Molecular formula analysis of fragment ions by isotope‐selective collision‐induced dissociation tandem mass spectrometry of pharmacologically active compounds. (December 2014)
- Record Type:
- Journal Article
- Title:
- Molecular formula analysis of fragment ions by isotope‐selective collision‐induced dissociation tandem mass spectrometry of pharmacologically active compounds. (December 2014)
- Main Title:
- Molecular formula analysis of fragment ions by isotope‐selective collision‐induced dissociation tandem mass spectrometry of pharmacologically active compounds
- Authors:
- Bianco, Giuliana
Buchicchio, Alessandro
Lelario, Filomena
Cataldi, Tommaso R.I. - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>The purpose of this work is to explore the mass fragment characterization of commonly used drugs through a novel approach, which involves isotope‐selective tandem mass spectrometry (MS/MS). Collision‐induced dissociation (CID) was performed with a low‐resolution linear ion trap mass spectrometer in positive electrospray ionization. Three pharmacologically active ingredients, i.e. omeprazole, meloxicam and brinzolamide, selected as model compounds in their own formulation, were investigated as a sodiated adduct [C<sub>17</sub>H<sub>19</sub>N<sub>3</sub>O<sub>3</sub>S + Na]<sup>+</sup> (omeprazole) and as protonated adducts, [C<sub>14</sub>H<sub>13</sub>N<sub>3</sub>O<sub>4</sub>S<sub>2</sub> + H]<sup>+</sup> and [C<sub>12</sub>H<sub>21</sub>N<sub>3</sub>O<sub>5</sub>S<sub>3</sub> + H]<sup>+</sup>, meloxicam and brinzolamide, respectively. Selecting a narrow window of ±0.5 <italic>m/z</italic> units, precursor ion fragmentation by CID‐MS/MS of isotopologues A + 0, A + 1 and A + 2 was found very useful to confirm the chemical formula of product ions, thus aiding the establishment of characteristic fragmentation pathways of all three examined compounds. The correctness of putative molecular formula of product ions was easily demonstrated by exploiting the isotope peak abundance ratios (i.e. I<sub>F+0</sub>/I<sub>F+1</sub> and I<sub>F+0</sub>/I<sub>F+2</sub>) as simple constraints in<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>The purpose of this work is to explore the mass fragment characterization of commonly used drugs through a novel approach, which involves isotope‐selective tandem mass spectrometry (MS/MS). Collision‐induced dissociation (CID) was performed with a low‐resolution linear ion trap mass spectrometer in positive electrospray ionization. Three pharmacologically active ingredients, i.e. omeprazole, meloxicam and brinzolamide, selected as model compounds in their own formulation, were investigated as a sodiated adduct [C<sub>17</sub>H<sub>19</sub>N<sub>3</sub>O<sub>3</sub>S + Na]<sup>+</sup> (omeprazole) and as protonated adducts, [C<sub>14</sub>H<sub>13</sub>N<sub>3</sub>O<sub>4</sub>S<sub>2</sub> + H]<sup>+</sup> and [C<sub>12</sub>H<sub>21</sub>N<sub>3</sub>O<sub>5</sub>S<sub>3</sub> + H]<sup>+</sup>, meloxicam and brinzolamide, respectively. Selecting a narrow window of ±0.5 <italic>m/z</italic> units, precursor ion fragmentation by CID‐MS/MS of isotopologues A + 0, A + 1 and A + 2 was found very useful to confirm the chemical formula of product ions, thus aiding the establishment of characteristic fragmentation pathways of all three examined compounds. The correctness of putative molecular formula of product ions was easily demonstrated by exploiting the isotope peak abundance ratios (i.e. I<sub>F+0</sub>/I<sub>F+1</sub> and I<sub>F+0</sub>/I<sub>F+2</sub>) as simple constraints in low‐resolution MS instrumentations. Copyright © 2014 John Wiley &amp; Sons, Ltd.</p> </abstract> … (more)
- Is Part Of:
- Journal of mass spectrometry. Volume 49:Number 12(2014:Dec.)
- Journal:
- Journal of mass spectrometry
- Issue:
- Volume 49:Number 12(2014:Dec.)
- Issue Display:
- Volume 49, Issue 12 (2014)
- Year:
- 2014
- Volume:
- 49
- Issue:
- 12
- Issue Sort Value:
- 2014-0049-0012-0000
- Page Start:
- 1322
- Page End:
- 1329
- Publication Date:
- 2014-12
- Subjects:
- Mass spectrometry -- Periodicals
543.65 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/jms.3468 ↗
- Languages:
- English
- ISSNs:
- 1076-5174
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5012.179500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3744.xml