One-Piece Triboelectric Nanosensor for Self-Triggered Alarm System and Latent Fingerprint Detection.

Tactile sensing is of great importance in developing human-machine interface, remote control, and security systems. Here, a self-triggered alarm system based on the one-piece triboelectric nanosensor (TENS) is reported. By using nitrocellulose (NC) membrane as the triboelectric material, the as-designed TENS can not only sensitively respond to physical contacts in a self-triggered mode but also securely detect the third-level details of latent fingerprint. The self-triggered idea based on the triboelectric nanogenerator is compatible with intelligent interactive interface. Besides, this TENS can be conveniently fabricated and integrated into arrays at a large scale due to its freestanding, simple, and low-cost characteristics. This work presents alternative perspectives for the practical applications of the multifunctionalized TENS.

Cytotoxicity and therapeutic effect of irinotecan combined with selenium nanoparticles.

Although chemotherapeutic drugs are widely applied for clinic tumor treatment, severe toxicity restricts their therapeutic efficacy. In this study, we reported a new form of selenium, selenium nanoparticles (Nano Se) which have significant lower toxicity and acceptable bioavailability. We investigated Nano Se as chemotherapy preventive agent to protect against toxicities of anticancer drug irinotecan and synergistically enhance the anti-tumor treatment effect in vitro and in vivo. The underlying mechanisms were also investigated. The combination of Nano Se and irinotecan showed increased cytotoxic effect with HCT-8 tumor cells likely by p53 mediated apoptosis. Nano Se inhibited growth of HCT-8 tumor cells partially through caspases mediated apoptosis. In vivo experiment showed Nano Se at a dose of 4 mg/kg/day significantly alleviated adverse effects induced by irinotecan (60 mg/kg) treatment. Nano Se alone treatment did not induce any toxic manifestations. The combination of Nano Se and irinotecan dramatically inhibited tumor growth and significantly induced apoptosis of tumor cells in HCT-8 cells xenografted tumor. Tumor inhibition rate was about 17.2%, 48.6% and 62.1% for Nano Se, irinotecan and the combination of Nano Se and irinotecan, respectively. The beneficial effects of Nano Se for tumor therapy were mainly ascribed to selectively regulating Nrf2-ARE (antioxidant responsive elements) pathway in tumor tissues and normal tissues. Our results suggest Nano Se is a promising selenium species with potential application in cancer treatment.

Spatially marking and quantitatively counting membrane immunoglobulin M in live cells via Ag cluster-aptamer probes.

A probe composed of an aptamer and a silver cluster, where the aptamer targets mIgM of live cells and the silver cluster provides fluorescent imaging and mass quantification of mIgM of live cells, is presented. This new probe simultaneously provides accurate spatial and mass information of mIgM in live cells.

Positively charged graphene oxide nanoparticle: precisely label the plasma membrane of live cell and sensitively monitor extracellular pH in situ.

Polyethylene glycol modified graphene oxide (GO-PEG) nanoparticles were prepared, which were positively charged and fairly stable in buffer solution. The GO-PEG nanoparticles possess a special affinity to the plasma membrane of live cells, and their yellowish-green fluorescence is sensitively responsive to the extracellular physiological solution in situ.

Blue two-photon fluorescence metal cluster probe precisely marking cell nuclei of two cell lines.

A bifunctional peptide was designed to in situ reduce Cu ions and anchor a Cu cluster. The peptide-Cu cluster probe, mainly composed of Cu14, emitted blue two-photon fluorescence under femtosecond laser excitation. Most important, the probe can specifically mark the nuclei of HeLa and A549 cells, respectively.

Diazonium functionalized graphene: microstructure, electric, and magnetic properties.

The unique honeycomb lattice structure of graphene gives rise to its outstanding electronic properties such as ultrahigh carrier mobility, ballistic transport, and more. However, a crucial obstacle to its use in the electronics industry is its lack of an energy bandgap. A covalent chemistry strategy could overcome this problem, and would have the benefits of being highly controllable and stable in the ambient environment. One possible approach is aryl diazonium functionalization. In this Account, we investigate the micromolecular/lattice structure, electronic structure, and electron-transport properties of nitrophenyl-diazonium-functionalized graphene. We find that nitrophenyl groups mainly adopt random and inhomogeneous configurations on the graphene basal plane, and that their bonding with graphene carbon atoms leads to slight elongation of the graphene lattice spacing. By contrast, hydrogenated graphene has a compressed lattice. Low levels of functionalization suppressed the electric conductivity of the resulting functionalized graphene, while highly functionalized graphene showed the opposite effect. This difference arises from the competition between the charge transfer effect and the scattering enhancement effect introduced by nitrophenyl groups bonding with graphene carbon atoms. Detailed electron transport measurements revealed that the nitrophenyl diazonium functionalization locally breaks the symmetry of graphene lattice, which leads to an increase in the density of state near the Fermi level, thus increasing the carrier density. On the other hand, the bonded nitrophenyl groups act as scattering centers, lowering the mean free path of the charge carriers and suppressing the carrier mobility. In rare cases, we observed ordered configurations of nitrophenyl groups in local domains on graphene flakes due to fluctuations in the reaction processes. We describe one example of such a superlattice, with a lattice constant nearly twice of that of pristine graphene. We performed comprehensive theoretical calculations to investigate the lattice and the electronic structure of the superlattice structure. Our results reveal that it is a thermodynamically stable, spin-polarized semiconductor with a bandgap of ∼0.5 eV. Our results demonstrate the possibility of controlling graphene's electronic properties using aryl diazonium functionalization. Asymmetric addition of aryl groups to different sublattices of graphene is a promising approach for producing ferromagnetic, semiconductive graphene, which will have broad applications in the electronic industry.

Spin-polarized semiconductors: tuning the electronic structure of graphene by introducing a regular pattern of sp3 carbons on the graphene plane.

First-principles calculations (generalized gradient approximation, density functional therory (DFT) with dispersion corrections, and DFT plus local atomic potential) are carried out on the stability and electronic structures of superlattice configurations of nitrophenyl diazonium functionalized graphene with different coverage. In the calculations, the stabilities of these structures are strengthened significantly since van der Waals interactions between nitrophenyl groups are taken into account. Furthermore, spin-polarized and wider-bandgap electronic structures are obtained when the nitrophenyl groups break the sublattice symmetry of the graphene. The unpaired quasi-localized p electrons are responsible for this itinerant magnetism. The results provide a novel approach to tune graphene's electronic structures as well as to form ferromagnetic semiconductive graphene.

Ag cluster-aptamer hybrid: specifically marking the nucleus of live cells.

Silver cluster-aptamer hybrids were mineralized via an artificially designed aptamer. The hybrids gave red emission when excited by light, and they successfully targeted the nucleus of live cells. This method is an effective approach to make cell target probes.

Graphene covalently binding aryl groups: conductivity increases rather than decreases.

Graphene functionalized via nitrophenyl groups covalently bonding to its basal plane is studied by Raman spectroscopy and electric transport measurements. The Raman spectra of functionalized graphene exhibit D mode and peaks derived from nitrophenyl groups, and the two fingerprints exhibit nearly the same distribution in the two-dimensional Raman maps over the whole graphene sheet. This result directly proves that the nitrophenyl groups bond to the graphene basal plane via σ-bonds. Electric transport measurements demonstrate that the modified graphene is significantly more conductive than intrinsic graphene. In the competition between charge transfer effect and scattering effect introduced by the nitrophenyl groups, the former one is dominant so that the conductivity of functionalized graphene is significantly enhanced as a result.

Nanoprobes: quantitatively detecting the femtogram level of arsenite ions in live cells.

In this report, nanoprobes which could detect the femtogram level of arsenite ions in subcellular organelle of live cells are disclosed. The nanoprobes are composed of ssDNA and single-wall carbon nanotubes (SWCNTs), and the ssDNA is marked by a dye molecule. In a live cell, trace arsenite ions could interact with nanoprobes and significantly decrease the emission of the nanoprobes. With the help of a confocal microscope and cryo-electron microscopy, the lysosome target of the arsenite ion and nanoprobe is well described in high spatial resolution.

The suppression of prostate LNCaP cancer cells growth by Selenium nanoparticles through Akt/Mdm2/AR controlled apoptosis.

The trace element Selenium is suggested having cancer prevention activity and used as food supplement. Previous results had shown Selenium nanoparticles are safer compared with other Selenium compounds like selenomethionine, sodium selenite and monomethylated Selenium, however, its anticancer activity and intrinsic mechanisms are still elusive. Here, we prepared Selenium nanoparticles and investigated its inherent anticancer mechanisms. We found Selenium nanoparticles inhibit growth of prostate LNCaP cancer cells partially through caspases mediated apoptosis. Selenium nanoparticles suppress transcriptional activity of androgen receptor via down-regulating its mRNA and protein expression. Moreover, Selenium nanoparticles activate Akt kinase by increasing its phosphorylation, promote Akt-dependent androgen receptor phosphorylation and Mdm2 regulated degradation through proteasome pathway. We suggest Selenium nanoparticles suppress prostate cancer cells growth by disrupting androgen receptor, implicating a potential application in cancer treatment.

Ag nanoparticles coated SWCNT with surface enhanced Raman scattering (SERS) signals.

We report here a simple method to fabricate the silver nanoparticles (AgNPs) coated DNA-SWCNTs that give SERS signals. Dynamic light scattering (DLS), atomic force microscopy (AFM), and high resolution transmission electron microscopy (HRTEM) suggested the products are dispersive and soluble in aqueous solution. The Raman scattering spectra show AgNPs coated SWCNTs have enhanced the Raman signal when compared with pure SWCNT. From the radial breathing mode (RBM) of the Raman spectra, we can disclose that this DNA-SWCNT has unique chirality, which implies that it could be a good nanoprobe for cell marking.

Synthesis and characterization of a grapevine nanostructure consisting of single-walled carbon nanotubes with covalently attached [60]fullerene balls.

A grapevine nanostructure based on single-walled carbon nanotubes (SWNTs) covalently functionalized with [60]fullerene (C60) has been synthesized and characterized in detail. Investigations into the ball-on-tube carbon nanostructure by ESR spectroscopy indicate a tendency for ground-state electron transfer from the SWNT to the C60 moieties. The cyclic-voltammetric response of the nanostructure film exhibits reversible multiple-step electrochemical reactions of the dispersed C60, which are strikingly similar to those of the C60 derivatives in solution, but with consistent negative shifts in the redox potential. This results from the covalent linkage of C60 to the surfaces of the SWNTs in the form of monomers and manifests the electronic interaction between the C60 and SWNT moieties.

Sensitive dopamine recognition by boronic acid functionalized multi-walled carbon nanotubes.

Boronic acid functionalized multi-walled carbon nanotubes (MWNTs) have been synthesized and used for sensitive dopamine (DA) detection using electrochemical methods in the presence of excess L-ascorbic acid (L-AA) via specific, reversible formation of a boronate ester between DA and the functionalized MWNTs.