Observation of new states decaying into Lambda+(c)pi(-)pi(+)

Using 13.7 fb(-1) of data recorded by the CLEO detector at the Cornell Electron Storage Ring, we investigate the spectrum of charmed baryons which decay into Lambda+(c)pi(-)pi(+) and are more massive than the Lambda+(c)(2625) baryon. We find evidence for two new states: one is broad and has an invariant mass roughly 480 MeV above that of the Lambda+(c) baryon; the other is narrow with an invariant mass of 596+/-1+/-2 MeV above the Lambda+(c) mass.     

Simultaneous NO and CO(2) measurement in human breath with a single IV-VI mid-infrared laser

A tunable diode laser absorption spectroscopy (TDLAS) system equipped with a IV-VI mid-IR laser operating near 5.2>mu;m was used to measure exhaled nitric oxide (eNO) and carbon dioxide (CO(2)) simultaneously in human breath over a single exhalation. Breath was sampled in real time, and eNO levels were measured from seven volunteers, two steroid-naive asthmatics and five nonasthmatics. Measured CO(2) levels were used as an internal standard to verify correct breath collection and calculate eNO values. Calculated eNO concentrations agreed well with reported values for asthmatic and nonasthmatic individuals.     

X-ray Crystallographic Structures of Neuroprotective Pyrimidine Derivatives: (I) the Mesylate Salt of BW1003C87 and (II) Sipatrigine Base

Abstract Drugs based on 5-phenyl-2,4 diamino pyrimidine and 6-phenyl-1,2,4 triazine derivatives are well known for their effects on the central nervous system. The study presented here provides detailed crystal structures of two pyrimidine derivatives which have neuroprotective properties in models of both grey and white matter ischemia. Recently published studies suggest that the compounds lamotrigine (a triazine derivative), and the two pyrimidines BW1003C87 (I) and sipatrigine (II) mediate their primary in vivo mode of action by inhibiting voltage-gated Na⁺ channels. The X-ray crystal structures will contribute valuable data for applications involving binding and modelling studies of the biological actions of these drugs. Graphical Abstract X-ray crystallographic structures of neuroprotective pyrimidine derivatives: (I) the mesylate salt of BW1003C87 and (II) sipatrigine base Rex A. Palmer*, Brian S. Potter, Michael J. Leach and Babur Z. Chowdhry Surface representations, [20] are a useful tool with respect to considerations employed for the purposes of drug design. Shown here are the neuroprotective drug molecules (a) BW1003C87 and (b) Sipatrigine Base (BW619C89) derived from their solid state structures reported in this paper. The molecules are viewed edge on to ring B with the two adjacent Cl atoms uppermost on the left.      

(24R)‐24,25‐Dihydroxycyclo­artan‐3‐one

In the title compound, C₃₀H₅₀O₃, the three six‐membered rings adopt chair, twist and twist‐boat conformations. The five‐membered ring is in a slightly distorted envelope conformation. The substituent on the five‐membered ring is in an extended conformation, with its two hydroxyl O atoms forming an intramolecular hydrogen bond. One of these O atoms also forms an intermolecular hydrogen bond with the oxy­gen of the carbonyl group in a neighbouring mol­ecule.     

Gadolinium nitride films deposited using a PEALD based process

Gadolinium nitride films have been deposited on Si(100) using a plasma-enhanced ALD (PEALD) based process. The deposition was carried out using tris(methylcyclopentadienyl)gadolinium {Gd(MeCp)₃} and remote nitrogen plasma, separated by argon pulses. Films were deposited at temperatures between 150 and 300 °C and capped with tantalum nitride to prevent post-deposition oxidation. Film composition was initially assessed using EDX and selected samples were subsequently depth profiled using medium energy ion scattering (MEIS) or AES. X-ray diffraction appears to show that the films are effectively amorphous. Films deposited at 200 °C were found to have a Gd:N ratio close to 1:1 and a low oxygen incorporation (～5%). Although the growth was affected by partial thermal decomposition of the Gd(MeCp)₃, it was still possible to obtain smooth (Ra.=～0.7 nm) films with good thickness uniformity (97%). Less successful attempts to deposit gadolinium nitride using thermal ALD with ammonia or mono-methyl-hydrazine are also reported.     

Application of Hildebrand's fluidity model to non-Newtonian solutions

Summary The fluidity model ofHildebrand has been applied to dilute aqueous polymer solutions exhibiting non-Newtonian behaviour. As for Newtonian fluids, it is found that the temperature dependence of apparent viscosity of non-Newtonian fluids is determined entirely by the temperature dependence of fluid density. However, whereas the parameters ofHildebrand's equation are constants, independent of the conditions of shear for Newtonian fluids, these parameters become shear-rate dependent for non-Newtonian fluids. The magnitude of the parameters and their variation with shear rate can be explained qualitatively in terms of interactions of polymer molecules and their behaviour in a shear field.

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Zusammenfassung Das Fließmodell vonHildebrand wird auf verdünnte wäßrige Polymerlösungen mit nicht-newtonschem Verhalten angewandt. Wie bei newtonschen Flüssigkeiten findet man hierfür, daß die Temperaturabhängigkeit der schergeschwindigkeitsabhängigen Viskosität ausschließlich durch die Temperaturabhängigkeit der Flüssigkeitsdichte bestimmt ist. Während jedoch die Parameter derHildebrandschen Gleichung für newtonsche Flüssigkeiten von den Scherbedingungen unabhängige Konstanten darstellen, werden diese bei nichtnewtonschen Flüssigkeiten schergeschwindigkeitsabhängig. Die Größe dieser Parameter und ihrer Variation mit der Schergeschwindigkeit kann qualitativ als eine Folge der Wechselwirkung der Polymermoleküle und ihres Verhaltens im Scherfeld gedeutet werden.

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Notation B Parameter inHildebrand's fluidity equation, eq. [1] (N^–1 m² s^–1) - K Consistency parameter in the power-law (Nm^–2 s ⁿ ) - n Flow behaviour index in the power-law (–) - T Temperature (K) - V Molar volume (m³ mol^–1) - V ₀ Intrinsic molar volume; parameter inHildebrand's fluidity equation, eq. [1] (m³ mol^–1) - Shear rate (s^–1) - Viscosity or apparent viscosity (Nm^–2 s) - Density (kg m^–3) - ₀ Intrinsic density; modified parameter inHildebrand's fluidity equation; eq. [5] (kg m^–3) - Shear stress (Nm^–2) With 4 figures and 1 table     

Novel Product Chemistry from Mechanistic Analysis of ent‐Copalyl Diphosphate Synthases from Plant Hormone Biosynthesis

An active‐site water molecule coordinated by conserved histidine and asparagine residues seems to serve as the catalytic base in all ent‐copalyl diphosphate synthases (CPSs). When these residues are substituted by alanine, the mutant CPSs produce stereochemically novel ent‐8‐hydroxy‐CPP. Given the requisite presence of CPSs in all land plants for gibberellin phytohormone biosynthesis, such plasticity presumably underlies the observed extensive diversification of the resulting labdane‐related diterpenoids.     

Photobleaching of photofrin II as a means of eliminating skin photosensitivity

One of the effects of using Photofrin II as a sensitizer in clinical photodynamic therapy is skin photosensitivity. Avoiding the harmful effect of this photosensitivity typically requires the patient to remain indoors during daylight hours for 4 weeks post injection. Photosensitivity can last up to 8 weeks. A possible method of quickly eliminating skin photosensitivity is the use of photobleaching to eliminate the DHE (dihematoporphyrin ether, the active agent in Photofrin II) from the skin. The Photofrin II was used as supplied (Photomedica, Raritan, NJ) and will be referred to as DHE. We report a series of experiments using Swiss mice which demonstrate the ability to reduce the period of photosensitivity to 1 week. The Swiss mice received 5 mg kg^-1 DHE intraperitoneal. Beginning at 24 h post injection they were given daily increasing light doses starting with 18 J cm^-2 (at 630 nm). Only the left hind feet were treated with light. At 7 days post injection both hind feet were treated with 135 J cm^-2. The pretreated left foot showed no reaction to this treatment whereas the right foot reacted as strongly as control mice which had received no pretreatment with light. The control mice were also injected 7 days prior to treatment. As a check for tolerance animals received a second injection of 5 mg kg^-1 DHE intraperitoneally 96 h after the conclusion of the bleaching protocol. Twenty-four h later the left hind foot (previously desensitized by light) reacted to 135 J cm^-2 as strongly as controls which had received the 5 mg kg^-1 of DHE but no pretreatment.     

Effect of substrate temperature on electrical and magnetic properties of epitaxial La1−x Pb x MnO3 films

Epitaxial La_1−x Pb _x MnO₃ (LPMO) thin films, grown on (100) SrTiO₃ substrates by laser ablation technique at different temperatures between 600 and 850°C, have been characterized for electrical and magnetic properties. The temperature dependence of resistivity showed that the metal-insulator transition temperature (T _MI) decreases with increasing substrate temperature, which has been attributed to decrease in Pb content in the filsm. The YBa₂Cu₃O _x /La_1−x MnO₃ heterostructures, exhibiting both superconductivity and ferromagnetism, have been fabricated.