Barakat Neamat T, El-Brashy Amina M, Fathy Mona E
Department of Pharmaceutical Analytical Chemistry, Faculty of Pharmacy, Mansoura University, Mansoura 35516, Egypt.
R Soc Open Sci. 2024 Jul 17;11(7):240829. doi: 10.1098/rsos.240829. eCollection 2024 Jul.
A green and sensitive factorial design-assisted reversed-phase high-performance liquid chromatography (RP-HPLC) approach with fluorimetric detection has been developed for simultaneous determination of cinnarizine and domperidone in pure materials, commercial single and combined tablets. Both drugs are co-formulated in one dosage form and are commonly used for the effective treatment of motion sickness in the ratio of 4 : 3 for cinnarizine and domperidone, respectively. To achieve the developed method's best performance and reliability, a 2 full factorial design was applied during the optimization of chromatographic conditions. Subsequently, isocratic elution on a C18 column with a mobile phase mixture of methanol and 0.02 M potassium dihydrogen phosphate buffer (85 : 15 v/v, pH 3.0) was performed to achieve the best separation. Moreover, the flow rate of 0.8 ml min was applied during the analysis with fluorescence detection at λ 283 nm/λ 324 nm. The elution process was time effective; it consumed less than 6 min for a complete run as retention time for cinnarizine and domperidone, was 4.5 and 3.5, respectively. Good linearity of the proposed method was achieved within the concentration ranges of 0.2-4.5 and 0.4-5.0 µg ml for domperidone and cinnarizine, respectively. The suggested approach was carefully validated according to the International Council for Harmonization (ICH) guidelines. Moreover, green analytical procedure index (GAPI), national environmental methods index (NEMI), analytical greenness (AGREE) and analytical eco-scale methods were applied to assess and confirm method greenness.
已开发出一种绿色且灵敏的析因设计辅助反相高效液相色谱(RP-HPLC)方法,并采用荧光检测,用于同时测定原料药、市售单方和复方片剂中的桂利嗪和多潘立酮。这两种药物共同制成一种剂型,通常以桂利嗪与多潘立酮4∶3的比例有效治疗晕动病。为实现所开发方法的最佳性能和可靠性,在色谱条件优化过程中应用了二水平全因子设计。随后,在C18柱上采用甲醇和0.02 M磷酸二氢钾缓冲液(85∶15 v/v,pH 3.0)的流动相混合物进行等度洗脱,以实现最佳分离。此外,分析过程中流速为0.8 ml/min,荧光检测波长为λ 283 nm/λ 324 nm。洗脱过程省时;一次完整运行耗时不到6分钟,因为桂利嗪和多潘立酮的保留时间分别为4.5分钟和3.5分钟。所提出方法在多潘立酮浓度范围为0.2 - 4.5 μg/ml、桂利嗪浓度范围为0.4 - 5.0 μg/ml内具有良好的线性。该建议方法已按照国际协调理事会(ICH)指南进行了仔细验证。此外,还应用了绿色分析程序指数(GAPI)、国家环境方法指数(NEMI)、分析绿色度(AGREE)和分析生态规模方法来评估和确认方法的绿色度。