Formulation and Evaluation of NabumetoneEmulgel for Topical Drug Delivery
Rashmi B Surekar, Twarita D Deshpande, Onkar V Jadhav, Anuj J Shinde
Abstract:
Nabumetone is commonly used to relieve pain and inflammation, especially in conditions like arthritis. However, its use through oral administration poses certain difficulties. These include its poor solubility in water, which limits its absorption, and a tendency to irritate the gastrointestinal tract, which may lead to discomfort or other side effects in patients. To overcome these limitations, the present investigation focused on developing a topical emulgel formulation. Carbopol 934 and Hydroxypropyl Methylcellulose K15M (HPMC K15M) were employed as gelling agents, and their concentrations were systematically varied to assess their influence on the drug release profile. Emulsion systems were systematically developed using light liquid paraffin as the oil component, Tween 80 as the primary surfactant, and an appropriate co-surfactant. To identify the optimal emulsification zone, pseudoternary phase diagrams were constructed and analyzed. The final emulgel was prepared by incorporating the optimized emulsion into gel bases containing different concentrations of the gelling agents (1.5%, 2.0%, and 2.5%). Comprehensive evaluation of the formulations indicated that the optimized batch, F2, exhibited favorable physicochemical stability in terms of pH, viscosity, and cumulative drug release percentage under ambient and accelerated storage conditions.
Keywords: Nabumetone, Emulgel, Topical Delivery, Rheumatoid Arthritis, Emulsion.
Refernces:
[1] Verma A, Singh S, Kaur R, Jain KU. (2013): Topical gels as drug delivery systems: a review. International Journal of Pharmaceutical Sciences Review and Research, 2(3): 374–382.
[2] Arti P, Panchaxari D, Anand G, Vinayak M. (2015): Formulation and characterization of meloxicam loaded emulgel for topical application. International Journal of Pharmaceutical Sciences, 7(11): 216–222.
[3] Arora R, Khan R, Ojha A, Upadhyaya K, Chopra H. (2017): Emulgel: a novel approach for hydrophobic drugs. International Journal of Pharmacy and Biological Sciences, 7(3): 43–60.
[4] Singla V, Saini S, Joshi B, Rana AC. (2012): Emulgel: a new platform for topical drug delivery. International Journal of Pharma and Bio Sciences, 3(1): 485–498.
[5] Benson Heather AE. (2005): Transdermal drug delivery: penetration enhancement techniques. Journal of Current Drug Delivery, 2(1): 23–33.
[6] Yadav SK, Mishra MK, Tiwari A, Shukla A. (2016): Emulgel: a new approach for enhanced topical drug delivery. International Journal of Current Pharmaceutical Research, 9(1): 15–19.
[7] Singh P, Bala R, Seth N, Kalia S. (2014): Emulgel: a novel approach to bioavailability enhancement. International Journal of Recent Advances in Pharmaceutical Research, 4(2): 35–47.
[8] Kute BS, Saudagar BR. (2013): Emulsified gel: a novel approach for delivery of hydrophobic drugs: an overview. Journal of Advanced Pharmacy Education & Research, 3(4): 368–376.
[9] Muzaffar F, Singh UK, Chauhan L. (2013): Review on microemulsion as futuristic drug delivery. International Journal of Pharmacy and Pharmaceutical Sciences, 5(3): 39–53.
[10] Lakshmi J, Kumar BA, Gupta S. (2013): Investigation of microemulsion as a potential carrier for advanced transdermal delivery: an overview. International Journal of Pharmaceutical Sciences Review and Research, 20(2): 51–59.
[11] Chittodiya P, Singh Tomar R, Ramchandan U, Manocha N. (2013): Topical gel – a review. International Journal of Pharmaceutical and Biological Archives, 4(4): 606–613.
[12] Kapoor D, Vyas RB, Lad C, Patel M, Lal B, Parmar R. (2014): Formulation, development and characterization of emulgel of NSAIDs. The Pharmaceutical and Chemical Journal, 1(3): 9–16.
[13] Sah AK, Jain SK, Pandey RS. (2011): Microemulsion-based hydrogel formulation of methoxsalen for the effective treatment of psoriasis. Asian Journal of Pharmaceutical and Clinical Research, 4(4): 140–145.
[14] Elmataeeshy ME, Sokar MS, Bahey-El-Din M, Shaker DS. (2018): Enhanced transdermal permeability of terbinafine through novel nanoemulgel formulation; development, in vitro and in vivo characterization. Future Journal of Pharmaceutical Sciences, 4(1): 18–28.
[15] Abd-allah FI, Dawaba HM, Ahmed AMS. (2010): Development of a microemulsion-based formulation to improve the availability of poorly water-soluble drugs. Drug Discovery and Therapy, 4(4): 257–266.
[16] Kaur LP, Guleri TK. (2013): Topical gel: a recent approach for novel drug delivery. Asian Journal of Biomedical and Pharmaceutical Sciences, 3(Fig 1): 1–5.
[17] Kumar KJR, Muralidharan S, Dhanaraj SA. (2012): Anti-fungal activity of microemulsion-based fluconazole gel for onychomycosis against Aspergillusniger. International Journal of Pharmacy and Pharmaceutical Sciences, 5(1): 3–9.
[18] Perioli L, Pagano C, Mazzitelli S, Rossi C, Nastruzzi C. (2008): Rheological and functional characterization of new anti-inflammatory delivery systems designed for buccal administration. International Journal of Pharmaceutics, 356(1–2): 19–28.
[19] Shahin M, Abdel Hady S, Hammad M, Mortada N. (2011): Novel jojoba oil-based emulsion gel formulations for clotrimazoledelivery. AAPS PharmSciTech, 12(1): 239–247.
[20] Kim BK, Cho AR, Park DJ. (2016): Enhancing oral bioavailability using preparations of apigenin-loaded W/O/W emulsions: in vitro and in vivo evaluations. Food Chemistry, 206: 85–91.
[21] Ahad A, Al-Saleh AA, Al-Mohizea AM, Al-Jenoobi FI, Raish M, Yassin AE, Alam MA. (2017): Pharmacodynamic study of eprosartanmesylate-loaded transfersomesCarbopol® gel under Dermaroller® on rats with methyl prednisolone acetate-induced hypertension. Biomedicine and Pharmacotherapy, 89: 177–184.
[22] Lobo MS, Costa P. (2001): Modeling and comparison of dissolution profiles. European Journal of Pharmaceutical Sciences, 13: 123.
[23] Ahmed OA, Badr-Eldin SM, Ahmed TA. (2013): Kinetic study of the in vitro release and stability of theophylline floating beads. International Journal of Pharmacy and Pharmaceutical Sciences, 5(1): 1–6.

