A new stability indicating RP-HPLC method for the estimation of Luliconazole in presence of internal standard

Luliconazole is an antifungal drug used for treating the skin infections. A new stability indicating RP-HPLC method has been developed for the estimation of Luliconazole in presence of internal standard using Zorbox C8 column (150 mm × 4.60 mm i. d. 5µm particle size) with PDA detector in pharmaceutical dosage forms. A mixture of acetonitrile, methanol and phosphate buffer (pH 4.5) was used for the chromatographic separation with a flow rate of 0.8 mL/min. and UV detection at 245 nm. Linearity was observed over the concentration range of 0.5-100 μg/mL with linear regression equation y = 0.0215x - 0.0018 (R2 = 0.9999). Forced degradation studies were performed and the method was validated as per ICH guidelines. The LOD and LOQ were found to be 0.1321 μg/mL and 0.4082 μg/mL respectively. The method was validated and found to be precise, accurate and robust.

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Publication Details

Journal
Research Journal of Pharmacy and Technology
Published
2025-05-07
DOI
https://doi.org/10.52711/0974-360x.2025.00340
Primary Topic
Veterinary medicine and infectious diseases
Type
article
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article

A new stability indicating RP-HPLC method for the estimation of Luliconazole in presence of internal standard

Mukthinuthalapati Mathrusri Annapurna, Priyanka Dehulkar
Research Journal of Pharmacy and Technology
Veterinary medicine and infectious diseases
article

A new stability indicating RP-HPLC method for the estimation of Luliconazole in presence of internal standard

Mukthinuthalapati Mathrusri Annapurna, Priyanka Dehulkar
article en

Abstract

Luliconazole is an antifungal drug used for treating the skin infections. A new stability indicating RP-HPLC method has been developed for the estimation of Luliconazole in presence of internal standard using Zorbox C8 column (150 mm × 4.60 mm i. d. 5µm particle size) with PDA detector in pharmaceutical dosage forms. A mixture of acetonitrile, methanol and phosphate buffer (pH 4.5) was used for the chromatographic separation with a flow rate of 0.8 mL/min. and UV detection at 245 nm. Linearity was observed over the concentration range of 0.5-100 μg/mL with linear regression equation y = 0.0215x - 0.0018 (R2 = 0.9999). Forced degradation studies were performed and the method was validated as per ICH guidelines. The LOD and LOQ were found to be 0.1321 μg/mL and 0.4082 μg/mL respectively. The method was validated and found to be precise, accurate and robust.

Research Journal of Pharmacy and Technology
GITAM University (IN)
Openalex Percentile: Top 87%
Veterinary medicine and infectious diseases
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