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- W2161582054 endingPage "463" @default.
- W2161582054 startingPage "453" @default.
- W2161582054 abstract "U.S. Food and Drug Administration issues certain guidelines for marketing of optically active drugs as some enantiomers racemize into human body, leading to the generation of other antipodes, which may be toxic or ballast to the human beings. Moreover, racemization reduces the administrated dosage concentration as optically active enantiomer converted into its inactive counter part. Therefore, the study of racemization of such type of drugs is an important and urgent need of today. This article describes in vitro and in vivo racemization of optically active drugs. The racemization process of various optically active drugs has been discussed considering the effect of different variables i.e. pH, temperature, concentration of the drug, ionic concentration, etc. Attempts have also been made to discuss the mechanisms of racemization. Besides, efforts have been made to suggest the safe dosages of such type of drugs too." @default.
- W2161582054 created "2016-06-24" @default.
- W2161582054 creator A5001106991 @default.
- W2161582054 creator A5035750388 @default.
- W2161582054 creator A5071872631 @default.
- W2161582054 creator A5084564947 @default.
- W2161582054 creator A5084842689 @default.
- W2161582054 date "2007-03-28" @default.
- W2161582054 modified "2023-10-09" @default.
- W2161582054 title "Role of racemization in optically active drugs development" @default.
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