Stratum-Confined Solid-State Reaction (SC-SSR) toward Colloidal Silicon-Based Hollow Nanostructures for Bioapplications.
Jeong Hun ChoiNitee KumariAmit KumarAnubhab AcharyaJungsoo AhnJaerim KimHyeonwoong HwangTaiha JooJong Kyu KimIn Su LeePublished in: Small (Weinheim an der Bergstrasse, Germany) (2023)
Silicon nanostructures (SiNSs) can provide multifaceted bioapplications; but preserving their subhundred nm size during high-temperature silica-to-silicon conversion is the major bottleneck. The SC-SSR utilizes an interior metal-silicide stratum space at a predetermined radial distance inside silica nanosphere to guide the magnesiothermic reduction reaction (MTR)-mediated synthesis of hollow and porous SiNSs. In depth mechanistic study explores solid-to-hollow transformation encompassing predefined radial boundary through the participation of metal-silicide species directing the in-situ formed Si-phase accumulation within the narrow stratum. Evolving thin-porous Si-shell remains well protected by the in-situ segregated MgO emerging as a protective cast against the heat-induced deformation and interparticle sintering. Retrieved hydrophilic SiNSs (<100 nm) can be conveniently processed in different biomedia as colloidal solutions and endocytosized inside cells as photoluminescence (PL)-based bioimaging probes. Inside the cell, rattle-like SiNSs encapsulated with Pd nanocrystals can function as biorthogonal nanoreactors to catalyze intracellular synthesis of probe molecules through C-C cross coupling reaction.
Keyphrases
- metal organic framework
- solid state
- quantum dots
- high temperature
- living cells
- room temperature
- molecularly imprinted
- induced apoptosis
- genetic diversity
- photodynamic therapy
- highly efficient
- fluorescent probe
- cell cycle arrest
- single cell
- high glucose
- ultrasound guided
- small molecule
- physical activity
- cell therapy
- diabetic rats
- mesenchymal stem cells
- reactive oxygen species
- light emitting
- tissue engineering
- electron transfer
- energy transfer
- endoplasmic reticulum stress
- cell death
- endothelial cells