Abstract
We have developed methods for the pharmaceutical analysis of the new domestic antiarrhythmic drug cardiocyclide in a solid dosage form (capsules). The main pharmacopoeial quality tests were carried out. The content of impurities in capsules was determined by thin-layer chromatography. UV spectrophotometry and gradient high-performance liquid chromatography were used for simultaneous assay, purity check, and quantitative analysis of the drug. The pharmacopoeial “Dissolution” test was carried out using UV spectrophotometry.
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