A Validated, Stability-Indicating, Eco-Friendly HPTLC Method for the Determination of Cinnarizine

被引:7
作者
Alqarni, Mohammed H. [1 ]
Shakeel, Faiyaz [2 ]
Foudah, Ahmed I. [1 ]
Aljarba, Tariq M. [1 ]
Mahdi, Wael A. [2 ]
Bar, Fatma M. Abdel [1 ,3 ]
Alshehri, Sultan [4 ]
Alam, Prawez [1 ]
机构
[1] Prince Sattam Bin Abdulaziz Univ, Coll Pharm, Dept Pharmacognosy, Al Kharj 11942, Saudi Arabia
[2] King Saud Univ, Coll Pharm, Dept Pharmaceut, Riyadh 11451, Saudi Arabia
[3] Mansoura Univ, Fac Pharm, Dept Pharmacognosy, Mansoura 35516, Egypt
[4] AlMaarefa Univ, Coll Pharm, Dept Pharmaceut Sci, Ad Diriyah 13713, Saudi Arabia
关键词
AGREE; cinnarizine; eco-friendly HPTLC; stability-indicating; validation; PHARMACEUTICAL-PREPARATIONS; BINARY-MIXTURE; CHROMATOGRAPHIC METHOD; LEAST-SQUARES; DOMPERIDONE; DIMENHYDRINATE; LC; SPECTROPHOTOMETRY; IMPURITIES; PLASMA;
D O I
10.3390/separations10020138
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The eco-friendly high-performance thin-layer chromatographic (HPTLC) approaches for measuring cinnarizine (CIN) are scant in reported databases. As a result, the current work has developed and validated an eco-friendly HPTLC technique for assessing CIN in commercial formulations. The proposed approach was based the use of ethyl alcohol-water (90:10 v/v) as the eco-friendly mobile phase. A wavelength of 197 nm was used to detect CIN. The greenness score of the current approach was measured using the Analytical GREENness (AGREE) approach. The current approach was linear for CIN measurement in 50-800 ng band(-1) range. The current approach for CIN measurement was validated successfully using ICH guidelines and was found to be linear, accurate (% recovery = 99.07-101.29%), precise (% CV = 0.80-0.95%), robust, sensitive (LOD = 16.81 ng band(-1) and LOQ = 50.43 ng band(-1)), specific, selective, stability-indicating, and eco-friendly. The AGREE score for the current approach was calculated to be 0.80, showing an excellent greenness characteristic of the present approach. Under forced degradation conditions, the current approach was successful in separating the CIN degradation product, demonstrating the stability-indicating qualities/selectivity of the present approach. The % assay of CIN in commercial tablet brands A and B was found to be 98.64 and 101.22%, respectively, suggesting the reliability of the present approach in the pharmaceutical analysis of CIN in commercial dosage forms. The obtained findings indicated that CIN in commercial formulations could be routinely determined using the current approach.
引用
收藏
页数:14
相关论文
共 48 条
[1]   Method development and validation for the simultaneous determination of cinnarizine and co-formulated drugs in pharmaceutical preparations by capillary electrophoresis [J].
Abdelal, A. A. ;
Kitagawa, S. ;
Ohtani, H. ;
El-Enany, N. ;
Belal, F. ;
Walash, M. I. .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2008, 46 (03) :491-497
[2]   Determination of the abused intravenously self-administered madness drops (Tropicamide) by liquid chromatography in rat plasma; an application to pharmacokinetic study and greenness profile assessment [J].
Abdelrahman, Maha M. ;
Abdelwahab, Nada S. ;
Hegazy, Maha A. ;
Fares, Michel Y. ;
EL-Sayed, Ghada M. .
MICROCHEMICAL JOURNAL, 2020, 159
[3]   Simultaneous determination of Cinnarizine and Domperidone by area under curve and dual wavelength spectrophotometric methods [J].
Abdelrahman, Maha M. .
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY, 2013, 113 :291-296
[4]   Simple spectrophotometric determination of cinnarizine in its dosage forms [J].
Abdine, H ;
Belal, F ;
Zoman, N .
FARMACO, 2002, 57 (04) :267-271
[5]  
Ahmed A.B., 2017, B FACULTY PHARM CAIR, V55, P163, DOI [10.1016/j.bfopcu.2017.01.003, DOI 10.1016/J.BFOPCU.2017.01.003]
[6]  
Al-Ghani A.M., 2021, CURR PHARM ANAL, V14, P161, DOI [10.22159/ajpcr.2021.v14i3.40384, DOI 10.22159/AJPCR.2021.V14I3.40384]
[7]   Simultaneous Determination of Caffeine and Paracetamol in Commercial Formulations Using Greener Normal-Phase and Reversed-Phase HPTLC Methods: A Contrast of Validation Parameters [J].
Alam, Prawez ;
Shakeel, Faiyaz ;
Ali, Abuzer ;
Alqarni, Mohammed H. ;
Foudah, Ahmed I. ;
Aljarba, Tariq M. ;
Alkholifi, Faisal K. ;
Alshehri, Sultan ;
Ghoneim, Mohammed M. ;
Ali, Amena .
MOLECULES, 2022, 27 (02)
[8]   Quantitative analysis of cabozantinib in pharmaceutical dosage forms using green RP-HPTLC and green NP-HPTLC methods: A comparative evaluation [J].
Alam, Prawez ;
Salem-Bekhit, Mounir M. ;
Al-Joufi, Fakhria A. ;
Alqarni, Mohammed H. ;
Shakeel, Faiyaz .
SUSTAINABLE CHEMISTRY AND PHARMACY, 2021, 21
[9]   NaDES as a green technological approach for the solubility improvement of BCS class II APIs: An insight into the molecular interactions [J].
Albertini, Beatrice ;
Bertoni, Serena ;
Sangiorgi, Stefano ;
Nucci, Giorgia ;
Passerini, Nadia ;
Mezzina, Elisabetta .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2023, 634
[10]   A THEORETICAL BASIS FOR A BIOPHARMACEUTIC DRUG CLASSIFICATION - THE CORRELATION OF IN-VITRO DRUG PRODUCT DISSOLUTION AND IN-VIVO BIOAVAILABILITY [J].
AMIDON, GL ;
LENNERNAS, H ;
SHAH, VP ;
CRISON, JR .
PHARMACEUTICAL RESEARCH, 1995, 12 (03) :413-420