Direct Detection of a Sulfonate Ester Genotoxic Impurity by Atmospheric-Pressure Thermal Desorption–Extractive Electrospray–Mass Spectrometry
Author(s) -
Neil A. Devenport,
Laura C. Sealey,
Faisal H. Alruways,
Daniel J. Weston,
James C. Reynolds,
Colin S. Creaser
Publication year - 2013
Publication title -
analytical chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.117
H-Index - 332
eISSN - 1520-6882
pISSN - 0003-2700
DOI - 10.1021/ac401054n
Subject(s) - chemistry , extractive electrospray ionization , mass spectrometry , detection limit , desorption electrospray ionization , desorption , chromatography , thermal desorption , electrospray , formic acid , analytical chemistry (journal) , atmospheric pressure , electrospray ionization , sample preparation in mass spectrometry , chemical ionization , ion , ionization , organic chemistry , adsorption , oceanography , geology
A direct, ambient ionization method has been developed using atmospheric pressure thermal desorption-extractive electrospray-mass spectrometry (AP/TD-EESI-MS) for the detection of the genotoxic impurity (GTI) methyl p-toluenesulfonate (MTS) in a surrogate pharmaceutical matrix. A custom-made thermal desorption probe was used to the desorb and vaporize MTS from the solid state, by rapid heating to 200 °C then cooling to ambient temperature, with a cycle time of 6 min. The detection of MTS using EESI with a sodium acetate doped solvent to generate the [MTS+Na](+) adduct ion provided a significant sensitivity enhancement relative to the [M+H](+) ion generated using a 0.1% formic acid solvent modifier. The MTS detection limit is over an order of magnitude below the long-term daily threshold of toxicological concern (TTC) of 1.5 μg/g and the potential for quantitative analysis has been determined using starch as a surrogate active pharmaceutical ingredient (API).
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