Two-photon fluorescence microscopy imaging of cellular oxidative stress using profluorescent nitroxides

A range of varying chromophore nitroxide free radicals and their nonradical methoxyamine analogues were synthesized and their linear photophysical properties examined. The presence of the proximate free radical masks the chromophore's usual fluorescence emission, and these species are described as profluorescent. Two nitroxides incorporating anthracene and fluorescein chromophores (compounds 7 and 19, respectively) exhibited two-photon absorption (2PA) cross sections of approximately 400 G.M. when excited at wavelengths greater than 800 nm. Both of these profluorescent nitroxides demonstrated low cytotoxicity toward Chinese hamster ovary (CHO) cells. Imaging colocalization experiments with the commercially available CellROX Deep Red oxidative stress monitor demonstrated good cellular uptake of the nitroxide probes. Sensitivity of the nitroxide probes to H(2)O(2)-induced damage was also demonstrated by both one- and two-photon fluorescence microscopy. These profluorescent nitroxide probes are potentially powerful tools for imaging oxidative stress in biological systems, and they essentially "light up" in the presence of certain species generated from oxidative stress. The high ratio of the fluorescence quantum yield between the profluorescent nitroxide species and their nonradical adducts provides the sensitivity required for measuring a range of cellular redox environments. Furthermore, their reasonable 2PA cross sections provide for the option of using two-photon fluorescence microscopy, which circumvents commonly encountered disadvantages associated with one-photon imaging such as photobleaching and poor tissue penetration.     

Synthesis and characterisation of photopolymerisable liquid crystals based on the π-extended fluorene core and their corresponding non-reactive analogues

We have synthesised a series of new reactive mesogens with photopolymerisable di-acrylates and their corresponding non-reactive analogues based on the π-conjugated aromatic core, fluorene (F)-di-[thiophene (T)-benzene (B)], using the Stille and Suzuki coupling reaction. The effect of lateral alkyl chains on the 9-position of the central fluorene moiety as well as α, ω- side alkyl chains attached to the π-conjugated aromatic core on the mesomorphism was investigated by utilising differential scanning calorimetry (DSC) and polarising optical microscopy (POM). A wide angle X-ray scattering (WAXS) study at the various temperatures was also carried out to reveal phase structures. Photopolymerisable di-acrylates connected directly to the rigid aromatic core showed higher phase transition temperatures, probably due to the induced dipole moment in comparison with those of a non-reactive methyl–ether counterpart.     

Substrate interaction effects on order to disorder transition behavior in block copolymer films

We present an overview of the recent progress on the phase transition in the block copolymer (BCP) films in terms of the interfacial interactions effects of the substrates and the χ (Flory-Huggins segmental interaction parameter) effects between the two blocks. For the BCP films thinner than a critical thickness (L_c) above which the transition is independent of film thickness, the order-to-disorder transition (ODT) increased or decreased with decreasing film thickness depending on the interfacial interaction types. The rapid and slow changes in the ODT were attributed to the relative magnitude of enthalpic contribution to χ between two blocks. Interestingly, a periodic amplification in the block composition for the BCP films suppressed the compositional fluctuation in the film geometry, resulting in the ODT shifts from the bulk ODTs above L_c. This effect of the BCP films was more illustrated by the ODT shift effects depending on the strength of the preferential interactions on the substrates. © 2013 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys, 2013     

The influence of alkaline reserve on the aging behavior of book papers

Degradation of cellulose under alkaline conditions is involved either involuntarily or deliberately in many different cellulose processing steps, such as pulping, bleaching, or aging within the viscose process, and the underlying chemistry has been the topic of numerous studies. When it comes to aging under alkaline conditions—either natural or accelerated (artificial)—the degradation processes are by far less investigated and understood. A prominent example of moderately alkaline cellulosic material is deacidified book paper from libraries which had undergone a mass-deacidification treatment. We studied their aging behavior under accelerated conditions in comparison to non-deacidified duplicates in order to better understand how the alkaline reserve, which was introduced by the deacidification treatment, affects the stability of the books on the long run. GPC analysis of cellulose and determination of carbonyl functionalities were performed, which were critical parameters to achieve a deeper insight into hydrolytic and oxidative changes of cellulose structure upon deacidification treatment and subsequent aging. Also, model book papers impregnated with different amounts of alkaline reserve were used to support the findings from the original book samples. Hydrolytic degradation rates of the original book papers were significantly reduced after mass deacidification compared to the non-deacidified duplicates. The beneficial effect of mass deacidification on cellulose stability was found to be strongly related to the amount of alkaline reserve deposited, independent of varying parameters of book papers. Although some indication of alkali-induced β-elimination was found (a minor decrease of the along-chain carbonyl content in the original deacidified book papers during aging), it did not occur to an extent that significantly influenced the molar mass of cellulose. The beneficial effect of retarded hydrolytic degradation by mass deacidification thus clearly outweighed possible negative alkalinity effects of the deposited alkaline reserve.     

Determination of PF‐04620110, a novel inhibitor of diacylglycerol acyltransferase‐1, in rat plasma using liquid chromatography–tandem mass spectrometry and its application in pharmacokinetic studies

In this study, we developed a method for the determination of PF‐04620110 (2‐{(1r,4r)‐4‐[4‐(4‐amino‐5‐oxo‐7,8‐dihydropyrimido[5,4‐f][1,4]oxazepin‐6(5H)‐yl)phenyl]cyclohexyl}acetic acid), a novel diacylglycerol acyltransferase 1 (DGAT‐1) inhibitor, in rat plasma and validated it using liquid chromatography–tandem mass spectrometry (LC‐MS/MS). Rat plasma samples were processed following a protein precipitation method by using acetonitrile and were then injected into an LC‐MS/MS system for quantification. PF‐04620110 and imipramine (internal standard) were separated using a Hypersil Gold C₁₈ column, with a mixture of acetonitrile and 10 mm ammonium formate (90:10, v/v) as the mobile phase. The ion transitions monitored in positive‐ion mode [M + H]⁺ of multiple‐reaction monitoring were m/z 397.0 → 260.2 for PF‐04620110 and m/z 280.8 → 86.0 for imipramine. The detector response was specific and linear for PF‐04620110 at concentrations within the range 0.05–50 µg/mL and the signal‐to‐noise ratios for the samples were ≥10. The intra‐ and inter‐day precision and accuracy of the method matched the acceptance criteria for assay validation. PF‐04620110 was stable under various processing and/or handling conditions. PF‐04620110 concentrations in the rat plasma samples could be measured up to 24 h after intravenous or oral administration of PF‐04620110, suggesting that the assay is useful for pharmacokinetic studies in rats. Copyright © 2013 John Wiley & Sons, Ltd.     

Poly(ethylene glycol)‐crosslinked fullerenes for high efficient phototherapy

Poly(ethylene glycol)‐crosslinked multimeric C₆₀ was developed for use in photothermal/photodynamic therapy of malignant cells. We showed that: (i) the tumor surface temperature on KB tumor‐bearing nude mice treated with multimeric C₆₀ reached about 44 °C; (ii) this hyperthermic condition and tremendous singlet oxygen generation from multimeric C₆₀ resulted in significant tumor volume regression in KB tumor‐bearing nude mice; and (iii) multimeric C₆₀ also efficiently inhibited arthritic progress in the arthritis‐induced DBA/1 J mice model. This multimeric C₆₀ may be useful for photothermal/photodynamic cell ablation in various malignant cells. Copyright © 2012 John Wiley & Sons, Ltd.     

Effective isolation of magnesium lithospermate B and its inhibition of aldose reductase and fibronectin on mesangial cell line

We developed an effective isolation method of magnesium lithospermate B from Salviae miltiorrhizae Radix and found for the first time that magnesium lithospermate B shows strong in vitro inhibition (IC50=0.04 microM) of aldose reductase (AR), 2.5 times than that of clinically used epalrestat (IC50=0.1 microM) and accumulation of fibronectin dose dependently.     

Harmonious Heterointerfaces Formed on 2D-Pt Nanodendrites by Facet-Respective Stepwise Metal Deposition for Enhanced Hydrogen Evolution Reaction

The performance of nanocrystal (NC) catalysts could be maximized by introducing rationally designed heterointerfaces formed by the facet- and spatio-specific modification with other materials of desired size and thickness. However, such heterointerfaces are limited in scope and synthetically challenging. Herein, we applied a wet chemistry method to tunably deposit Pd and Ni on the available surfaces of porous 2D−Pt nanodendrites (NDs). Using 2D silica nanoreactors to house the 2D-PtND, an 0.5-nm-thick epitaxial Pd or Ni layer ( e - Pd or e -Ni ) was exclusively formed on the flat {110} surface of 2D−Pt, while a non-epitaxial Pd or Ni layer ( n - Pd or n -Ni ) was typically deposited at the {111/100} edge in absence of nanoreactor. Notably, these differently located Pd/Pt and Ni/Pt heterointerfaces experienced distinct electronic effect to influence unequally in electrocatalytic synergy for hydrogen evolution reaction (HER). For instance, an enhanced H₂ generation on the Pt{110} facet with 2D-2D interfaced e -Pd deposition and faster water dissociation on the edge-located n -Ni overpowered their facet-located counterparts in respective HER catalysis. Therefore, a feasible assembling of the valuable heterointerfaces in the optimal 2D n -Ni/e-Pd/Pt catalyst overcame the sluggish alkaline HER kinetics, with a catalytic activity 7.9 times higher than that of commercial Pt/C.     

A General Strategy Toward pH-Resistant Phenolic Fluorophores for High-Fidelity Sensing and Bioimaging Applications

Aryl alcohol-type or phenolic fluorophores offer diverse opportunities for developing bioimaging agents and fluorescence probes. Due to the inherently acidic hydroxyl functionality, phenolic fluorophores provide pH-dependent emission signals. Therefore, except for developing pH probes, the pH-dependent nature of phenolic fluorophores should be considered in bioimaging applications but has been neglected. Here we show that a simple structural remedy converts conventional phenolic fluorophores into pH-resistant derivatives, which also offer “medium-resistant” emission properties. The structural modification involves a single-step introduction of a hydrogen-bonding acceptor such as morpholine nearby the phenolic hydroxyl group, which also leads to emission bathochromic shift, increased Stokes shift, enhanced photo-stability and stronger emission for several dyes. The strategy greatly expands the current fluorophores’ repertoire for reliable bioimaging applications, as demonstrated here with ratiometric imaging of cells and tissues.