TY - JOUR
T1 - Enhanced NLCs
T2 - Elevating therapeutic and diagnostic performance through covalent dye integration
AU - Borga, Joana
AU - Yañez, Osvaldo
AU - Urra, Gabriela
AU - Bustos, Daniel
AU - Morales, Javier O.
AU - Pinho, Sonia L.C.
N1 - Publisher Copyright:
© 2025 The Authors.
PY - 2025/12
Y1 - 2025/12
N2 - Nanostructured lipid carriers (NLCs) are widely investigated as versatile drug delivery systems. In this study, we aimed to design, synthesize, and characterize a novel fluorescently labeled NLC platform incorporating a rhodamine B–oleic acid conjugate (Rd-OA) as a proof-of-concept model for future therapeutic applications. NLCs were prepared using Precirol® ATO 5, oleic acid and Rd-OA, and Tween® 20 (T20) or Tween® 80 (T80). The resulting nanoparticles exhibited sizes of 350–500 nm, narrow polydispersity indices (<0.2), and highly negative zeta potentials (∼–30 mV), confirming stable colloidal properties. Rd-OA was efficiently integrated (100 % incorporation efficiency) with different concentrations. Molecular dynamics simulations provided atomic-level structural insights, revealing surfactant-dependent differences in component organization consistent with experimental data. NLCs were stable over a period of three months. In vitro assays in keratinocytes cells demonstrated a concentration-dependent cytotoxicity effect influenced by Rd-OA content, while fluorescence microscopy confirmed efficient cellular internalization of the NLCs. Collectively, these findings support the developed fluorescent NLC system as a stable, reproducible, and traceable platform suitable for future adaptation in drug delivery and imaging applications.”
AB - Nanostructured lipid carriers (NLCs) are widely investigated as versatile drug delivery systems. In this study, we aimed to design, synthesize, and characterize a novel fluorescently labeled NLC platform incorporating a rhodamine B–oleic acid conjugate (Rd-OA) as a proof-of-concept model for future therapeutic applications. NLCs were prepared using Precirol® ATO 5, oleic acid and Rd-OA, and Tween® 20 (T20) or Tween® 80 (T80). The resulting nanoparticles exhibited sizes of 350–500 nm, narrow polydispersity indices (<0.2), and highly negative zeta potentials (∼–30 mV), confirming stable colloidal properties. Rd-OA was efficiently integrated (100 % incorporation efficiency) with different concentrations. Molecular dynamics simulations provided atomic-level structural insights, revealing surfactant-dependent differences in component organization consistent with experimental data. NLCs were stable over a period of three months. In vitro assays in keratinocytes cells demonstrated a concentration-dependent cytotoxicity effect influenced by Rd-OA content, while fluorescence microscopy confirmed efficient cellular internalization of the NLCs. Collectively, these findings support the developed fluorescent NLC system as a stable, reproducible, and traceable platform suitable for future adaptation in drug delivery and imaging applications.”
KW - Bioimaging
KW - Drug delivery
KW - Fluorescent nanocarriers
KW - In silico modeling
KW - Lipid-based nanoparticles
UR - http://www.scopus.com/inward/record.url?scp=105018763407&partnerID=8YFLogxK
U2 - 10.1016/j.jddst.2025.107612
DO - 10.1016/j.jddst.2025.107612
M3 - Article
AN - SCOPUS:105018763407
SN - 1773-2247
VL - 114
JO - Journal of Drug Delivery Science and Technology
JF - Journal of Drug Delivery Science and Technology
M1 - 107612
ER -