This phase evaluates to develop accurate, plain, UV spectrophotometric method which is empty extraction techniques, and smaller time and highly delicate technique. This study illustrates a simple, accurate, exact and cost effective UV-visible spectrophotometric plan for the estimation of Azelaic acid in pure and drug formulations. The analytically useful working groups in Azelaic acid have not been adequately exploited for designing appropriate, visible spectrophotometric methods accordingly still offer a scope to expand more visible spectrophotometric methods accompanying better sensitivity, selectivity, accuracy and accuracy. The method is established the measurement of absorbance of Azelaic acid solution in Phosphate safeguard pH 6.8 at 204nm in the wavelength range of 200-400nm. When using sure media and concentration ranges of 10–50µ g/ml, the process complies with Beer’s Lambert’s standard. Calculations were still performed for the slope, intercept, and equivalence coefficient. The presence of coarse excipients in tablets did not impair the process, according to the results of the percentage improvement investigation. In accordance with the approvals set forth by the Worldwide Conference on Harmonization (ICH), determinants such as extent of object, precision, accuracy, and feeling studies, which includes limit of discovery and limit of quantitation, were examined. The proposed form was found to be natural, accurate, precise and expeditious for the routine determination of Azelaic acid in pure and drug formulation.
Author(s) Details:
T. V. Kadam,
Department
of Pharmaceutics, KVN Naik SPS's Institute of Pharmaceutical Education and
Research, Canada Corner, Nashik, India.
A.
B. Darekar,
Department
of Pharmaceutics, KVN Naik SPS's Institute of Pharmaceutical Education and
Research, Canada Corner, Nashik, India.
Please see the link here: https://stm.bookpi.org/ACPR-V3/article/view/12769
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