Department of Pharmaceutical Chemistry, Amity Institute of Pharmacy, Lucknow, Amity University Uttar Pradesh, Noida, India.
Amity Institute of Pharmacy, Amity University Maharashtra, Panvel, Mumbai, India.
Biomed Chromatogr. 2024 Nov;38(11):e5994. doi: 10.1002/bmc.5994. Epub 2024 Sep 3.
The present study utilized Analytical Quality by Design (AQbD) approach to develop a stability-indicating high-performance liquid chromatography (HPLC) method for estimating evogliptin tartrate using design expert software. The key parameters were methodically optimized, contours were plotted, and stability was evaluated using various forced degradation conditions. Using an Agilent HPLC system with a photo diode array (PDA) detector along with Fortis C18 column (250 × 4.6 mm, 5 μm) effectively separated the drug from its degradants. The mobile phase used was methanol: water (pH adjusted to 3.0, 76:24; v/v) at 0.8 mL/min flow rate. Evogliptin was eluted at 2.98 min, at a detection wavelength of 267 nm. The proposed method was found to be specific, precise, linear and robust. The drug was sensitive to acidic, basic, oxidative, thermal, and photodegradation resolving six degradation products. Thus, the developed AQbD-based stability-indicating HPLC method is applicable in analyzing evogliptin in bulk, tablet dosage form and stability samples.
本研究采用分析质量源于设计(AQbD)方法,使用设计专家软件开发了一种用于估算依格列汀酒石酸盐的稳定性指示高效液相色谱(HPLC)方法。使用各种强制降解条件,系统地优化了关键参数、绘制了等高线,并对稳定性进行了评估。使用配备光电二极管阵列(PDA)检测器的安捷伦 HPLC 系统和 Fortis C18 柱(250×4.6mm,5μm)有效地将药物与其降解产物分离。所用的流动相为甲醇:水(pH 值调整至 3.0,76:24;v/v),流速为 0.8mL/min。依格列汀在 2.98 分钟时洗脱,检测波长为 267nm。该方法被证明具有专属性、精确性、线性和稳健性。该药物对酸性、碱性、氧化、热和光降解敏感,可解析六种降解产物。因此,开发的基于 AQbD 的稳定性指示 HPLC 方法适用于分析原料药、片剂制剂和稳定性样品中的依格列汀。