272 resultados para ICP


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Macromolecular conjugates of two kinds of natural polysaccharides, that from Panax quinquefolium linn (PQPS) and Ganoderma applanatum pat (GAPS), with gadolinium-diethylenetriaminepenta-acetic acid (Gd-DTPA) have been synthesized and characterized by means of FTIR, elementary analysis and ICP-AES. Their stability was investigated by competition study with Ca2+, EDTA (ethylenediaminetetraacetic acid) and DTPA. Polysaccharide-bound complexes exhibit T-1 relaxivities of 1.5-1.7 times that of Gd-DTPA in D2O at 25degreesC and 9.4T. MR imaging of Sprague-Dawley (SD) rats showed remarkable enhancement in rat liver and kidney after i.v. injection of these two complexes: liver parenchyma 60.9+/-5.6%, 57.8+/-7.4% at 65-85 min; kidney 144.9+/-14.5%, 199.9+/-25.4% at 10-30 min for PQPS-GdDTPA, GAPS-Gd-DTPA at gadolinium dose of 0.083 and 0.082 mmol/kg, respectively. Our preliminary in vivo and in vitro study indicates that the two kinds of polysaccharide-bound complexes are potential tissue-specific contrast agents for MRI.

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研究了常乐(用于肥料添加剂的一种混合稀土硝酸盐)对Wistar大鼠肝脏中7种常见酶(ALT,ICD,AST,LAP,ALP,γGT ,CHE)活性的变化,并用电感耦合等离子体质谱(ICP MS)测定了稀土在肝脏中的累积情况。结果表明,稀土对多种酶表现出低剂量激活、高剂量抑制的小剂量刺激作用 (Hormesis),但产生刺激作用的剂量随酶的种类不同而不同 ,并表现出明显的性别差异

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Two Meinhard microconcentric nebulizers, model AR30-07-FM02 and AR 30-07-FM005, were employed as a self-installed micro-sampling system for inductively coupled plasma-mass spectrometry (ICP-MS). The FM02 nebulizer at 22 muL/min of solution uptake rate gave the relative standard deviations of 7.6%, 3.0%, 2.7%, 1.8% for determinations (n = 10) of 20 mug/L Be, Co, In and Bi, respectively, and the detection limits (3s) of 0.14, 0.10, 0.02 and 0.01 mug/L for Be, Co In and Bi, respectively. The mass intensity of In-115 obtained by this micro-sampling system was 60% of that by conventional pneumatic nebulizer system at 1.3 mL/min. The analytical results for La, Ce, Pr and Nd in 20 muL Wistar rat amniotic fluid obtained by the present micro-sampling system were precisely in good agreement with those obtained using conventional pneumatic nebulization system.

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Arabinogalactan-Gd-DTPA was synthesized by the reaction of diethylenetriaminepenta-acetic acid (DTPA) bisanhydride with polysaccharide in dry DMSO and characterized by FTIR, elemental analysis and ICP-AES. Its stability was investigated by competition with Ca2+, EDTA, DTPA. The t(1)-relaxivity is 8.06 mmol(-1) . L . s(-1) in D2O, 8.48 mmol(-1) . L . s(-1) in 0.725 mmol . L-1 BSA, respectively. t(1)-weighted MR imaging of rat kidney and liver showed a remarkable enhancement post injection of Arabinogalactan-Gd-DTPA. The results indicate that the arabinogalactan-Gd-DTPA is a potential contrast agent for MRI.

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The metabolic accumulation and species of rare earth in rat liver were investigated by ICP-MS and chromatography after the rats were fed by a low dose of mixed rare earth for a long time or the administration of a high dose of lanthanum for a short time. It was found that the content of rare earth in the liver increased with the arising of dose of drug delivery. Their accumulation rate was different, for example, La>Ce>Nd>Pr. The protein which could combine,with rare earth specially were not gotten through chromatography. It was suggested that rare earth could bind to many proteins voluntarily, such as some important enzymes and it might be separated from the combined proteins under certain conditions.

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用2种微量雾化器组装成微量进样系统与常规气动雾化方式的ICP MS的分析性能作了详细比较。FM0 2雾化器在22μL min低提升率下,20μg L的Be、Co、In和Bi进行10次平行测定的RSD分别为7.6%、30%、2.7%和1.8%;检出限分别为0.14、0.10、0.02和0.01μg L;115In的信号强度达到常规气动雾化器1.3mL min提升速率下的60%,显示了良好的分析性能。对20μLWistar鼠的羊水样品中La、Ce、Pr和Nd4种元素的测定结果与常规进样系统的结果完全吻合

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碳电极表面的修饰在电化学和材料科学中很重要 .最近 ,通过层与层电子间的相互作用来自组装修饰玻碳电极已引起人们的关注 [1] .运用这种方法可将一些功能团修饰到电极表面 ,赋予电极一些新的功能 [2 ] .过渡金属取代的多金属氧酸盐不仅在配位环境 ,而且在催化活性方面都类似于金属卟啉和其它大环配体金属配合物 [3] .将其修饰到玻碳电极表面已有文献报道 [4 ] .由于修饰电极的厚度可控、成分可调及具有良好的电催化活性 ,在生物传感器和电子器件等方面具有潜在的应用前景 .取代型夹心型多金属氧酸盐具有大摩尔质量和高电荷密度 ,表现出优秀的磁性和催化活性 [5] ,将成为玻碳电极表面的修饰材料 .我们首次制备了四铁取代的夹心型钨砷酸盐 Na12 [Fe4 ( H2 O) 2 ( As2 W15O56 ) 2 ]·41 H2 O,通过元素分析 ,IR,UV和 NMR对其进行了表征 ,并通过自组装将其修饰到玻碳电极表面形成多层膜 .此修饰电极对 NO- 2 和 H2 O2 具有电催化活性 ,可望成为检测 NO- 2 和 H2 O2 浓度的探针 .1 实验部分1 .1 仪器和试剂  ICP- AES等离子体发射光谱仪 ...

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采用 ICP-MS、微量蛋白层析分离技术 ,研究了长时间、低剂量混合稀土及短时间、高剂量硝酸镧分别对大鼠及小鼠作用后 ,稀土在鼠肝中的代谢累积及其物种分布 .结果表明 ,鼠肝中各稀土含量随给药剂量的增加而增大 ,其累积速度大小顺序为 La>Ce>Nd>Pr;经柱层析分离未得到与稀土特异结合的鼠肝蛋白 ;稀土可与多种鼠肝蛋白 (包括多种重要的酶 )结合 ,在一定条件下 ,稀土与其结合蛋白可发生解离

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合成了阿拉伯半乳聚糖修饰的 DTPA钆配合物 ,用红外光谱、元素分析、 ICP-AES等手段进行了表征 ,用竞争性方法研究了其在水溶液中的稳定性 ,测试了其在水中及 BSA溶液中的弛豫性能 ,并进行了体内成像实验 .结果表明 ,其弛豫效率是目前临床所用造影剂 Gd-DTPA的 1 .5~ 2 .0倍 ,对肝脏和肾脏 MRI信号具有良好的增强效果 ,是比较好的潜在磁共振成像造影剂

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分别从体内作用和体外作用两个方面研究了镧对鼠肝脏中的胆碱脂酶、异柠檬酸脱氢酶、谷丙转氨酶活性的影响 ,同时用电感耦合等离子质谱 (ICP -MS)研究了镧在肝脏中的累积情况 .结果表明 :经尾静脉注射后镧在肝脏中有明显的累积现象 ,其累积量随给药剂量的增大而增加 ;镧对上述三种酶的活性均表现出低剂量激活 ,高剂量抑制的Hormesis效应

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研究了地质样品中超痕量Au、Pt和Pd的测定方法。采用C 4 1 0阴离子交换树脂在 1 .5mol LHCl条件下对Au、Pt、Pd的吸附率分别为 91 .2 %、1 0 0 .0 %、95 .7%。共存离子除Ge4+ 、Cr6 + 、Ti4+ 外 ,无显著性干扰。用ICP MS测定Au、Pt、Pd的检出限分别为 0 .2 7、0 .4 0和 0 .1 9μg L。当n =8时 ,Au的RSD为 1 9.2 % ;Pt的RSD为 2 8.1 % ;Pd的RSD为 1 5 .6%。

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用电感耦合等离子体原子发射光谱法 (ICP AES)测定了 11种东北大豆中大量、小量和微量元素。比较了两种湿法消解方法 ,HNO3 HClO4,HNO3 H2 SO4和干灰化法对分析结果的影响。由于大豆含有较多的油脂 ,用混合酸消解时费时较长且需加入较多的酸 ,从而可能产生较高的背景空白 ,因此对大豆样品的前处理采用干灰法较为合适。大豆中钾和磷是大量元素 ,本工作还研究了钾和磷对其他元素测定的影响。结果表明 ,大豆中钾和磷对其他微量元素的测定没有影响。结果还表明 ,这 11种大豆中的各微量元素的含量没有显著性差异

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Three selenium-containing catalytic antibodies mHB4, mHB5 and mHB7 which acted as mimics of cytosolic glutathione peroxidase(cGPX), were prepared by chemically introducing selenium into monoclonal antibodies HB4, HB5 and HB7. HB4. HB5 and HB7 were raised against a GSH derivative GSH-S-DNP dibenzyl ester, The cGPX activity of mHB4, mHB5, mHB7 were 170, 1 867, 32 U/mu mol, respectively. The cGPX activity of mHB5 was 0, 32 fold of natural rabbit liver cGPX and 1. 51 fold of m4A4. About two atoms of selenium existed in each of mHB5 molecule determined by inductively-coupled plasma/mass spectroscopy (ICP-MS), The optimal activity of mHB5 was at between pH 8. 4 and 8, 8, The reaction catalyzed by mHB5 involved a Ping-Pong mechanism. At pH 7. 0 and 37 degreesC, the apparent second-order rate constants for reaction of mHB5 with H2O2 and t-ROOH were as followed: k(+1) (H2O2) = 9. 71 x 10(6) L/(mol min), k(+1)(t-ROOH) = 5. 99 x 10(5) L/(mol.min). Rate accelerations (k(cat)/K-m/k(uncat)) 9. 8 x 10(6) and 3.7 x 10(5) fold those of the uncatalytic reaction were observed.

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The effect of LB monolayers on the mixed crystal was investigated by using X-ray photoelectron spectroscopy (XPS), Transmission electron microscopy (TEM), and Inductively coupled plasma-atomic emission spectroscopy (ICP-AES). The results show that LB monolayer has selectivity for the different nucleation ions with equal charge numbers and about the same ion radius. The selectivity is dependent on the head groups of monolayer. The monolayer and the doped ions have also an effect on the crystal morphology. (C) 2000 Published by Elsevier Science B.V. All rights reserved.

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Matrix effects arising from ethanol, propanol, glycerol, acetic acid, ethylenediamine and triethanolamine in inductively coupled plasma mass spectrometry have been studied. Addition of ethanol, propanol, glycerol, acetic acid, ethylenediamine and triethanolamine into solution has an enhancement effect on the signal intensity of analyte with ionization potential between 9 and 11 eV. The ethylenediamine and triethanolamine have higher enhancement effect on the signal intensity of Hg than that of ethanol, propanol, glycerol and acetic acid. Addition of ethylenediamine and triethanolamine into solution has a suppression effect on the signal intensity of Ph and Sr. The mechanism of the enhancement or suppression was investigated. The signal enhancement of Hg in the presence of ethylenediamine and triethanolamine is not caused by improved degree of ionization of Hg and nebulization efficiency. The suppression effects of Ph and Sr in the presence of ethylenediamine and triethanolamine are due to decrease of atomization efficiency of these elements. A method for the determination of Hg in the biological standard samples Ly ICP-MS was developed.