• 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
  • Record number

    2561522