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To detect the amount of rifampicin in bulk and medicinal dosage formulations, an accurate and costeffective
UV spectrophotometric technique has been developed using the area under the peak to
estimate the presence of rifampicin. This range of wavelengths (300–356 nm) was chosen. The method
showed linearity in the 2–22 μg/mL range, with R2 being2 0.9996. The developed method’s linearity,
detection limit, quantification limit, precision, repeatability, and accuracy were all statistically and
experimentally validated. The suggested methodology can be used for routine quality control analysis
of rifampicin in pure form and in capsule dosage form, as demonstrated by the satisfactory recovery
percentage results. This study explores the str
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