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Sepsis-induced acute kidney injury (AKI) is a common in clinic. Circular RNAs (circRNAs) play significant roles in ameliorating AKI. The purpose of this study was aimed to identify the role of circ_0074371 and the potential action mechanism in sepsis-induced AKI.AKI patients and healthy individual serum samples were collected and the relative expression of circ_0074371 was measured by real-time polymerase chain reaction (RT-PCR). HK2 cells were treated with different dose (0, 2.5, 5 and 10 μg/ml) lipopolysaccharide (LPS) to establish the AKI cell model. The cell viability and apoptosis of HK2 cells were detected using cell counting kit-8 (CCK-8) and flow cytometry, respectively. The contents of malondialdehyde (MDA), and superoxide dismutase (SOD) were evaluated using the relative commercial kits. The IL-1β and TNF-α levels in cell culture supernatants were measured by ELISA. The interaction relationship between miR-330-5p and circ_0074371 or ELK1 was predicted by Targetscan database and further confirmed by the dual-luciferase reporter assay system.The circ_0074371 expression was up-regulated in sepsis patients and LPS-induced HK2 cells. Silencing circ_0074371 promoted HK2 cells viability and inhibited the HK2 cells apoptosis. miR-330-5p inhibitor weakened circ_0074371 inhibitor-induced cell viability, apoptosis and oxidative stress. Further mechanism analysis showed that circ_0074371 acted as a sponge for miR-330-5p to increase ELK1 expression level. Importantly, miR-330-5p downregulation or ELK1 upregulation reversed the action of circ_0074371 knockdown on LPS-induced HK2 cells.Knockdown of circ_0074371 ameliorated LPS-induced HK2 cells apoptosis, inflammation and oxidative stress via regulating miR-330-5p/ELK1, opening a new window into the pathogenesis AKI.

Carbon dots (CDots) coupled with visible light exposure were found highly effective in the inactivation of bacterial pathogens.

Five novel halophilic archaeal strains, named BND22T, ZY10T, ZY41T, ZY58T, and ZY43T, were isolated from the coastal saline sediment of the intertidal zone located in Qingdao and the natural sea salt produced from Huanghua marine solar saltern, PRChina. These five strains demonstrated the typical morphology and growth characteristics of haloarchaea. The comparison of 16S rRNA gene revealed that strain BDN22T was associated with Salinirubellus salinus ZS-35-S2T (95.2% similarity), strain ZY10T was related to Halosegnis rubeus F17-44T (95.1% similarity), both strains ZY41T and ZY58T were closely related to Haloglomus irregulare F16-60T (98.1% and 98.2% similarities, respectively), and strain ZY43T was close to Natronomonas salina YPL13T (98.0% similarity). In addition to the 16S rRNA gene, the rpoB′ gene is undoubtedly another important molecular marker for the identification of halophilic archaea, and concatenated-conserved-protein phylogeny was widely used in archaeal classification in recent years. Phylogenetic and phylogenomic analyses based on rpoB′ genes and 122 concatenated archaeal protein genes showed that these haloarchaea construct three different clades and gathered together with the current members of Haloarculaceae. Strains BND22T and ZY10T formed two distinct clades separated from Salinirubellus salinus ZS-35-S2T and Halosegnis members, strains ZY41T and ZY58T clustered with Haloglomus irregulare F16-60T, and strain ZY43T gathered with the current members of Natronomonas. The ANI, DDH, and AAI values of these five strains against phylogenetic neighbours were no more than 91%, 45%, and 92%, respectively, far below the cut-off values for species delineation, supporting their placements in new taxa. Based on the phenotypic, chemotaxonomic, phylogenetic, and phylogenomic properties, these five strains represent five novel taxa of the family Haloarculaceae, Halorarius litoreus gen. nov., sp. nov. (type strain BND22T = CGMCC 1.18780T = JCM 34966T), Halorarius halobius sp. nov. (type strain ZY10T = CGMCC 1.17475T = JCM 34319T), Haloglomus halophilum sp. nov. (type strain ZY41T = CGMCC 1.17030T = JCM 34161T), Haloglomus salinum sp. nov. (type strain ZY58T = CGMCC 1.17216T = JCM 34163T), and Natronomonas marina sp. nov. (type strain ZY43T = CGMCC 1.17202T = JCM 34162T). This is the first report of description of a novel haloarchaeon isolated from a marine intertidal zone.

A filamentous cell-shaped halophilic archaeon (strain AD-1T) was isolated from Aiding Salt Lake, PR China. Its colonies on HCM7 agar plates were pinkish white, 1–4 mm (diameter), elevated and round. The optimum conditions for growth were observed at 42 °C, 4.3 M NaCl, 0.01 M MgCl2 and pH 7. Strain AD-1T could hydrolyse Tween 60, Tween 80, starch and gelatin. Phylogenetic analysis based on 16S rRNA gene, rpoB′ and the concatenated 484 single-copy orthologous proteins revealed that strain AD-1T formed a clade with Halocatena pleomorpha SPP-AMP-1T. The average nucleotide identity and in silico DNA–DNA hybridization values between strain AD-1T and Halocatena pleomorpha SPP-AMP-1T were both below the species delineation thresholds (95~96 and 70 %, respectively). The major phospholipids of strain AD-1T were phosphatidic acid, phosphatidylglycerol and phosphatidylglycerol phosphate methyl ester, while the major glycolipids were sulphated galactosyl mannosyl glucosyl diether, galactosyl mannosyl glucosyl diether and glucosyl mannosyl glucosyl diether. The phenotypic, phylogenetic and genome-based analyses suggested that strain AD-1T (=CGMCC 1.13724T=JCM 32960T) represents a novel species, for which the name Halocatena salina sp. nov. is proposed.

Understanding the cellular uptake and exocytosis processes of nanoparticles (NPs) is essential for developing the nanomedicines and assessing the health risk of nanomaterials. Considerable efforts have been made to reveal how physicochemical properties of NPs influence these processes. However, little attention has been paid to how cell type impacts these processes, especially exocytosis. Herein, the uptake and exocytosis of the carbon dots (CDs) obtained from the carbonization of citric acid with polyethylenimine (PEI) oligomers (CDs-PEI) in five human cell lines (HeLa, A549, BEAS-2B, A431, and MDA-MB-468) are analyzed to understand how cell type influences the fate of CDs in cells. The cell division is taken into account by the correction of cell number for accurate quantification of the uptake and exocytosis of CDs-PEI. The results indicate that the cell type significantly affects the cellular uptake, trafficking, and exocytosis of CDs-PEI. Among the cell types investigated, MDA-MB-468 cells have the greatest capacity for both uptake and exocytosis, and HeLa cells have the least capacity. The kinetics of the exocytosis largely follows a single exponential decay function, with the remaining CDs-PEI in cells reaching plateaus within 24 h. The kinetic parameters are cell-dependent but insensitive to the initial intracellular CDs-PEI content. Generally, the Golgi apparatus pathways are more important in exocytosis than the lysosomal pathway, and the locations of CDs-PEI in the beginning of exocytosis are not correlated with their exocytosis pathways. The findings on the cell type-dependent cellular uptake and exocytosis reported here may be valuable to the future design of high-performance and safe CDs and related nanomaterials in general.

Six novel halophilic archaeal strains of XZYJT10

The prevention of viral transmission is an important step to address the spread of viral infections. Using the enveloped vesicular stomatitis virus (VSV) as a model, this study explored the antiviral functions of the specifically designed and prepared carbon dots (CDots). The CDots were prepared using small carbon nanoparticles with surface functionalization-passivation by oligomeric polyethylenimine (PEI). The results indicated that the PEI-CDots were readily activated by visible light to effectively and efficiently inactivate VSVs under various combinations of experimental conditions (viral titer, dot concentration, and treatment time). The photodynamically induced viral structural protein degradation and genomic RNA degradation were observed, suggesting the mechanistic origins, leading to the inactivation of virus. The results suggested CDots as a class of promising broad-spectrum antiviral agents for disinfection of viruses.

Three halophilic archaeal strains, NEN8

Aim To synthesize qualitative evidence on nurses' and midwives' experiences in the provision of surgical abortion care. We address three specific questions: (a) what are the experiences of nurses and midwives in surgical abortion care? (b) what are their responses and coping strategies? (c) what are the deficiencies in surgical abortion care? Design Qualitative studies were synthesized using Thomas and Harden's qualitative thematic synthesis method. Data sources Electronic databases, including PubMed, Embase, CINAHL, PsycINFO, Scopus and Web of Science were searched. Grey literature using ProQuest was searched. The databases were searched from inception to 5 August 2020. Review methods The SPIDER (Sample, Phenomenon of Interest, Design, Evaluation and Research type) search tool was used in the literature search. Data synthesis was conducted using the three-stage thematic synthesis method described by Thomas and Harden. Results 966 studies were identified in the initial search and 18 studies were included. Four analytical themes were generated: 'Providing abortion care requires high emotional labour'; 'Professionalism of abortion care providers'; 'Initiatives in professional development' and 'Improving directions for high-quality abortion care'. Conclusion Nurses and midwives indicated that they require support to enhance psychological health and improve professional skills. Hospital managers should organize regular debriefing or structured group workshops for exchange of practical experiences and strengthening emotional support. More research is required to establish comprehensive training related to abortion care for nurses and midwives. The findings demonstrate that optimization of abortion services should start from hospital management models, pain management and bereavement care. Impact Understanding the experiences of nurses and midwives in abortion provision will inform future clinical practice in surgical abortion care, which would be helpful in improving the professionalism and confidence of abortion providers. Our findings have implications for the training, development of policies and standards for surgical abortion care for nurses and midwives.

Carbon dots (CDots) are defined as surface-passivated small carbon nanoparticles, with the effective passivation generally achieved by organic functionalization. Photoexcited CDots are both potent electron donors and acceptors, and their characteristic bright and colorful fluorescence emissions make them excellent fluorescence sensors for organic analytes and metal ions. For the latter extraordinarily low detection limits based on extremely efficient quenching of fluorescence intensities by the targeted metal cations have been observed and reported in the literature. However, all of the dot samples in those reported studies were made from “one-pot” carbonization of organic precursors mostly under rather mild processing conditions, unlikely to be sufficient for the required level of carbonization. Those dot samples should therefore be more appropriately considered as “nano-carbon/organic hybrids”, characterized structurally as being highly porous and spongy, which must be playing a dominating role in the reported sensing results. In this study, we compared the dot samples from carbonization syntheses under similarly mild and also more aggressive processing conditions with the classically defined and structured CDots for the fluorescence sensing of copper(II) cations in aqueous solutions. The observed dramatic decoupling between quenching results for fluorescence intensities and lifetimes of the carbonization samples, with the former being extraordinary and the latter within the diffusion controlled limit, suggested that the quenching of fluorescence intensities was greatly affected by the higher local quencher concentrations than the bulk associated with the porous and spongy sample structures, especially for the sample from carbonization under too mild processing conditions. The major differences between the classical CDots and the nano-carbon/organic hybrids are highlighted, and the tradeoffs between sensitivity and accuracy or reproducibility in the use of the latter for fluorescence sensing are discussed.

Carbon dots (CDots) are strongly absorptive over the visible spectrum, with the effective photon-harvesting driving rich excited state processes and properties. In this work, spectroscopic probing of these processes and properties is coupled with the evaluation of the photoinduced bactericidal function of CDots, aimed toward making correlations among the findings from the former and those from the latter on the inactivation of bacterial pathogens. Within the general mechanistic framework for CDots, the observed effective and efficient antibacterial activities of the CDots under visible light are attributed to major contributions by the initially photo-generated electrons and holes that are trapped at passivated surface defect sites of the dots, in addition to the traditional reactive oxygen species (ROS) produced in the emissive excited states from the recombination of the redox pairs. Such major contributions to the inactivation of the bacteria by the separated redox species in CDots can not be quenched by ROS scavengers commonly used in the study of photodynamic effects with classical molecular photosensitizers, thus making light-activated CDots uniquely potent antimicrobial agents. The characteristic features of photoexcited CDots and their related mechanistic implications are discussed in reference to the similar behaviors and mechanistic model of conventional semiconductor quantum dots.

Carbon dots (CDots) exploit and enhance the intrinsic properties of small carbon nanoparticles. Their optical absorptions and photoinduced redox characteristics are competitive with those of conventional semiconductor quantum dots at one end and fullerenes and other carbon nanomaterials at the other. Highlighted in this mini review are the effective photon harvesting over a broad spectral range by CDots and their subsequent excited-state charge transfer processes and interactions, which have enabled their use as sensors, for photodynamic effects, and in various energy conversion technologies.

For addressing the ever increasing challenge of multidrug-resistant (MDR) bacterial infections, specifically designed and prepared carbon dots (CDots) of small carbon nanoparticles with surface functionalization–passivation by oligomeric polyethylenimine were found to be readily activated by visible light to effectively and efficiently inactivate MDR bacterial strains. The inactivation was evaluated under various combinations of experimental conditions (dot concentrations, light intensities, and treatment times), with the results collectively suggesting CDots as a new class of promising agents for combating MDR bacteria. Mechanistic origins and implications of the observed strong antibacterial actions as relevant to the photoexcited state processes in CDots and the photodynamically induced cellular damages leading to the death of the bacterial cells were explored, with the results discussed.

The antiviral function of carbon dots (CDots) with visible light exposure was evaluated, for which the model bacteriophages MS2 as a surrogate of small RNA viruses were used. The results show clearly that the visible light-activated CDots are highly effective in diminishing the infectivity of MS2 in both low and high titer samples to the host E. coli cells, and the antiviral effects are dot concentration- and treatment time-dependent. The action of CDots apparently causes no significant damage to the structural integrity and morphology of the MS2 phage or the breakdown of the capsid proteins, but does result in the protein carbonylation (a commonly used indicator for protein oxidation) and the degradation of viral genomic RNA. Mechanistically the results may be understood in the framework of photodynamic effects that are associated with the unique excited state properties and processes of CDots. Opportunities for potentially broad applications of CDots coupled with visible/natural light in the prevention and control of viral transmission and spread are highlighted and discussed.

This study aimed to address the significant problems of bacterial biofilms found in medical fields and many industries. It explores the potential of classic photoactive carbon dots (CDots), with 2,2′-(ethylenedioxy)bis (ethylamine) (EDA) for dot surface functionalization (thus, EDA-CDots) for their inhibitory effect on B. subtilis biofilm formation and the inactivation of B. subtilis cells within established biofilm. The EDA-CDots were synthesized by chemical functionalization of selected small carbon nanoparticles with EDA molecules in amidation reactions. The inhibitory efficacy of CDots with visible light against biofilm formation was dependent significantly on the time point when CDots were added; the earlier the CDots were added, the better the inhibitory effect on the biofilm formation. The evaluation of antibacterial action of light-activated EDA-CDots against planktonic B. subtilis cells versus the cells in biofilm indicate that CDots are highly effective for inactivating planktonic cells but barely inactivate cells in established biofilms. However, when coupling with chelating agents (e.g., EDTA) to target the biofilm architecture by breaking or weakening the EPS protection, much enhanced photoinactivation of biofilm-associated cells by CDots was achieved. The study demonstrates the potential of CDots to prevent the initiation of biofilm formation and to inhibit biofilm growth at an early stage. Strategic combination treatment could enhance the effectiveness of photoinactivation by CDots to biofilm-associated cells.

Foodborne pathogens have long been recognized as major challenges for the food industry and repeatedly implicated in food product recalls and outbreaks of foodborne diseases. This study demonstrated the application of a recently discovered class of visible-light-activated carbon-based nanoparticles, namely, carbon dots (CDots), for photodynamic inactivation of foodborne pathogens. The results demonstrated that CDots were highly effective in the photoinactivation of Listeria monocytogenes in suspensions and on stainless steel surfaces. However, it was much less effective for Salmonella cells, but treatments with higher CDot concentrations and longer times were still able to inactivate Salmonella cells. The mechanistic implications of the observed different antibacterial effects on the two types of cells were assessed, and the associated generation of intracellular reactive oxygen species (ROS), the resulting lipid peroxidation, and the leakage of nucleic acid and proteins from the treated cells were analyzed, with the results collectively suggesting CDots as a class of promising photodynamic inactivation agents for foodborne pathogens. IMPORTANCE Foodborne infectious diseases have long been recognized as major challenges in public health. Contaminations of food processing facilities and equipment with foodborne pathogens occur often. There is a critical need for new tools/approaches to control the pathogens and prevent such contaminations in food processing facilities and other settings. This study reports a newly established antimicrobial nanomaterials platform, CDots coupled with visible/natural light, for effective and efficient inactivation of representative foodborne bacterial pathogens. The study will contribute to promoting the practical application of CDots as a new class of promising nanomaterial-based photodynamic inactivation agents for foodborne pathogens.

Carbon dots (CDots) are small carbon nanoparticles with effective surface passivation by organic functionalization. In the reported work, the surface functionalization of preexisting small carbon nanoparticles with N-ethylcarbazole (NEC) was achieved by the NEC radical addition. Due to the major difference in microwave absorption between the carbon nanoparticles and organic species such as NEC, the nanoparticles could be selectively heated via microwave irradiation to enable the hydrogen abstraction in NEC to generate NEC radicals, followed by in situ additions of the radicals to the nanoparticles. The resulting NEC-CDots were characterized by microscopy and spectroscopy techniques including quantitative proton and 13C NMR methods. The optical spectroscopic properties of the dot sample were found to be largely the same as those of CDots from other organic functionalization schemes. The high structural stability of NEC-CDots benefiting from the radical addition functionalization is highlighted and discussed.

Hexagonal boron nitride (h-BN) and exfoliated nanosheets (BNNs) not only resemble their carbon counterparts graphite and graphene nanosheets in structural configurations and many excellent materials characteristics, especially the ultra-high thermal conductivity, but also offer other unique properties such as being electrically insulating and extreme chemical stability and oxidation resistance even at elevated temperatures. In fact, BNNs as a special class of 2-D nanomaterials have been widely pursued for technological applications that are beyond the reach of their carbon counterparts. Highlighted in this article are significant recent advances in the development of more effective and efficient exfoliation techniques for high-quality BNNs, the understanding of their characteristic properties, and the use of BNNs in polymeric nanocomposites for thermally conductive yet electrically insulating materials and systems. Major challenges and opportunities for further advances in the relevant research field are also discussed.

Foodborne pathogens have long been recognized as major challenges for the food industry and repeatedly implicated in food product recalls and outbreaks of foodborne diseases. This study demonstrated the application of a recently discovered class of visible-light-activated carbon-based nanoparticles, namely, carbon dots (CDots), for photodynamic inactivation of foodborne pathogens. The results demonstrated that CDots were highly effective in the photoinactivation of Listeria monocytogenes in suspensions and on stainless steel surfaces. However, it was much less effective for Salmonella cells, but treatments with higher CDot concentrations and longer times were still able to inactivate Salmonella cells. The mechanistic implications of the observed different antibacterial effects on the two types of cells were assessed, and the associated generation of intracellular reactive oxygen species (ROS), the resulting lipid peroxidation, and the leakage of nucleic acid and proteins from the treated cells were analyzed, with the results collectively suggesting CDots as a class of promising photodynamic inactivation agents for foodborne pathogens. IMPORTANCE Foodborne infectious diseases have long been recognized as major challenges in public health. Contaminations of food processing facilities and equipment with foodborne pathogens occur often. There is a critical need for new tools/approaches to control the pathogens and prevent such contaminations in food processing facilities and other settings. This study reports a newly established antimicrobial nanomaterials platform, CDots coupled with visible/natural light, for effective and efficient inactivation of representative foodborne bacterial pathogens. The study will contribute to promoting the practical application of CDots as a new class of promising nanomaterial-based photodynamic inactivation agents for foodborne pathogens.

Boron nitride nanosheets (BNNs) are pursued for their high thermal conductivity yet electrical insulation and their extreme thermal and chemical stabilities for a variety of applications. For high-quality BNNs, a number of exfoliation approaches under different processing conditions were evaluated. Three more effective methods were identified, including method-A based on refluxing and vigorous sonication in isopropyl alcohol, method-B involving ball-milling in urea, and method-C with the aid of ammonia in hydrothermal processing. These methods produced BNNs of apparently different structural and morphological characteristics, with those from the first two being smaller pieces, more defective, and their polymeric nanocomposites exhibiting relatively lower thermal conductive performance. The method-C yielded BNNs of obviously better quality, as also made evident by the observed high thermal diffusivities of their corresponding polymeric nanocomposites. Correlations of exfoliation approaches and conditions w...

Carbon dots (CDots) for their excellent optical and other properties have been widely pursued for potential biomedical applications, in which a more comprehensive understanding on the cellular behaviors and mechanisms of CDots is required. For such a purpose, two kinds of CDots with surface passivation by 3-ethoxypropylamine (EPA-CDots) and oligomeric polyethylenimine (PEI-CDots) were selected for evaluations on their uptakes by human cervical carcinoma HeLa cells at three cell cycle phases (G0/G1, S and G2/M), and on their different internalization pathways and translocations in cells. The results show that HeLa cells could internalize both CDots by different pathways, with an overall slightly higher internalization efficiency for PEI-CDots. The presence of serum in culture media could have major effects, significantly enhancing the cellular uptake of EPA-CDots, yet markedly inhibiting that of PEI-CDots. The HeLa cells at different cell cycle phases have different behaviors in taking up the CDots, which are also affected by the different dot surface moieties and serum in culture media. Mechanistic implications of the results and the opportunities associated with an improved understanding on the cellular behaviors of CDots for potentially the manipulation and control of their cellular uptakes and translocations are discussed.

Carbon dots (CDots) exploit unique properties of small carbon nanoparticles, which represent the often under-appreciated zero-dimensional carbon allotrope. The carbon nanoparticles in CDots could be modified by a selected organic chromophore of desired strong red/near-IR absorption in the dot synthesis to obtain a specific type of hybrid CDots. The reported results show that these hybrid CDots derived from the modification of core carbon nanoparticles by selected dyes or other chromophoric species represent a highly versatile and effective platform for CDots of desired optical properties and photoinduced redox characteristics in a by-design fashion.

Producing carbon nanomaterials adjustably on a large scale with existing manufacturing methods is a promising direction. Here, multiwalled carbon nanotubes (MWCNTs) were grown on stainless steel substrate using a self-built V-type flame burner under atmospheric pressure. The surface structure of mirror and wiredrawing stainless steel substrates was observed by scanning electron microscopy. Carbon nanotubes only grow on calcined wiredrawing stainless steel substrate. X-ray diffraction was used to investigate the crystallinity of MWCNTs synthesized on substrates that were heated at 400 °C, 600 °C, and 800 °C, indicating that the calcining temperature of the substrate affects the properties of MWCNTs growth. Products grown on the substrate calcined at 600 °C are optimal. Scanning electron microscopy, X-ray diffraction and X-ray photoelectron spectroscopy were employed to examine the morphology and chemical compositions of substrates calcined at different temperatures before growing carbon nanotubes. It was found that the morphology of the substrate surface is a key factor in controlling the growth of MWCNTs. Uniform particles with glossy boundaries are available for MWCNTs synthesis. Energy-dispersive spectroscopy was performed on single metallic particles found inside the nanotubes, clarifying that iron nanoparticles provide active sites for carbon nanotube growth on stainless steel instead of oxidation iron and other elements. A better understanding of the growth of carbon nanotubes on stainless steel using a V-type flame burner can help to adjust the properties of carbon nanotubes deposited on the required constructions, and provide additional insight into realization of large-scale and low-cost constructions covered with carbon nanotubes.

Background: Carbon dots (CDots) have recently been demonstrated their effective visible light-activated antimicrobial activities toward bacteria. This study was to evaluate and understand the roles of the surface functionalities in governing the antimicrobial activity of CDots. Methods: Using the laboratory model bacteria Bacillus subtilis, the photo-activated antimicrobial activities of three groups of CDots with specifically selected different surface functionalization moieties were evaluated and compared. The first group consisting of CDots with surface functionalization by 2,2-(ethylenedioxy)bis(ethylamine) (EDA) vs. 3-ethoxypropylamine (EPA), was evaluated to determine the effect of different terminal groups/charges on their photo-activated antibacterial activities. The second group consisting of CDots functionalized with oligomeric polyethylenimine (PEI) and those prepared by the carbonization of PEI – citric acid mixture, was to evaluate the effects of dot surface charges vs. fluorescent quantum yields on their antimicrobial activities. The third group consisting of CDots functionalized with PEI of 1,200 vs. 600 in average molecular weight was evaluated for the effect of molecular weight of surface passivation molecular on their antimicrobial activities. Results: The results indicated the EDA-CDots in the first group was more effective and was attributed to the positive charges from the protonation of the amino groups (–NH2) being more favorable to interactions with bacterial cells. The evaluation of the second group CDots suggested the same surface charge effect dominating the antibacterial performance over the fluorescent quantum yields. The evaluation of the third group CDots functionalized with PEI of 1,200 vs. 600 in average molecular weight, indicated the latter was significantly more effective. Conclusions: The results from this study highlighted the dominant role of surface functionalities in governing CDots’ light activated antimicrobial activity and should have significant implications to the further design and development of CDots as a new class of visible light-activated antibacterial agents.

Carbon dots (CDots), generally small carbon nanoparticles with surface passivation by a soft corona-like layer of mostly organic species, have been actively pursued for potential applications in optoelectronics, including various functions that have been served by some popular fullerene derivatives. For the preparation of CDots, chemical functionalization of pre-processed and selected small carbon nanoparticles by organic molecules, so far mostly molecules with primary and secondary amine groups, has been an effective method. In this study, carbon nanoparticles were functionalized by N-ethylcarbazole (NEC) under microwave-assisted reaction conditions for NEC-CDots, analogous but with advantages to the CDots of surface functionalization by poly(N-vinylcarbazole) (PVK, which holds a special place in optoelectronics). NEC molecules can apparently be activated under the reaction conditions for reactive functionalities such as radicals to bind to surface carbons of the nanoparticles, consistent with the observed high stability of NEC-CDots. These dots, likely with a unique surface passivation scheme, exhibited optical properties and photoinduced redox characteristics similar to those found in other high-performance CDots. The potentially broad applicability of the new functionalization approach is discussed, so are implications of the unique surface passivation of carbon nanoparticles by the carbazole moieties.

In the vast research field on carbon nanostructures, a seemingly broadly accepted family configuration of nanoscale carbon allotropes is such that fullerenes take the zero-dimensional dot spot, in perfect harmony with one-dimensional carbon nanotubes and two-dimensional graphene nanosheets. More recently, however, a threat to the nice “family value” has been the emergence of small carbon nanoparticles, which are carbon particles of a few nanometers in size without any defined crystal structures or largely amorphous and populated with abundant surface and other defects. The growing experimental evidence has revealed the unique and/or advantageous optical and photoexcited state properties and photoinduced redox characteristics of the small carbon nanoparticles, elevating them to the position of being able to compete with fullerenes for the title of nanoscale carbon allotrope at the zero-dimension. Moreover, a related supporting argument is that fullerenes are molecules, nanoscale in their sizes but not necessarily “nanomaterials” strictly speaking. In this presentation, relevant experimental results of the nanoparticles and fullerenes will be compared for a fair assessment and judgment of their title competition, and more importantly their shared structural features and electronic properties and also their enormous potential in the development of materials for a variety of technological applications will be highlighted.

Carbon dots were originally found and reported as surface-passivated small carbon nanoparticles, where the effective surface passivation was the chemical functionalization of the carbon nanoparticles with organic molecules. Understandably, the very broad optical absorptions of carbon dots are largely the same as those intrinsic to the carbon nanoparticles, characterized by progressively decreasing absorptivities from shorter to longer wavelengths. Thus, carbon dots are generally weak absorbers in the red/near-IR and correspondingly weak emitters with low quantum yields. Much effort has been made on enhancing the optical performance of carbon dots in the red/near-IR, but without meaningful success due to the fact that optical absorptivities defined by Mother Nature are in general rather inert to any induced alterations. Nevertheless, there were shockingly casual claims in the literature on the major success in dramatically altering the optical absorption profiles of “carbon dots” by simply manipulating the dot synthesis to produce samples of some prominent optical absorption bands in the red/near-IR. Such claims have found warm receptions in the research field with a desperate need for carbon dots of the same optical performance in the red/near-IR as that in the green and blue. However, by looking closely at the initially reported synthesis and all its copies in subsequent investigations on the “red/near-IR carbon dots”, one would find that the “success” of the synthesis by thermal or hydrothermal carbonization processing requires specific precursor mixtures of citric acid with formamide or urea. In the study reported here, the systematic investigation included precursor mixtures of citric acid with not only formamide or urea but also their partially methylated or permethylated derivatives for the carbonization processing under conditions similar to and beyond those commonly used and reported in the literature. Collectively all of the results are consistent only with the conclusion that the origins of the observed red/near-IR optical absorptions in samples from some of the precursor mixtures must be molecular chromophores from thermally induced chemical reactions, nothing to do with any nanoscale carbon entities produced by carbonization.

Carbon dots (CDots) are defined as surface-passivated small carbon nanoparticles, with the effective passivation generally achieved by organic functionalization. Photoexcited CDots are both potent electron donors and acceptors, and their characteristic bright and colorful fluorescence emissions make them excellent fluorescence sensors for organic analytes and metal ions. For the latter extraordinarily low detection limits based on extremely efficient quenching of fluorescence intensities by the targeted metal cations have been observed and reported in the literature. However, all of the dot samples in those reported studies were made from "one-pot" carbonization of organic precursors mostly under rather mild processing conditions, unlikely to be sufficient for the required level of carbonization. Those dot samples should therefore be more appropriately considered as "nano-carbon/organic hybrids", characterized structurally as being highly porous and spongy, which must be playing a dominating role in the reported sensing results. In this study, we compared the dot samples from carbonization syntheses under similarly mild and also more aggressive processing conditions with the classically defined and structured CDots for the fluorescence sensing of copper(ii) cations in aqueous solutions. The observed dramatic decoupling between quenching results for fluorescence intensities and lifetimes of the carbonization samples, with the former being extraordinary and the latter within the diffusion controlled limit, suggested that the quenching of fluorescence intensities was greatly affected by the higher local quencher concentrations than the bulk associated with the porous and spongy sample structures, especially for the sample from carbonization under too mild processing conditions. The major differences between the classical CDots and the nano-carbon/organic hybrids are highlighted, and the tradeoffs between sensitivity and accuracy or reproducibility in the use of the latter for fluorescence sensing are discussed.

Carbon dots, generally referring to small carbon nanoparticles with various levels of surface passivation, have emerged as a new class of quantum dot-like fluorescent nanomaterials. Since the original report in 2006, carbon dots have been investigated by many research groups worldwide, with major advances already made in their syntheses, structural and mechanistic understandings, and evaluations for biocompatibilities and potential bio-applications. In this article, representative studies responsible for these advances in the development and understanding of carbon dots are reviewed, and those targeting the use of carbon dots as high-performance yet nontoxic fluorescence agents for optical bioimaging in vitro and in vivo are highlighted and discussed.

High-quality boron nitride nanosheets (BNNs) characterized by large aspect ratios and less defective surfaces and structures are in demand for thermal management and other uses that exploit the uniquely advantageous properties of boron nitride, such as being highly thermally conductive yet electrically insulating and extreme chemical and thermal stabilities. In this study, an ammonia-assisted exfoliation processing method was developed and applied to the preparation of high-quality BNNs. As a demonstration of the excellent potential of these nanomaterials, the BNNs were dispersed in polyethylene polymers for nanocomposite films of superior thermal transport performance at levels significantly beyond the state of the art in the literature. Effects of crosslinking in the nanocomposite film structure on thermal transport were also explored and favorable outcomes were achieved.

Nanoscale carbon has been a major cornerstone in the extremely broad and active research filed of nanoscience and nanotechnology. Among carbon allotropes, fullerenes have often been considered as representing zero-dimensional carbon nanomaterials, despite the fact that they are stoichiometrically defined molecules of distinct electronic structures, different in some fundamental aspects from the carbon nanomaterials in other dimensions. Unlike fullerenes, carbon nanotubes and graphene nanosheets are nanomaterials with the inevitable presence of defects, among other structural features and related properties similar to those found in small carbon nanoparticles. Thus, the nanoparticles should more logically be considered as carbon nanomaterials at the zero-dimension. Various comparisons of the small carbon nanoparticles with fullerenes, carbon nanotubes, and graphene nanosheets are highlighted, especially on their optical properties and redox characteristics. The similarities and differences in electronic transitions and their associated various applications between the zero-, one-, and two-dimensional carbon allotropes are discussed.

Carbon dots (CDots) are generally defined as small carbon nanoparticles with various surface passivation schemes. For the definition, the synthesis with the use of pre-existing small carbon nanoparticles for chemical functionalization obviously eliminates any issues or complications with the structures of carbon cores in the dots, thus “classical.” Results based on amidation chemistry for the functionalization of small carbon nanoparticles are presented and discussed in more detail, and other modes of functionalization for CDots with somewhat different surface structures are highlighted. Also presented and discussed are the optical properties (absorptions and photoluminescence emissions) and photoinduced redox characteristics of CDots from the classical synthesis, which may be considered as references for those of other dot samples, and the mechanistic framework for the photoexcited state properties and processes in CDots.

Carbon-based/carbon-derived hybrid dots or simply carbon hybrid dots share similar structural features with CDots, but the core in individual dots is a broadly defined mixture of nanoscale carbon with other elements, molecules, and/or nanomaterials. Among the carbon hybrid dots highlighted are the following: (1) “host–guest” CDots, in which the carbon core hosts the selected organic dye species as guest, primarily for the purpose of extending the spectral coverage into the red/near-IR for improved bioimaging and other applications; (2) CDots of the core carbon nanoparticles doped with an inorganic salt, combined with the typical organic functionalization–passivation, for substantially enhanced fluorescence performance and related photoexcited state properties; (3) various nanoscale carbon–TiO2 mixtures/composites as cores in the hybrid dots, corresponding to very different photoexcited state properties and redox characteristics; and (4) similar dot configurations to some of those in (3) for the incorporation of magnetic elements into dot structures for optical–magnetic dual-modality hybrid dots.

The overwhelming majority of the dot samples in studies reported in the literature were prepared by “one-pot” carbonization of organic molecules or mixtures. Unfortunately, the equal majority of the carbonization processes were under conditions insufficient for the necessary level of carbonization to ensure the dominance of nanoscale carbon domains (equivalent in functions to the small carbon nanoparticles in the general definition of CDots) in the produced dot samples. As highlighted and discussed, the insufficient carbonization resulted in the substantial contamination of dye-like species/mixtures formed as chemical reaction products in the carbonization processing, including the dominating contamination in the claimed “red/near-IR carbon quantum dots” from thermal reactions of specific precursor organic mixtures. Also discussed critically are some of the reported preparations of “graphene quantum dots” by similar carbonization syntheses and the fact that the original concept and definition of graphene quantum dots were misunderstood or misrepresented in those studies.

Carbon dots as a new carbon nanomaterials platform have been pursued extensively for a variety of potential applications, with many conceptually innovative demonstrations already in the literature. Highlighted here are some representative examples for the relevant application concepts and topics, though hardly comprehensive. The purpose is to limit the presentation to include only those application-related studies based on dot samples prepared primarily with pre-existing carbon nanoparticles, so as not to increase or create more confusions related to the growing concerns in the research community on dot samples contaminated substantially or even predominantly with dye-like species/mixtures produced in some carbonization syntheses.

Provided in this chapter is a historical account of the investigations and experimental observations, the debates and controversies, and the deliberate and systematic efforts that were associated with or led to the discovery of carbon dots (CDots). The story began in the year 2000 with the reported observation of bright and colorful photoluminescence emissions in functionalized carbon nanotubes, followed by the serious concerns in the relevant research community that the observed emissions could be due to “carbonaceous impurities” in the carbon nanotube samples. The debates and related extensive investigations for exploring and validating the emissions and their defect-derived mechanistic origins are highlighted. The phenomenological and mechanistic resemblances between chemically functionalized defects in carbon nanotubes and small carbon nanoparticles are discussed. It was the recognition and experimental verification of such resemblances that led to the invention of CDots and made the largely ignored (or unwanted and to be eliminated) “ugly” carbon nanoparticles a distinct and highly valuable member of the carbon nanomaterials family.

Background Transesophageal echocardiography may be used to assess pulmonary veins for atrial fibrillation ablation. No study focused on the role of transthoracic echocardiography (TTE) in evaluating the diameter and anatomy of pulmonary veins. Methods Among 142 atrial fibrillation patients (57.7% men; mean age, 60.5) hospitalised for catheter ablation, we assessed pulmonary veins and compared the measurements by TTE with cardiac computed tomography (CT) before ablation. Among 17 patients who had follow-up examinations, the second measurements were also studied. Results TTE identified and determined the diameters of 140 (98.6%) right and 140 (98.6%) left superior PVs, and 136 (95.7%) right and 135 (95.1%) left inferior PVs. A separate middle PV ostia was identified in 14 out of the 22 patients (63.6%) for the right side and in 2 out of 4 (50.0%) for the left side. The PV diameters before ablation assessed by CT vs. TTE were 17.96 vs. 18.07 mm for right superior, 15.92 vs. 15.51 mm for right inferior, 18.54 vs. 18.42 mm for left superior, and 15.56 vs. 15.45 mm for left inferior vein. The paired differences between the assessments of CT and TTE were not significant (P ≥ 0.31) except for the right inferior vein with a CT-minus-TTE difference of 0.41 mm (P = 0.018). The follow-up PV diameters by both CT (P ≥ 0.069) and TTE (P ≥ 0.093) were not different from baseline measurements in the 17 patients who had follow-up measurements. Conclusions With a better understanding of PV anatomy in TTE imaging, assessing PV diameters by non-invasive TTE is feasible. However, the clear identification of anatomic variation might still be challenging.

Carbon dots (CDots) are characterized by their optical properties including strong absorptions and bright and colorful fluorescence emissions in the visible spectrum and by their photoinduced redox...

BACKGROUND Lower respiratory tract illness is a major cause of morbidity and mortality in children worldwide, however, information about the epidemiological and clinical characteristics of LRTIs caused by HMPV and HBoV in China is limited. OBJECTIVES Human bocavirus (HBoV) and human metapneumovirus (HMPV) are two important viruses for children with lower respiratory tract infections (LRTI). We aimed to assay the correlation between viral load and clinical characteristics of HBoV and HMPV with LRTI in Changsha, China. METHODS Nasopharyngeal aspirates (NPAs) from children with LRTI were collected. Real-time PCR was used to screen HBoV and HMPV. Analyses were performed using SPSS 16.0 software. RESULTS Pneumonia was the most frequent diagnosis. There was no significant difference between HBoV- and HMPV-positive patients in age (P = .506) or hospitalization duration (P = .280); 24.1% and 18.2% were positive for HBoV and HMPV. HBoV infections peaked in summer (32.2%), and HMPV infections peaked in winter (28.9%). The HBoV-positive patients had a shorter hospitalization duration than the HBoV-negative patients (P = .021), and the HMPV-positive patients had a higher prevalence of fever than the HMPV-negative patients (P = .002). The HBoV viral load was significantly higher among patients aged

Carbon-based hybrid nanostructures, especially carbon hybrid dots with metal oxides, are important to both fundamental studies and technological applications. In this work, carbon–TiO2 hybrid dots in two different structural configurations were prepared and investigated comparatively for their optical properties and photoinduced redox characteristics, and the results suggested major differences. In the configuration of small carbon nanoparticles each coated/doped with only a small amount of TiO2, the TiO2 played the role of enhancing the surface passivation effect in conjunction with organic surface functionalization agents for the hybrid dots to exhibit a much improved performance over that of their corresponding neat carbon dots. In the other configuration, however, the hybrid dots of TiO2 nanocrystals each composited with nanoscale carbon domains were apparently similar to dye-sensitized TiO2 nanoparticle systems, with the carbon domains providing the dye function for the harvesting of visible photons. While combining nanoscale carbon and TiO2 for various applications has been a popular topic in the recent literature, the results reported here provide new insights into the different structural configurations or arrangements between the carbon and TiO2 and their associated effects on the optical and photoinduced redox properties of the hybrid nanostructures. Significant implications of the results on an understanding of the mechanistic relationships between the hybrid nano-structures/configurations and optical/redox properties are highlighted, and opportunities in the further exploration of carbon–metal oxide hybrid dots and their applications are discussed.

Carbon “quantum” dots or carbon dots, generally defined as small carbon nanoparticles with various surface passivation schemes, have emerged to represent a rapidly advancing and expanding research field. A wide variety of technological applications of carbon dots have been pursued, including especially their uses as fluorescence probes or sensors. In the work reported here, carbon dots obtained from the surface chemical functionalization of small carbon nanoparticles with 2,2′-(ethylenedioxy)bis(ethylamine) (EDA) were selected as structurally compact and defined fluorescence probes, and their interactions with nitrotoluene compounds were studied on the basis of fluorescence quenching in steady-state and time-resolved measurements. The fluorescence quenching of the carbon dots by the nitrotoluenes, which are commonly used as signature compounds for nitroaromatic explosives, was found to be extremely efficient in ambient solution, though still at the very upper-limit of diffusion-control. There were some static quenching contributions at high nitrotoluene quencher concentrations, especially for the compound that is more electron deficient, which could be rationalized in terms of some near-neighbor charge transfer interactions. Mechanistic implications of the results and the potential for carbon dots to serve as highly sensitive fluorescence probes in the detection of nitroaromatic explosives are discussed.

Boron nitride film could be developed for unique thermal management needs that require electrical insulation and also for applications that benefit from the other advantageous properties of boron nitride. In this work the two related major issues on the neat boron nitride films were identified, including the quality of the precursor boron nitride nanosheets (BNNs) and the dispersion of the BNNs relevant to the film fabrication. These issues were explored by examining various solvent systems and experimental conditions for the exfoliation of commercially acquired hexagonal boron nitride into BNNs and their ability to form relatively stable dispersions. The more stable dispersions were used for the fabrication of neat films of BNNs, and the results suggested that the films were too brittle to serve the film functions as those performed by their carbon-based counterparts. As an alternative approach, a small amount of graphene oxides (GOs) was used as binder for BNNs-GOs composite films of significantly improved mechanical characteristics. Thermal and electrical conductivities in these films were evaluated, so was the tuning of the conductivity ratios via thermal annealing of the as-fabricated films. The challenges and opportunities with the development of BNNs-derived neat boron nitride films are discussed, and their potential technological applications are highlighted.

Host–guest carbon dots (G@CDots) represent a new platform in the rapidly advancing and expanding research field of carbon “quantum” dots or carbon dots, enabling the development of novel carbon hybrid nanostructures of unique and/or advantageous properties and capabilities beyond those of conventional carbon dots. In this study, the red/near-IR emissive dye nile blue (NB) was selected as the guest, and NB@CDots were prepared in a microwave-assisted one-pot thermal carbonization synthesis with oligomeric polyethylene glycols (PEGs) as the precursor and also surface passivation species in the resulting host–guest dots. The NB@CDots exhibited unique and/or favorable characteristics, including especially the bright red/near-IR fluorescence emissions, with the observed fluorescence quantum yield due to the guest nile blue species more than an order of magnitude higher than that of free nile blue molecules, all in aqueous solutions. The higher fluorescence intensities were coupled with a longer fluorescence lifetime, and also accompanied by excellent photochemical stability, making the NB@CDots high-performance fluorescence probes for bioimaging-sensing and related applications. Indeed, their potential in this regard was explored and demonstrated in the fluorescence imaging of live stem cells. The NB@CDots were also evaluated in cytotoxicity assays, and the results suggested their being nontoxic. Excellent opportunities in further development of the host–guest carbon dots platform for high-performance yet nontoxic fluorescence probes are discussed.