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Synthesis of mesoporous silica nanoparticles by sol–gel as nanocontainer for future drug delivery applications
Author(s) -
Naiara I. Vazquez,
Z. González,
B. Ferrari,
Yolanda Castro
Publication year - 2017
Publication title -
boletín de la sociedad española de cerámica y vidrio
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.462
H-Index - 24
eISSN - 2173-0431
pISSN - 0366-3175
DOI - 10.1016/j.bsecv.2017.03.002
Subject(s) - tetraethyl orthosilicate , mesoporous silica , materials science , chemical engineering , zeta potential , dynamic light scattering , mesoporous material , nanoparticle , transmission electron microscopy , nanotechnology , specific surface area , particle size , chemistry , organic chemistry , catalysis , engineering
Development of mesoporous silica nanoparticles as carriers for drug delivery systems has increased exponentially during the last decade. The present work is focused on the synthesis of silica carriers by sol–gel from tetraethyl orthosilicate (TEOS) as precursor of silica and cetyltrimethylammonium bromide (CTAB) as pore generating agent. The synthesis conditions were modified varying the molar ratio of water/TEOS, NH3/TEOS and amount of CTAB. The silica particles were characterized by scan electron microscopy techniques (FESEM), high resolution transmission electron microscopy (HR-TEM), N2 adsorption–desorption isotherms, Zeta-potential and Dynamic Light Scattering (DLS). The results show that the specific surface area and the porosity of silica particles were strongly affected by the addition of CTAB and the amount of H2O. The dispersion and stability of silica mesoporous particles is achieved in spite of the high surface reactivity. The synthesis formulation affects considerably to the particle morphology, which changes from spheres to rods when the molar ratio of H2O increases. A maximum specific surface area of 1480 m2/g was obtained with pore sizes ranging 2.5–2.8 nm

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