Formulation and evaluation of microemulsion containing griseofulvin

https://doi.org/10.53730/ijhs.v6nS3.8245

Authors

  • Trupti Shinde Department of Pharmaceutical Quality Assurance, P.D.E.A’s Sankarrao Ursal College of Pharmaceutical Sciences and Research Centre, Kharadi, Pune, Maharashtra, India
  • Vijaya Barge Department of Pharmaceutical Quality Assurance, P.D.E.A’s Sankarrao Ursal College of Pharmaceutical Sciences and Research Centre, Kharadi, Pune, Maharashtra, India
  • Amit Kasabe Department of Pharmaceutical Quality Assurance, P.D.E.A’s Sankarrao Ursal College of Pharmaceutical Sciences and Research Centre, Kharadi, Pune, Maharashtra, India
  • Manisha Sukre Department of Pharmaceutical Quality Assurance, P.D.E.A’s Sankarrao Ursal College of Pharmaceutical Sciences and Research Centre, Kharadi, Pune, Maharashtra, India
  • Mansi Kandge Department of Pharmaceutical Quality Assurance, P.D.E.A’s Sankarrao Ursal College of Pharmaceutical Sciences and Research Centre, Kharadi, Pune, Maharashtra, India

Keywords:

griseofulvin, microemulsion, particle size, zeta potential, scanning electron microscopy

Abstract

The aim of the following research is to formulate a microemulsion containing drug Griseofulvin. Griseofulvin is an antifungal agent which inhibits the mitosis. It is recommended orally for treatment of fungal disease.  It is used to treat skin infections such as jock itch, athletes foot and ringworm. Also it is used to treat the fungal infections of scalp, toenails and fingernails. Griseofulvin is a BCS II class drug. It is highly lipophilic poorly soluble drug with low oral bioavailability. The present aim was to increase the solubility by microemulsion system for topical delivery. Microemulsions are clear, stable and isotropic liquid. They show advantages such as spontaneous preparation, scale up, ease of preparation, improving drug solubility of hydrophobic drugs. It is also used to increase the bioavailability of drug. These also aim at controlling the bioavailability of various drug molecules. The review put forward the development in microemulsion containing system. They improve solubility, chemical stability and oral bioavailability of poorly water soluble drugs. There is formulation of four different batches. The batches differ in quantity of surfactant and co- surfactants.

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References

International Agency for Research on Cancer. IARC Monographs on the Evaluation of Carcinogenic Risks to Humans. Vol. 79. Lyon, France: IARC Press; 2001. p. 75-89.

Tanaka Y, Waki R, Nagata S. Species differences in the dissolution and absorption of

griseofulvin and albendazole, biopharmaceutics classification system class II drugs, in the gastrointestinal tract. Drug Metab Pharmacokinet 2013;28(6):485-90.

Aggarwal N, Goindi S, Khurana R. Formulation, characterization and evaluation of an optimized microemulsion formulation of griseofulvin for topical application. Colloids Surf B Biointerfaces 2013;105:158-66.

Moghimipour E, Salimi A, Hassanvand S. Permeability assessment of griseofulvin microemulsion through rat skin. Int J Pharm Chem Biol Sci 2013;3(4):1061-5.

U.S. National Library of Medicine. Griseofulvin-Griseofulvin Tablet; 2016. Available from: http://www.dailymed.nlm.nih.gov/dailymed/ drugInfo.cfm?setid=6149c044-58bb-402c-a4b5-18b96dd9b3b9. [Last accessed on 2016 Jan 11].

Lahenmeier DW. Safety evaluation of topical applications of ethanol on the skin and inside the oral cavity. J Occup Med Toxicol 2008;3:26.

Shinde U, Pokharkar S, Modani S. Design and evaluation of microemulsion gel system of nadifloxacin. Indian J Pharm Sci 2012;74(3):237-47.

Kumar A, Kushwaha V, 11. Júnior AA, Baldo JB. The behavior of zeta potential of silica suspensions. N J Glass Ceram 2014;4:29-37

Sharma PK. Pharmaceutical microemulsion: Formulation, characterization and drug deliveries across skin. Int J Drug Dev Res 2014;6(1):1-21.

T.P. Hoar and J.H. Schulman. Transparent water-in-oil dispersions, the oleopathic hydro micelle. Nature 1943; 152: 102–103.

J. H. Schulman et al. Mechanism of formation and structure of micro emulsions by electron microscopy. The Journal of Physical Chemistry 1959; 63: 1677–1680.

Danielsson and B. Lindman. The definition of a microemulsion, Colloids and Surfaces 1981; 3: 391–392.

Shinoda K and Lindman B. Organised surfactant systems: Microemulsions. Langmuir 1987; 3: 135–149.

M. Jayne Lawrencea and Gareth D. Reesb. Microemulsion-based media as novel drug delivery systems. Advanced Drug Delivery Reviews 2000; 45: 89–121.

Kumar. K. Senthil et al. Microemulsions as Carrier for Novel Drug Delivery: A Review. International Journal of Pharmaceutical Sciences Review and Research 2011; 10: 37-45.

Patel R. Mrunali. Microemulsions: As Novel Drug Delivery Vehicle. 2007; 5.

Madhav. S and Gupta. D. A review on microemulsion based system. International Journal of Pharmaceutical Sciences and Research 2011; 2 (8): 1888.

Shiokawa T. et al. Effect of Polyethylene Glycol Linker Chain Length of Folate-Linked Microemulsions Loading Aclacinomycin A on Targeting Ability and Antitumor Effect In itro and In vivo. Clinical Cancer Research 2005; p11.

Talegaonkar S and Mishra P. Intranasal delivery: An approach to bypass the blood brain barrier. Indian Journal of Pharmacology 2004; 36: 140-147.

Hasse. A. and Keipert S. Development and characterisation of microemulsions for ocular application. European Journal of Pharmaceutics and Biopharmaeutics 1997; 43; 179–183.

Malmsten. M. Microemulsions in pharmaceuticals In Handbook of Microemulsion. Science and Technology. Marcel Dekker. Inc. New York. 1999; p 755.

Published

01-06-2022

How to Cite

Shinde, T., Barge, V., Kasabe, A., Sukre, M., & Kandge, M. (2022). Formulation and evaluation of microemulsion containing griseofulvin. International Journal of Health Sciences, 6(S3), 9206–9215. https://doi.org/10.53730/ijhs.v6nS3.8245

Issue

Section

Peer Review Articles