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J Pharm Biomed Anal ; 247: 116256, 2024 Sep 01.
Article in English | MEDLINE | ID: mdl-38850847

ABSTRACT

A long-term stability study using high performance liquid chromatography (HPLC) revealed an unidentified impurity in the bromhexine hydrochloride injection, which was employed as a mucolytic agent. Investigations into stress degradation and elemental impurities revealed one of the elemental impurities Fe3+ in this injection as the primary generator of these impurities. This impurity, named N-carboxymethyl bromhexine, was a product formed during drug-excipient interaction between bromhexine and tartaric acid with Fe3+. The structure of the impurity was identified through ultra-high-performance liquid chromatography with diode array detector (UHPLC-DAD), liquid chromatograph mass spectrometer (LC-MS). Further, the formation mechanism of the impurity was discussed. Overall, this study elucidates the cause, origin, and mechanism of an unknown impurity in bromhexine hydrochloride injection, providing a basis for quality control for bromhexine hydrochloride injections and drug products containing both amine and tartaric acid.


Subject(s)
Bromhexine , Drug Contamination , Excipients , Bromhexine/chemistry , Bromhexine/analysis , Chromatography, High Pressure Liquid/methods , Excipients/chemistry , Excipients/analysis , Tartrates/chemistry , Tartrates/analysis , Mass Spectrometry/methods , Drug Stability , Quality Control
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