Lipid-polymer hybrid nanoparticles as a targeted drug delivery system for melanoma treatment

Aiming to target vitamin D receptors (VDR) expressed in melanoma cells, vitamin D(3)functionalized hybrid lipid-polymer nanoparticles (HNP-VDs) comprising a poly(lactic-co-glycolic acid) (PLGA) core and a lipid shell composed of hydrogenated soy phosphatidylcholine (HSPC), cholesterol (CHOL) and 1,2-disteroyl-sn-glycero-3-phosphaethanolamine-N[succinyl(polyethyleneglycol)-2000 (DSPE-PEG(2000)) were synthesized. The nanocarriers were optimized to a lipid surface area coverage of 97%.In vitrodrug release studies showed an initial burst release in the first 24 h followed by diffusive transport. Finally, cellular uptake experiments demonstrated that the HNP-VDs efficiently targeted B16 melanoma cells, thus resulting in a promising vehicle to deliver therapeutics for the melanoma treatment.

Automated summary

In this study, vitamin D(3) functionalized hybrid lipid-polymer nanoparticles were synthesized to target melanoma cells. The nanoparticles showed efficient cellular uptake and hold promise as a delivery vehicle for melanoma treatment.