Scholarlink

Abstract <p>Gilteritinib (<b>GTB</b>) is used for the treatment of refractory or relapsed acute myeloid leukemia and inhibits several receptor tyrosine kinases, including FMS-like tyrosine kinase 3 and AXL. The main objective of the current study was to determine how GTB degrades under forced conditions (hydrolysis, oxidation, and photolysis) in accordance with ICH Q1A and Q1B criteria. Zeneth software was used to predict the in-silico deterioration profile of GTB before the study was carried out. GTB was found to be stable under hydrolytic (acidic, basic, and neutral) and photolytic degradation conditions, but it was labile under oxidative (H<sub>2</sub>O<sub>2</sub>) conditions, producing three novel degradation products. The degradation products were identified and separated using a Phenomenex Gemini C18 column (250 × 4.6 mm, 5 µm) in a reversed-phase high-performance liquid chromatography with a gradient program. Mobile phases consisted of 10 mM ammonium formate with 0.01% acetic acid (pH unadjusted, %A) and methanol (%B). High-resolution mass spectrometry was used for the structural elucidation of the degradation products. The resulting data enabled the proposal of a mechanism for the formation of the degradation products. Using in silico techniques (DEREK Nexus, SARAH Nexus, and ProTox-3.0), the toxicity and mutagenicity of GTB and its degradation products were predicted. In summary, this study highlights safety monitoring and storage conditions for GTB.</p>

错误：搜索内容不能为空，请输入英文关键词
错误：关键词超出字数限制，请精简
高级检索

Separation of Oxidative Degradation Products of the Anti-Cancer Drug Gilteritinib Fumarate by Liquid Chromatography with Photodiode Array and Mass Spectrometric Detection

  • 期刊论文

  • 发表日期：

    2025年4月1日

查看全文
  • Pushpa Pilli,
  • Sowmya Chaganti,
  • Vijaya Madhyanapu Golla,
  • Hema Sree Kommalapati,
  • Bhukya Vijay Nayak,
  • Gananadhamu Samanthula

摘要

Abstract

Gilteritinib (GTB) is used for the treatment of refractory or relapsed acute myeloid leukemia and inhibits several receptor tyrosine kinases, including FMS-like tyrosine kinase 3 and AXL. The main objective of the current study was to determine how GTB degrades under forced conditions (hydrolysis, oxidation, and photolysis) in accordance with ICH Q1A and Q1B criteria. Zeneth software was used to predict the in-silico deterioration profile of GTB before the study was carried out. GTB was found to be stable under hydrolytic (acidic, basic, and neutral) and photolytic degradation conditions, but it was labile under oxidative (H2O2) conditions, producing three novel degradation products. The degradation products were identified and separated using a Phenomenex Gemini C18 column (250 × 4.6 mm, 5 µm) in a reversed-phase high-performance liquid chromatography with a gradient program. Mobile phases consisted of 10 mM ammonium formate with 0.01% acetic acid (pH unadjusted, %A) and methanol (%B). High-resolution mass spectrometry was used for the structural elucidation of the degradation products. The resulting data enabled the proposal of a mechanism for the formation of the degradation products. Using in silico techniques (DEREK Nexus, SARAH Nexus, and ProTox-3.0), the toxicity and mutagenicity of GTB and its degradation products were predicted. In summary, this study highlights safety monitoring and storage conditions for GTB.