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Development of span 80–tween 80 based fluid-filled organogels as a matrix for drug delivery

BACKGROUND: Organogels are defined as 3-dimensional networked structures which immobilize apolar solvents within them. These gelled formulations are gaining importance because of their ease of preparation and inherent stability with improved shelf life as compared to the ointments. AIM: Development...

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Detalles Bibliográficos
Autores principales: Bhattacharya, Charulata, Kumar, Nikhil, Sagiri, Sai S., Pal, Kunal, Ray, Sirsendu S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3341720/
https://www.ncbi.nlm.nih.gov/pubmed/22557927
http://dx.doi.org/10.4103/0975-7406.94822
Descripción
Sumario:BACKGROUND: Organogels are defined as 3-dimensional networked structures which immobilize apolar solvents within them. These gelled formulations are gaining importance because of their ease of preparation and inherent stability with improved shelf life as compared to the ointments. AIM: Development of span 80–tween 80 mixture based organogels for the first time by fluid-filled fiber mechanism. MATERIALS AND METHODS: Span 80 and tween 80 were used as surfactant and co-surfactant, respectively. The surfactant mixtures were dissolved in oil followed by the addition of water which led to the formation of organogels at specific compositions. The formulations were analyzed by microscopy, X-ray diffraction (XRD), time-dependent stability test and accelerated thermal stability test by thermocycling method. Ciprofloxacin, a fourth-generation fluoroquinolone, was incorporated within the organogels. The antimicrobial activity of the drug loaded organogels and in vitro drug release from the gels was also determined. RESULTS AND CONCLUSIONS: Microscopic results indicated that the gels contained clusters of water-filled spherical structures. XRD study indicated the amorphous nature of the organogels. The release of the drug was found to be diffusion controlled and showed marked antimicrobial property. In short, the prepared organogels were found to be stable enough to be used as pharmaceutical formulation.