富马酸伏诺哌赞的hplc -密度法测定稳定性。

IF 2.4 4区 医学 Q3 CHEMISTRY, MEDICINAL
Mitalben S Parmar, Dimal A Shah, Usmangani K Chhalotiya
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引用次数: 0

摘要

目的:建立富马酸伏诺哌赞的高效薄层色谱分析方法。采用碱性强制降解动力学研究了富马酸伏诺哌赞的降解速率。材料与方法:以硅胶60f254预包被的铝填充薄层色谱板为固定相,甲醇:甲苯:三乙胺(6:4:1 . 0 v/v/v)为流动相。以267nm波长为吸光度模式进行检测。采用HPTLC/MS分析方法检测碱性降解物。结果:富马酸伏诺哌赞的谱带紧凑(Rf值为0.43±0.1)。回归分析表明,在200 ~ 1200 ng/波段范围内,峰面积与浓度呈良好的线性关系(R2 = 0.9996)。富马酸伏诺哌赞标准加样法测定的准确度为99.72% ~ 101.74%。在水解、氧化、热和光解等不同胁迫条件下进行了强制降解稳定性研究。在碱性条件下观察了其降解过程,发现其符合一级降解动力学。用HPTLC-MS分析确定了碱降解物可能的结构。该方法已成功地应用于合成混合物中药物的测定。结论:建立了一种简便、精确、准确的富马酸伏诺哌赞的定量方法。进行了强制降解研究。该方法可用于富马酸伏诺哌赞的质量控制和稳定性样品评价。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Stability indicating HPTLC - densitometric method for estimation of vonoprazan fumarate.

Objectives: High performance thin layer chromatography method was developed and validated for analysis of vonoprazan fumarate. An Alkaline forced degradation kinetic study was performed to find out probable rate of degradation of vonoprazan fumarate.

Material and methods: Aluminum packed TLC plates precoated with silica gel 60 F 254 were used as stationary phase and Methanol: Toluene: triethylamine (6: 4: 0.1 v/v/v) was used as mobile phase. The detection was carried out at 267 nm wavelength as absorbance mode. HPTLC/MS analysis study was performed to detect alkaline degradant.

Results: A compact band (Rf value of 0.43 ± 0.1) was obtained for vonoprazan fumarate. Regression analysis shows a good linear relationship (R2 = 0.9996) between peak area and concentration in the range 200-1200 ng/band. The accuracy determined by standard addition method for vonoprazan fumarate and percentage recovery was found to be 99.72% - 101.74%. Forced degradation stability study was performed under different stress conditions including hydrolytic, oxidative, thermal and photolytic. Degradation was observed under alkaline condition and it was found to follow first order degradation kinetic. The possible structure of base degradants was also determined using HPTLC-MS analysis. The method was successfully applied for the estimation of drug in synthetic mixture.

Conclusion: A New, Simple, precise and accurate method has been developed and validated for the quantification of vonoprazan fumarate. Forced degradation studies were performed. The method can be used for quality control and stability sample evaluation of vonoprazan fumarate.

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来源期刊
CiteScore
6.80
自引率
0.00%
发文量
82
审稿时长
4.5 months
期刊介绍: The aim of Drug Development and Industrial Pharmacy is to publish novel, original, peer-reviewed research manuscripts within relevant topics and research methods related to pharmaceutical research and development, and industrial pharmacy. Research papers must be hypothesis driven and emphasize innovative breakthrough topics in pharmaceutics and drug delivery. The journal will also consider timely critical review papers.
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