Fluconazole Ocular Inserts: Formulation and In -Vitro Evaluation

Journal Title: Journal of Pharmaceutical Sciences and Research - Year 2010, Vol 2, Issue 11

Abstract

[i][/i]The eye presents unique opportunities and challenges when it comes to the delivery of Pharmaceuticals. While absorption by this route is bungling, there are few side effects with conventional ocular dosage forms like eye drops and eye suspensions. Several polymeric systems have been used to fabricate ocular inserts for better ocular bioavailability and retention of drug for which gelling systems have shown advantages of convenient administration and increased contact time. Fluconazole ocular films were prepared using film forming polymers namely; Hydroxy propyl methyl cellulose, poly vinyl pyrrolidine and poly vinyl alcohol. PEG-400 was incorporated as plasticizer. Solvent casting technique was followed to prepare fluconazole ocular inserts. Seven formulations were formulated .The prepared ocular inserts were characterized by means of film thickness, weight variation, folding endurance and surface pH, and  in- vitro drug release to determine the amount of drug release from selected film formulae using excised goat cornea. Ocular inserts prepared were smooth and passed all the evaluation tests performed. Formulation F5 shows a maximum cumulative percentage drug release of 69.02 % at the end of 2 hours through excised goat cornea. The drug in the films was found to be active against selected fungal species as was proved by microbial efficacy studies. 

Authors and Affiliations

Purna Chandra Rao. M , Nappinnai. M , Raju. S , Uma Maheshwara Rao. V , Venkateshwara Reddy. B

Keywords

Related Articles

INCIDENCE OF CHLAMYDIAL INFECTION IN WOMEN

 With the emergence of AIDS in the 1980s sexually transmitted disease (STDs) received increased attention.The most common agent is Chlamydia trachomatis (CT), Nesseria gonorrhea and etc. CT commonlycauses non-gonoco...

Formulation and Evaluation of Levofloxacin Using Different Types and Concentrations of Superdisintegrants

Levofloxacin is a fluoroquinolone anti bacterial drug effective in the treatment of bacterial conjunctivitis. Levofloxacin is a synthetic chemotherapeutic antibiotic of the fluoroquinolone drug class. The objective of th...

Extracellular synthesis of silver nanoparticles using leaves of Euphorbia hirta and their antibacterial activities

Aqueous extract of shade dried leaves of Euphorbia hirta (L) was used for the synthesis of silver (Ag) nanoparticles. UV-visible spectroscopy studies were carried out to assess the formation Ag nanoparticles. Scanning E...

Preparation and Evaluation of Ethyl Cellulose Microspheres Containing Diclofenac Sodium by Novel W/O/O Emulsion Method

The aim of present study was to formulate and evaluate microencapsulated controlled release preparations of a highly water/soluble drug, Diclofenac Sodium by (water in oil) in oil emulsion technique. Ethylcellulose, a bi...

Synthesis and Evalution of Amide Prodrugs of Diclofenac

“Prodrugs Approach” is a versatile approach in solving the problems associated with drug molecules. Diclofenac is a pain reliever in variety of painful conditions but it has some side effects i.e. absorption, toxicity, d...

Download PDF file
  • EP ID EP113425
  • DOI -
  • Views 103
  • Downloads 0

How To Cite

Purna Chandra Rao. M, Nappinnai. M, Raju. S, Uma Maheshwara Rao. V, Venkateshwara Reddy. B (2010). Fluconazole Ocular Inserts: Formulation and In -Vitro Evaluation. Journal of Pharmaceutical Sciences and Research, 2(11), 693-699. https://europub.co.uk/articles/-A-113425