Niosomes play an important role in novel drug delivery systems and it can increase the bioavailability and modify the pharmacokinetic property of drug.Topically used niosomal formulations increase the residence time and decrease the systemic circulation . The core objective of the study is to formulate the Nigella sativa niosomes for topical application. The niosomes of Nigella sativa was prepared by hand shaking method with various ratios of cholesterol and span. The formulated niosomes were characterized by Size, Shape, Entrapment efficiency, in-vitro drug release study, release kinetics study and Anti microbial activity. TEM study analyses showed that the formulated niosomes were spherical in shape. Among the formulations, formulation 5 (F5) showed a 98.99% cumulative percentage of drug release at the end of 24thhr. The in vitro release profile of optimized formulation5 (F5) was fitted with various kinetic equations and it was best fit with zero order kinetics and the korsmeyer model explained the release pattern of the drug and it followed the non fickian diffusion. The optimized formulation (F5) was effective against P. aeruginosa. The best formulation was selected based on the evaluation parameters and it is more stable. The Nigella sativa niosomal gel was formulated by incorporating the optimized formulation with carbopol. The carbopol was selected for this formulation, because of its hydrophilic nature and also to improve the residence time of the drug at the absorption site of the skin . The prepared gel was evaluated for physical appearance, pH, Rheological study, Drug content and Stability studies. From the study, it was concluded that the prepared niosomal gel may be enhancing the penetration of drug and providing a sustained pattern of drug release for topical application and to improve the antimicrobial activity.
Keywords: Nigella sativa, Niosomes, in -vitro study, Carbopol, Topical gel, Anti microbial activity
Full HTML:
References
Vyas, S. P.; Khar, R. K. Niosomes,Targeted and Controlled. Drug Deliv. Syst. 2002, 258–260.
Kareparamban, J. A.; Nikam, P. H.; Jadhav, A. P.; Kadam, V. J. Phytosome A Novel Revolution in Herbal Drugs. IntJResPharma Chem. 2012, 2 (2), 299–300.
Babita Rani, V.; Nagpal, M.; Sandeep Arora, P. Potential Carrier for Herbal Drugs, Int J Res Rev Pharma App Sci. 2012, 2 (3), 567–569.
Acharya, N. S.; Parihar, G. V.; Acharya, S. R. Phytosome: A Novel Approach for Delivering Herbal Extract with Improved Bioavailability,IJPS.2011;2(1), 145–148.
Arunothayanun, P.; Bernard, M. S.; Craig, D. Q. M.; Uchegbu, I. F.; Florence, A. T. Theeffectofprocessingvariablesonthephysicalcharacteristicsofnon-ionicsurfactantvesicles(niosomes)formedfromahexadecyldiglycerolether,ELSEVEIR. Int. J. Pharm. 2000, 201 (1), 7–14. DOI: 10.1016/s0378-5173(00)00362-8
Khandare, J. N.; Hemant, J. B.; Ramesh, U. R. Preparation and Evaluation of Nimesulide Niosomes for Topical Application. Indian Drugs April 2001, 38 (4), 197–201.
Thiboutot. D, M. Straus, J.S.: Diseases of the sebaceous glands. In Dermatologyingeneralmedicine.Sixthedition.New York:the McGrawhill Com; Vol. 1. Freedberg, I. M. et al., Eds., 2003, pp 675–685.
Mutabagani, A.; El-Mahdy, S. A. A Study of the Anti-Inflammatory Activity of Nigella sativa L. and Thymoquinone in Parts. Saudi Pharm. J. 1997, 5 (2), 110–113.
Toama, M. A.; El-Alfy, T. S.; El-Fatatry, H. M. Antimicrobial Activity of the Volatile Oil of Nigella sativa Linneaus Seeds. Antimicrob. Agents Chemother. 1974, 6 (2), 225–226. DOI: 10.1128/AAC.6.2.225
Banker, G. S.; Rhodes, C. T., Eds. Modern Pharmaceutics New York: MarcelDekker 2002, 4, 182.
Yamini, K.; Onesimus, T. Preparation and Evaluation of Herbal Anti-Acne Gel. Int. J. Pharm. Biol. Sci. 2013, 4 (2) (April–June), 956–960.
Jamal, M. A.; Perinbam, K.; Vahitha, V.; Devanesan, S.; Janaki Raman, K. K. Effect of Excipients on Pharmaceutical Parameters on Topical Gel Loaded with Povidone Iodine, Honey and Aloe vera. Int. J. Pharma Bio Sci., 10 (5). DOI: 10.22376/ijpbs/lpr.2020.10.5.P111-117
Miss. Shital, G.; Mr. Tulsidas, N.; Mr. Sunil, B. Formulation and Evaluation of Topical Herbal Gel for Rheumatoid Arthritis Using Some Medicinal Plants. Int. J. Pharma Bio Sci., 11 (3). DOI: 10.22376/ijpbs.2020.11.3.p50-55
Srikanth, K.; Nappinnai, M.; Gupta, V. R. M.; Suribabu, J. Niosomes: Aprominent Tool for Transdermal Drug Delivery. Res. J. Pharm. Biol. Chem. Sci. 2010, 1 (2), 308–316.
Solanki, A. B., J.R. Parikh,R. H. Parikh, and M. R. Patel, Evaluation of Different Compositions of Niosomes to Optimize Aceclofenac Transdermal Delivery. Asian J. Pharm. Sci. 2010, 5 (3), 87–95.
Kamboj, V. P. Herbal Medicine. Curr. Sci. 2000, 78 (1), 35–36.
Firthouse, P. U. M., S.M. Halith,S.U.Wahab,M.Sirajudeen,andS.K.Mohideen,“Formulation and evaluation of miconazolenio somes. Int. J. Pharm. Technol. Research 2011, 3 (2), 1019–1022.
Solanki, A. B., J.R. Parikh,R. H. Parikh, and M. R. Patel, Evaluation of Different Compositions of Niosomes to Optimize Aceclofenac Transdermal Delivery. Asian J. Pharm. Sci. 2010, 5 (3), 87–95.
GyatiShilakariAsthana, A.A.; Singh, D.; Sharma, P. K. Etodolac Containing Topical Niosomal Gel:Formulation Development and Evaluation. J. Drug Deliv., 2016, 1–8
UpasanaBhalani, K. S. Preparation and Evaluation of Topical Gel OfNigella Sativa (Kalonji). Int. J. Res. Dev. Pharm. L. Sci 2015, 4 (4), 1669–1672.
SorlinSelvaJoice, P.; Rubina Reichal, C.; Thirumoorthy, N.; Sangeetha, M. Formulation and Evaluation of Tetracycline Niosomal Topical Gel Drug Delivery System WJPPS, 6 (8), 2644–2657.
ManjushaMalhotra; Jain. N.K, Niosomes as Drug Carriers. Indian Drugs March 1994, 31 (3), 81–85.
Shinde, U. A.; Kanojiya, S. S. Serratiopeptidase Niosomal Gel with Potential in Topical Delivery. J. Pharm. (Cairo) 2014, 2014, 382959. DOI: 10.1155/2014/382959
RaymondCRowe, PaulJSheskey andMarianEQuinn.HandbookofPharmaceutical Excipients; Pharmaceutical Press and the American Pharmaceutical Association, 2009, p 6.
Garima Singhal, R. B.; Kasariya, K.; Sharma, A. R.; PalSingh, R. Biosynthesis of Silver Nanoparticles Using Ocimum Sanctum(Tulsi)Leaf Extract and Screening Its Antimicrobial Activity. J. Nanopart. Res., 2011 (13), 2981–2988.
Martin, A. Physical Pharmacy,Kinetics. First Indian Reprint.NewDelhi:B.I Waverly, 1994.
Hossain, M. A.; Kabir, M. J.; Salehuddin, S. M.; Rahman, S. M. M.; Das, A. K.; Singha, S. K.; Alam, M. K.; Rahman, A. Antibacterial Properties of Essential Oils and Methanol Extracts of Sweet Basil Ocimum basilicum Occurring in Bangladesh. Pharm. Biol. 2010, 48 (5), 504–511. DOI: 10.3109/13880200903190977
Carstensen, J. T.; Rhodes, C. T. Drug Stability Principles and Practices, 3rd ed,Marcel Dekker, Int New York, 2008, pp 415–481.