TY - JOUR
T1 - Probing the coverage of nanoparticles by biomimetic membranes through nanoplasmonics
AU - Cardellini, Jacopo
AU - Ridolfi, Andrea
AU - Donati, Melissa
AU - Giampietro, Valentina
AU - Severi, Mirko
AU - Brucale, Marco
AU - Valle, Francesco
AU - Bergese, Paolo
AU - Montis, Costanza
AU - Caselli, Lucrezia
AU - Berti, Debora
PY - 2023/6/15
Y1 - 2023/6/15
N2 - Although promising for biomedicine, the clinical translation of inorganic nanoparticles (NPs) is limited by low biocompatibility and stability in biological fluids. A common strategy to circumvent this drawback consists in disguising the active inorganic core with a lipid bilayer coating, reminiscent of the structure of the cell membrane to redefine the chemical and biological identity of NPs. While recent reports introduced membrane-coating procedures for NPs, a robust and accessible method to quantify the integrity of the bilayer coverage is not yet available. To fill this gap, we prepared SiO2 nanoparticles (SiO2NPs) with different membrane coverage degrees and monitored their interaction with AuNPs by combining microscopic, scattering, and optical techniques. The membrane-coating on SiO2NPs induces spontaneous clustering of AuNPs, whose extent depends on the coating integrity. Remarkably, we discovered a linear correlation between the membrane coverage and a spectral descriptor for the AuNPs’ plasmonic resonance, spanning a wide range of coating yields. These results provide a fast and cost-effective assay to monitor the compatibilization of NPs with biological environments, essential for bench tests and scale-up. In addition, we introduce a robust and scalable method to prepare SiO2NPs/AuNPs hybrids through spontaneous self-assembly, with a high-fidelity structural control mediated by a lipid bilayer.
AB - Although promising for biomedicine, the clinical translation of inorganic nanoparticles (NPs) is limited by low biocompatibility and stability in biological fluids. A common strategy to circumvent this drawback consists in disguising the active inorganic core with a lipid bilayer coating, reminiscent of the structure of the cell membrane to redefine the chemical and biological identity of NPs. While recent reports introduced membrane-coating procedures for NPs, a robust and accessible method to quantify the integrity of the bilayer coverage is not yet available. To fill this gap, we prepared SiO2 nanoparticles (SiO2NPs) with different membrane coverage degrees and monitored their interaction with AuNPs by combining microscopic, scattering, and optical techniques. The membrane-coating on SiO2NPs induces spontaneous clustering of AuNPs, whose extent depends on the coating integrity. Remarkably, we discovered a linear correlation between the membrane coverage and a spectral descriptor for the AuNPs’ plasmonic resonance, spanning a wide range of coating yields. These results provide a fast and cost-effective assay to monitor the compatibilization of NPs with biological environments, essential for bench tests and scale-up. In addition, we introduce a robust and scalable method to prepare SiO2NPs/AuNPs hybrids through spontaneous self-assembly, with a high-fidelity structural control mediated by a lipid bilayer.
KW - Biomimetic nanoparticles
KW - Extracellular vesicles
KW - Gold nanoparticles
KW - Membrane-coated nanoparticles
KW - Nano-bio interface
KW - Nanomedicine
KW - Nanoplasmonics
KW - Silica nanoparticles
U2 - 10.1016/j.jcis.2023.02.073
DO - 10.1016/j.jcis.2023.02.073
M3 - Article
C2 - 36842416
AN - SCOPUS:85149057277
SN - 0021-9797
VL - 640
SP - 100
EP - 109
JO - Journal of Colloid and Interface Science
JF - Journal of Colloid and Interface Science
ER -