Green analytical quality by design RP-HPLC technique with fluorimetric detection for simultaneous assay of cinnarizine and dompridone

被引:0
|
作者
Barakat, Neamat T. [1 ]
El-Brashy, Amina M. [1 ]
Fathy, Mona E. [1 ]
机构
[1] Mansoura Univ, Fac Pharm, Dept Pharmaceut Analyt Chem, Mansoura 35516, Egypt
来源
ROYAL SOCIETY OPEN SCIENCE | 2024年 / 11卷 / 07期
关键词
cinnarizine; domperidone; full factorial design; high-performance liquid chromatography; greenness; co-formulated tablets; PHARMACEUTICAL-PREPARATIONS; SPECTROPHOTOMETRIC METHODS; DOMPERIDONE; FORMULATIONS; VALIDATION;
D O I
10.1098/rsos.240829
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 23 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-1 was applied during the analysis with fluorescence detection at lambda ex 283 nm/lambda em 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 mu g ml-1 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.
引用
收藏
页数:19
相关论文
共 50 条
  • [1] Analytical Quality by Design Approach in RP-HPLC Method Development for the Assay of Etofenamate in Dosage Forms
    Peraman, R.
    Bhadraya, K.
    Reddy, Y. Padmanabha
    Reddy, C. Surayaprakash
    Lokesh, T.
    INDIAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2015, 77 (06) : 751 - 757
  • [2] A Novel Analytical Method for Simultaneous Quantification of Silodosin and Tadalafil by RP-HPLC
    Gupta, Ajay
    Mishra, S. K.
    JOURNAL OF PHARMACEUTICAL RESEARCH INTERNATIONAL, 2021, 33 (39B) : 193 - 202
  • [3] Exploring Analytical Quality by Design (AQbD) Enabled RP-HPLC Method for Carvedilol
    Randive, Krantisinha Hanumant
    Maste, Meenaxi Maruti
    Kempwade, Amolkumar Ashok
    INDIAN JOURNAL OF PHARMACEUTICAL EDUCATION AND RESEARCH, 2024, 58 (02) : 651 - 660
  • [4] Environmental benign RP-HPLC method for the simultaneous estimation of anti-hypertensive drugs using analytical quality by design
    Dharuman, Naveenarani
    Lakshmi, Karunanidhi Santhana
    Krishnan, Manikandan
    GREEN CHEMISTRY LETTERS AND REVIEWS, 2023, 16 (01)
  • [5] Analytical Quality by Design Approach for Simultaneous Determination of Phytomarkers Orientin, Quercetin and Piperine in Nilaveembu Kudineer by RP-HPLC Method
    Sivagami, B.
    Sailaja, B.
    ORIENTAL JOURNAL OF CHEMISTRY, 2025, 41 (01) : 293 - 302
  • [6] Analytical quality by design approach to RP-HPLC method development and validation for simultaneous estimation of esomeprazole and naproxen in modified-release dosage form
    Urmi, Khandokar Farjana
    Nawaz, Md. Saddam
    Islam, S. M. Ashraful
    FUTURE JOURNAL OF PHARMACEUTICAL SCIENCES, 2022, 8 (01)
  • [7] Green RP-HPLC methods for assay and related substances in rivaroxaban tablets
    Nakov, Natalija
    Anastasova, Liljana
    Gjorgievska, Marija Zafirova
    Acevska, Jelena
    Brezovska, Katerina
    Petkovska, Rumenka
    Dimitrovska, Aneta
    ACTA CHROMATOGRAPHICA, 2024, 36 (04) : 371 - 382
  • [8] Deduction of the operable design space of RP-HPLC technique for the simultaneous estimation of metformin, pioglitazone, and glimepiride
    Marie, Aya A.
    Hammad, Sherin F.
    Salim, Mohamed M.
    Elkhodary, Mahmoud M.
    Kamal, Amira H.
    SCIENTIFIC REPORTS, 2023, 13 (01)
  • [9] Stability Indicating Assay for the Determination of Bilastine in Bulk Drug and Method Development Validation by RP-HPLC Using Analytical Quality by Design Approaches
    Nayak, Anjali
    Alwin, R. Maria Danish
    Sangeetha, G.
    Sowmya, C. Y.
    Reddy, Yashwanth V.
    Dang, Raman
    INDIAN JOURNAL OF PHARMACEUTICAL EDUCATION AND RESEARCH, 2024, 58 (02) : s582 - s590
  • [10] Validated Stability Indicating and Assay Method Development of Linagliptin in Formulation by RP-HPLC Using Quality by Design
    Ganorkar, Anvesha, V
    Askarkar, Sonali S.
    Gupta, Krishna R.
    Umekar, Milind J.
    ORBITAL-THE ELECTRONIC JOURNAL OF CHEMISTRY, 2020, 12 (02): : 48 - 61