TY - JOUR
T1 - Internalization and cytotoxicity analysis of silicon-based microparticles in macrophages and embryos
AU - Fernández-Rosas, Elisabet
AU - Gómez, Rodrigo
AU - Ibañez, Elena
AU - Barrios, Lleonard
AU - Duch, Marta
AU - Esteve, Jaume
AU - Plaza, José A.
AU - Nogués, Carme
PY - 2010/6/1
Y1 - 2010/6/1
N2 - Microchips can be fabricated, using semiconductor technologies, at microscopic level to be introduced into living cells for monitoring of intracellular parameters at a single cell level. As a first step towards intracellular chips development, silicon and polysilicon microparticles of controlled shape and dimensions were fabricated and introduced into human macrophages and mouse embryos by phagocytosis and microinjection, respectively. Microparticles showed to be non-cytotoxic for macrophages and were found to be localized mainly inside early endosomes, in tight association with endosomal membrane, and more rarely in acidic compartments. Embryos with microinjected microparticles developed normally to the blastocyst stage, confirming the non-cytotoxic effect of the particles. In view of these results silicon and polysilicon microparticles can serve as the frame for future intracellular chips development and this technology opens the possibility of real complex devices to be used as sensors or actuators inside living cells. © 2009 Springer Science+Business Media, LLC.
AB - Microchips can be fabricated, using semiconductor technologies, at microscopic level to be introduced into living cells for monitoring of intracellular parameters at a single cell level. As a first step towards intracellular chips development, silicon and polysilicon microparticles of controlled shape and dimensions were fabricated and introduced into human macrophages and mouse embryos by phagocytosis and microinjection, respectively. Microparticles showed to be non-cytotoxic for macrophages and were found to be localized mainly inside early endosomes, in tight association with endosomal membrane, and more rarely in acidic compartments. Embryos with microinjected microparticles developed normally to the blastocyst stage, confirming the non-cytotoxic effect of the particles. In view of these results silicon and polysilicon microparticles can serve as the frame for future intracellular chips development and this technology opens the possibility of real complex devices to be used as sensors or actuators inside living cells. © 2009 Springer Science+Business Media, LLC.
KW - Cytotoxicity
KW - MEMS
KW - Microparticle
KW - Polysilicon
KW - Silicon
UR - https://www.scopus.com/pages/publications/77952890067
U2 - 10.1007/s10544-009-9393-6
DO - 10.1007/s10544-009-9393-6
M3 - Article
SN - 1387-2176
VL - 12
SP - 371
EP - 379
JO - Biomedical Microdevices
JF - Biomedical Microdevices
ER -