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61.
X‐ray crystal structures are reported for Na6[RuO2{TeO4(OH)2}2]·16H2O and Na5[Ag{TeO4(OH)2}2]·16H2O which contain respectively RuVI and AgIII coordinated to chelating bidentate tellurate ([TeO4(OH)2]4−) groups. Na6[RuO2{TeO4(OH)2}2]·16H2O: Space group P1¯, Z = 2, lattice dimensions at 120 K; a = 6.9865(1), b = 8.7196(2), c = 11.7395(2)Å, α = 74.008(1), β = 79.954(1), γ = 88.514(1)°; R1 = 0.025. Na5[Ag{TeO4(OH)2}2]·16H2O: Space group P1¯, Z = 2, lattice dimensions at 120 K; a = 5.888(1), b = 8.932(1), c = 12.561(2)Å, α = 98.219(6), β = 97.964(9), γ = 93.238(14)°; R1 = 0.047. 相似文献
62.
Hector Rene Vega-Carrillo M. R. Martinez-Blanco Victor Martin Hernandez-Davila Jose Manuel Ortiz-Rodriguez 《Journal of Radioanalytical and Nuclear Chemistry》2009,281(3):615-618
Artificial neural networks have been applied to unfold the neutron spectra and to calculate the effective dose, the ambient equivalent dose, and the personal dose equivalent for 252Cf, 241Am–Be, and 239Pu–Be neutron sources. The count rates that these neutron sources produce in a Bonner Sphere Spectrometer with a 6LiI(Eu) were utilized as input in both artificial neural networks. Spectra and the ambient dose equivalent were also obtained with BUNKIUT code and the UTA4 response matrix. With both procedures spectra and ambient dose equivalent agrees in less than 10%. The Artificial neural network technology is an alternative procedure to unfold neutron spectra and to perform neutron dosimetry. 相似文献
63.
Margarita Suárez Hector Novoa Yamila Verdecia Amaury Alvarez Rolando Pérez Dolores Molero Norbert M. Blaton Nazario Martín 《Tetrahedron》2006,62(7):1365-1371
Unprecedented 2-iminium chloride salts of 5,8-dihydro-2H-pyrido[3,2-e][1,3]thiazines derivatives (8) were easily synthesized in one step from the corresponding o-chloroformyl-1,4-dihydropyridine (2) and thiourea. The structural study has been carried out by X-ray crystallography and theoretical calculations at the B3LYP/6-31G* levels and reveal that the new salts exhibit appropriate structural features to behave as calcium channel modulators. 相似文献
64.
Hector?Pool Gabriel?Luna-Barcenas David?Julian?McClements Sandra?MendozaEmail author 《Journal of nanoparticle research》2017,19(9):324
In this study, pH-sensitive nanospheres were fabricated using a polymethacrylate-based copolymer to encapsulate, protect, and release catechin, and thereby overcome its poor water solubility and low oral bioaccessibility. The polymer used was a polymethacrylic acid-co-ethyl acrylate 1:1 copolymer that dissolves above pH 5.5, and so can be used to retain and protect bioactives within the stomach but releases them in the small intestine. Catechin-loaded nanospheres were fabricated using the solvent displacement method. Physicochemical characterization of the nanospheres indicated that they were relatively small (d = 160 nm) and had a high negative charge (ζ = ? 36 mV), which meant that they had good stability to aggregation under physiological conditions (pH 7.2). Catechin was trapped within the nanospheres at an encapsulation efficiency of about 51% in an amorphous state. A simulated gastrointestinal study showed that catechin was slowly released under gastric conditions (pH 2.5), but rapidly released under small intestine conditions (pH 7.2). The observed improvement in the antioxidant activity and bioaccessibility of catechin after encapsulation was attributed to the fact that it was in an amorphous state and had good water dispersibility. This study provides useful information for the formulation of novel delivery systems to improve the dispersibility, bioaccessibility, and bioactivity of catechin and potentially other active components. These delivery systems could be used to improve the efficacy of bioactive components in foods, supplements, and pharmaceutical products. 相似文献
65.
Figueroa H Peddi D Osborne JM Wilson BM Pesaru RR Kurva B Ramaraju S Milletti MC Heyl DL 《Journal of chemical information and modeling》2012,52(5):1298-1307
Human islet amyloid polypeptide (hIAPP) forms cytotoxic fibrils in type-2 diabetes and insulin is known to inhibit formation of these aggregates. In this study, a series of insulin-based inhibitors were synthesized and assessed for their ability to slow aggregation and impact hIAPP-induced membrane damage. Computational studies were employed to examine the underlying mechanism of inhibition. Overall, all compounds were able to slow aggregation at sufficiently high concentrations (10× molar excess); however, only two peptides showed any inhibitory capability at the 1:1 molar ratio (EALYLV and VEALYLV). The results of density functional calculations suggest this is due to the strength of a salt bridge formed with the Arg11 side chain of hIAPP and the inhibitors' ability to span from the Arg11 to past the Phe15 residue of hIAPP, blocking one of the principal amyloidogenic regions of the molecule. Unexpectedly, slowing fibrillogenesis actually increased damage to lipid membranes, suggesting that the aggregation process itself, rather than the fibrilized peptide, may be the cause of cytotoxicity in vivo. 相似文献
66.
B Hadwen GR Broder D Morganti A Jacobs C Brown JR Hector Y Kubota H Morgan 《Lab on a chip》2012,12(18):3305-3313
We describe a new device concept for digital microfluidics, based on an active matrix electrowetting on dielectric (AM-EWOD) device. A conventional EWOD device is limited by the number of electrical connections that can be made practically, which restricts the number and type of droplet operations. In an AM-EWOD, the patterned electrodes of a conventional EWOD device are replaced by a thin film transistor (TFT) array, as found in a liquid crystal display (LCD), facilitating independent control of each electrode. The arrays can have many thousand individually addressable electrodes, are fully reconfigurable and can be programmed to support multiple simultaneous operations. Each element is 210 μm × 210 μm in size and contains a circuit that measures the electrical impedance of the liquid above it. This is used to determine the presence and size of a droplet, a method that can improve assay reliability and accuracy. This sensor provides feedback, error detection and closed loop control of an assay sequence. We describe the design, fabrication and testing of a 64 × 64 format AM-EWOD device with impedance sensor functionality. A colorimetric assay is implemented on the device and used to measure glucose in human blood serum. Results are compared with the same assay performed on a microtitre plate. 相似文献
67.
Mandal S Reber AC Qian M Liu R Saavedra HM Sen S Weiss PS Khanna SN Sen A 《Dalton transactions (Cambridge, England : 2003)》2012,41(18):5454-5457
The dimeric Zintl ion [Hg(2)(As(7))(2)](4-) has been synthesized with high crystalline yield from the reaction of an ethylendiamine solution of the intermetallic Zintl phase K(3)As(7) with diphenyl mercury. Single crystal X-ray diffraction of [K(2,2,2-crypt)](4)[Hg(2)As(14)], 1 (2,2,2-crypt = 4,7,13,16,21,24-hexaoxa-1,10-diazabicyclo[8.8.8]-hexacosane), reveals that the cluster anion exhibits a Hg-Hg bond and the compound has been further characterized using Raman spectroscopy, cyclic voltammetry and its band gap energy was measured. Theoretical studies provide a microscopic understanding of the bonding in this unusual compound. 相似文献
68.
Triffo SB Huang HH Smith AW Chou ET Groves JT 《Journal of the American Chemical Society》2012,134(26):10833-10842
This study examines the dynamic co-localization of lipid-anchored fluorescent proteins in living cells using pulsed-interleaved excitation fluorescence cross-correlation spectroscopy (PIE-FCCS) and fluorescence lifetime analysis. Specifically, we look at the pairwise co-localization of anchors from lymphocyte cell kinase (LCK: myristoyl, palmitoyl, palmitoyl), RhoA (geranylgeranyl), and K-Ras (farnesyl) proteins in different cell types. In Jurkat cells, a density-dependent increase in cross-correlation among RhoA anchors is observed, while LCK anchors exhibit a more moderate increase and broader distribution. No correlation was detected among K-Ras anchors or between any of the different anchor types studied. Fluorescence lifetime data reveal no significant F?rster resonance energy transfer in any of the data. In COS 7 cells, minimal correlation was detected among LCK or RhoA anchors. Taken together, these observations suggest that some lipid anchors take part in anchor-specific co-clustering with other existing clusters of native proteins and lipids in the membrane. Importantly, these observations do not support a simple interpretation of lipid anchor-mediated organization driven by partitioning based on binary lipid phase separation. 相似文献
69.
Dulce María Soler Yanet Rodríguez Hector Correa Ailed Moreno Lila Carrizales 《Radiation Physics and Chemistry》2012,81(8):1249-1253
This study is aimed of producing pilot batches of hydrogel wound dressings by gamma radiation and evaluating their shelf stability. Six batches of 3L capacity were prepared based on poly(vinyl pyrrolidone), agar and polyethylene glycol and they were dispensed in polyester trays, covered with polyester films and sealed in two types of materials: polyethylene bags and vacuum polyethylene bags. Dressings were formed in a single step process for the hydrogel formation and sterilization at 25–30 kGy gamma radiation dose in a JS-9500 Gamma Irradiator (Nordion, Canada). The six batches were initially physicochemical characterized in terms of dimensions and appearance, gel fraction, morphology analysis, hydrogel strength, moisture retention capability and swelling capacity. They were kept under two storage conditions: room temperature (T: 30±2 °C/RH: 70± 5%) and refrigerated temperature (T: 5±3 °C) during 24 months and sterility test was performed. The appearance of membranes was transparent, clear, uncut and flexible; the gel fraction of batches was higher than 75% and the hydrogel surface showed a porous structure. There was a slow decrease of the compression rate 20% until 7 h and about 70% at 24 h. Moisture retention capability in 5 h was similar for all the batches, about 40% and 60% at 37 °C and at room temperature respectively. The swelling of hydrogels in acidic media was strong and in alkaline media the weight variation remains almost stable until 24 h and then there is a loss of weight. The six batches remained sterile during the stability study in the conditions tested. The pilot batches were consistent from batch to batch and remained stable during 24 months. 相似文献
70.
Multi-way partial least-squares (N-PLS) is combined to the residual bi-linearization procedure (RBL) for the direct analysis of metabolites of polycyclic aromatic hydrocarbons in urine samples. Metabolite analysis is carried out via a two-step experimental procedure based on solid-phase extraction and room temperature fluorescence spectroscopy. Excitation-emission matrices are recorded from octadecyl (C18) membranes that serve as solid substrates for sample extraction and spectroscopic measurements. Excellent metabolite recoveries were obtained in all cases, which varied from 96.2 ± 1.35% (9-hydroxyphenanthrene) to 99.7 ± 0.49% (3-hydroxybenzo[a]pyrene). Background correction of extraction membranes is carried out with a new alternating least-squares (ALS) procedure adapted to second order data. The performance of N-PLS/RBL is compared to the well-established multivariate curve resolution-alternating least-squares (MCR-ALS) algorithm. Both algorithms provided similar analytical figures of merit, including their ability to handle unknown interference in urine samples. With only 10 mL of sample, the limits of detection varied between 0.06–0.08 ng mL−1 (1-hydroxypyrene) and 0.016–0.018 ng mL−1 (2-hydroxyfluorene). When compared to previously reported univariate calibration data, the limits of detection via N-PLS/RBL and MCR-ALS are approximately one order of magnitude higher. This was somehow expected due to the effect of unexpected components in multivariate figures of merit, i.e. a more realistic approach to the analysis of metabolites in human urine samples. 相似文献