呋喃唑酮在凡纳滨对虾组织中代谢动力学研究

运用液相色谱-串联质谱法研究了呋喃唑酮药饵多次给药后在凡纳滨对虾体内的药物代谢动力学.研究结果表明：呋喃唑酮代谢物在血淋巴、肝胰脏、肌肉组织中的代谢过程均符合二室模型,其动力学方程分别为C血液=414.107×e^-0.092t＋124.451×e^-0.005t,C肝胰腺=1625.563×e^-0.019t＋125.700,C肌肉=120.434×e^-0.019t＋71.579×e^-0.001t.凡纳滨对虾血淋巴和肝胰腺中呋喃唑酮代谢物浓度在4h达到高峰,肌肉中药物浓度在2h达到最大值;最高峰时血淋巴、肝胰腺和肌肉中药物浓度平均为570.6μg·L^-1、1948.6μg·kg-1和210.0μg·kg-1.在血淋巴、肝胰腺和肌肉组织中呋喃唑酮代谢物浓度的吸收半衰期（t1/2α）分别为7.497h、36.206h和36.484h,消除半衰期（t1/2β）分别为132.525 h、1 000 479.217 h和505.637 h,总表观分布容积（V1/F）分别为55.775 L·kg^-1、17.16 L·kg^-1和161.574L·kg^-1.说明给药后呋喃唑酮代谢物在凡纳滨对虾体内消除缓慢,残留严重,尤其以肝胰脏残留最为明显.     

DF/HF化学激光器HYLTE喷管的副喷管质量流量系数

对DF/HF化学激光器HYLTE喷管的副喷管质量流量进行了数值和理论计算,得出入口滞止压力在0.01~0.4MPa之间、喉道半高度在0.1~0.9mm之间的喷管的氘气,氢气和氦气质量流量系数,总结出质量流量系数随入口滞止压力和喉道高度的变化规律,并给出拟合公式,为副喷管的设计提供依据。     

Zur Anreicherung der stabilen Isotope des Schwefels durch Fest-Flüissig-Austausch unter Verwendung von Ionenaustauschern

An verschiedenen Systemen chemischer Verbindungen wurden Versuche zur Anreicherung des stabilen Isotopes ³⁴S unter Verwendung der Ionenaustauscher Wofatit L 150, SBW und SBK nach den Methoden der Frontalchromatographie und der Bandenverdrāngungschromatographie ausgeführt. Beim Isotopenaustauschsystem Hydrogensulfit (am Ionenaustauscher)/Schwefeldioxid (in wäβriger Lösung) wurden Verfahrensweise und Betriebsparameter hinsichtlich des Anreicherungsgrades optimiert. Mit Hilfe einer einfachen Methode gelang es, aus den Versuchsergebnissen Werle für den elementaren Trennfaktor und die Trennstufenhöhe zu berechnen.     

The Influence of the Flow-Pattern on Column Leaching Experiments: Formulation and Measurement by Radiotracer

The leaching of microconstituents from granular solid wastes is often studied by column experiments. The underlying assumption is that the flow is of the one-compartment or “backmix” type. The influence of small deviations from this ideal situation on the outcome of the leaching experiment depends slightly on the specific mass-transfer function of the trace involved. The deviation itself may be measured by a simple separate radiotracer experiment.     

Unique ion beam scattering technique on depth profile determination

Abstract

By combination of energy and time of flight detection in ERDA or NRA measurement, the particles' masses can be determined, additionally to the depth information. This leads to unique depth profile determination even for complex targets. Combination with th concept of Jacobi transformations results in extremely fast measurements. In this paper, a way is shown how this concept can be realized even for accelerators ofenergies as low as about 1 MeV.     

A new method for the determination of the 34S/32S ratio of water-soluble sulphur in soil

A new method for the determination of the ³⁴S/³²S ratio of water-extractable sulphate in soil is described. Soils are extracted directly with deionized water, which is evaporated down. The remaining residue is then rehydrated and transferred to tin cups containing an adsorbent and mixed with an oxygen donor (V₂O₅). Samples are then analysed using a continuous flow isotope ratio mass spectrometer. The new method requires around 10?g soil per determination, compared to much larger amounts (up to kilograms) of soil required for the previous methods. Sample preparation and subsequent analysis is quick and efficient. The method is demonstrated using a number of soils collected from around the world to provide a range of determined δ³⁴S values. The δ³⁴S values of water-extractable sulphur were broadly similar to those of the soil total sulphur.     

Separation and Analysis of o.p'-DDD and its Lipophilic Metabolite,O.P'-DDE,in Tissue,Faeces and Plasma

Abstract

An analytical procedure based on electron capture gas chromatography for the determination of o,p′-DDD, a drug used for the treatment of Cushing′s syndrome, is presented. Detection of a metabolite, identified as o,p′-DDE, is also described.     

Transformation of macromonomers into ring‐opening polymerization macroinitiators: A detailed initiation efficiency study

In the present study, n‐butyl acrylate macromonomer (BAMM) (M_n = 1900 g mol^?1; PDI = 1.96) has been synthesized via a high‐temperature polymerization process. Subsequently, the olefinic termini of the BAMM have been transformed into a diol via a dihydroxylation process using KMnO₄ as an oxidizing agent. The OH‐terminated macroinitiator pBA(OH)₂ has subsequently been employed for the ring‐opening polymerization (ROP) of ε‐caprolactone via various catalytic systems, that is, organo‐(1,5,7‐triazabicyclo[4.4.0]dec‐5‐ene), metal (tin(II) 2‐ethylhexanoate), and enzymatic catalysis (Novozym® 435). The obtained pBA‐b‐pCL block copolymers and the initiation efficiency of the BAMM macroinitiator have been investigated via size exclusion chromatography (SEC), electrospray ionization–mass spectrometry (ESI‐MS) hyphenated with SEC and liquid chromatography at the critical conditions of both poly(ε‐caprolactone) (pCL) and pBA. The in vitro enzyme catalysis (eROP) approach proved to be the most efficient catalysis system due to minor transesterification side reactions during the polymerization process. However, side reactions such as transesterifications occur in each catalytic system and—while they cannot be suppressed—they can be minimized. The species generated during the eROP process include the desired block copolymer pBA‐b‐pCL as main species as well as pCL homopolymer and residual macroinitiator pBA(OH)₂. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012     

Z=18—82原子的同步辐射内壳层光电离积分截面的计算和讨论

此文计算了Ｚ＝１８－８２的原子在北京同步辐射４Ｂ９Ａ束线的白色Ｘ光照射下的光电离积分截面Ｇ值。结果表明，有三个Ｇ值较大的区域，Ｚ＝１８－２０，３９－４７和５９－８２，最大值分别为３．８×１０－６，１．６×１０－５和３．５×１０－５ｐｈｏｔｏｎｓ·ｃｍ２／ｓ。同时，估计了平衡时主要多重电荷态离子数目，分析了用同步辐射和离子阱进行多重电荷态实验的新的候选原子，讨论了有关实验方法和技术。     

解析电喷雾质谱法对感冒药中对乙酰氨基酚的快速检测

基于常压质谱的直接、快速、无需样品预处理检测的优势,该文拓展了其在药物质检领域的应用。采用自行搭建的解析电喷雾(DESI)装置,对常用感冒药对乙酰氨基酚片进行快速质谱检测,无需样品预处理,直接获得药片中有效成分的分子结构信息。为克服基质差异对定量分析的影响,以淀粉为基质构建对乙酰氨基酚模拟药片,在优化的基础上进行定量实验。针对实际药片中高浓度对乙酰氨基酚检测的需要,研究了其在较高浓度范围的定量关系,结果显示,方法对0.35～4.52 mg/mm²范围内的对乙酰氨基酚具有较好的线性关系(r²=0.998 2),定量下限为1.903 ng/mm²,检出限为0.237 ng/mm²,加标回收率为102%～114%。对3种市售的对乙酰氨基酚片进行直接检测,与厂家提供的标准数据相比,相对标准偏差(RSD)为7.2%～12%,表明方法具有较好准确度。该工作很好地证明了DESI-MS在药品快检中的优势,从而为药品质检提供了潜在的高效、可靠的检测手段。