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WORLD JOURNAL OF PHARMACOLOGICAL RESEARCH AND TECHNOLOGY A Review on Bioavailability Enhancement
2014
WJPRT
unpublished
The U.S Food and Drug administration defines bioavailability as "The rate and extent to which the active drug ingredient or therapeutic moiety is absorbed from a drug product and become available at the site of drug action." Many studies illustrate that difference in manufacturing procedures, as well as the composition of the dosage form; can affect the bioavailability of a drug product. The importance of bioavailability is related to the drug action. A pharmacological response occur when drug
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