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Spontaneous Emulsification as a Low-Energy Strategy for Designing and Optimizing Resveratrol-Loaded Nanostructured
Nicoly T R Britto1, Lilian R S Montanheri1, Juliane N B D Pelin1
1Department of Pharmaceutical Sciences, Federal University of Sao Paulo, Diadema 09913-030, São Paulo, Brazil.
This study developed stable nanostructured lipid carriers (NLCs) using a low-energy, solvent-free method. These NLCs efficiently encapsulate bioactive compounds like resveratrol for sustained release, offering a sustainable drug delivery platform.
Area of Science:
- Materials Science
- Pharmaceutical Technology
- Nanotechnology
Background:
- Nanostructured lipid carriers (NLCs) are advanced delivery systems for lipophilic drugs, offering high encapsulation and controlled release.
- Conventional methods for NLC production often involve high energy input and organic solvents, posing limitations for large-scale and sustainable manufacturing.
Purpose of the Study:
- To develop and optimize nanostructured lipid carriers (NLCs) using a low-energy, solvent-free spontaneous emulsification method.
- To evaluate the encapsulation efficiency, particle characteristics, colloidal stability, and in vitro release profile of resveratrol (RVL)-loaded NLCs.
- To demonstrate the viability of spontaneous emulsification as a sustainable alternative for NLC production.
Main Methods:
- NLCs were formulated using cetearyl alcohol (solid lipid) and Kolliphor RH 40 (surfactant) via spontaneous emulsification.
- A Box-Behnken design was employed for optimizing formulation and process parameters, with particle size and uniformity assessed by laser diffraction.
- Resveratrol was encapsulated, and the resulting NLCs were characterized using techniques including DSC/Thermogravimetry, FTIR, and TEM. Stability was assessed over 90 days.
Main Results:
- Optimized NLCs achieved 99% resveratrol encapsulation efficiency, with a mean particle size of 90 nm, a polydispersity index of 0.2, and a zeta potential of -37 mV.
- The NLCs exhibited excellent colloidal stability for 90 days at 8 °C, confirmed by characterization techniques.
- Differential scanning calorimetry/thermogravimetry and FTIR confirmed successful active compound incorporation and nanocarrier composition. Transmission electron microscopy visualized the nanocarrier morphology.
- In vitro studies demonstrated a delayed and sustained release profile for resveratrol from the NLCs.
Conclusions:
- Spontaneous emulsification is a viable, low-energy, and solvent-free method for producing stable and efficient nanostructured lipid carriers.
- The developed NLCs show significant potential as a platform for delivering bioactive compounds, including pharmaceuticals and cosmetic ingredients.
- This approach offers a sustainable and scalable alternative to conventional high-energy methods for NLC fabrication.
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