Key result
Advanced analytical methods enable quality control and standardization across 15 recently approved cardiovascular drugs.
Why the study?
Spectrophotometric, chromatographic, and bioanalysis methods are important for quality control and standardization of recently approved cardiovascular drugs but have not been comprehensively reviewed.
Analytical methods such as spectrophotometry and chromatography are essential for the quality control and standardization of recently approved cardiovascular drugs.
Supports QC standardization of recent CV drugs; extends analytical literature but leaves optimal methods open.
Background Heart Study has been operating for more than 40 years, and throughout that time it has found a number of risk variables that interact negatively to have an overall negative effect on cardiovascular disease (CVD) with an estimated 17.9 million deaths per year, CVD is the world's leading cause of death. Main body In the current study, we present spectrophotometric, chromatographic analysis and bioanalysis methods for qualitative and quantitative evaluation of 15 drugs, including small and large molecules, that the U.S. FDA approved between 2015 and June 2020 to treat CVD’s and in the current review work, they were presented. Short conclusion The review's conclusion is that spectroscopic, chromatographic and bioanalysis methods play important role in quality control and standardization of recently approved drugs from 2015 to 2020 for treating CVD’s in its bulk, pharmaceutical dosage form, synthetic mixture or human/rat plasma.
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Gharge et al. (2023) conducted a review in Cardiovascular diseases. Analytical methods (spectrophotometric, chromatographic, and bioanalysis) was evaluated. Spectroscopic, chromatographic, and bioanalysis methods play an important role in the quality control and standardization of 15 recently approved cardiovascular drugs from 2015 to 2020.
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