Title of article
Prodrugs of NSAIDs: A Review
Author/Authors
Shah, Kamal Institute of Pharmaceutical Research - GLA University, Mathura, U.P.- 281406, India , Gupta, Jeetendra K. Institute of Pharmaceutical Research - GLA University, Mathura, U.P.- 281406, India , Chauhan, Nagendra S. Drugs Testing Laboratory Avam Anusandhan Kendra,Raipur (CG),India , Upmanyu, Neeraj School of Pharmacy & Research - Peoples University, Bhopal, M.P.- 462037, India , Shrivastava, Sushant K. Department of Pharmaceutics - Institute of Technology - Banaras Hindu University, Varanasi U.P.- 221005, India , Mishra, Pradeep Institute of Pharmaceutical Research - GLA University, Mathura, U.P.- 281406, India
Pages
50
From page
146
To page
195
Abstract
Intoroduction:
Prodrug approach deals with chemical biotransformation or enzymatic conversion or involves inactive or less active bio-reversible derivatives of active drug molecules. They have to pass through enzymatic or chemical biotransformation before eliciting their pharmacological action.
Methods & Materials:
The two different pharmacophores combine to give synergistic activity or may help in targeting the active drug to its target. Prodrug super seeds the problems of prodrug designing, for example solubility enhancement, bioavailability enhancement, chemical stability improvement, presystemic metabolism, site specific delivery, toxicity masking, improving patient acceptance, or eradicating undesirable adverse effects.
Results:
As an outcome the search for a prodrug or mutual prodrug with reduced toxicity has continued during recent years. This present review emphasizes the common help to revamp physiochemical, pharmaceutical and therapeutic effectiveness of drugs.
Conclusion:
This gives the researcher a common platform where they can find prodrugs of commonly used NSAIDs to overcome the gastrointestinal toxicity (irritation, ulcergenocity and bleeding).
Farsi abstract
فاقد چكيده فارسي
Keywords
Prodrug , Synergistic , NSAIDs , Ulcergenocity , Gastrointestinal toxicity , Enzymatic attack
Journal title
Open Medicinal Chemistry Journal
Serial Year
2017
Full Text URL
Record number
2561522
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