TY - JOUR
T1 - Porous Silicon Nanodiscs for Targeted Drug Delivery
AU - Alhmoud, Hashim
AU - Delalat, Bahman
AU - Elnathan, Roey
AU - Cifuentes-Rius, Anna
AU - Rogers, Mary-Louise
AU - Chaix, Arnaud
AU - Durand, Jean-Olivier
AU - Voelcker, Nicholas
PY - 2015/2/18
Y1 - 2015/2/18
N2 - There is a strong demand for techniques that allow the fabrication of biocompatible porous nanoparticles for drug delivery applications. In this work, a new method to fabricate size- and shape-controlled porous silicon (pSi) nanodiscs is described. The process relies on a combination of colloidal lithography and metal-assisted chemical etching. Height and diameter of the pSi nanodiscs can be easily adjusted. The nanodiscs are degradable in physiological milieu and are nontoxic to mammalian cells. In order to highlight the potential of the pSi nanodiscs in drug delivery, an in vitro investigation that involved loading of nanodiscs with the anticancer agent camptothecin and functionalization of the nanodisc periphery with an antibody that targets receptors on the surface of neuroblastoma cells is carried out. The thus-prepared nanocarriers are found to selectively attach to and kill cancer cells.
AB - There is a strong demand for techniques that allow the fabrication of biocompatible porous nanoparticles for drug delivery applications. In this work, a new method to fabricate size- and shape-controlled porous silicon (pSi) nanodiscs is described. The process relies on a combination of colloidal lithography and metal-assisted chemical etching. Height and diameter of the pSi nanodiscs can be easily adjusted. The nanodiscs are degradable in physiological milieu and are nontoxic to mammalian cells. In order to highlight the potential of the pSi nanodiscs in drug delivery, an in vitro investigation that involved loading of nanodiscs with the anticancer agent camptothecin and functionalization of the nanodisc periphery with an antibody that targets receptors on the surface of neuroblastoma cells is carried out. The thus-prepared nanocarriers are found to selectively attach to and kill cancer cells.
UR - http://www.scopus.com/inward/record.url?scp=84922855797&partnerID=8YFLogxK
U2 - 10.1002/adfm.201403414
DO - 10.1002/adfm.201403414
M3 - Article
SN - 1616-301X
VL - 25
SP - 1137
EP - 1145
JO - Advanced Functional Materials
JF - Advanced Functional Materials
IS - 7
ER -