UNASSIGNED: The presence of metastatic disease in the cervical lymph nodes can affect the recurrence and survival of patients with thyroid cancer. Parathyroid gland injury during surgery can result in hypoparathyroidism, particularly with total thyroidectomy. Injection of carbon nanoparticles into the thyroid will label draining lymph nodes and aid in the visualization of metastatic cervical lymph nodes during a radical operation, sparing accidental damage to the parathyroid glands. Although reported to be useful during surgery, the safety of nanocarbon particles has rarely been investigated, and adverse side effects need to be studied.
UNASSIGNED: The author describes five patients with thyroid cancer who had carbon secretions in the trachea or mucosa after carbon nanoparticles were injected into the thyroid. A patient with carbon secretions in the trachea mucosa recovered but had progressive dyspnoea. Surgical treatment was performed, and a mass was found in the trachea mucosa. After excluding all other possibilities, the author concluded that the mass was caused by nanocarbon suspension.
UNASSIGNED: To the author\'s knowledge, there are no reports on nanocarbon suspension into the mucosa and no consensus has yet been reached on the precise injection site, depth, or dose for injecting carbon nanoparticles before thyroidectomy.
UNASSIGNED: The author suggests that the most appropriate injection depth of nanocarbon suspensions should be no more than 3 mm of the thyroid gland thickness to avoid deep injection into the trachea.

Overactive or dysregulated cytokine expression is a hallmark of many acute and chronic inflammatory diseases. This is true for acute or chronic infections, neurodegenerative diseases, autoimmune diseases, cardiovascular diseases, cancer, and others. Cytokines such as interleukin-6 (IL-6) are known therapeutic targets and biomarkers for such inflammatory diseases. Platforms for cytokine detection are, therefore, desirable tools for both research and clinical applications. Single-walled carbon nanotubes (SWCNT) are versatile nanomaterials with near-infrared fluorescence that can serve as transducers for optical sensors. When functionalized with an analyte-specific recognition element, SWCNT emission may become sensitive and selective toward the desired target. SWCNT-aptamer sensors are easily assembled, inexpensive, and biocompatible. In this work, we introduced a nanosensor design based on SWCNT and a DNA aptamer specific to IL-6. We first evaluated several SWCNT-aptamer constructs based on this simple direct complexation method, wherein the aptamer both solubilizes the SWCNT and confers sensitivity to IL-6. The sensor limit of detection, 105 ng/mL, lies in the relevant range for pathological IL-6 levels. Upon investigation of sensor kinetics, we found rapid response within seconds of antigen addition which continued over the course of 3 h. We found that this sensor construct is stable and the aptamer is not displaced from the nanotube surface during IL-6 detection. Finally, we investigated the ability of this sensor construct to detect macrophage activation caused by bacterial lipopolysaccharides (LPS) in an in vitro model of disease, finding rapid and sensitive detection of macrophage-expressed IL-6. We are confident that further development of this sensor will have novel implications for diagnosis of acute and chronic inflammatory diseases, in addition to contributing to the understanding of the role of cytokines in these diseases.

Overactive or dysregulated cytokine expression is hallmark of many acute and chronic inflammatory diseases. This is true for acute or chronic infection, neurodegenerative diseases, autoimmune diseases, cardiovascular disease, cancer, and others. Cytokines such as interleukin-6 (IL-6) are known therapeutic targets and biomarkers for such inflammatory diseases. Platforms for cytokine detection are therefore desirable tools for both research and clinical applications. Single-walled carbon nanotubes (SWCNT) are versatile nanomaterials with near-infrared fluorescence that can serve as transducers for optical sensors. When functionalized with an analyte-specific recognition element, SWCNT emission may become sensitive and selective towards the desired target. SWCNT-aptamer sensors are easily assembled, inexpensive, and biocompatible. In this work, we introduced a nanosensor design based on SWCNT and a DNA aptamer specific to IL-6. We first evaluated several SWCNT-aptamer constructs based on this simple direct complexation method, wherein the aptamer both solubilizes the SWCNT and confers sensitivity to IL-6. The sensor limit of detection, 105 ng/mL, lies in the relevant range for pathological IL-6 levels. Upon investigation of sensor kinetics, we found rapid response within seconds of antigen addition which continued over the course of three hours. We found that this sensor construct is stable, and the aptamer is not displaced from the nanotube surface during IL-6 detection. Finally, we investigated the ability of this sensor construct to detect macrophage activation caused by bacterial lipopolysaccharides (LPS) in an in vitro model of disease, finding rapid and sensitive detection of macrophage-expressed IL-6. We are confident further development of this sensor will have novel implications for diagnosis of acute and chronic inflammatory diseases, in addition to contributing to the understanding of the role of cytokines in these diseases.

Efficient water-solubilization of nanocarbons is desirable for both their biological and material applications, but so far has mainly relied on covalent modifications or amphiphiles featuring ionic side-chains. Here, we report a facile 2-4-step synthesis of pyridinium-based, bent aromatic amphiphiles with modular nonionic side-chains (i.e., CH3 and CH2CH2(OCH2CH2)2-Y (Y = OCH3, OH, and imidazole)). The new amphiphiles quantitatively self-assemble into ≈2 nm-sized aromatic micelles in water independent of the side-chain. Importantly, efficient water-solubilization and nonionic surface modification of various nanocarbons (e.g., fullerene C60, carbon nanotubes, and graphene nanoplatelets) are achieved through noncovalent encircling with the bent amphiphiles. The resultant imidazole-modified nanocarbons display a pH-responsive surface charge, as evidenced by NMR and zeta-potential measurements. In addition, solubilization of a nitrogen-doped nanocarbon (i.e., graphitic carbon nitride) in the form of 10-30 nm-sized stacks is also demonstrated using the present amphiphiles.

Nanocarbon materials have become extraordinarily compelling for their significant potential in the cutting-edge science and technology. These materials exhibit exceptional physicochemical properties due to their distinctive low-dimensional structures and tailored surface characteristics. An attractive direction at the forefront of this field involves the spatially resolved chemical functionalization of a diverse range of nanocarbons, encompassing carbon nanotubes, graphene, and a myriad of derivative structures. In tandem with the technological leaps in lithography, these endeavors have fostered the creation of a novel class of nanocarbon materials with finely tunable physical and chemical attributes, and programmable multi-functionalities, paving the way for new applications in fields such as nanoelectronics, sensing, photonics, and quantum technologies. Our review examines the swift and dynamic advancements in nanocarbon chemical patterning. Key breakthroughs and future opportunities are highlighted. This review not only provides an in-depth understanding of this fast-paced field but also helps to catalyze the rational design of advanced next-generation nanocarbon-based materials and devices.

In the present study, a hybrid cotton fabric with an enhanced ultraviolet (UV) shielding property was developed by coating with functionally activated nanocarbon (FACN) which was grafted by polyaniline (PANI) using in situ polymerization. In light of this, Teff hay biomass was used to establish the activated nanocarbon (ANC), that was subsequently given a surface functionalization using a silane coupling agent. Using the response surface (RSM) statistical analysis, the study was optimized for the weight percent of ANC and PANI with respect to the cotton fabric that was found to offer remarkable UV protection, with an ultraviolet protection factor (UPF) of 64.563, roughly 17 times more than that of primitive cotton (UPF = 3.7). The different characterization techniques, such as UV absorption, Fourier transform infrared (FTIR), scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), and thermal behavior studies were investigated. In addition, the basic textile properties on optimized hybrid material were found to be appreciably increased. The results suggested that activated FACN made from Teff hay could be an effective alternative organic source material for developing UV protective hybrid cotton fabrics.

In this paper, we report on novel polyimide (PI) nanocomposites filled with binary mixtures of metal oxide (either TiO2 or ZrO2) nanoparticles and nanocarbon (either carbon nanofibers (CNFs) or functionalized carbon nanotubes (CNTfs)). The structure and morphology of the materials obtained were comprehensively studied. An exhaustive investigation of their thermal and mechanical properties was performed. We revealed a synergistic effect of the nanoconstituents with regard to a number of functional characteristics of the PIs compared with single-filler nanocomposites, including thermal stability, stiffness (below and above glass transition temperature), yield point, and temperature of flowing. Moreover, the possibility of manipulating the properties of the materials by choosing a proper combination of the nanofillers was demonstrated. The results obtained can become a platform in the design of PI-based engineering materials with tailored characteristics capable of operating in extreme conditions.

This work aimed to study the thermal and crystalline properties of poly (1,4-phenylene sulfide)@carbon char nanocomposites. Coagulation-processed nanocomposites of polyphenylene sulfide were prepared using the synthesized mesoporous nanocarbon of coconut shells as reinforcement. The mesoporous reinforcement was synthesized using a facile carbonization method. The investigation of the properties of nanocarbon was completed using SAP, XRD, and FESEM analysis. The research was further propagated via the synthesis of nanocomposites through the addition of characterized nanofiller into poly (1,4-phenylene sulfide) at five different combinations. The coagulation method was utilized for the nanocomposite formation. The obtained nanocomposite was analyzed using FTIR, TGA, DSC, and FESEM analysis. The BET surface area and average pore volume of the bio-carbon prepared from coconut shell residue were calculated to be 1517 m2/g and 2.51 nm, respectively. The addition of nanocarbon to poly (1,4-phenylene sulfide) led to an increase in thermal stability and crystallinity up to 6% loading of the filler. The lowest glass transition temperature was achieved at 6% doping of the filler into the polymer matrix. It was established that the thermal, morphological, and crystalline properties were tailored by synthesizing their nanocomposites with the mesoporous bio-nanocarbon obtained from coconut shells. There is a decline in the glass transition temperature from 126 °C to 117 °C using 6% filler. The measured crystallinity was decreased continuously, with the mixing of the filler exhibiting the incorporation of flexibility in the polymer. So, the loading of the filler into poly (1,4-phenylene sulfide) can be optimized to enhance its thermoplastic properties for surface applications.

Developing efficient platinum (Pt)-based electrocatalysts is enormously significant for fuel cells. Herein, we report an integrated electrocatalyst of ultralow-Pt alloy encapsulated into nitrogen-doped nanocarbon architecture for efficient oxygen reduction reaction. This hybrid Pt-based catalyst achieves a mass activity of 3.46 A mgpt-1 at the potential of 0.9 V vs. RHE with a negligible stability decay after 10,000 cycles. More importantly, this half-cell activity can be expressed at full cell level with a high Pt utilization of 10.22 W mgPt-1cathode and remarkable durability after 30,000 cycles in single-cell. Experimental and theoretical investigations reveal that a highly strained Pt structure with an optimal Pt-O binding energy is induced by the incorporation of Co/Ni into Pt lattice, which would account for the improved reaction kinetics. The synergistic catalysis due to nitrogen-doped nanocarbon architecture and active Pt component is responsible for the enhanced catalytic activity. Meanwhile, the strong metal-support interaction and optimized hydrophilic properties of nanocarbon matrix facilitate efficient mass transport and water management. This work may provide significant insights in designing the low-Pt integrated electrocatalysts for fuel cells and beyond.

Selective hydrogenation of nitroaromatics to the corresponding anilines is a key topic for research in fine chemical industrial fields. Nanocarbon materials with good chemical stability, high electrical conductivity, and good mechanical performance have been regarded as promising candidates in the catalytic field, and have shown a wide range of applications in recent years. Controllable synthesis on the structure, morphology, and active sites of nanocarbon-based catalysts is vital to the development of highly efficient catalysts. In this mini-review, we summarize the recent progresses of nanocarbon materials by focusing on the synthesis approaches and their corresponding nanostructures, including carbon nanofibers, carbon nanotubes, graphene, porous carbon, carbon spheres, and metal organic framework-derived carbon materials. The design and catalytic performance of these nanocarbon materials have been systematically discussed. Finally, the emerging challenges and future prospective for developing advanced nanocarbon-based catalysts are outlined.