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61.
In bottom-viewed inductively coupled plasma-atomic emission spectrometry (BV-ICP-AES), emission from the central channel of the plasma is measured axially from the bottom of the plasma. A straight quartz tube was used as a hollow light pipe (HLP) to collect plasma emission in this study. The HLP also serves as an injector for aerosols transport and injection into the ICP. The optical characteristics of HLPs with the original reflective surface and roughened outer surface are reported. The roughened HLP is effective in rejecting light beams that are not in line with the HLP. The transmission efficiency of the HLP, however, is high (> 70%) for light beams from a source that has the same dimension as the entrance of the HLP and is flush with the HLP. The HLP is effective in rejecting background emission from the core of the plasma that encircles the plasma central channel and yet efficient in light collection from the central channel of the plasma. 相似文献
62.
Yanpeng Liu Dr. Houzong Yao Dr. Man-Kit Tse Shu Chen Dr. Shek-Man Yiu Prof. Dr. Guangyu Zhu 《欧洲无机化学杂志》2023,26(3):e202200763
Platinum-based complexes are among the most widely utilized cancer therapeutics. Current Pt(II) drugs face some challenges including toxicity and drug resistance. To solve these issues, great efforts have been devoted to developing nonclassical platinum complexes, such as Pt(IV) prodrugs, that act via mechanisms distinct from those of the approved drugs. Compared with active Pt(II) counterparts, Pt(IV) complexes are relatively inert. Although direct interactions between Pt(IV) complexes and nucleotides have been reported, the reaction is slow due to the kinetic inertness of Pt(IV) complexes. Herein, we design and synthesize a Pt(IV) monotrifluoromethyl complex, in which the chloride ligand that is trans to trifluoromethyl ligand is reactive. The Pt(IV) monotrifluoromethyl complex is very stable in water but displays high reactivity towards various substrates including buffer components and 5’-dGMP. The study of reaction mechanism reveals that this Pt(IV) complex reacts with phosphate via SN2 nucleophilic substitution pathway, which is different from Pt(II) drugs. The Pt(IV) monotrifluoromethyl complex is cytotoxic in human ovarian cancer cells. Our work reports an example of a reactive organometallic Pt(IV) complex that can directly interact with nucleophiles and implies its potential as an anticancer agent. 相似文献
63.
Zhi-Hai Rong Qian Zhao Zhi-Xi Wu Tao Zhou Chi Kong Tse 《The European Physical Journal B - Condensed Matter and Complex Systems》2016,89(7):166
Zero-determinant strategies, which can unilaterally define a linear relationship between two individuals’ long-term payoff, have drawn much attention to comprehend the emergence of cooperation among individuals with repeated interactions. A subset of zero-determinant strategies, extortion strategy, can let an extortioner’s surplus exceed her opponent’s by a fixed percentage. On the other hand, the dual generosity strategy can ensure that a complier’s payoff is never larger than her opponent’s. In the framework of the prisoner’s dilemma game driven by payoff aspiration, we investigate in this paper the evolution of generosity strategy, in competition with extortion and unconditional defection strategies. We show that extortioners act as a catalyst to induce more defectors to change to compliers. Such influence will enhance when extortioners become more greedy. At a low aspiration level where individuals are easy to be satisfied with their current payoffs, different strategies can coexist. With the increase of aspiration level, unsatisfied individuals are likely to turn to compliers and build long-term reciprocity with their neighbors. However, at a high aspiration level, individuals are difficult to be satisfied with their payoffs and may randomly change their behaviors. Thus proper aspiration level promotes the emergence of generous behavior in the spatial prisoner’s dilemma game. 相似文献
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65.
A sensitive and simple liquid chromatography-tandem mass spectrometry method for the determination of midazolam and 1'-hydroxymidazolam in human plasma has been developed and validated with a dynamic range of 0.1-250 ng/mL. The analysis was based on semi-automated liquid-liquid extraction followed by evaporation of the extraction solvent, reconstitution and chromatography on a reversed-phase C(18) column. The mobile phase consists of 5 mm ammonium acetate and methanol and runs in gradient at a flow rate of 0.25 mL/min with column temperature of approximately 20 degrees C. The entire column effluent was transferred into the LC-MS/MS interface operated in positive electrospray ionization mode. The chromatographic run time was 4.3 min per injection, with retention times for midazolam, 1'-hydroxymidazolaml and the internal standard, triazolam, of 2.5, 2.3 and 2.1 min, respectively. The intra-day and inter-day precision (RSD %) and accuracy (bias %) of the quality control samples were <15.0% and within +/-13%, respectively. The current method has been applied to a clinical drug-drug interaction study in human. 相似文献
66.
A liquid chromatographic method with tandem mass spectrometric detection (LC-MS/MS) for the determination of N-methyl-4-isoleucine-cyclosporin (NIM811) was developed and validated over the concentration range 1-2500 ng/mL in human whole blood using a 0.05 mL sample volume. NIM811 and the internal standard, d(12)-cyclosporin A (d(12)-CsA), were extracted from blood using MTBE via liquid-liquid extraction. After evaporation of the organic solvent and reconstitution, a 10 microL aliquot of the resulting extract was injected onto the LC-MS/MS system. Chromatographic separation of NIM811 and internal standard was performed using a Waters Symmetry RP-8 (50 x 4.6 mm, 3 microm particle size) column. The mobile phase consists of 10 mm ammonium acetate in water (A) and acetonitrile (B), with 45% B from 0 to 0.2 min, 45 to 85% B from 0.2 to 0.8 min and 85% B from 0.8 to 2.2 min. The total run time was 3.5 min with a flow rate of 0.8 mL/min. The method was validated for sensitivity, linearity, reproducibility, stability, dilution integrity and recovery. The precision and accuracy of quality control samples at low (2.00 ng/mL), medium (20.0 and 400 ng/mL) and high (2000 ng/mL) concentrations were in the range 1.1-4.3% relative standard deviation (RSD) and -2.5-10.0% (bias), respectively, from three validation runs. The method has been used to measure the exposure of NIM811 in human subjects. 相似文献
67.
68.
B-SERIES METHODS CANNOT BE VOLUME-PRESERVING 总被引:1,自引:0,他引:1
Volume preservation is one of the qualitative characteristics common to many dynamical systems. However, it has been proved by Kang and Shang that e.g. Runge–Kutta (RK) methods can not preserve volume for all linear source-free ODEs (let alone nonlinear ODEs). On the other hand, certain so-called Exponential Runge–Kutta (ERK) methods do preserve volume for all linear source-free ODEs. Do such ERK methods perhaps also preserve volume for all nonlinear ODEs? Here we prove that the answer to this question is negative; B-series methods (which include RK, ERK and several more classes of methods) cannot preserve volume for all source-free ODEs. The proof is presented via the theory of K-loops, which is an extension of the theory of classical rooted trees. 相似文献
69.
K. Yurekli R. Krishnamoorti M. F. Tse K. O. McElrath A. H. Tsou H.‐C. Wang 《Journal of Polymer Science.Polymer Physics》2001,39(2):256-275
The linear and nonlinear melt viscoelastic properties for a series of carbon black‐filled polymer composites were studied. Complementary tapping‐mode atomic force microscopy (AFM) studies were used to examine the dispersion and structural correlations of the filler particles in these composites. The low‐frequency dependence of the linear viscoelastic moduli gradually changes from liquidlike behavior for the unfilled polymer to pseudosolid character for composites with more than 9 vol % carbon black filler. The plateau modulus, inferred from the linear viscoelastic response, exhibits a somewhat discontinuous change at about 9 vol % filler. On the basis of the linear viscoelastic response, we postulate that the carbon black filler forms a continuous percolated network structure beyond 9 vol % filler, considerably lower than that expected from theoretical calculations for overlapping spheres and ellipsoids. We suggest that the lower threshold for percolation is due to the polymer mediation of the filler structure, resulting from the low functionality of the polymer and, consequently, few strong polymer–filler interactions, allowing for long loops and tails that can either bridge filler particles or entangle with one another. Furthermore, the strain amplitude for the transition from linear behavior to nonlinear behavior of the modulus for the composites with greater than 9 vol % filler is independent of frequency, and this critical strain amplitude decreases with increasing filler concentration. Complementary AFM measurements suggest a well‐dispersed carbon black structure with the nearest neighbor distance showing a discontinuous decrease at about 9 vol % filler, again consistent with the formation of a filler network structure beyond 9 vol % carbon black. © 2000 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 39: 256–275, 2001 相似文献
70.
Rate constants for three dimethylbenzaldehydes and two trimethylphenols have been determined for the OH reactions at 298±2 K and atmospheric pressure using a relative rate method. The OH reaction rate constants were placed on an absolute basis using the literature rate constant for 1,2,4-trimethylbenzene of (3.25±0.5)×10−11 cm3 molecule−1s−1). The measured rate constants were (in units of cm3 molecule−1 s−1) 2,4-dimethyl-benzaldehyde, (4.32±0.67)×10−11; 2,5-dimethylbenzaldehyde, (4.37±0.68)×10−11; 3,4-dimethylbenzaldehyde, (2.14±0.34)×10−11; and 2,3,5- trimethylphenol, (12.5±1.9)×10−11, 2,3,6-trimethylphenol, (11.8±1.8)×10−11. Using an average OH concentration of 8.7×105 molecule cm−3, the estimated atmospheric lifetimes are ca. 7.5 h for 2,4- and 2,5-dimethylbenzaldehydes, ca. 15 h for 3,4-dimethylbenzaldehyde, ca. 2.5 h for 2,3,5- and 2,3,6-trimethylphenols. The reactivities of the trimethylphenols exceed those of the dimethyl-benzaldehydes by more than a factor of 3. © 1997 John Wiley & Sons, Inc. Int J Chem Kinet 29: 523–525, 1997. 相似文献