Nanocarbons with different dimensions (e.g., 0D fullerenes and carbon nanodots, 1D carbon nanotubes and graphene nanoribbons, 2D graphene and graphene oxides, and 3D nanodiamonds) have attracted enormous interest for applications ranging from electronics, optoelectronics, and photovoltaics to sensing, bioimaging, and therapeutics due to their unique physical and chemical properties. Among them, nanocarbon-based theranostics (i.e., therapeutics and diagnostics) is one of the most intensively studied applications, as these nanocarbon materials serve as excellent biosensors, versatile drug/gene carriers for specific targeting in vivo, effective photothermal nanoagents for cancer therapy, and promising fluorescent nanolabels for cell and tissue imaging. This review provides a systematic overview of the latest theranostic applications of nanocarbon materials with a comprehensive comparison of the characteristics of different nanocarbon materials and their influences on theranostic applications. We first introduce the different carbon allotropes that can be used for theranostic applications with their respective preparation and surface functionalization approaches as well as their physical and chemical properties. Theranostic applications are described separately for both in vitro and in vivo systems by highlighting the protocols and the studied biosystems, followed by the toxicity and biodegradability implications. Finally, this review outlines the design considerations for nanocarbon materials as the key unifying themes that will serve as a foundational first principle for researchers to study, investigate, and generate effective, biocompatible, and nontoxic nanocarbon materials-based models for cancer theranostics applications. Finally, we summarize the review with an outlook on the challenges and novel theranostic protocols using nanocarbon materials for hard-to-treat cancers and other diseases. This review intends to present a comprehensive guideline for researchers in nanotechnology and biomedicine on the selection strategy of nanocarbon materials according to their specific requirements.
CONTENTSRelated Molecules by Different Nano-54 carbon Materials W 55 2.2. Nanocarbons for in Vitro Bioimaging AD 56 2.2.1. In Vitro Imaging by Graphene AD 57 2.2.2. In Vitro Imaging by Carbon Nanotubes AF 58 2.2.3. In Vitro Imaging by Fullerenes AH 59 2.2.4. In Vitro Imaging by Carbon Nanohorns AI 60 2.2.5. In Vitro Imaging by Nanodiamonds AJ
Over the past decade, carbon dots have ignited a burst of interest in many different fields, including nanomedicine, solar energy, optoelectronics, energy storage, and sensing applications, owing to their excellent photoluminescence properties and the easiness to modify their optical properties through doping and functionalization. In this review, the synthesis, structural and optical properties, as well as photoluminescence mechanisms of carbon dots are first reviewed and summarized. Then, we describe a series of designs for carbon dot-based sensors and the different sensing mechanisms associated with them. Thereafter, we elaborate on recent research advances on carbon dot-based sensors for the selective and sensitive detection of a wide range of analytes, including heavy metals, cations, anions, biomolecules, biomarkers, nitroaromatic explosives, pollutants, vitamins, and drugs. Lastly, we provide a concluding perspective on the overall status, challenges, and future directions for the use of carbon dots in real-life sensing.
In
this work, we reported the synthesis of an engineered novel
nanocarrier composed of biodegradable charged polyester vectors (BCPVs)
and graphene quantum dots (GQDs) for pancreatic cancer (MiaPaCa-2
cells) therapy applications. Such a nanocarrier was utilized to co-load
doxorubicin (DOX) and small interfering ribonucleic acid (siRNA),
resulting in the formation of GQD/DOX/BCPV/siRNA nanocomplexes. The
resulting nanocomplexes have demonstrated high stability in physiologically
mimicking media, excellent K-ras downregulation activity, and effective
bioactivity inhibition for MiaPaCa-2 cells. More importantly, laser
light was used to generate heat for the nanocomplexes via the photothermal
effect to damage the cells, which was further employed to trigger
the release of payloads from the nanocomplexes. Such triggered release
function greatly enhanced the anticancer activity of the nanocomplexes.
Preliminary colony formation study also suggested that GQD/DOX/BCPV/siRNA
nanocomplexes are qualified carrier candidates in subsequent in vivo
tests.
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