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首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Study on forced degradation behaviour of dofetilide by LC-PDA and Q-TOF/MS/MS: Mechanistic explanations of hydrolytic, oxidative and photocatalytic rearrangement of degradation products
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Study on forced degradation behaviour of dofetilide by LC-PDA and Q-TOF/MS/MS: Mechanistic explanations of hydrolytic, oxidative and photocatalytic rearrangement of degradation products

机译:用LC-PDA和Q-TOF / MS / MS的Dofetilide强制降解行为的研究:水解,氧化和光催化重排降解产物的机械解释

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A solution and solid state forced decomposition study was carried on dofetilide under diverse stress conditions of hydrolysis, oxidation, photolysis and thermal as per International Council for Harmonisation guidelines (ICH) Q1A(R2) to understand its degradation behaviour. A total of eight degradation products (DPs) were identified and separated on reversed phase kromasil 100 C8 column (4.6 mm x 250 mm x5 mu m) using gradient elution with ammonium acetate (10 mM, pH 6.2) and acetonitrile as mobile phase. The detection wavelength was selected as 230 nm. The high performance liquid chromatography (HPLC) study found that the drug was susceptible to hydrolytic stress condition, but it was highly unstable to photolytic and oxidative conditions. The solid drug was stable in thermal and photolytic conditions. Initially comprehensive mass fragmentation pattern of the drug was accomplished with the LC/ESI/QTOF/MS/MS studies in positive ionization mode. The same was followed for all the eight degradation products to characterise their structure. The DP4 was N-oxide and the structure was confirmed by LC/APCI/QTOF/MS/MS in positive ionization mode. The complete mass fragmentation pattern of the drug and its DPs were established which in turn helped the characterisation of their structures. The mechanistic pathway for the formation of all the DPs was explained. (C) 2019 Elsevier B.V. All rights reserved.
机译:根据国际委员会协调指南(ICH)Q1A(R2)的水解,氧化,光解和热,在水解,氧化,光解和热的各种胁迫条件下进行溶液和固态强制分解研究,以了解其降解行为。使用梯度洗脱在乙酸铵(10mM,pH6.2)和乙腈作为流动相的梯度洗脱时鉴定出总共八种降解产物(DPS)并分离在反相Kromasil 100c8柱(4.6mm×250mmx5μm)上。检测波长被选为230nm。高效液相色谱(HPLC)研究发现,该药物易受水解应激状况的影响,但对光解和氧化条件非常不稳定。固体药物在热和光溶解条件下稳定。最初通过阳性电离模式的LC / ESI / QTOF / MS / MS研究完成了该药物的初始综合质量碎片模式。所有八种降解产品都是相同的,以表征其结构。 DP4是N-氧化物,通过LC / APCI / QTOF / MS / MS在正电离模式中确认该结构。建立了药物及其DPS的完整质量碎片模式,反过来有助于其结构表征。解释了形成所有DP的机械途径。 (c)2019 Elsevier B.v.保留所有权利。

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