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Development and validation of different spectrophotometric and chromatographic methods for determination of clotrimazole and hydrocortisone in a topical cream
Michel Yousry Fares (1,*)
, Maha Mohamed Abdelrahman (2) , Hamdy Mohamed Abdel-Rahman (3) , Nada Sayed Abdelwahab (4) (1) Pharmaceutical Chemistry Department, Faculty of Pharmacy, Nahda University, Sharq El-Nile, 62511 Beni-Suef, Egypt
(2) Analytical Chemistry Department, Faculty of Pharmacy, Beni-Suef University, 62514 Beni-Suef, Egypt
(3) Medicinal Chemistry Department, Faculty of Pharmacy, Assiut University, 71526 Assiut, Egypt
(4) Analytical Chemistry Department, Faculty of Pharmacy, Beni-Suef University, 62514 Beni-Suef, Egypt
(*) Corresponding Author
Received: 31 Aug 2017 | Revised: 07 Oct 2017 | Accepted: 08 Oct 2017 | Published: 31 Dec 2017 | Issue Date: December 2017
Abstract
In this study, we developed and validated different spectrophotometric and chromatographic methods for determination of clotrimazole (CLO) and hydrocortisone (HDC) in their combined dosage form. The developed spectrophotometric methods were first derivative spectrophotometry (1D) by measuring the peak amplitude at 247.4 and 236.2 nm for CLO and HDC, respectively, second derivative of ratio spectra (2DD) at 225.4 nm for CLO and 269 nm for HDC, dual wavelength spectrophotometry (DW) by measuring absorbance difference between 225.4 and 264 nm for CLO and between 228 and 247 nm for HDC determination, advanced absorbance subtraction method (AAS) between 225.4 and 264 nm and mean centering of ratio spectra (MCR) spectrophotometric method in the range of 232-265 nm. On the other hand, the proposed chromatographic method was Ultra Performance Liquid Chromatography method (UPLC) using acetonitrile:water (50:50, v:v) as a mobile phase and the peaks were detected at 228 nm. All these methods were successfully applied to determine the two studied drugs in pure forms; laboratory prepared mixtures and combined dosage form. Methods validations were carried out regarding linearity, accuracy, precision and selectivity. The spectrophotometric methods exhibited a linear dynamic range over 5-40 and 5-45 µg/mL for CLO and HDC, respectively, and over 3-35 and 5-50 µg/mL for UPLC method. Sensitive and selective spectrophotometric and UPLC methods for the determination of clotrimazole and hydrocortisone in their topical formulation were successfully developed and validated. The developed methods were statistically confirmed to be accurate, precise and reproducible.
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DOI: 10.5155/eurjchem.8.4.371-377.1646
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Citations
[1]. Maha M. Abdelrahman, Selvia M. Adly, Nourudin W. Ali, Nada S. Abdelwahab
Development and Validation of Different Spectrophotometric and High-Performance Thin-Layer Chromatographic Methods for the Determination of Fosinopril Sodium, Hydrochlorothiazide, and Chlorothiazide as Hydrochlorothiazide Impurity
JPC - Journal of Planar Chromatography - Modern TLC 32(5), 411, 2019
DOI: 10.1556/1006.2019.32.5.9
[2]. Mahmoud Mohamed Abbas, Amira Mabrouk El-Kosasy, Lobna Abd El-Aziz Hussein, Nancy Magdy Hanna
Universal procedures for spectrophotometric determination of anticoccidial drugs; application to multi-ingredient veterinary formulation and computational investigations for multivariate analysis
European Journal of Chemistry 12(4), 368, 2021
DOI: 10.5155/eurjchem.12.4.368-376.2144
[3]. Kanaka Parvathi Kannaiah, Abimanyu Sugumaran, Hemanth Kumar Chanduluru
Simultaneous estimation of crotamiton and hydrocortisone by RP-UPLC using green analytical principles embedded analytical quality by design (AQbD) method
Microchemical Journal 184, 108166, 2023
DOI: 10.1016/j.microc.2022.108166
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DOI Link: https://doi.org/10.5155/eurjchem.8.4.371-377.1646
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European Journal of Chemistry 2017, 8(4), 371-377 | doi: https://doi.org/10.5155/eurjchem.8.4.371-377.1646 | Get rights and content
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