| Literature DB >> 32093358 |
Eliana B Souto1,2, Aleksandra Zielinska1, Selma B Souto3, Alessandra Durazzo4, Massimo Lucarini4, Antonello Santini5, Amélia M Silva6,7, Atanas G Atanasov8,9,10,11, Conrado Marques12,13,14, Luciana N Andrade15,16, Patricia Severino12,13,14.
Abstract
In this work, we developed a solid lipid nanoparticle (SLN) formulation with (+)-limonene 1,2-epoxide and glycerol monostearate (Lim-SLNs), stabilized with Poloxamer® 188 in aqueous dispersion to modify the release profile of the loaded monoterpene derivative. We also evaluated the role of SLNs in lipid peroxidation and cytotoxicity in a spontaneously transformed aneuploid immortal keratinocyte cell line from adult human skin (the HaCaT cell line). For the cell viability assay, the colorimetric 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay was used. Lim-SLNs with a loading capacity and encapsulation efficiency of 0.39% and 63%, respectively, were produced by high pressure homogenization. A mean particle size of 194 ± 3.4 nm and polydispersity index of 0.244 were recorded for the loaded Lim-SLNs, as compared to 203 ± 1.5 nm (PI 0.213) for the non-loaded (blank) SLNs. The loading of the monoterpene derivative into glycerol monostearate SLNs fitted into the zero-order kinetics, and ameliorated both lipid peroxidation and cytotoxicity in a keratinocyte cell line. A promising formulation for antioxidant and anti-tumoral activities is here proposed.Entities:
Keywords: (+)-limonene 1,2-epoxide; HaCaT cell line; Imwitor 900K-SLN; cytotoxicity; lipid peroxidation; monoterpene
Year: 2020 PMID: 32093358 DOI: 10.3390/ijms21041449
Source DB: PubMed Journal: Int J Mol Sci ISSN: 1422-0067 Impact factor: 5.923