TY - JOUR
T1 - Characterization of Synthetic and Natural Product Pharmaceuticals by Functional Group Analysis using Electrospray Ionization-Ion Trap Mass Spectrometry
T2 - A Mini-Review
AU - Smyth, W. Franklin
AU - McClean, Stephen
AU - Massaro, C. Flavia
AU - Smyth, Thomas J.
AU - Brooks, Peter
AU - Robledo, Virginia Rodríguez
N1 - Publisher Copyright:
© 2015, Copyright © Taylor & Francis Group, LLC.
PY - 2015/11/22
Y1 - 2015/11/22
N2 - This mini-review is concerned with the characterization of synthetic and natural product pharmaceuticals by functional group analysis using electrospray ionization-ion trap mass spectrometry. Studies of the electrospray ionization–ion trap mass spectrometry behavior of selected synthetic and natural product pharmaceuticals of low molecular mass have shown certain characteristic fragmentations in that functional groups are generally cleaved from ring systems either as even electron inorganic or organic molecules such as H2O, CO, CO2, alcohols, carboxylic acids, or as odd electron entities such as methoxy and methyl. This is particularly energetically favorable in the former case with the standard heat of formation at 298.15 K of the ejected neutral molecule having a relatively high negative value. Fragmentation of pharmaceuticals involving the generation of odd electron entities such as the methyl radical is structure dependent and is to a large extent correlated with the stability of the newly formed free radical ions. The fragmentation data therefore provides useful information on the structure of these pharmaceuticals, their degradation products and metabolites. In some cases, the cleaving of functional groups may parallel the production of certain metabolites. In addition, electrospray ionization-ion trap mass spectrometry data on even and odd electron mass losses may be cross-referenced with data obtained from unknown analytes such as bioactive molecules isolated from natural sources which can then be of value in their structural characterization, assisting in the dereplication process. This mini-review on functional group analysis of selected pharmaceuticals by electrospray ionization-ion trap mass spectrometry provides examples of drug characterization following cleavage from ring systems of even electron molecules (e.g., hypnotic drugs, coumarins, phloroglucinols, and polyphenols) and odd electron entities (e.g., the alkaloid tetrandrine). Parallels between the cleaving of functional groups as even electron mass losses and the metabolic reactions of the macrocyclic antibiotic rifapentine are also discussed.
AB - This mini-review is concerned with the characterization of synthetic and natural product pharmaceuticals by functional group analysis using electrospray ionization-ion trap mass spectrometry. Studies of the electrospray ionization–ion trap mass spectrometry behavior of selected synthetic and natural product pharmaceuticals of low molecular mass have shown certain characteristic fragmentations in that functional groups are generally cleaved from ring systems either as even electron inorganic or organic molecules such as H2O, CO, CO2, alcohols, carboxylic acids, or as odd electron entities such as methoxy and methyl. This is particularly energetically favorable in the former case with the standard heat of formation at 298.15 K of the ejected neutral molecule having a relatively high negative value. Fragmentation of pharmaceuticals involving the generation of odd electron entities such as the methyl radical is structure dependent and is to a large extent correlated with the stability of the newly formed free radical ions. The fragmentation data therefore provides useful information on the structure of these pharmaceuticals, their degradation products and metabolites. In some cases, the cleaving of functional groups may parallel the production of certain metabolites. In addition, electrospray ionization-ion trap mass spectrometry data on even and odd electron mass losses may be cross-referenced with data obtained from unknown analytes such as bioactive molecules isolated from natural sources which can then be of value in their structural characterization, assisting in the dereplication process. This mini-review on functional group analysis of selected pharmaceuticals by electrospray ionization-ion trap mass spectrometry provides examples of drug characterization following cleavage from ring systems of even electron molecules (e.g., hypnotic drugs, coumarins, phloroglucinols, and polyphenols) and odd electron entities (e.g., the alkaloid tetrandrine). Parallels between the cleaving of functional groups as even electron mass losses and the metabolic reactions of the macrocyclic antibiotic rifapentine are also discussed.
KW - Cleavage from ring systems
KW - Electrospray ionization ion trap mass spectrometry
KW - Fragmentation
KW - Functional group analysis
KW - Natural product pharmaceuticals
KW - Pharmaceutical characterization
UR - http://www.scopus.com/inward/record.url?scp=84940530533&partnerID=8YFLogxK
U2 - 10.1080/00032719.2015.1045590
DO - 10.1080/00032719.2015.1045590
M3 - Article
AN - SCOPUS:84940530533
SN - 0003-2719
VL - 48
SP - 2661
EP - 2675
JO - Analytical Letters
JF - Analytical Letters
IS - 17
ER -