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ABSTRACT
Objective: Atorvastatin calcium exhibits poor bioavailability due to its low water solubility
the solubility, leading to improved drug absorption and bioavailability. Enhance wound healing
efficacy, provide controlled drug release and offer localized delivery, ultimately improving
Methods: Atorvastatin calcium nanocrystals (NCs) were prepared by 23 factorial design and
solvent antisolvent precipitation method. The influences of three formulation excipients such as
stabilizer (Pluronic F-127), solvent antisolvent ration and stirring time on the characterization of
NCs were investigated. Aloe vera-carbopol gel was added to the chosen F8 nanosuspension
formulation, and the mixture was stirred at 800 rpm in a magnetic stirrer to create Nanogel (NG).
The prepared ATC NG was evaluated for their Transparency, smoothness and relative density,
pH, moisture content, rheological behavior, spreadability, drug stability and permeability tests in
an ex vivo model.
Results: Compared to the pure drug, the improved formulation NCs exhibited much higher
saturation solubility and a much faster dissolving rate. The ATC loaded aloe-carbopol gel (AG)
and ATC nanoparticle loaded gel (ANG) is clear and viscous. The pH was found to be 6.5 which
is nearly neutral and it does not cause any tingling or irritation when applied on the skin. The
dynamic viscosity of the ANG is found to be 8500 cp which shows the thickness of the gel and it
will stays in the place where it will be applied. Based on the results of drug permeation
hours whereas the ANG showed a release of 400±18 µg/cm2. The results of the stability tests
showed that there were no detectable changes in the product after storage for up to 90 days.
Conclusion: This study shows that the formulation of ATC based Nanogel have sustain
release activity and may be useful in solving the limitations of conventional drug delivery
system. Patient compliance will be more because topical administration of these Nanogel is less
Nanogel.