Stimuli Responsive In Situ Gelling Systems Loaded with PLGA Nanoparticles of Moxifloxacin Hydrochloride for Effective Treatment of Periodontitis.
Animals
Anti-Bacterial Agents
/ chemistry
Delayed-Action Preparations
/ chemistry
Drug Delivery Systems
/ methods
Female
Gels
Moxifloxacin
/ chemistry
Nanoparticles
/ chemistry
Particle Size
Periodontitis
/ drug therapy
Polylactic Acid-Polyglycolic Acid Copolymer
/ chemistry
Rats
Rats, Sprague-Dawley
Treatment Outcome
Viscosity
nanoparticles
periodontitis
quality by design
thermo-responsive gels
γ-scintigraphy
Journal
AAPS PharmSciTech
ISSN: 1530-9932
Titre abrégé: AAPS PharmSciTech
Pays: United States
ID NLM: 100960111
Informations de publication
Date de publication:
22 Jan 2020
22 Jan 2020
Historique:
received:
15
08
2019
accepted:
17
12
2019
entrez:
24
1
2020
pubmed:
24
1
2020
medline:
17
6
2020
Statut:
epublish
Résumé
The objectives of the present research work were systematic development of novel in situ gel formulation containing nanoparticles for localised delivery of moxifloxacin against bacterial periodontitis. PLGA nanoparticles were prepared and optimised in a systematic manner. Factor screening was performed with the help of half-factorial design to identify the influential factors, while response surface optimisation of the nanoparticles was conducted using central composite design. The optimum nanoparticle formulation was chosen on the basis of lower particle size, higher drug entrapment and controlled drug release characteristics up to 1 week time period, while the optimum in situ gel was selected on the basis of faster gelling and higher viscosity and gel strength properties for improved retention in the periodontium. In vivo histopathological studies and in vivo gamma scintigraphy studies revealed the extended release, superior efficacy and enhanced retention of nanoparticle-loaded in situ gelling system. Results obtained from in vivo histopathological studies after 1 week treatment with in situ gel formulation containing nanoparticles of moxifloxacin were found to be better than with 3 weeks treatment of marketed gel formulation. Overall, the studies ratify successful development of an effective site-specific drug delivery system with enhanced biopharmaceutical attributes for the periodontitis treatment.
Identifiants
pubmed: 31970603
doi: 10.1208/s12249-019-1613-7
pii: 10.1208/s12249-019-1613-7
doi:
Substances chimiques
Anti-Bacterial Agents
0
Delayed-Action Preparations
0
Gels
0
Polylactic Acid-Polyglycolic Acid Copolymer
1SIA8062RS
Moxifloxacin
U188XYD42P
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM