Abstract:
Problem Statement: Periodontal (gum) diseases are a “chronic inflammatory
disease and infection” that destroy the tissue that support the teeth and finally,
tooth loss. It involves the absorption of Alveolar bone, periodontal ligaments and
formation of Pocket or space between tooth and gum is called as “Periodontitis”.
The major cause is growth of microorganism in the pockets and release enzyme,
toxins and stimulation of body’s immune response. Periodontitis is a very
common and, is widely regarded as the second most common disease worldwide.
In the United states has a prevalence of 30-50% of the population, but about 10%
have severe form. This severe form is known as periodontitis.
• Purpose: The objective of this study was to resolve the problems in different
dosage form which are given in systemic root. Topical site-specific delivery of
ornidazole was reduced the side effects occurs by the systemic drug delivery like
hypersensitivity, gastrointestinal intolerance and bacterial resistance because of
ornidazole have a longer half-life 12 to 14 hrs. Nanoparticles loaded film having
a potential to deliver small amount of drug with prolonged period of time.
• Methods: The Chitosan containing ornidazole nanoparticles was prepared by
Ionic gelation mechanism using 1% Acetic acid. The nanoparticles were evaluated for Particle size, Zeta potential, Drug content, antimicrobial study and
In-vitro drug release study. After preparation of nanoparticles they have loaded
in film. Nanoparticle loaded film was formulated by solvent casting method
using ethyl cellulose as a polymer, Dichloromethane as a solvent and Dibutyl
phthalate as a plasticizer. The film was evaluated for thickness uniformity,
folding endurance, weight uniformity, surface pH, swelling index, Surface
morphology study with scanning electron microscopy, In-vitro drug release
study, antibacterial study, FT-IR study of film and comparison study with
marketed formulation.
• Results: The optimized batch of nanoparticles was selected using Design of
Experiment (DOE) Software7. F1 to F9 batch was prepared and evaluate all
batches such as particle size, Drug content and In-vitro drug release study. After
prepared F1-F9 batches, Design of experiment software 7 was applied and select
the optimized batch. F2 have optimized batch, they have maximum drug release
82% and minimum inhibitory concentration. Optimized nanoparticles were
loaded in ethyl cellulose film and they evaluate such parameters. In-vitro
antibacterial of formulated nanoparticle containing ethyl cellulose film of
ornidazole have similar activity as compare to standard drug sample. In compare
to marketed formulation (Chlorhexidine mouth- wash) fabricated film have
better antibacterial activity. The surface morphological study by scanning
electron microscopy show that the molecules are uniformly distributed with
nanoparticle in the formulation.
• Conclusion: Chitosan nanoparticles loaded ethyl cellulose film combination is
the better carrier among the others for the preparation of ornidazole periodontal
film for prolonged the drug action up to 7days.