Cancer has nowadays become one of the leading causes of death worldwide.Conventional anticancer approaches are associated with different limitations.Therefore,innovative methodologies are being investigated,and severa...Cancer has nowadays become one of the leading causes of death worldwide.Conventional anticancer approaches are associated with different limitations.Therefore,innovative methodologies are being investigated,and several researchers propose the use of remotely activated nanoparticles to trigger cancer cell death.The idea is to conjugate two different components,i.e.,an external physical input and nanoparticles.Both are given in a harmless dose that once combined together act synergistically to therapeutically treat the cell or tissue of interest,thus also limiting the negative outcomes for the surrounding tissues.Tuning both the properties of the nanomaterial and the involved triggering stimulus,it is possible furthermore to achieve not only a therapeutic effect,but also a powerful platform for imaging at the same time,obtaining a nano-theranostic application.In the present review,we highlight the role of nanoparticles as therapeutic or theranostic tools,thus excluding the cases where a molecular drug is activated.We thus present many examples where the highly cytotoxic power only derives from the active interaction between different physical inputs and nanoparticles.We perform a special focus on mechanical waves responding nanoparticles,in which remotely activated nanoparticles directly become therapeutic agents without the need of the administration of chemotherapeutics or sonosensitizing drugs.展开更多
Highly mesoporous Zn O and g-Al2O3nanowires（NWs） are both synthesized by a hydrothermal method using commercially available porous anodic aluminium oxide（AAO） as template. AAO membrane acts as template for Zn O NW...Highly mesoporous Zn O and g-Al2O3nanowires（NWs） are both synthesized by a hydrothermal method using commercially available porous anodic aluminium oxide（AAO） as template. AAO membrane acts as template for Zn O NWs and both as template and precursor for g-Al2O3 NWs. The formation of intermediate phases of porous Zn6Al2（OH）16CO3and boehmite（g-Al OOH） were observed, both occurring during the hydrothermal synthesis of porous Zn O and g-Al2O3 NWs, respectively, and disappearing after annealing at 600 C. This novel template-assisted hydrothermal process leads to the formation of porous Zn O and g-Al2O3NWs（specific surface area of 192 m2 g 1and 263 m2 g 1, respectively）, showing pore sizes around 4 nm in diameter. The influence of the reaction parameters on the nanostructure morphology was also investigated. A Zn O seed layer, deposited on the AAO channels prior to the hydrothermal synthesis, leads to more compact Zn O nanowires（99 m2 g-1） protecting the AAO host from the chemical attack of the precursor solution.展开更多
Correction to:Nano-Micro Lett.(2021)13:11 https://doi.org/10.1007/s40820-020-00537-8 In the original publication figures 7 and 11 need to be updated with correct values.The correct version of Figs.7 and 11 is provided...Correction to:Nano-Micro Lett.(2021)13:11 https://doi.org/10.1007/s40820-020-00537-8 In the original publication figures 7 and 11 need to be updated with correct values.The correct version of Figs.7 and 11 is provided in this correction.The original article has been corrected.展开更多
基金the European Research Council(ERC)under the European Union’s Horizon 2020 research and innovation programme(Grant Agreement No 678151-Project Acronym“TROJANANOHORSE”-ERC starting Grant)the Politecnico di Torino and the Moschini Spa Company through a seed funding of Proof-of-Concept Grant No.16417.
文摘Cancer has nowadays become one of the leading causes of death worldwide.Conventional anticancer approaches are associated with different limitations.Therefore,innovative methodologies are being investigated,and several researchers propose the use of remotely activated nanoparticles to trigger cancer cell death.The idea is to conjugate two different components,i.e.,an external physical input and nanoparticles.Both are given in a harmless dose that once combined together act synergistically to therapeutically treat the cell or tissue of interest,thus also limiting the negative outcomes for the surrounding tissues.Tuning both the properties of the nanomaterial and the involved triggering stimulus,it is possible furthermore to achieve not only a therapeutic effect,but also a powerful platform for imaging at the same time,obtaining a nano-theranostic application.In the present review,we highlight the role of nanoparticles as therapeutic or theranostic tools,thus excluding the cases where a molecular drug is activated.We thus present many examples where the highly cytotoxic power only derives from the active interaction between different physical inputs and nanoparticles.We perform a special focus on mechanical waves responding nanoparticles,in which remotely activated nanoparticles directly become therapeutic agents without the need of the administration of chemotherapeutics or sonosensitizing drugs.
文摘Highly mesoporous Zn O and g-Al2O3nanowires（NWs） are both synthesized by a hydrothermal method using commercially available porous anodic aluminium oxide（AAO） as template. AAO membrane acts as template for Zn O NWs and both as template and precursor for g-Al2O3 NWs. The formation of intermediate phases of porous Zn6Al2（OH）16CO3and boehmite（g-Al OOH） were observed, both occurring during the hydrothermal synthesis of porous Zn O and g-Al2O3 NWs, respectively, and disappearing after annealing at 600 C. This novel template-assisted hydrothermal process leads to the formation of porous Zn O and g-Al2O3NWs（specific surface area of 192 m2 g 1and 263 m2 g 1, respectively）, showing pore sizes around 4 nm in diameter. The influence of the reaction parameters on the nanostructure morphology was also investigated. A Zn O seed layer, deposited on the AAO channels prior to the hydrothermal synthesis, leads to more compact Zn O nanowires（99 m2 g-1） protecting the AAO host from the chemical attack of the precursor solution.
文摘Correction to:Nano-Micro Lett.(2021)13:11 https://doi.org/10.1007/s40820-020-00537-8 In the original publication figures 7 and 11 need to be updated with correct values.The correct version of Figs.7 and 11 is provided in this correction.The original article has been corrected.
