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Separation of tolperisone and its degradation products by a dual cyclodextrin capillary electrophoresis system to study their potential role in allergic events.

Authors :
Lakatos, Péter P.
Ignáth, Zsuzsanna
Csernák, Orsolya
Boldizsár, Imre
Szökő, Éva
Tábi, Tamás
Source :
Journal of Pharmaceutical & Biomedical Analysis. Jan2025, Vol. 252, pN.PAG-N.PAG. 1p.
Publication Year :
2025

Abstract

Tolperisone is a centrally acting muscle relaxant that has been used for the treatment of post-stroke spasticity and low back pain. Recently, the safety of tolperisone pharmaceutical products has been reassessed due to growing concerns over allergic adverse events. Reactive degradants of tolperisone may be responsible for these hypersensitivity reactions. By forming adducts with proteins, they may act as haptens that could evoke allergic reactions. The objective of this study was to examine the presence of these degradants in tolperisone pharmaceutical products and to assess their reactivity to elucidate their possible role in the pro-allergic effect of tolperisone. For this purpose, capillary electrophoresis UV detection (CE-UV) method was developed and validated for the quantification of degradants. A dual cyclodextrin system was applied to achieve the appropriate migration order enabling the analysis of 2-methyl-1-(4-methylphenyl)prop-2-en-1-one (MMP) and 1-(4-methylphenyl)propan-1-one (MMPO) in the presence of high concentrations of tolperisone. MMP was identified as the main degradant in forced degradation tests of the active pharmaceutical ingredient. Differences in MMP content of tolperisone products by different manufacturers have also been found, highlighting the role of formulation in their stability. High reactivity of MMP was demonstrated as rapid and almost complete adduct formation with cysteine was found. This degradant thus might be responsible for the allergic adverse effects of tolperisone even when it is present in trace amounts in tablets by readily reacting with proteins in vivo. • A CE-UV method was developed for the analysis of tolperisone degradants. • 2-Methyl-1-(4-methylphenyl)prop-2-en-1-one (MMP) was found as the main degradant. • High reactivity of MMP to cysteine was demonstrated. • MMP might be responsible for allergic adverse events associated with tolperisone. • Formulation of tolperisone products determines their stability and thus MMP content. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
07317085
Volume :
252
Database :
Academic Search Index
Journal :
Journal of Pharmaceutical & Biomedical Analysis
Publication Type :
Academic Journal
Accession number :
180629504
Full Text :
https://doi.org/10.1016/j.jpba.2024.116532