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Processing of Lipid Nanodispersions into Solid Powders by Spray Drying
Denise Steiner1,2, Leonie V Schumann1, Heike Bunjes1,2
1Institut für Pharmazeutische Technologie und Biopharmazie, Technische Universität Braunschweig, Mendelssohnstraße 1, 38106 Braunschweig, Germany.
Pharmaceutics
|November 26, 2022
Summary
Spray drying effectively preserves lipid nanocarriers for oral drug delivery. Optimized conditions maintain nanoparticulate properties and enable amorphous matrix formation for enhanced bioavailability of poorly soluble active pharmaceutical ingredients (APIs).
Area of Science:
- Pharmaceutical Technology
- Materials Science
- Chemical Engineering
Background:
- Lipid nanodispersions are effective carriers for poorly water-soluble active pharmaceutical ingredients (APIs), improving bioavailability.
- Oral administration of APIs is preferred by patients, necessitating the development of solid dosage forms from nanocarrier systems.
- Spray drying offers a potential method for producing stable, solid-state nanocarrier formulations.
Purpose of the Study:
- To evaluate spray drying as a method for producing stable lipid nanodispersions for oral drug delivery.
- To investigate the influence of matrix materials and drying parameters on the nanoparticulate properties of lipid nanodispersions.
- To assess the redispersibility and particle size of spray-dried lipid nanoemulsions loaded with an active pharmaceutical ingredient.
Main Methods:
- Preparation of lipid nanodispersions using various solid lipids and oils.
- Spray drying of nanodispersions using lactose and SDS as matrix materials.
- Characterization of nanoparticulate properties, including particle size and redispersibility.
- Investigation of the effect of drying air inlet temperature on matrix formation and particle stability.
- Development of a tristearin suspension probe to measure particle temperature exposure during spray drying.
Main Results:
- Nanoparticulate properties of lipid nanodispersions were maintained during spray drying using lactose and SDS as matrix materials.
- Spray-dried lipid nanoemulsions loaded with fenofibrate showed good redispersibility with particle sizes below 300 nm at 26.8 wt.% lipid content.
- Optimal drying air inlet temperatures of 110 °C or above facilitated the formation of an amorphous lactose matrix around lipid particles.
- The tristearin probe indicated that particle temperatures during spray drying could exceed the measured outlet temperature.
Conclusions:
- Spray drying is a viable technology for producing stable, solid lipid nanocarrier systems for oral administration of poorly water-soluble APIs.
- Lactose in combination with SDS is an effective matrix system for spray drying lipid nanodispersions, preserving their nanoparticulate integrity.
- Controlling spray drying temperature is crucial for achieving an amorphous matrix and ensuring the stability and redispersibility of the nanocarriers.
- Further investigation into the precise temperature experienced by lipid particles during spray drying is warranted.

