The purpose of this
work was the assembly of multicomponent nano-bioconjugates
based on mesoporous silica nanoparticles (MSNs), proteins (bovine
serum albumin, BSA, or lysozyme, LYZ), and gold nanoparticles (GNPs).
These nano-bioconjugates may find applications in nanomedicine as
theranostic devices. Indeed, MSNs can act as drug carriers, proteins
stabilize MSNs within the bloodstream, or may have therapeutic or
targeting functions. Finally, GNPs can either be used as contrast
agents for imaging or for photothermal therapy. Here, amino-functionalized
MSNs (MSN–NH
2
) were synthesized and characterized
through various techniques (small angle X-rays scattering TEM, N
2
adsorption/desorption isotherms, and thermogravimetric analysis
(TGA)). BSA or lysozyme were then grafted on the external surface
of MSN–NH
2
to obtain MSN–BSA and MSN–LYZ
bioconjugates, respectively. Protein immobilization on MSNs surface
was confirmed by Fourier transform infrared spectroscopy, ζ-potential
measurements, and TGA, which also allowed the estimation of protein
loading. The MSN–protein samples were then dispersed in a GNP
solution to obtain MSN–protein–GNPs nano-bioconjugates.
Transmission electron microscopy (TEM) analysis showed the occurrence
of GNPs on the MSN–protein surface, whereas almost no GNPs
occurred in the protein-free control samples. Fluorescence and Raman
spectroscopies suggested that proteins–GNP interactions involve
tryptophan residues.