Development of a novel synergistic thermosensitive gel for vaginal candidiasis: An in vitro, in vivo evaluation

[Display omitted] ► An oil phase of Itraconazole and tea tree oil was developed by the method of co-solvency (using chloroform) which was used further to develop a nanoemulsion. ► Optimized nanoemulsion was then converted into mucoadhesive and thermosensitive gels. ► Optimized gel was evaluated prec...

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Published inColloids and surfaces, B, Biointerfaces Vol. 103; pp. 275 - 282
Main Authors Mirza, Mohd. Aamir, Ahmad, Sayeed, Mallick, Md. Nasar, Manzoor, Nikhat, Talegaonkar, Sushama, Iqbal, Zeenat
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.03.2013
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Online AccessGet full text
ISSN0927-7765
1873-4367
1873-4367
DOI10.1016/j.colsurfb.2012.10.038

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Abstract [Display omitted] ► An oil phase of Itraconazole and tea tree oil was developed by the method of co-solvency (using chloroform) which was used further to develop a nanoemulsion. ► Optimized nanoemulsion was then converted into mucoadhesive and thermosensitive gels. ► Optimized gel was evaluated preclinically and the promising results pave the ways for clinical evaluations. The singular aim of the proposed work is the development of a synergistic thermosensitive gel for vaginal application in subjects prone to recurrent vaginal candidiasis and other microbial infections. The dual loading of Itraconazole and tea tree oil in a single formulation seems promising as it would elaborate the microbial coverage. Despite being low solubility of Itraconazole in tea tree oil, a homogeneous, transparent and stable solution of both was created by co-solvency using chloroform. Complete removal of chloroform was authenticated by GC–MS and the oil solution was used in the development of nanoemulsion which was further translated into a gel bearing thermosensitive properties. In vitro analyses (MTT assay, viscosity measurement, mucoadhesion, ex vivo permeation, etc.) and in vivo studies (bioadhesion, irritation potential and fungal clearance kinetics in rat model) of final formulation were carried out to establish its potential for further clinical evaluation.
AbstractList The singular aim of the proposed work is the development of a synergistic thermosensitive gel for vaginal application in subjects prone to recurrent vaginal candidiasis and other microbial infections. The dual loading of Itraconazole and tea tree oil in a single formulation seems promising as it would elaborate the microbial coverage. Despite being low solubility of Itraconazole in tea tree oil, a homogeneous, transparent and stable solution of both was created by co-solvency using chloroform. Complete removal of chloroform was authenticated by GC–MS and the oil solution was used in the development of nanoemulsion which was further translated into a gel bearing thermosensitive properties. In vitro analyses (MTT assay, viscosity measurement, mucoadhesion, ex vivo permeation, etc.) and in vivo studies (bioadhesion, irritation potential and fungal clearance kinetics in rat model) of final formulation were carried out to establish its potential for further clinical evaluation.
[Display omitted] ► An oil phase of Itraconazole and tea tree oil was developed by the method of co-solvency (using chloroform) which was used further to develop a nanoemulsion. ► Optimized nanoemulsion was then converted into mucoadhesive and thermosensitive gels. ► Optimized gel was evaluated preclinically and the promising results pave the ways for clinical evaluations. The singular aim of the proposed work is the development of a synergistic thermosensitive gel for vaginal application in subjects prone to recurrent vaginal candidiasis and other microbial infections. The dual loading of Itraconazole and tea tree oil in a single formulation seems promising as it would elaborate the microbial coverage. Despite being low solubility of Itraconazole in tea tree oil, a homogeneous, transparent and stable solution of both was created by co-solvency using chloroform. Complete removal of chloroform was authenticated by GC–MS and the oil solution was used in the development of nanoemulsion which was further translated into a gel bearing thermosensitive properties. In vitro analyses (MTT assay, viscosity measurement, mucoadhesion, ex vivo permeation, etc.) and in vivo studies (bioadhesion, irritation potential and fungal clearance kinetics in rat model) of final formulation were carried out to establish its potential for further clinical evaluation.
The singular aim of the proposed work is the development of a synergistic thermosensitive gel for vaginal application in subjects prone to recurrent vaginal candidiasis and other microbial infections. The dual loading of Itraconazole and tea tree oil in a single formulation seems promising as it would elaborate the microbial coverage. Despite being low solubility of Itraconazole in tea tree oil, a homogeneous, transparent and stable solution of both was created by co-solvency using chloroform. Complete removal of chloroform was authenticated by GC-MS and the oil solution was used in the development of nanoemulsion which was further translated into a gel bearing thermosensitive properties. In vitro analyses (MTT assay, viscosity measurement, mucoadhesion, ex vivo permeation, etc.) and in vivo studies (bioadhesion, irritation potential and fungal clearance kinetics in rat model) of final formulation were carried out to establish its potential for further clinical evaluation.The singular aim of the proposed work is the development of a synergistic thermosensitive gel for vaginal application in subjects prone to recurrent vaginal candidiasis and other microbial infections. The dual loading of Itraconazole and tea tree oil in a single formulation seems promising as it would elaborate the microbial coverage. Despite being low solubility of Itraconazole in tea tree oil, a homogeneous, transparent and stable solution of both was created by co-solvency using chloroform. Complete removal of chloroform was authenticated by GC-MS and the oil solution was used in the development of nanoemulsion which was further translated into a gel bearing thermosensitive properties. In vitro analyses (MTT assay, viscosity measurement, mucoadhesion, ex vivo permeation, etc.) and in vivo studies (bioadhesion, irritation potential and fungal clearance kinetics in rat model) of final formulation were carried out to establish its potential for further clinical evaluation.
Author Mirza, Mohd. Aamir
Mallick, Md. Nasar
Iqbal, Zeenat
Ahmad, Sayeed
Manzoor, Nikhat
Talegaonkar, Sushama
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/23201748$$D View this record in MEDLINE/PubMed
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Keywords Pseudo ternary phase diagram
Mucoadhesion
MTT assay
Tea tree oil
Itraconazole
Language English
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Snippet [Display omitted] ► An oil phase of Itraconazole and tea tree oil was developed by the method of co-solvency (using chloroform) which was used further to...
The singular aim of the proposed work is the development of a synergistic thermosensitive gel for vaginal application in subjects prone to recurrent vaginal...
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SubjectTerms Adhesiveness - drug effects
animal models
Animals
Antifungal Agents - pharmacology
candidiasis
Candidiasis, Vulvovaginal - drug therapy
Cell Death - drug effects
chloroform
colloids
Drug Synergism
Emulsions - chemistry
Female
fungi
gas chromatography-mass spectrometry
gels
Gels - pharmacology
Gels - therapeutic use
HeLa Cells
Humans
in vivo studies
Itraconazole
Itraconazole - pharmacology
Itraconazole - therapeutic use
Itraconazole - toxicity
Kinetics
Materials Testing - methods
MTT assay
Mucoadhesion
Mucus - drug effects
nanoemulsions
Nanoparticles - chemistry
Particle Size
Pseudo ternary phase diagram
Rats
solubility
Surface-Active Agents - chemistry
Tea tree oil
Tea Tree Oil - pharmacology
Tea Tree Oil - therapeutic use
Tea Tree Oil - toxicity
Temperature
Transition Temperature
viscosity
Viscosity - drug effects
Title Development of a novel synergistic thermosensitive gel for vaginal candidiasis: An in vitro, in vivo evaluation
URI https://dx.doi.org/10.1016/j.colsurfb.2012.10.038
https://www.ncbi.nlm.nih.gov/pubmed/23201748
https://www.proquest.com/docview/1286947647
https://www.proquest.com/docview/2000084890
Volume 103
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