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A LC-MS/MS method for simultaneous estimation of a novel anti-diabetic combination of saxagliptin and dapagliflozin using a polarity switch approach: application to in vivo rat pharmacokinetic study

机译:LC-MS / MS方法通过极性转换方法同时评估沙格列汀和达格列净的新型抗糖尿病组合:在体内大鼠药代动力学研究中的应用

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Diabetes and its associated concerns constitute a major growing health issue in modern society. In the current work we report a highly sensitive, selective and specific LC-MS/MS method for the estimation of a novel anti-diabetic combination of saxagliptin (SAX) and dapagliflozin (DAP) in rat plasma. An Agilent Eclipse Plus C18 column (150 mm × 4.6 mm, 3.6 μm) with gradient elution using 0.01% ammonia solution and acetonitrile as the mobile phase was used for the chromatographic separation. The ion transitions were quantified in positive and negative polarity using a polarity switching approach. A solid phase extraction process was used as the sample preparation approach. The method provided good linearity over the range of 0.2–80 ng mL?1 for SAX and 5–2000 ng mL?1 for DAP. The method was validated according to US FDA bioanalytical guidelines and successfully applied in a preclinical study for simultaneous quantification of SAX and DAP in SD rats. The developed analytical method can also be utilized for the future clinical applications of both the drugs in combined dosage form.
机译:糖尿病及其相关问题构成了现代社会日益严重的健康问题。在当前的工作中,我们报告了一种高灵敏度,选择性和特异性的LC-MS / MS方法,用于估计大鼠血浆中沙格列汀(SAX)和达格列净(DAP)的新型抗糖尿病组合。使用0.01%氨溶液和乙腈作为流动相进行梯度洗脱的Agilent Eclipse Plus C18色谱柱(150 mm×4.6 mm,3.6μm)用于色谱分离。使用极性切换方法以正负极性定量离子迁移。固相萃取过程用作样品制备方法。该方法在SAX的0.2–80 ng mL?1和DAP的5–2000 ng mL?1范围内提供了良好的线性。该方法已根据美国FDA的生物分析指南进行了验证,并成功地应用于临床前研究中,同时定量SD大鼠中的SAX和DAP。所开发的分析方法还可用于两种药物在组合剂型中的未来临床应用。

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