Development and validation of UV spectrophotometric method for orbifloxacin assay and dissolution studies

Abstract

New, simple and cost effective UV-spectrophotometric method was developed for the estimation of orbifloxacin in pharmaceutical formulation. Orbifloxacin was estimated at 290 nm in 0.5 M hydrochloric acid. Linearity range was found to be 1.0-6.0 μg mL-1. The method was tested and validated for various parameters according to main guidelines. The proposed method was successfully applied for the determination of orbifloxacin in tablets. The results demonstrated that the procedure is accurate, precise and reproducible, while being simple, economical and less time consuming. It can be suitably applied for the estimation of orbifloxacin in routine quality control and dissolution studies.

Keywords

• Medicamentos/controle de qualidade
• Medicamentos/dissolução
• Método analítico
• Orbifloxacino/determinação
• Espectrofotometria na região do UV/controle de qualidade/validação