Preparation and In-Vitro Evaluation of Thermosensitive In-Situ Gel with Different Concentrations of Levofloxacin for Periodontal Applications
摘要
Periodontitis is a chronic inflammatory disease which can ultimately lead to tooth loss. This research aimed to develop a thermosensitive in-situ gel (ISG) for the localized administration and study the effect of varying concentrations (Conc.) of levofloxacin (Lvx) within periodontal pockets.
Methods25 mixtures of different concentrations of poloxamer (Polx) 407 (16%-20%) and Polx188 (1%-4%) were formulated; four were selected: P2 (Polx 407 17%), P14 (Polx 407 19% and Polx 188 3%), P19 (Polx 407 19% and Polx188 2%), and P22 (Polx 407 17% and Polx188 1%). Mucoadhesive polymers were added to the chosen four formulations (Methyl Cellulose (MC) 0.25%-1%, Hydroxypropyl methylcellulose (HPMC) 0.1%-0.3%, Gellan gum (GG) 0.2%-0.6%, Chitosan (Chts) 0.5%-1.5%, Carbopol (Car) 0.05%-0.15%), resulted in 60 combinations. After assessing factors such as viscosity and gelation, three formulations were chosen: A7 (Polx407 17% GG 0.2%), A10 (Polx407 17% Chts 0.5%), and A19 (Polx407 17% Polx188 1% HPMC 0.1%) for further investigations. the antibacterial effects of various Conc. of Lvx (0.5%-5%) on these formulations, specifically incorporating them into the A10 (Polx407 17% Chts 0.5%) formulation.
ResultsAll tested concentrations of levofloxacin exhibited impressive inhibition zones ranging from 31 to 45 mm in comparison to positive control (14-15mm). 0.5% and 1% Conc. of Lvx where chosen, which were then incorporated, resulting in six formulations for evaluation Lvx, resulting in six final formulations. These were evaluated for drug release, antibacterial activity, and stability.
ConclusionsFormulations F1 and F2 exhibited sustained Lvx release and demonstrated significant efficacy against bacteria. In conclusion, F1 and F2 promise to develop a prolonged-release ISG for delivering Lvx in treating periodontitis.