Identification, Synthesis, and Characterization of N-Formyl Mirabegron: A New Degradation Product Formed by Formic Acid Impurity in Pharmaceutical Excipients.

IF 2.1 Q3 PHARMACOLOGY & PHARMACY Advances in Pharmacological and Pharmaceutical Sciences Pub Date : 2024-12-10 eCollection Date: 2024-01-01 DOI:10.1155/adpp/4971456
Bashir Daoud Agha Dit Daoudy, Mohammad Ammar Al-Khayat, Ghassan Abo Chameh, Mohammad Amer Al Mardini
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引用次数: 0

Abstract

This study demonstrated the impact of formic acid (FAc), a common reactive impurity in pharmaceutical excipients, on the stability of mirabegron (MB). The investigation of MB-excipient compatibility tests revealed the formation of a new degradation product, FAc-DP, at 0.2% after 7 days of isothermal stress at 55°C. FAc-DP was synthesized and characterized as N-formyl MB using liquid chromatography-mass spectrometry (LC-MS) and both 1D and 2D nuclear magnetic resonance spectroscopy (NMR).

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N-Formyl Mirabegron 的鉴定、合成和表征:一种由药用辅料中的甲酸杂质形成的新降解产物。
本研究证实了药用辅料中常见的活性杂质甲酸(FAc)对米拉米格隆(MB)稳定性的影响。mb -赋形剂相容性试验的研究表明,在55°C等温胁迫7天后,在0.2%的浓度下形成了一种新的降解产物facc - dp。采用液相色谱-质谱联用(LC-MS)、一维和二维核磁共振波谱(NMR)对FAc-DP进行了表征,并鉴定为n -甲酰基MB。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.30
自引率
3.60%
发文量
0
审稿时长
17 weeks
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