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Development and Evaluation of Etodolac-Loaded Niosomal Gel for Sustained Drug Release
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: Niosomes, vesicular systems formed
from non-ionic surfactants, offer benefits such as
enhanced stability, controlled drug release, and
improved skin penetration. This study aimed to
formulate and evaluate niosomal gels for etodolac, a
nonsteroidal anti-inflammatory drug, to achieve
sustained drug release and enhanced topical
application. The study involves the preparation of
niosomal suspensions with varying concentrations
of surfactants (Span 60) and cholesterol, followed
by incorporation into a gel base of carbopol 934.
The formulation was evaluated for physical
appearance, viscosity, pH, irritancy,drug content and
diffusion studies. The optimized formulation (F4)
demonstrated good homogeneity, spreadability and
a pH range suitable for skin application. It showed
sustained drug release of 83.8% at the end of 6
hours in diffusion studies, demonstrating better
performance compared to the marketed Etodolac
gel. Entrapment efficiency for the optimized
formulation was 77%, and the gel was non-irritant
based on the HET-CAM assay. In conclusion, this
study suggests etodolac loaded niosomal gel was
successfully developed and can be a promising
strategy for providing localized and sustained drug
delivery, minimizing systemic side effects and
enhancing patient compliance.
Title: Development and Evaluation of Etodolac-Loaded Niosomal Gel for Sustained Drug Release
Description:
: Niosomes, vesicular systems formed
from non-ionic surfactants, offer benefits such as
enhanced stability, controlled drug release, and
improved skin penetration.
This study aimed to
formulate and evaluate niosomal gels for etodolac, a
nonsteroidal anti-inflammatory drug, to achieve
sustained drug release and enhanced topical
application.
The study involves the preparation of
niosomal suspensions with varying concentrations
of surfactants (Span 60) and cholesterol, followed
by incorporation into a gel base of carbopol 934.
The formulation was evaluated for physical
appearance, viscosity, pH, irritancy,drug content and
diffusion studies.
The optimized formulation (F4)
demonstrated good homogeneity, spreadability and
a pH range suitable for skin application.
It showed
sustained drug release of 83.
8% at the end of 6
hours in diffusion studies, demonstrating better
performance compared to the marketed Etodolac
gel.
Entrapment efficiency for the optimized
formulation was 77%, and the gel was non-irritant
based on the HET-CAM assay.
In conclusion, this
study suggests etodolac loaded niosomal gel was
successfully developed and can be a promising
strategy for providing localized and sustained drug
delivery, minimizing systemic side effects and
enhancing patient compliance.
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