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LC、LC-MS/TOF 和 MS(n) 研究鉴定和表征奈非那韦甲磺酸盐的降解产物。

LC, LC-MS/TOF and MS(n) studies for the identification and characterization of degradation products of nelfinavir mesylate.

机构信息

Department of Pharmaceutical Chemistry, SVKM's NMIMS, School of Pharmacy and Technology Management, Near Bank of Tapi River, Agra-Mumbai Road Babulde, Shirpur Dist., Dhule 425405, Maharashtra, India.

出版信息

J Pharm Biomed Anal. 2011 Jun 1;55(3):435-45. doi: 10.1016/j.jpba.2011.02.020. Epub 2011 Feb 24.

Abstract

The objective of the present investigation was to separate, identify and characterize the major degradation products (DPs) of nelfinavir mesylate generated under hydrolytic, oxidative, photolytic and thermal stress conditions as advised in International Conference on Harmonization (ICH) guideline Q1A(R2). The drug was found to degrade under acidic, basic, oxidative and photolytic stress, while it was stable in neutral and thermal stress conditions. A total of three degradation products were formed, which were separated on a C-18 column employing a gradient HPLC method. A complete mass fragmentation pathway of the drug was first established with the help of multi-stage (MS(n)) and MS/TOF accurate mass studies. Then stressed samples were subjected to LC-MS/TOF studies, which provided their fragmentation pattern and accurate masses. The mass spectral data were employed to characterize the DPs and assign structures to them. The total information was also used to establish the degradation pathway of the drug. The degradation products were identified as 3-hydroxy-N-((2R,3R)-3-hydroxy-1-(phenylthio)butan-2-yl)-2-methylbenzamide and (3S,4aS,8aS)-N-tert-butyl-2-((2R,3R)-2-hydroxy-3-(3-hydroxy-2-methylbenzamido)-4-(phenylsulfinyl)butyl)decahydroisoquinoline-3-carboxamide.

摘要

本研究的目的是按照国际协调会议(ICH)指南 Q1A(R2)的建议,分离、鉴定和表征奈非那韦甲磺酸盐在水解、氧化、光解和热应力条件下生成的主要降解产物(DPs)。研究发现,该药物在酸性、碱性、氧化和光解条件下会降解,而在中性和热应力条件下稳定。总共形成了三种降解产物,它们在 C-18 柱上采用梯度 HPLC 方法分离。首先借助多级(MS(n))和 MS/TOF 精确质量研究,建立了药物的完整质谱碎裂途径。然后对受应力的样品进行 LC-MS/TOF 研究,提供其碎裂模式和精确质量。质谱数据用于表征 DPs 并为其分配结构。总信息还用于建立药物的降解途径。鉴定出的降解产物为 3-羟基-N-((2R,3R)-3-羟基-1-(苯硫基)丁-2-基)-2-甲基苯甲酰胺和(3S,4aS,8aS)-N-叔丁基-2-((2R,3R)-2-羟基-3-(3-羟基-2-甲基苯甲酰胺基)-4-(苯亚磺酰基)丁基)十氢异喹啉-3-甲酰胺。

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