An insight of non-steroidal anti-inflammatory drug mefenamic acid: A review
DOI:
https://doi.org/10.30574/gscbps.2019.7.2.0066Keywords:
Anti-inflammatory drugs, Mefenamic acid, Rheumatoid arthritis, Dosage formulationsAbstract
This review focuses on the design, synthesis and pharmacological effects of non-steroidal anti-inflammatory (NSAIDs) mefenamic acid which is an anthranilic acid derivative. Mefenamic acid is a non-steroidal anti-inflammatory drug used to treat pain, including menstrual pain. Exploitation of the prodrug approach has the potential to achieve a reduction of mefenamic acid GI (gastrointestinal) intolerance, enhance its bioavailability, mask its unpleasant sensation and prolong its duration of action. Mefenamic acid, an effective NSAID has always been used as an anti-inflammatory and analgesic agent. A brief note on various marketed formulations of mefenamic acid provides an insight of the potential capability of this drug and its future scope.
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References
Winder CV. (1966). Experimental observations on flufenamic, mefenamic, and meclofenamic acids. I. Pharmacology. Annals of Physical and Rehabilitation Medicine, Suppl. 7-16.
Sriamomsak P, Limmatvapirat S, Piriyaprasarth S, Mansukmanee P and Huang Z. (2015). A new emulsifying formulation of mefenamic acid with enhanced drug dissolution. Asian Journal of Pharmaceutical Sciences, 10(2), 121-127.
Patel KC and Pramanik S. (2014). Formulation and characterization of Mefenamic acid loaded polymeric nanoparticles. World Journal of Pharmacy and Pharmaceutical Sciences, 3(6), 1391-1405.
Shah K, Shrivastava SK and Mishra P. (2014). Formulation and evaluation of suspensions: Mefenamic acid prodrugs. Pakistan Journal of Pharmaceutical Sciences, 27(4), 917-923.
Ansel HC and Popovish NK (1995). Pharmaceutical dosage forms and drug delivery system, sixth edition. BI Waverly Pvt. Ltd., New Delhi, India, 253-254.
Shah K, Shrivastava SK and Mishra P. (2013). Evaluation of mefenamic acid mutual prodrugs. Medicinal Chemical Research, 22(1), 70-77.
Usman M, Ali I, Bibi H, Iqbal J and Iqbal K. (2012) Preparation and evaluation of controlled release tablets containing Mefenamic acid. Journal of Clinical and Experimental Pharmacolology, 2(1), 107.
Kumar L and Verma R. (2010). In vitro evaluation of topical gel prepared using natural polymer. International Journal of Drug Delivery 2, 58-63.
Shah SU, Shah KU, Rehman A and Khan GM. (2011). Investigating the in vitro drug release kinetics from controlled release diclofenac potassium-ethocel matrix tablets and the influence of co-excipients on drug release patterns. Pakistan Journal of Pharmaceutical Sciences, 24(2), 183-192.
Khullar R, Kumar D, Seth N and Saini S. (2012). Formulation and evaluation of mefenamic acid emulgel for topical delivery. Saudi Pharmaceutical Journal, 20(1), 63-67.
Steiger M. (2004).Topical emulsion, gel composition comprising diclofenac sodium. European Patent Specification no. WO/2004/017998).
Mohamed MI. (2004). Optimization of chlorphenesinemulgel formulation. AAPS Journal, 6 (3), 81-87.
Gupta A, Mishra AK, Singh AK, Gupta V and Bansal P. (2010). Formulation and evaluation of topical gel of diclofenac sodium using different polymers. Drug Invention Today, 2(5), 250-253.
Stanos, SP. (2007). Topical agents for the management of musculoskeletal pain. Journal of Pain Symptom Management, 33(3), 342-355.
Jain A, Deveda P, Vyas N, Chauhan J, Khambete H and Jain S. (2011). Development of antifungal emulsion based gel for topical fungal infection(s). International Journal of Pharmaceutical Research and Development, 2 (12), 18-25.
Shuhaib B and Suja C. (2019).Studies on formulation and characterization of topical emulgel containing microsponges of mefenamic acid. European Journal of Pharmaceutical and Medical Research, 6(1), 314-326.
Embil K and Nacht S. (1996). The microsponge delivery system (MDS): a topical delivery system with reduced irritancy in-cooperating multiple triggering mechanism for the release of actives. Journal of Microencapsulation, 13(5): 575-588.
Comoglo T, Gonul N and Baykara T. (2003). Preparation and in vitro evaluation of modified release ketoprofen microsponges. Farmaco, 58(2), 101-106.
Ali N, Mitra J, Mohammad-Reza S and Siavoosh D. (2005). The effect of formulation type on the release of benzoyl peroxide from microsponges. Iranian Journal of Pharmaceutical Sciences, 1(3), 131-142.
Mahaparale PR, Nikam SA and Chavan MS. (2018). Development and evaluation of terbinafine hydrochloride polymeric microsponges for topical drug delivery. Indian Journal of Pharmaceutical Sciences, 80(6), 1086-1092.
Mandava SS and Thavva V. (2014). Novel approach: microsponge drug delivery system. International Journal of Pharmaceutical Sciences and Research, 3(4), 967-980.
Swetha A, Rao GM, Ramana VK, Niyaz BB and Reddy KV. (2011). Formulation and in vitro evaluation of etodolac entrapped in microsponge based drug delivery system. International Journal of Pharmacy, 1(2) 73-80.
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