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LC/DAD 和 MS/MS 法测定达格列净的化学稳定性。

Determination of the Chemical Stability of Dapagliflozin by LC/DAD and MS/MS Methods.

机构信息

Department of Pharmacy, Faculty of Pharmacy, Universidad de Concepción, Concepción 4030000, Chile.

出版信息

J Chromatogr Sci. 2022 Oct 3;60(8):741-749. doi: 10.1093/chromsci/bmab120.

Abstract

A simple and fast stability-indicating liquid chromatographic method with diode array detection (DAD) was developed and validated for the determination of dapagliflozin (DAPA) in bulk and tablets, in the presence of its major degradation products (DP). The drug was subjected to hydrolytic, oxidative, photolytic, thermal and humidity/thermal stress conditions, showing significant degradation under humidity/thermal with the formation of two DP, which were preliminarily identified by liquid chromatography with diode array detector coupled with electrospray ionization-tandem mass spectrometry (HPLC-DAD-ESI-MS/MS). Chromatographic separation of dapagliflozin and its DP was achieved with a core-shell RP-18 column, using acetonitrile and water as mobile phase in isocratic elution mode. The described method was linear over a range of 50-150 μg/mL. For precision, the relative standard deviation (RSD) was <1.3%, the recovery was 99.64-100.11%, and the assay demonstrated adequate selectivity. The degradation kinetics of dapagliflozin was evaluated corresponding to first-order under thermal and humidity/thermal stress conditions. Dapagliflozin was well resolved from its drug products showing the power of stability-indicating of the method. The results showed that the proposed method was found to be suitable for routine analysis, quantitative determination and the stability study of dapagliflozin in pharmaceutical samples.

摘要

建立并验证了一种简单、快速的含二极管阵列检测的稳定性指示液相色谱法,用于在存在主要降解产物(DP)的情况下测定达格列净(DAPA)的含量。该药物分别进行了水解、氧化、光解、热和湿度/热稳定性试验,在湿度/热条件下发生显著降解,形成两种 DP,通过二极管阵列检测液相色谱-电喷雾串联质谱(HPLC-DAD-ESI-MS/MS)初步鉴定。达格列净及其 DP 的色谱分离在核壳 RP-18 柱上实现,采用乙腈和水作为流动相,以等度洗脱模式。该方法在 50-150μg/mL 范围内呈线性。精密度方面,相对标准偏差(RSD)<1.3%,回收率为 99.64%-100.11%,且方法具有足够的选择性。达格列净在热和湿度/热稳定性条件下的降解动力学符合一级动力学。该方法能很好地区分达格列净与其制剂,表明该方法具有较强的专属性。结果表明,该方法适用于药品中达格列净的常规分析、定量测定和稳定性研究。

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