Journal of Pharmaceutical and Biomedical Analysis, volume 190, pages 113533

HPLC/ESI-MS identification of diastereomers of Impurity E – Degradation products of cefaclor

Publication typeJournal Article
Publication date2020-10-01
scimago Q2
wos Q2
SJR0.584
CiteScore6.7
Impact factor3.1
ISSN07317085, 1873264X
Drug Discovery
Spectroscopy
Pharmaceutical Science
Clinical Biochemistry
Analytical Chemistry
Abstract
A seven years old sample of cefaclor stored in room conditions, as a solid, has been analyzed by using high performence liquid chromatography/electrospray ionization-mass spectrometry. As a result of the sample degradation process, two diastereomers of Impurity E have been found to have formed. It is reasonable to assume that the diastereomers are formed due to the isomerization of C6 carbon atom. They have almost identical fragmentation patterns in both positive and negative ion mode. On the other hand, the diastereomers have different efficiencies of formation of dimer ions, under ESI conditions, especially in negative ion mode.

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