Decagram-Scale Synthesis of Multicolor Carbon Nanodots: Self-Tracking Nanoheaters with Inherent and Selective Anticancer Properties
journal contributionposted on 2022-01-05, 15:48 authored by Nicolò Mauro, Mara Andrea Utzeri, Alice Sciortino, Fabrizio Messina, Marco Cannas, Radian Popescu, Dagmar Gerthsen, Gianpiero Buscarino, Gennara Cavallaro, Gaetano Giammona
Carbon nanodots (CDs) are a new class of carbon-based nanoparticles endowed with photoluminescence, high specific surface area, and good photothermal conversion, which have spearheaded many breakthroughs in medicine, especially in drug delivery and cancer theranostics. However, the tight control of their structural, optical, and biological properties and the synthesis scale-up have been very difficult so far. Here, we report for the first time an efficient protocol for the one-step synthesis of decagram-scale quantities of N,S-doped CDs with a narrow size distribution, along with a single nanostructure multicolor emission, high near-infrared (NIR) photothermal conversion efficiency, and selective reactive oxygen species (ROS) production in cancer cells. This allows achieving targeted and multimodal cytotoxic effects (i.e., photothermal and oxidative stresses) in cancer cells by applying biocompatible NIR laser sources that can be remotely controlled under the guidance of fluorescence imaging. Hence, our findings open up a range of possibilities for real-world biomedical applications, among which is cancer theranostics. In this work, indocyanine green is used as a bidentate SOx donor which has the ability to tune surface groups and emission bands of CDs obtained by solvothermal decomposition of citric acid and urea in N,N-dimethylformamide. The co-doping implies various surface states providing transitions in the visible region, thus eliciting a tunable multicolor emission from blue to red and excellent photothermal efficiency in the NIR region useful in bioimaging applications and image-guided anticancer phototherapy. The fluorescence self-tracking capability of SOx–CDs reveals that they can enter cancer cells more quickly than healthy cell lines and undergo a different intracellular fate after cell internalization. This could explain why sulfur doping entails pro-oxidative activities by triggering more ROS generation in cancer cells when compared to healthy cell lines. We also find that oxidative stress can be locally enhanced under the effects of a NIR laser at moderate power density (2.5 W cm–2). Overall, these findings suggest that SOx–CDs are endowed with inherent drug-independent cytotoxic effects toward cancer cells, which would be selectively enhanced by external NIR light irradiation and helpful in precision anticancer approaches. Also, this work opens a debate on the role of CD surface engineering in determining nanotoxicity as a function of cell metabolism, thus allowing a rational design of next-generation nanomaterials with targeted anticancer properties.
tune surface groupsspearheaded many breakthroughsprecision anticancer approachesnarrow size distributionmoderate power densityguided anticancer phototherapydifferent intracellular fatecd surface engineeringallows achieving targeted5 w cmphotothermal conversion efficiencygood photothermal conversionexcellent photothermal efficiencyworld biomedical applicationstunable multicolor emissiontargeted anticancer propertieshealthy cell linesmulticolor carbon nanodotsbased nanoparticles endowedenter cancer cellsnir region usefulcancer cells>, photothermalvisible regionemission bandsbiological propertiesbioimaging applicationscell metabolismcell internalizationcancer theranosticsx tracking nanoheaterstracking capabilitytight controlthus elicitingthus allowingsynthesis scalesub ><step synthesissolvothermal decompositionselectively enhancedscale synthesisscale quantitiesremotely controlledrational designoxidative stressesoxidative stressoxidative activitiesnir lasernew classlocally enhancedindocyanine greenhigh neargeneration nanomaterialsfluorescence imagingfirst timefindings suggestfindings openefficient protocole .drug deliverydetermining nanotoxicitycould explaincitric acid> sub>- dimethylformamide