, USA
ThermoFinnigan
"""Purpose:
To develop and evaluate a quantitative high performance liquid chromatography UV and tandem mass spectrometric method (HPLC-UV-MS/MS) for simultaneous determination of nutritional nucleotides and nucleosides in infant formula.
Methods:
Infant formula samples were centrifugated after acid protein precipitation and filtered before analysis. Separation was achieved on an Acclaim C30 reversed phase column using an Ultimate RSLC UHPLC system. UV and selected reaction monitoring (SRM) were used in series to provide the flexibility for routine and trace quantitation purposes.
Results:
Total chromatographic resolution for ten nucleotides and nucleosides was achieved within 12 minutes. Linearity was achieved from 20 to 4000 ppb with coefficient of determination (r2) greater than 0.999 for each analyte. Precision was evaluated at 50 ppb and 2000 ppb and was achieved within 5% RSD and accuracy within the range from 90.3% (guanosine 5т-phosphate, GMP, 2000ppb) to 112% (GMP, 50 ppb). Powdered and liquid infant formula samples were successfully analyzed using this method.""; null; Purpose:; To develop and evaluate a quantitative high performance liquid chromatography UV and tandem mass spectrometric method (HPLC-UV-MS/MS) for simultaneous determination of nutritional nucleotides and nucleosides in infant formula.; Methods:; Infant formula samples were centrifugated after acid protein precipitation and filtered before analysis. Separation was achieved on an Acclaim C30 reversed phase column using an Ultimate RSLC UHPLC system. UV and selected reaction monitoring (SRM) were used in series to provide the flexibility for routine and trace quantitation purposes.; Results:; Total chromatographic resolution for ten nucleotides and nucleosides was achieved within 12 minutes. Linearity was achieved from 20 to 4000 ppb with coefficient of determination (r2) greater than 0.999 for each analyte. Precision was evaluated at 50 ppb and 2000 ppb and was achieved within 5% RSD and accuracy within the range from 90.3% (guanosine 5т-phosphate; GMP; 2000ppb) to 112% (GMP; 50 ppb). Powdered and liquid infant formula samples were successfully analyzed using this method."; null; Purpose:; To develop and evaluate a quantitative high performance liquid chromatography UV and tandem mass spectrometric method (HPLC-UV-MS/MS) for simultaneous determination of nutritional nucleotides and nucleosides in infant formula.; Methods:; Infant formula samples were centrifugated after acid protein precipitation and filtered before analysis. Separation was achieved on an Acclaim C30 reversed phase column using an Ultimate RSLC UHPLC system. UV and selected reaction monitoring (SRM) were used in series to provide the flexibility for routine and trace quantitation purposes.; Results:; Total chromatographic resolution for ten nucleotides and nucleosides was achieved within 12 minutes. Linearity was achieved from 20 to 4000 ppb with coefficient of determination (r2) greater than 0.999 for each analyte. Precision was evaluated at 50 ppb and 2000 ppb and was achieved within 5% RSD and accuracy within the range from 90.3% (guanosine 5т-phosphate; GMP; 2000ppb) to 112% (GMP; 50 ppb). Powdered and liquid infant formula samples were successfully analyzed using this method.; "Nucleosides (adenosine, cytosine, guanosine, inosine, uridine) and their monophosphate nucleotides (AMP, CMP, GMP, IMP and UMP respectively) are the building blocks of nucleic acids, and are fully involved in essential cell functions such as energy production, transfer and storage, cellular signaling, as well as enzymatic activities."; "Purpose:
To develop and evaluate a quantitative high performance liquid chromatography UV and tandem mass spectrometric method (HPLC-UV-MS/MS) for simultaneous determination of nutritional nucleotides and nucleosides in infant formula.
Methods:
Infant formula samples were centrifugated after acid protein precipitation and filtered before analysis. Separation was achieved on an Acclaim C30 reversed phase column using an Ultimate RSLC UHPLC system. UV and selected reaction monitoring (SRM) were used in series to provide the flexibility for routine and trace quantitation purposes.
Results:
Total chromatographic resolution for ten nucleotides and nucleosides was achieved within 12 minutes. Linearity was achieved from 20 to 4000 ppb with coefficient of determination (r2) greater than 0.999 for each analyte. Precision was evaluated at 50 ppb and 2000 ppb and was achieved within 5% RSD and accuracy within the range from 90.3% (guanosine 5т-phosphate, GMP, 2000ppb) to 112% (GMP, 50 ppb). Powdered and liquid infant formula samples were successfully analyzed using this method."
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