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Background: Application of hepatoprotectants, such as drugs or cytokines, can reduce drug-induced hepatotoxicity (DIH). Due to species-specific differences and abnormal cell polarity and drug-metab...

Drug-induced hepatotoxicity (DIH) in preclinical tests will help reduce drug attrition and development costs. However, the concordance between preclinical animal safety data and human clinical hepa...

Many categories of drugs can induce hepatotoxicity, so improving the prediction of toxic drugs is important. In vitro models using human hepatocytes are more accurate than in vivo animal models. Good in vitro models require an abundance of metabolic enzyme activities and normal cellular polarity. However, none of the in vitro models can completely simulate hepatocytes in the human body. There are two ways to overcome this limitation: enhancing the metabolic function of hepatocytes and changing the cultural environment. In this review, we summarize the current state of research, including the main characteristics of in vitro models and their limitations, as well as improved technology and developmental prospects. We hope that this review provides some new ideas for hepatotoxicity research.

Classical contact lithography involves patterning of surfaces by embossing or by transfer of ink. We report direct lithographic transfer of parts of sacrificial stamps onto counterpart surfaces. Using sacrificial stamps consisting of the block copolymer polystyrene-block-poly(2-pyridine) (PS-b-P2VP), we deposited arrays of nanostructured submicron PS-b-P2VP dots with heights of about 100 nm onto silicon wafers and glass slides. The sacrificial PS-b-P2VP stamps were topographically patterned with truncated-pyramidal contact elements and penetrated by spongy-continuous nanopore systems. The spongy nature of the sacrificial PS-b-P2VP stamps supported formation of adhesive contact to the counterpart surfaces and the rupture of the contact elements during stamp retraction. The submicron PS-b-P2VP dots generated by sacrificial stamping can be further functionalized, examples include loading submicron PS-b-P2VP dots with dyes and attachment of gold nanoparticles to their outer surfaces. The arrays of submicron PS-b-P2VP dots can be integrated into setups for advanced optical microscopy, total internal reflection fluorescence microscopy or Raman microscopy. Arrays of nanostructured submicron block copolymer dots may represent a preconcentration platform for locally resolved sensing and locally resolved monitoring of cellular interactions or might be used as microreactor arrays in lab-on-chip configurations., ACS Applied Nano Materials 2018

A titanium sulfonate ligand is synthesized for surface coordination of black phosphorus (BP). In contrast to serious degradation observed from the bare BP, the BP after surface coordination exhibits excellent stability during dispersion in water and exposure to air for a long period of time, thereby significantly extending the lifetime and spurring broader application of BP.

A novel 12.5Gbps quarter rate CDR is presented in this paper. For lock acquisition depends on the frequency tracking loop (FLL loop) and recovered clock jitter depends on the phase tracking loop (PLL loop) without one impacting the other, the CDR gets both short lock acquisition and low clock jitter. Moreover, a novel frequency band switch (FBS) is proposed, which switches the band of VCO. Meanwhile, the FBS ensures proper switching of dual loops to prevent false locking, without another lock detector, reducing the power consumption. Realized in 55-nm CMOS technology, the CDR consumes 15.2mW with a 1.2V supply.

High overpotentials, particularly an issue of common anode materials, hamper the process of water electrolysis for clean energy generation. Thanks to immense research efforts up to date oxygen evolution electrocatalysts based on earth-abundant elements work efficiently and stably in neutral and alkaline regimes. However, non-noble metal-based anode materials that can withstand low pH regimes are considered to be an indispensable prerequisite for the water splitting to succeed in the future. All oxygen evolving electrodes working durably and actively in acids contain Ir at least as an additive. Due to its scarcity and high acquisition costs noble elements like Pt, Ru and Ir need to be replaced by earth abundant elements. We have evaluated a Ni containing stainless steel for use as an oxygen-forming electrode in diluted H2SO4. Unmodified Ni42 steel showed a significant weight loss after long term OER polarization experiments. Moreover, a substantial loss of the OER performance of the untreated steel specimen seen in linear sweep voltammetry measurements turned out to be a serious issue. However, upon anodization in LiOH, Ni42 alloy was rendered in OER electrocatalysts that exhibit under optimized synthesis conditions stable overpotentials down to 445 mV for 10 mA cm-2 current density at pH 0. Even more important: The resulting material has proven to be robust upon long-term usage (weight loss: 20 mug/mm2 after 50 ks of chronopotentiometry at pH 1) towards OER in H2SO4. Our results suggest that electrochemical oxidation of Ni42 steel in LiOH (sample Ni42Li205) results in the formation of a metal oxide containing outer zone that supports solution route-based oxygen evolution in acidic regime accompanied by a good stability of the catalyst., arXiv admin note: text overlap with arXiv:1712.01100

Insect-inspired capillary submicron stamping and subsequent surface-limited metal-assisted chemical etching (MACE) with ammonium bifluoride as HF source is employed for high-throughput production of ordered topographically patterned silicon (tpSi). Insect feet often possess hairy contact elements through which adhesive secretion is deployed. Thus, arrays of adhesive secretion drops remain as footprints on contact surfaces. Stamps for insect-inspired capillary submicron stamping having surfaces topographically patterned with contact elements mimic the functional principles of such insect feet. They contain spongy continuous nanopore networks penetrating the entire stamps. Any ink (organic, aqueous) may be supplied from the backside of the nanoporous stamps to the contact elements. We generated ordered arrays of AgNO3 dots extending mm^2 on Si by manual stamping with cycle times of a few seconds under ambient conditions; at higher load ordered holey AgNO3 films were obtained. Surface-limited MACE correspondingly yielded either macroporous tpSi or Si pillar arrays. Inkjet printing of polymer solutions onto tpSi yielded patterns of polymer blots conformally covering the tpSi. Such blot patterns could potentially represent a starting point for the development of persistent and scratch-resistant identity labels or QR codes on silicon surfaces.

A novel oxygen evolution reaction (OER) catalyst (3D S235-P steel) based on steel S235 substrate has been successfully prepared via a facile one-step surface modification. The standard Carbon Manganese steel was phosphorizated superficially leading to the formation of a unique 3D interconnected nanoporous surface with high specific area which facilitates the electrocatalytically initiated oxygen evolution reaction. The prepared 3D S235-P steel exhibits enhanced electrocatalytic OER activities in alkaline regime confirmed by a low overpotential ({\eta}=326 mV at j=10 mA cm-2) and a small Tafel slope of 68.7 mV dec-1. Moreover, the catalyst was found to be stable under long-term usage conditions functioning as oxygen evolving electrode at pH 13 as evidenced by the sufficient charge to oxygen conversion rate (Faradaic efficiency: 82.11% and 88.34% at 10 mA cm-2 and 5 mA cm-2, respectively). In addition, it turned out that the chosen surface modification renders steel S235 into an OER electrocatalyst sufficiently and stable to work in neutral pH condition. Our investigation revealed that the high catalytic activities are likely to stem from the generated Fe/(Mn) hydroxide/oxo-hydroxides generated during the OER process. The phosphorization treatment is therefore not only an efficient way to optimize the electrocatalytic performance of standard Carbon-Manganese steel, but also enables for the development of low cost and abundant steels in the field of energy conversion., Comment: ChemSusChem, 2018, published online

Spatial self-phase modulation (SSPM) experiments on two-dimensional (2D) black phosphorus (BP) nanoflake suspensions are performed with focused femtosecond pulsed lasers at 350-1160 nm. In the broadband region, the slope of the SSPM ring number versus laser intensity varies from 0.99 to 0.34, which is larger than 0.25 in MoS2. We deduce the portion of the fluid globe (ξ) to be 0.0067, which is a constant independent of laser intensity, when the laser intensity is above 10 W/cm2. The nonlinear refractive index of BP is measured to be ∼10(-5) cm2 W(-1), and the third-order nonlinear susceptibility is χ(3)∼10(-8) esu at multiple wavelengths.

Dense layers of overlapping three-dimensional (3D) gold nanodendrites characterized by high specific surfaces as well as by abundance of sharp edges and vertices creating high densities of SERS hotspots are promising substrates for SERS-based sensing and catalysis. We have evaluated to what extent structural features of 3D gold nanodendrite layers can be optimized by the initiation of 3D gold nanodendrite growth at gold particles rationally positioned on silicon wafers. For this purpose, galvanic displacement reactions yielding 3D gold nanodendrites were guided by hexagonal arrays of parent gold particles with a lattice constant of 1.5 micrometers obtained by solid-state dewetting of gold on topographically patterned silicon wafers. Initiation of the growth of dendritic features at edges of the gold particles resulted in the formation of 3D gold nanodendrites while limitation of dendritic growth to the substrate plane was prevented. The regular arrangement of the parent gold particles supported the formation of dense layers of overlapping 3D gold nanodendrites that were sufficiently homogeneous within the resolution limits of Raman microscopes. Consequently, SERS mapping experiments revealed a reasonable degree of uniformity. The proposed preparation algorithm comprises only bottom-up process steps that can be carried out without use of costly instrumentation.

Components of technical systems and devices often require self-lubricating properties, which are implemented by means of dry lubricants. However, continuous lubricant coatings on the components' surfaces often suffer from poor adhesion, delamination and crack propagation. The replacement of continuous coatings with dense ordered arrays of microparticles consisting of dry lubricants may overcome these drawbacks. Using the well-established solid lubricant MoS2 as model system, we demonstrate that the sliding capability of polymeric monoliths can be significantly enhanced by integration of arrays of micron-sized dry lubricant microparticles into their contact surfaces. To synthesize the MoS2 microparticle arrays, we first prepared ordered hexagonal arrays of ammonium tetrathiomolybdate (ATM) microparticles on Si wafers by molding against poly(dimethylsiloxane) templates followed by high-temperature conversion of the ATM microparticles into MoS2 microparticles under Ar/H2 atmosphere in the presence of elemental sulfur. Finally, the obtained large-scale hexagonal MoS2 microparticle arrays were transferred to the surfaces of polymer monoliths under conservation of the array ordering. Self-lubrication of components of technical systems by incorporation of dry lubricant microparticle arrays into their contact surfaces is an example for overcoming the drawbacks of continuous functional coatings by replacing them with microparticle arrays., In press