Comparative Investigation on in vitro release of extemporaneously prepared norfloxacin semisolid formulations with marketed silver sulfadiazine 1% cream, USP using model independent approach

Authors

  • K Dua Lecturer, Dept. of Pharmaceutical Technology, School of Pharmacy & Allied Health Sciences, International Medical University, Bukit Jalil, Malaysia
  • K Pabreja Lecturer, Dept. of Life Sciences, School of Pharmacy & Allied Health Sciences, International Medical University, Bukit Jalil, Malaysia.
  • MV Ramana Professor, VIT University, Vellore, Tamilnadu, India

Keywords:

Semisolid, Ointments, Norfloxacin

Abstract

Objective

In an attempt for better treatment of bacterial infections, various semisolid formulations containing 5%w/w of norfloxacin were prepared and evaluated for in vitro drug release and in vitro skin permeabilityusing dialysis membrane and rat abdominal skin respectively. The in vitro diffusion and permeationprofile of the prepared formulation was compared with marketed silver sulfadiazine cream 1%, USPusing model independent approach.

Methods

Various semisolid formulations were prepared with different dermatological bases usingstandard procedures. In vitro diffusion and permeation studies were carried out using Keshary-Chein(KC) type diffusion cell using dialysis membrane and rat abdominal skin respectively.

Results

The f1 lower than 15 and f2 higher than 50 indicated similarities in the in vitro diffusion andpermeation profiles of the extemporaneously prepared selected semisolid formulations and marketedsilver sulfadiazine 1% cream, USP.

Conclusion

Amongst all the semisolid formulations prepared, carbopol gel base was found to be most suitabledermatological base for norfloxacin, the results obtained for in vitro diffusion, and in vitro skinpermeation studies are comparable with that of marketed silver sulphadiazine 1% cream, USP.

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References

M. W. Benner, P. M. Bencon and W. D. James, In; Topical Antibiotics in Dermatology, 5th Ed., McGraw Hill Co., NY, 1999, pp. 25-27.

G. J. Murakawa and D. Sable, Quinolones in Dermatology, Clinical Dermatol., 21(1) (2003) pp. 56-63.

Martindale, The Extra Pharmacopoeia, 29th Ed., Reynolds, J.E.F.(Eds.),The Pharmaceutical Press, London (1989).

Y. K. S. Rathore, P. K. Chatterjee, S. C. Mathur, Sunderlal and P. D. Sethi, Indian Drugs 27 (1990) 215-217.

K. Florey, Analytical Profiles of Drug Substances, Academic Press, Inc., New York, 1991, Vol. 20, pp. 557-600.

V. Rajni and P. R. P. Verma, Diffusion study of ibuprofen from ointment base, Ind. J. Pharm. Sci. 57 (1995) 1-6.

A. Mohammed, S. Yasmin and A. Asgar, Matrix type transdermal drug delivery systems of metoprolol tartrate, Acta. Pharm. 53 (2003) 119-125.

F. W. Ezzedeen, F. A. Shihab and E. J. Husain, Percutanous diffusion of cefalexin, sulfamethoxazole and diphenhydramine from ointments, Pharmazie 45 (1990) 512–514.

V. Sanna, A. T. Peana and M. D. Moretti, Effect of vehicle on diclofenac sodium permeation from new topical formulations: in vitro and in vivo studies, Curr. Drug Deliv. 6(1) (2009) 93-100.

A. E. Nagia, M. E. Hanan and F. B. Gehan, Formulation and evaluation of meloxicam gels for topical administration, Saudi Pharm. J. 14(3-4) (2006) 155-62.

S. Singh, B. Gajra, M. Rawat and M. S. Muthu, Enhanced transdermal delivery of ketoprofen from bioadhesive gels, Pak. J. Pharm. Sci. 22(2) (2009) 193-198.

J. W. Moore and H. H. Flanner, Mathematical comparison of dissolution profiles, Pharm. Technol. 20 (1996) 64-74.

P. Costa and J. M. Sousa Lobo, Modeling and comparison of dissolution profiles, Eur. J. Pharm. Sci. 13 (2001)123-133.

FDA, Guidance for industry: dissolution testing of immediate release solid oral dosage forms, (BP1), Centre for drug evaluation and research, Food and drug administration, 1997, Rockville, MD, P9. http://www.fda.gov/cder/guidance.

N. H. Parikh , A. Babar and F. M. Plakogiannis, Medicament release from ointment bases: II. Testosterone: in vitro release and effects of additives on its release, Drug Development and Industrial Pharmacy 12(14) (1986) 2493-2509.

B. Perez-Marcos, R. Iglesias and J. L. Gomez-Amoxa, Mechanical and drug release properties of atenolol-Carbopol hydrophilic matrix tablets, J. Controlled Rel. 17(3) (1991) 267-276.

V. V. Dhavse and P. D. Amin, Formulation and evaluation of topical bases of ketoprofen, East Pharm. (1997) 133–135.

Published

2010-12-20

How to Cite

1.
Dua K, Pabreja K, Ramana M. Comparative Investigation on in vitro release of extemporaneously prepared norfloxacin semisolid formulations with marketed silver sulfadiazine 1% cream, USP using model independent approach. Ars Pharm [Internet]. 2010 Dec. 20 [cited 2024 May 18];51(4):177-85. Available from: https://revistaseug.ugr.es/index.php/ars/article/view/4876

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Original Articles