Abstract
Introduction: Cyclooxygenase (COX), in literature, known as prostaglandin-endoperoxide
synthase (PTGS), is an enzyme that is responsible for the formation of prostanoids, including thromboxane
and prostaglandins from arachidonic acid. COX-1 does housekeeping activity, whereas COX-
2 induces inflammation. Continuous rise in COX-2 gives birth to chronic pain-associated disorders,
i.e., arthritis, cardiovascular complications, macular degeneration, cancer, and neurodegenerative disorders.
Despite their potent anti-inflammatory effects, the detrimental effects of COX-2 inhibitors coexist
in healthy tissues. Non-preferential NSAIDs cause gastrointestinal discomfort, whereas selective
COX-2 inhibitors exert higher cardiovascular risk and renal impairment on chronic use.
Methods: This review paper covers key patents published between 2012-2022 on NSAIDs and coxibs,
highlighting their importance, mechanism of action, and patents related to formulation and drug combination.
So far, several drug combinations with NSAIDS have been used in clinical trials to treat
chronic pain besides combating the side effects.
Conclusion: Emphasis has been given on the formulation, drug combination, administration routesmodification,
and alternative routes, i.e., parenteral, topical, and ocular DEPOT, improving its riskbenefit
ratio of NSAIDs to improvise their therapeutic availability and minimize the adverse effects.
Considering the wide area of research on COX-2 and ongoing studies, and future scope of view for
the better use of the NSAIDs in treating debilitating disease-associated algesia.
Keywords:
Selective COX-2 inhibitors, formulations, prostaglandins, tyrosine kinase, epithelial to mesenchymal transition (EMT), combination therapy, novel drug delivery design, NSAIDs.
Graphical Abstract
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