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991.
Maysa Faisal Suyagh Godwill Iheagwaram Prashant Laxman Kole Jeff Millership Paul Collier Henry Halliday James C. McElnay 《Analytical and bioanalytical chemistry》2010,397(2):687-693
A selective and sensitive high-performance liquid chromatography method with UV detection for the determination of metronidazole in dried blood spots (DBS) has been developed and validated. DBS samples [spiked or patient samples] were prepared by applying blood (30 µL) to Guthrie cards. Discs (6 mm diameter) were punched from the cards and extracted using water containing the internal standard, tinidazole. The extracted sample was chromatographed without further treatment using a reversed phase system involving a Symmetry® C18 (5 µm, 3.9?×?150 mm) preceded by a Symmetry® guard column of matching chemistry and a detection wavelength of 317 nm. The mobile phase comprised acetonitrile/0.01?M phosphate solution (KH2PO4), pH 4.7, 15:85, v/v, with a flow rate of 1 mL/min. The calibration was linear over the range 2.5–50 mg/mL. The limits of detection and quantification were 0.6 and 1.8 µg/mL, respectively. The method has been applied to the determination of 203 DBS samples from neonatal patients for a phamacokinetic/pharmacodynamic study. 相似文献
992.
Ragothaman Yennamalli Naidu Subbarao Thorsten Kampmann Ross P. McGeary Paul R. Young Bostjan Kobe 《Journal of computer-aided molecular design》2009,23(6):333-341
Dengue and related flaviviruses represent a significant global health threat. The envelope glycoprotein E mediates virus attachment
to a host cell and the subsequent fusion of viral and host cell membranes. The fusion process is driven by conformational
changes in the E protein and is an essential step in the virus life cycle. In this study, we analyzed the pre-fusion and post-fusion
structures of the dengue virus E protein to identify potential novel sites that could bind small molecules, which could interfere
with the conformational transitions that mediate the fusion process. We used an in silico virtual screening approach combining
three different docking algorithms (DOCK, GOLD and FlexX) to identify compounds that are likely to bind to these sites. Seven
structurally diverse molecules were selected to test experimentally for inhibition of dengue virus propagation. The best compound
showed an IC50 in the micromolar range against dengue virus type 2.
Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users. 相似文献
993.
Paul Reece Monique Bremer Robert Stones Christopher Danks Sabine Baumgartner Victoria Tomkies Claudia Hemetsberger Nathalie Smits Walter Lubbe 《Analytical and bioanalytical chemistry》2009,394(7):1845-1851
A bioinformatics approach to developing antibodies to specific proteins has been evaluated for the production of antibodies
to heat-processed specified risk tissues from ruminants (brain and eye tissue). The approach involved the identification of
proteins specific to ruminant tissues by interrogation of the annotation fields within the Swissprot database. These protein
sequences were then interrogated for peptide sequences that were unique to the protein. Peptides were selected that met these
criteria as close as possible and that were also theoretically resistant to either pepsin or trypsin. The selected peptides
were synthesised and used as immunogens to raise monoclonal antibodies. Antibodies specific for the synthetic peptides were
raised to half of the selected peptides. These antibodies have each been incorporated into a competitive enzyme-linked immunosorbent
assay (ELISA) and shown to be able to detect the heat-processed parent protein after digestion with either pepsin or trypsin.
One antibody, specific for alpha crystallin peptide (from bovine eye tissue), was able to detect the peptide in canned meat
products spiked with 10% eye tissue. These results, although preliminary in nature, show that bioinformatics in conjunction
with enzyme digestion can be used to develop ELISA for proteins in high-temperature processed foods and demonstrate that the
approach is worth further study. 相似文献
994.
阳离子表面活性剂Aliquat 336对水中双酚A的浊点萃取及作用机制 总被引:2,自引:1,他引:2
研究了阳离子表面活性剂Aliquat 336(三辛基甲基氯化铵)浊点萃取水中双酚A(BPA)后以高效液相色谱测定的方法.探讨了Aliquat 336与Na_2SO_4/NaCl用量、pH值、萃取时间等因素对萃取效果的影响,经条件实验选定各因素水平如下:0.8 g/L Aliquat 336,4.0 g/L Na_2SO_4,超声萃取15 min,pH和对萃取影响不大,故不予调节.结果表明: 在此选定条件下,本方法富集效率高(BPA在胶束相-水相分配系数达10~4),萃取效率稳定(相对标准偏差均小于10%),其对BPA在不同水质、不同加标浓度下的回收率均大于90%,去离子水中检出限为0.34 μg/L.本方法操作简单、方便、成本低,易于推广.同时以胶束粒径与Zeta电位分析等确证盐含量对阳离子表面活性剂胶束形成的决定性作用,并结合影响因子分析,推测Aliquat 336浊点萃取过程中BPA可能存在静电作用、阳离子-π键等疏水分配以外的作用机制. 相似文献
995.
Fang L Park JY Cui Y Alivisatos P Shcrier J Lee B Wang LW Salmeron M 《The Journal of chemical physics》2007,127(18):184704
The mechanical and electrical properties of CdTe tetrapod-shaped nanocrystals have been studied with atomic force microscopy. Tapping mode images of tetrapods deposited on silicon wafers revealed that they contact the surface with three of its arms. The length of these arms was found to be 130+/-10 nm. A large fraction of the tetrapods had a shortened vertical arm as a result of fracture during sample preparation. Fracture also occurs when the applied load is a few nanonewtons. Compression experiments with the atomic force microscope tip indicate that tetrapods with the shortened vertical arm deform elastically when the applied force was less than 50 nN. Above 90 nN additional fracture events occurred that further shortened the vertical arm. Loads above 130 nN produced irreversible damage to the other arms as well. Current-voltage characteristics of tetrapods deposited on gold revealed a semiconducting behavior with a current gap of approximately 2 eV at low loads (<50 nN) and a narrowing to about 1 eV at loads between 60 and 110 nN. Atomistic force field calculations of the deformation suggest that the ends of the tetrapod arms are stuck during compression so that the deformations are due to bending modes. Empirical pseudopotential calculation of the electron states indicates that the reduction of the current gap is due to electrostatic effects, rather than strain deformation effects inside the tetrapod. 相似文献
996.
Saveyn P Van der Meeren P Cocquyt J Drakenberg T Olofsson G Olsson U 《Langmuir : the ACS journal of surfaces and colloids》2007,23(21):10455-10462
Lipid freezing in dilute sonicated vesicular dispersions was studied using differential scanning calorimetry (DSC) and 1H NMR. For charged, anionic, or cationic lipids, approximately half of the lipids remain in a fluid state when cooled 20 degrees C below the main chain melting temperature. With a zwitterionic phospholipid, on the other hand, essentially no supercooling of the liquid state was observed. The observations are analyzed in terms of the nucleation and growth of flat solid domains in originally fluid spherical vesicles. As the solid domains grow, the remaining fluid domain is deformed, resulting in a curvature stress. Depending on the vesicle size and the bilayer bending rigidity, the solid domain growth may terminate as the gain in cohesive free energy is balanced by the curvature stress of the remaining fluid domain. It is argued that high bending rigidities are required for having a significant supercooling, which is why it is only observed for charged lipids. 相似文献
997.
A theoretical analysis of coherent anti-Stokes Raman scattering (CARS) spectroscopy of gas-phase resonances using femtosecond lasers is performed. The time-dependent density matrix equations for the femtosecond CARS process are formulated and manipulated into a form suitable for solution by direct numerical integration (DNI). The temporal shapes of the pump, Stokes, and probe laser pulses are specified as an input to the DNI calculations. It is assumed that the laser pulse shapes are 70 fs Gaussians and that the pulses are Fourier-transform limited. A single excited electronic level is defined as an effective intermediate level in the Raman process, and transition strengths are adjusted to match the experimental Raman polarizability. The excitation of the Raman coherence is investigated for different Q-branch rotational transitions in the fundamental 2330 cm(-1) band of diatomic nitrogen, assuming that the pump and Stokes pulses are temporally overlapped. The excitation process is shown to be virtually identical for transitions ranging from Q2 to Q20. The excitation of the Raman coherences is also very efficient; for laser irradiances of 5x10(17) W/m2, corresponding approximately to a 100 microJ, 70 fs pulse focused to 50 microm, approximately 10% of the population of the ground Raman level is pumped to the excited Raman level during the impulsive pump-Stokes excitation, and the magnitude of the induced Raman coherence reaches 40% of its maximum possible value. The theoretical results are compared with the results of experiments where the femtosecond CARS signal is recorded as a function of probe delay with respect to the impulsive pump-Stokes excitation. 相似文献
998.
Pham TN Griffin JM Masiero S Lena S Gottarelli G Hodgkinson P Filip C Brown SP 《Physical chemistry chemical physics : PCCP》2007,9(26):3416-3423
(2h)J(NN) hydrogen-bond mediated J couplings are measured in the solid state for two synthetic deoxyguanosine derivatives by (15)N MAS NMR spin-echo experiments. The use of rotor-synchronised Hahn-echo pulse train (RS-HEPT) (1)H decoupling, with a duty cycle of 6%, allows spin-echo durations out to 200 ms, hence enabling the accurate determination of J couplings as small as 3.8 Hz. A single-crystal X-ray diffraction structure exists for the shorter alkyl chain derivative dG(C(3))(2): the observation of significantly different (2h)J(NN) couplings, 6.2 +/- 0.4 and 7.4 +/- 0.4 Hz, for the two resolved N7 resonances is to be expected given the NH...N hydrogen-bonding distances of 2.91 and 2.83 A for the two distinct molecules in the asymmetric unit cell. For the longer alkyl chain derivative, dG(C(10))(2), for which there is no single-crystal diffraction structure, a (15)N refocused INADEQUATE spectrum (Pham et al., J. Am. Chem. Soc., 2005, 127, 16018-16019) has demonstrated the presence of N2-H...N7 intermolecular hydrogen-bonds indicative of a quartet-like structure. The (2h)J(NN) hydrogen-bond mediated J coupling of 5.9 +/- 0.2 Hz is at the lower end of the range (5.9-8.2 Hz) of (2h)J(NN) couplings determined from solution-state NMR of guanosine quartets in quadruplex DNA. A full discussion of the determination of error bars on the fitted parameters is given; specifically, error bars determined by a non-linear fitting (using the covariance matrix) or in a Monte-Carlo fashion are found to give effectively identical results. 相似文献
999.
Glassy carbon electrodes modified with (5-amino-1,10-phenanthroline)bis(bipyridine)ruthium(II) chloride hydrate, [(bpy)2Ru(5-phenNH2)]Cl2·H2O, are shown to oxidize hydrazine with excellent sensitivity. The presence of an amine group on the ruthenium complex facilitates electropolymerization onto the electrode surface. Using cyclic voltammetry, a large catalytic current is observed upon oxidation of hydrazine in phosphate buffer (pH 5.0), compared to the current obtained from the ruthenium-modified electrode with no hydrazine present. The sensitivity of cyclic voltammetry is sufficient for obtaining a linear calibration curve for hydrazine over the range of 10−5 to 10−2 M. Hydrodynamic amperometry was used to determine the working potential for flow injection analysis. The limit of detection for hydrazine was determined to be 8.5 μM using FIA. The thickness of these films was shown to increase linearly with the number of electropolymerization cycles, in the range of 1000-2500 nm for 5-20 cycles, respectively, using Rutherford backscattering spectrometry (RBS). RBS analysis also suggests that the film is multilayered with the outermost layers containing a high ruthenium concentration, followed by layers where the concentration of ruthenium decreases linearly and approaches zero at the electrode surface. 相似文献
1000.
The reactions of syn-1-haloethyl p-chlorophenyl sulfoxides (halogen = Cl, Br) with main-group organometallic reagents (n-BuMgCl, MeLi, n-BuLi, s-BuLi, and t-BuLi) in THF and PhMe solvents were examined. Product distributions were analyzed to determine the extent of competing sulfoxide ligand exchange, halogen-metal exchange, and deprotonation reaction pathways. A combination of t-BuLi in PhMe was optimal for initiation of sulfoxide ligand exchange from syn-1-chloroethyl p-chlorophenyl sulfoxide. 相似文献