低钾血症116例临床分析

对116例低钾血症患者进行了血清钾的测定及心电图检查,并分析了其临床特点。结果显示,轻、中度低血钾占90.5%,心电图异常患者占94.8%;经补钾等治疗,7 d内患者可恢复正常。表明血清钾的测定及心电图的检查,有助于低钾血症患者早期诊断及治疗。     

急性脑梗死患者心电图特征与病情分型及其预后状况的关系

为探讨急性脑梗死患者心电图特征与病情分型及其预后状况的关系,选择2016年1月~2019年6月期间本院神经内科住院部收治的急性脑梗死患者110例作为研究对象,全部患者采用心电图检查。急性脑梗死患者心电图异常率为72.73%,其中缺血性ST-T改变占45.00%,窦性心动过速和室性早搏各占11.25%,心房颤动占7.50%,房性早搏和左心室肥厚各占6.25%。轻型组心电图异常率为52.63%,明显低于中型组的82.22%和重型组的85.19%,比较差异具有统计学意义(P<0.05)。大梗死灶组、小梗死灶组心电图异常率分别为88.89%和79.41%,明显高于腔隙性脑梗死组的41.94%,比较差异具有统计学意义(P<0.05)。心电图异常组死亡率明显高于心电图正常组,比较差异具有统计学意义(P<0.05)。提示急性脑梗死患者心电图异常主要表现为缺血性ST-T改变、窦性心动过速、室性早搏、心房颤动、房性早搏和左心室肥厚等,其异常率对病情分型及其预后状况具有重要的评估价值。     

(-)-Epicatechin-3-gallate, a green tea polyphenol is a potent agent against UVB-induced damage in HaCaT keratinocytes

(-)-Epicatechin-3-gallate (ECG) is a polyphenolic compound similar to (-)-epigallocatechin-3-gallate (EGCG) which is abundant in green tea. Numerous workers have proposed that EGCG protects epidermal cells against UVB-induced damage. However, little has been known about whether ECG protects keratinocytes against UVB-induced damage. We decided to investigate the protective effects and underlying mechanisms of ECG on UVB-induced damage. Cell viability was determined by the MTT assay. Activation of ERK1/2, p38 and JNK was analyzed by Western blotting. Intracellular H2O2 production and DNA content was analyzed by flow cytometry. Lipid peroxidation was assayed by colorimetry. In our study, we found that ECG dose-dependently attenuated UVB-induced keratinocyte death. Moreover, ECG markedly inhibited UVB-induced cell membrane lipid peroxidation and H2O2 generation in keratinocytes, suggesting that ECG can act as a free radical scavenger when keratinocytes were photodamaged. In parallel, H2O2-induced the activation of ERK1/2, p38 and JNK in keratinocytes could be inhibited by ECG. UVB-induced pre-G1 arrest leading to apoptotic changes of keratinocytes were blocked by ECG. Taken together, we provide here evidence that ECG protects keratinocytes from UVB-induced photodamage and H2O2-induced oxidative stress, possibly through inhibition of the activation of ERK1/2, p38 and JNK and/or scavenging of free radicals.     

Recursive Wavelet Peak Detection of Analytical Signals

A novel algorithm, entitled recursive wavelet peak detection (RWPD), is proposed to detect both normal and overlapped peaks in analytical signals. Recursive peak detection is based on continuous wavelet transforms (CWTs), which can be used to obtain initial peak positions even for overlapped peaks. Genetic algorithm (GA) and Gaussian fitting are used to refine peak parameters (peak positions, widths, and heights). Finally, area of peaks can be calculated by numeric integration. Simulated and ultrahigh performance liquid chromatographic ion trap time-of-flight mass spectrometry (UPLC-IT-TOF-MS) data sets have been analyzed by RWPD, MassSpecWavelet, and peakfit package by Tom O’Haver. Results show that RWPD can obtain more accurate positions and smaller relative fitting errors than MassSpecWavelet and peakfit, especially in overlapped peaks. RWPD is a convenient tool for peak detection and deconvolution of overlapped peaks, and it has been developed in R programming language and is available at https://github.com/zmzhang/RWPD.

     

纳米铂修饰玻碳电极对邻苯二酚的电化学氧化及测定

应用循环伏安法研究了邻苯二酚在纳米铂修饰玻碳(PtNPs/GC)电极上的电化学氧化行为。实验表明,PtNPs/GC电极对邻苯二酚有很强的电催化作用,其伏安扫描氧化峰电流随着温度的升高而增大,但氧化峰电位略有负移。常温下,邻苯二酚能自发在电极表面发生聚合反应,生成具有导电性的聚合膜,其催化氧化电流与邻苯二酚浓度在1.0×10-6mol/L~5.0×10-5mol/L范围内呈良好的线性关系,检出限为2.9×10-7mol/L。     

Spatial characterization of analyte emission and excitation temperature in an inductively coupled plasma

Vertical, lateral and radial profiles of analyte emission in an inductively coupled plasma have been measured using photodiode array spatial profiling spectrometers. These profiles have been measured for both neutral atom and ionic lines of several elements. Neutral atom lines can be sub-divided into two basic groups on the basis of their vertical spatial emission characteristics. One group in which the peak vertical position of emission correlates positively with normal temperature and a second group in which the peak vertical position of emission correlates negatively with normal temperature. Utilizing radially resolved emission intensities and vertical and radial profiles of neutral atom excitation temperature, the caracteristic emission patterns of both groups of neutral atom lines can be explained. Analyte ionic line spatial emission characteristics, both vertically and radially, are shown to be relatively species independent and radial emission intensity ratio maps of ionic and neutral atom lines of the same element are presented that indicate the potential importance of plasma boundary regions as regions of major non-LTE behavior.     

1.5th- and 2.5th-order derivative adsorption voltammetry of the cobalt(II)—2-(5′-bromo-2′-pyridylazo)-diethylaminophenol system

On the basis of the adsorptive characteristics of the cobalt(II) complex with 2-(5′-bromo-2′-pyridylazo)diethylaminophenol at a hanging mercury drop electrode in NH₃NH₄Cl, a more sensitive method for the determination of cobalt based on 1.5th- and 2.5th-order derivative adsorption voltammetry has been developed. The detection limit is one order of magnitude lower than that of normal linear-sweep adsorption voltammetry. The equations of the 1.5th- and 2.5th-order derivative of current with respect to time, peak potential and distance from peak to peak are discussed.     

Localization of electrochemically generated radicals as a function of their structure and the nature of the solvent

The electrooxidation of different perfluorocarboxylic acids has been investigated in the presence of ethylene, on electrodes with different adsorbing power [platinum and glassy carbon (GC)] in different solvents. It has been shown that the reaction zone of the ECG radicals is determined by their solubility; depending on this, it can be limited to the electrode surface or encompass the entire volume of the solution. The concept of the solubility of the ECG radicals made it possible to establish some regularities in the formation of cross combination products in the Kolbe electrosynthesis of different perfluorocarboxylic acids.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 5, pp. 1134–1141, May, 1991.     

常规二脉冲叠加四阶跃微分伏安法研究─准可逆电极过程的理论和验证

推导并验证了新型阶跃伏安技术─常规二脉冲叠加四阶跃微分伏安法准可逆电极过程的理论电流方程式,同时研究了各项参数如扫描增量(E_s)、脉冲高度(△E)、传递系数(α)对峰电流函数(ψ_p)、峰电流(i_p)、峰电位(E_p)和半峰宽(W_1/2)的影响。运用理论ψ_p-lgk_s图和单纯形优化计算测量了及Zn(Ⅱ)/Zn(Hg)-NaNO3体系的K_s及α值,结果与文献值一致。     

Evaluation of diastolic phase by left ventricular volume curve using S2-gated equilibrium method in radioisotope angiography

S2-gated (the second heart sound) method was designed by authors. In 6 normal subjects and 16 patients (old myocardial infarction 12 cases, hypertension 2 cases and aortic regurgitation 2 cases), radioisotope (RI) angiography using S2-gated equilibrium method was performed. In RI angiography, 99mTc-human serum albumin (HSA) 555MBq (15 mCi) as tracer, PDP11/34 as minicomputer and PCG/ECG synchronizer (Metro Inst.) were used. Then left ventricular (LV) volume curve by S2-gated and electrocardiogram (ECG) R wave-gated method were obtained. Using LV volume curve, left ventricular ejection fraction (EF), mean ejection rate (mER, s-1), mean filling rate (mFR, s-1) and rapid filling fraction (RFF) were calculated. mFR indicated mean filling rate during rapid filling phase. RFF was defined as the filling fraction during rapid filling phase among stroke volume. S2-gated method was reliable in evaluation of early diastolic phase, compared with ECG-gated method. There was the difference between RFF in normal group and myocardial infarction (MI) group (p less than 0.005). RFF in 2 groups were correlated with EF (r = 0.82, p less than 0.01). RFF was useful in evaluating MI cases who had normal EF values. The comparison with mER by ECG-gated and mFR by S2-gated was useful in evaluating MI cases who had normal mER values. mFR was remarkably lower than mER in MI group, but was equal to mER in normal group approximately. In conclusion, the evaluation using RFF and mFR by S2-gated method was useful in MI cases who had normal systolic phase indices.     

Self-assembled monolayers of peptide nucleic acids on gold surfaces: a spectroscopic study

We have characterized self-assembled monolayers (SAMs) of thiol-derivatized peptide nucleic acid (PNA) chains adsorbed on gold surfaces by using reflection absorption infrared spectroscopy (RAIRS) and X-ray photoemission spectroscopy (XPS) techniques. We have found that the molecular orientation of PNAs strongly depends on surface coverage. At low coverage, PNA chains lie flat on the surface, while at high coverage, PNA molecules realign their molecular axes with the surface normal and form SAMs without the need of co-immobilization of spacers or other adjuvant molecules. The change in the molecular orientation has been studied by infrared spectroscopy and it has been confirmed by atomic force microscopy (AFM). PNA immobilization has been followed by analyzing the N(1s) XPS core-level peak. We show that the fine line shape of the N(1s) core-level peak at optimal concentration for biosensing is due to a chemical shift. A combination of the above-mentioned techniques allow us to affirm that the structure of the SAMs is stabilized by molecule-molecule interactions through noncomplementary adjacent nucleic bases.     

Differentialthermoanalyse von Polyäthylen

Polyethylene (PE) samples pretreated in different ways were investigated by means of normal and isothermal DTA. Changes caused by the pretreatment were manifested as follows: In contrast to non-treated PE, the normal DTA curves taken under the influence of oxygen exhibited an isolated oxidation peak between 200 and 300°, the peak area decreasing with the increasing effect of the pretreatment on the structure of the PE. In isothermal DTA the induction times and activation energies of oxidative thermal degradation were reduced. The peak area of the oxidation peak can also be used to characterize mixtures of high and low-density PE; the amount of high-density PE is obtained quantitatively from the melting peak area measured from the peak tip up to the peak end.     

常规二脉冲叠加四阶跃微分伏安法研究：—可逆电极过程的理论和验证

推导并验证了提出的新型阶跃伏安技术－常规二脉冲叠加四阶跃微分伏安法可逆电极过程听理论电流方程，同时研究了各项参数如扫描增量（Es)、脉冲高度（△E）、脉冲周期（T）等对实验的影响，理论与实验结果一致。     

Parcel model for peak shapes in chromatography numerical verification of the temporal distortion effect to peak asymmetry

The traditional plate concept has been reassessed and improved to a parcel matrix model, which can be used to imitate the chromatographic behavior of a hypothetic column on a computer worksheet. Under programmed conditions, various peak shapes (nearly Gaussian, and with prolonged or fronting tails) are generated. The peak tailing has been separated into two major fractions: spatial and temporal. The former fraction is caused by the retention nature of a column, whereas the latter is induced by the observer's relative position and the changing of the zone broadening rate. The temporal distortion effect can be identified qualitatively and quantitatively through a normalized peak-overlapping process. In general, a chromatographic peak may carry a prolonged (or normal type) tail under linear isotherms, while both prolonged and fronting tails will appear under non-linear conditions. The temporal distortion is proved to be significant, and may be regarded as the major cause of peak asymmetry in most cases. This is in contrast to the conclusions of many previous studies. The model is also eligible to simulate chromatographic peaks for various injection sizes.     

Digestion-free determination of heavy metals (Pb, Cd, Cu) in honey using anodic stripping differential pulse voltammetry and potentiometric stripping analysis

Experiments have been carried out to assess the potential of differential pulse voltammetry and potential stripping analysis for determining Pb, Cu and Cd directly in dissolved honey samples using a flow-through cell. With the hanging mercury drop electrode Pb alone can be determined only if the electrode is first modified in-situ with Triton X 100 to increase the separation between the Pb peak and a broad, interfering adsorption peak which overlaps the Cu peak. If the (more sensitive) thin film mercury electrode is used the interference encountered is less so also Cu and Cd can be determined. With potentiometric stripping analysis Cu and Pb can be determined using normal procedures. The determination of Cd, however, can only be carried out if the concentration of the oxidizing agent [Hg(II)] in solution is decreased. A good agreement has been obtained between the values found and those obtained after high pressure digestion of the samples.     

Optimization of cyclical electrical field flow fractionation

Cyclical electrical field flow fractionation (CyElFFF) is a variation on electrical field flow fractionation (ElFFF) where cyclical electrical fields are used instead of steady DC fields to increase the effective field experienced by particles in the flow channel. Even though the effective field increases more than 20-fold compared to normal ElFFF, the retention and resolution in CyElFFF has not been shown to be better than in ElFFF. In this paper we report how one can optimize operational parameters in CyElFFF to obtain good retention and resolution in CyElFFF. The effects of offset voltage, frequency, flowrate, concentration of particles and sample size on retention, resolution and retained peak/void peak ratio have been observed. The results obtained from these experiments were analyzed and suggestions have been made to improve both retention and resolution. A 4-fold improvement in retention without a significant increase in band broadening is reported.     

Optical properties of transparent copper nanorod and nanowire arrays embedded in anodic alumina oxide

Transparent copper nanorod/nanowire arrays and anodic alumina oxide composite films have been prepared by alternating current electrodeposition, and their linear optical properties have been systematically characterized by absorption spectra. In the experimental spectra, there exist transverse and longitudinal resonance peaks, which are caused by the surface-plasmon resonance along the diameter and the length of the copper nanorods, respectively. The transverse resonance peak is affected by the diameter and aspect ratio of the nanorod. The longitudinal resonance peak appears at longer wavelength when a polarized light illuminates the film with an angle of incidence of about 70 degrees , where the angle is defined with respect to the surface normal. Moreover, the longitudinal resonance mode is sensitive to the polarization direction when compared with the transverse resonance mode.     

低温陈化法制备SO_4~(2-)/WO_3-TiO_2固体超强酸及性能研究

0引言固体超强酸的研制是近20年来催化领域中的热点研究课题之一。起初,人们所研制的SO42-/MxOy型固体超强酸中,MxOy多为ZrO2。近年来,研究者们为得到高酸强度和高催化活性的固体超强酸催化剂,以ZrO2为主体,引入第二组分、第三组分组成复合型催化剂,这方面的研究者颇多[1~4],也     

8—氮鸟嘌呤的极谱伏安行为

用循环伏安法（ＣＶ）、电流采样极诸法（ＳＣＰ，即ＴＡＳＴ）、常规脉冲极谱法（ＮＰＰ）、微分脉冲极谱法（ＤＰＰ）、线性扫描伏安法（ＬＳＶ）、Ｏｓｔｅｒｙｏｕｎｇ方波伏安法（ＯＳＷＶ）和计时库仑法（ＣＣ）等电化学技术研究了抗癌药物８－氮鸟嘌呤（８－ａｚａｇｕａｎｉｎｅ，ｇｕａｎａｚｏｌｏ，简称８－ＡＧ）的极谱伏安行为．在 ０． １ｍｏｌ／Ｌ Ｈ２ＳＯ４底液中，８－ＡＧ有一良好的还原峰，峰电位（Ｅｐ）在－０． ９５Ｖ（ｖｓ．Ａｇ／ＡｇＣｌ，下同）附近，８－ＡＧ浓度在４×１０－６～８×１０－４ｍｏｌ／Ｌ范围内．峰高与浓度有良好的线性关系，线性相关系数ｒ＝０．９９９９～０．９９１０，检出限为１× １０－６ｍｏｌ／Ｌ．实验证明了该峰具有吸附性．本文提出了电极反应机理，它包括：酸性介质中８－ＡＧ的质子化、质子化的８－ＡＧ在汞电极上吸附以及完全不可逆的两电子还原过程．同时用量子化学计算方法（全略微分重叠法即ＣＮＤＯ／２）对８－ＡＧ和鸟嘌呤的各原子的净电荷以及Ｗｉｂｅｒｇ键级进行了计算，从理论上解释了８－ＡＧ的电化学还原机理。     

Reciprocal derivative constant-current stripping analysis

Reciprocal derivative constant-current stripping analysis (RD-CCSA) is based on the measurement of dt/dE converted from a derivative signal, dE/dt, vs. electrode potential (E) during the stripping of analyte under galvanostatic conditions from a mercury-film electrode after preconcentration. The potential transient signal (E-t) in normal chronopotentiometric stripping analysis (CPSA) is converted in RD-CCSA into a stripping peak (dT/dE)(p) the height of which is proportional to the bulk concentration of analyte in solution. The theory of RD-CCSA has been derived, and validated by the good correlation obtained between the theory and experimental data. Compared with normal CPSA, RD-CCSA is more sensitive and has higher resolution. The detection limit for cadmium is 6 x 10(-10)M. Simultaneous determination of Cd(2+), In(3+), and Tl(+) (for which the differences between the stripping peak potentials are 58 and 50 mV, respectively) which is impossible for normal CPSA, voltammetry or differential pulse polarography, has become possible with RD-CCSA.