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Updated: Jan 25, 2026

Solid Lipid Nanoparticles SLNs for Intracellular Targeting Applications
Published on: November 17, 2015
Improved synthesis and characterization of cholesteryl oleate-loaded cationic solid lipid nanoparticles with high
Marc Suñé-Pou1, María J Limeres2, Isaac Nofrerias3
1Service of Development of Medicines (SDM), Faculty of Pharmacy, University of Barcelona, Avda. Joan XXIII, s/n 08028, Barcelona, Spain; Department of Molecular Biology, Institute of Parasitology and Biomedicine "López-Neyra" (IPBLN-CSIC), PTS, 18016, Granada, Spain; Pharmacotherapy, Pharmacogenetics and Pharmaceutical Technology Research Group. IDIBELL-UB, Duran i Reynals Hospital, 3ª level, Gran Via de l'Hospitalet 199, 08908, Hospitalet de Llobregat, Barcelona, Spain.
Abstract:
The development of new nanoparticle formulations that are capable of high transfection efficiency without toxicity is essential to provide new tools for gene therapy. However, the issues of complex, poorly reproducible manufacturing methods, and low efficiencies during in vivo testing have prevented translation to the clinic. We have previously reported the use of cholesteryl oleate as a novel excipient for solid lipid nanoparticles (SLNs) for the development of highly efficient and nontoxic nucleic acid delivery carriers. Here, we performed an extensive characterization of this novel formulation to make the scale up under Good Manufacturing Practice (GMP) possible. We also describe the complete physicochemical and biological characterization of cholesteryl oleate-loaded SLNs to ensure the reproducibility of this formula and the preservation of its characteristics before and after the lyophilization process. We defined the best manufacturing method and studied the influence of some parameters on the obtained nanoparticles using the Quality by Design (ICH Q8) guideline to obtain cholesteryl oleate-loaded SLNs that remain stable during storage and guarantee in vitro nucleic acid delivery efficacy. Our results indicate that this improved formulation is suitable for gene therapy with the possibility of scale-up the manufacturing of nanoparticles under GMP conditions.
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