Stimuli-Responsive in situ Spray Gel of Miconazole Nitrate for Vaginal Candidiasis.
Cytotoxicity
Improved antifungal efficacy
In situ spray gel
Miconazole nitrate
Stimuli-sensitive polymers
Sustained release
Vaginal candidiasis
Journal
Journal of pharmaceutical sciences
ISSN: 1520-6017
Titre abrégé: J Pharm Sci
Pays: United States
ID NLM: 2985195R
Informations de publication
Date de publication:
02 2023
02 2023
Historique:
received:
12
07
2022
revised:
05
09
2022
accepted:
06
09
2022
pubmed:
13
9
2022
medline:
18
1
2023
entrez:
12
9
2022
Statut:
ppublish
Résumé
Vaginal candidiasis is a common form of infection in women caused by Candida species. Due to several drawbacks of conventional treatments, the current research is attempted to formulate and optimize a miconazole nitrate-loaded in situ spray gel for vaginal candidiasis. The stimuli-responsive (pH and thermo-responsive) polymers selected for the in situ gel were chitosan and poloxamer 407, respectively, whereas hydroxypropyl methylcellulose (HPMC) was introduced in the formulation to further improve the mucoadhesive property. The dispersion of each polymer was carried out using the cold method, whereas the optimization of the formulation was achieved using Box-Behnken statistical design considering viscosity and gelation temperature as dependent variables. Present design achieved the optimized outcome with HPMC, poloxamer and chitosan at 0.52% (w/v), 18.68% (w/v) and 0.41% (w/v), respectively. Evaluation of drug-excipients compatibility was performed using differential scanning calorimetry, Fourier transform infrared spectroscopy, and thermogravimetric analysis where the results showed the absence of any chemical interaction between the polymers and drug component. The optimized formulation showed gelation temperature at 31°C allowing in situ phase transition in a vaginal environment; pH of 4.21 is suitable for use in the vaginal cavity, and appropriate viscosity (290 cP) at storage temperature (below 30°C) would allow spraying at ease, whereas strong mucoadhesive force (22.4±0.513 g) would prevent leaking of the formulation after application. The drug release profile showed sustained release up to 24 h with a cumulative drug release of 81.72%, which is significantly better than the marketed miconazole nitrate cream. In addition, an improved antifungal activity could be correlated to the sustained release of the drug from the formulation. Finally, the safety of the formulation was established while tested on HaCaT cell lines. Based on our findings, it could be concluded that the in situ hydrogel formulation using stimuli-responsive polymers could be a viable alternative to the conventional dosage form that can help to reduce the frequency of administration with ease of application to the site of infection, thus will provide better patient compliance.
Identifiants
pubmed: 36096286
pii: S0022-3549(22)00398-7
doi: 10.1016/j.xphs.2022.09.002
pii:
doi:
Substances chimiques
Miconazole
7NNO0D7S5M
Delayed-Action Preparations
0
Chitosan
9012-76-4
Antifungal Agents
0
Poloxamer
106392-12-5
Gels
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
562-572Informations de copyright
Copyright © 2022 American Pharmacists Association. Published by Elsevier Inc. All rights reserved.