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使用液相色谱/电喷雾电离/四极杆飞行时间串联质谱法对鲁拉西酮的碱性和氧化应激降解产物进行结构表征

Structural characterization of alkaline and oxidative stressed degradation products of lurasidone using LC/ESI/QTOF/MS/MS.

作者信息

Kumar Talluri M V N, Dharavath Shireesha, Kalariya Pradipbhai D, Prasanth B, Srinivas R

机构信息

Department of Pharmaceutical Analysis, National Institute of Pharmaceutical Education & Research, IDPL R&D Campus, Balanagar, Hyderabad 500037, India.

Department of Pharmaceutical Analysis, National Institute of Pharmaceutical Education & Research, IDPL R&D Campus, Balanagar, Hyderabad 500037, India.

出版信息

J Pharm Biomed Anal. 2015 Feb;105:1-9. doi: 10.1016/j.jpba.2014.11.035. Epub 2014 Nov 26.

Abstract

A selective, accurate, precise and robust stability indicating liquid chromatography assay method was developed for the monitoring of a novel antipsychotic drug, lurasidone, in the presence of its degradation products (DPs). Also, we investigated degradation behavior of the drug under various stressed conditions such as hydrolytic (acidic, basic and neutral), oxidation, photolytic and thermal. The drug was found to be degraded under base hydrolytic and oxidative conditions, while it was stable in acid and neutral hydrolytic, photolytic and thermal conditions. The method showed adequate separation of lurasidone and its DPs on Xterra C18 (150 mm × 4.6 mm i.d., 3.5 μm) column using 20 mM ammonium formate (pH 3.0): acetonitrile as a mobile phase in gradient elution mode at a flow rate of 0.6 mL/min. This method was extended to liquid chromatography electrospray ionization quadrupole time-of-flight mass spectrometry (LC/ESI/QTOF/MS/MS) for structural characterization of DPs. A total of five DPs were characterized by LC/ESI/QTOF/MS/MS studies. Most probable mechanisms for the formation of DPs were proposed. The developed method was validated in terms of specificity, linearity, accuracy, precision, and robustness as per International Conference on Harmonization Guideline Q2 (R1).

摘要

开发了一种选择性、准确、精密且稳健的稳定性指示液相色谱测定方法,用于在存在降解产物(DPs)的情况下监测新型抗精神病药物鲁拉西酮。此外,我们研究了该药物在各种强制条件下的降解行为,如水解(酸性、碱性和中性)、氧化、光解和热解。发现该药物在碱性水解和氧化条件下降解,而在酸性和中性水解、光解和热解条件下稳定。该方法在Xterra C18(150 mm×4.6 mm内径,3.5μm)柱上,使用20 mM甲酸铵(pH 3.0):乙腈作为流动相,以0.6 mL/min的流速在梯度洗脱模式下,实现了鲁拉西酮及其DPs的充分分离。该方法扩展至液相色谱电喷雾电离四极杆飞行时间质谱(LC/ESI/QTOF/MS/MS),用于DPs的结构表征。通过LC/ESI/QTOF/MS/MS研究共鉴定出5种DPs。提出了DPs形成的最可能机制。根据国际协调会议指南Q2(R1),对所开发的方法在特异性、线性、准确性、精密度和稳健性方面进行了验证。

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