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排序方式: 共有986条查询结果,搜索用时 15 毫秒
1.
In this study we report the levels of 3-methoxy-4-hydroxyphenylglycol, 3,4-dihydroxyphenylacetic acid, homovallinic acid, tryptophan, 5-hydroxyindole-3-acetic acid and serotonin in lumbar cerebrospinal fluid (CSF) from patients with multiple sclerosis, cerebrovascular disease and muscular tension headache the later, as healthy controls. The separation of these substances was performed on a reversed phase column by ion pair high performance liquid chromatography and detection was made by a glassy carbon electrode set at +900 mV vs Ag+/AgCl. The whole separation was achieved within 25 min. Concentrations of all substances (10-1000 pmole/L) were linearly proportional to areas obtained. The system is sensitive, stable and reproducible. The significance of CSF levels of these metabolites from patients groups compared with healthy controls are discussed. 相似文献
2.
I. H. Qureshi M. S. Chaudhary S. Ahmad 《Journal of Radioanalytical and Nuclear Chemistry》1982,68(1-2):209-218
Instrumental neutron activation analysis technique has been used to determine the concentration levels of 12 trace elements
in human head hair samples collected from 105 individuals living in various areas of Rawalpindi-Islamabad. The data show that
the average concentrations of Mn, Co, Ag and Au are higher in the female group as compared to the male group. Four individuals
were found to have elevated levels of Se due to the use of anti-dandruff shampoos, whereas two individials had elevated levels
of Hg. 相似文献
3.
An electrolytic device for decomposition of water has been developed which readily gives hydrogen and oxygen for isotopic measurement with a mass spectrometer. A 20-mul sample can be decomposed quantitatively in 10 min with good reproducibility. The results produced are comparable with those obtained by reduction with uranium. 相似文献
4.
5.
Rashid A. Zeineh George Kyriakidis A. Rashid Bhatti 《Applied biochemistry and biotechnology》1986,13(2):111-117
Virion polypeptides (35 S), methionine-labeled and purified by CsCl gradient centrifugation, were separated by SDS-gel electrophoresis. Analysis of their band pattern was performed by scanning the images of the SDS-gels shown on a 35-mm slide. The densitometric tracings revealed the presence of 17 protein bands, although only 15 of them were visible to the naked eye. The high sensitivity and resolving capacities of the soft-laser scanning densitometer enabled us to detect trace amounts of protein bands separated in SDS-gels and to obtain a resolution compatible to that of electrophoresis. Fourfold electronic amplification of the densitometric tracings, produced by a computer, generated new information regarding the pattern of the electrophoregram. The facility to amplify peaks of importance is particularly advantageous when faint or overlapping protein bands revealed on a gel are assessed. 相似文献
6.
T. Jabbar M. S. Subhani K. Khan A. Rashid S. D. Orfi A. Y. Khan 《Journal of Radioanalytical and Nuclear Chemistry》2003,258(1):143-149
A study on the concentration of natural and fallout radionuclides in environmental samples collected from different localities of Islamabad was performed. For the determination of gamma-emitters such as 238U, 232Th, 40K and 137Cs high purity germanium (HPGe) detector was used while for the analysis of 90Sr, a beta-emitter, liquid scintillation counting system was used. The indoor absorbed dose rate was measured by a CaF2 : Dy thermoluminescence detector. Other radiation parameters were also determined to evaluate the radiation hazard. All the results were well within the permissible limits showing that there is no radiation hazard in the environment of Islamabad. 相似文献
7.
8.
M. S. Chaudhary S. Ahmad A. Mannan I. H. Qureshi 《Journal of Radioanalytical and Nuclear Chemistry》1984,83(2):387-396
An instrumental neutron activation analytical (INAA) technique is described for the determination of 26 toxic and other trace elements in Eastern Coal (NBS SRM-1632a), local coal and its ash. The coal ash was produced by heating coal at 750°C in a muffled furnace. The transfer of these elements to the environment on the complete compustion of coal is estimated from the difference between the elemental concentration of coal and its ash. 相似文献
9.
Shah BH Siddiqui A Qureshi KA Khan M Rafi S Ujan VA Yakoob MY Yaqub Y Rasheed H Saeed SA 《Experimental & molecular medicine》1999,31(1):42-46
Our previous studies have shown that subthreshold concentrations of two platelet agonists exert synergistic effects on platelet aggregation. Here we studied the mechanism of synergistic interaction of 5-hydroxytryptamine (5-HT) and epinephrine mediated platelet aggregation. We show that 5-HT had no or little effect on aggregation but it did potentiate the aggregation response of epinephrine. The synergistic interaction of 5-HT (1-5 microM) and epinephrine (0.5-2 microM) was inhibited by alpha2-adrenoceptor blocker (yohimbine; IC50= 0.4 microM), calcium channel blockers (verapamil and diltiazem with IC50 of 10 and 48 mM, respectively), PLC inhibitor (U73122; IC50=6 microM) and nitric oxide (NO) donor, SNAP (IC50=1.6 microM)). The data suggest that synergistic effects of platelet agonists are receptor-mediated and occur through multiple signalling pathways including the activation PLC/Ca2+ signalling cascades. 相似文献
10.
High-performance liquid chromatography separated successively and quantitatively the food flavoring agents pyrimidines, purines and nucleosides, followed by nucleotides, then by polyphenols and finally by pyrazines with a reversed-phase octadecylsilica (μBondapak C18) column and various proportions of methanol, water, acetic acid and tetrabutylammonium phosphate (PIC A). The polar solvent (solvent A) was water—acetic acid—PIC A (97.5:1.5:1.0) and the relatively non-polar solvent (solvent B) was methanol—acetic acid—PIC A (97.5:1.5:1.0). Purines, pyrimidines, and nucleosides were eluted with solvent A. Nucleotides were eluted with a mixture of solvents A and B (9:1). Polyphenols were separated with a gradient starting at 10% solvent B and finishing at 25% solvent B, and finally the pyrazines were removed successively from the column with a gradient starting at 25% solvent B and finishing at 45% solvent B. The resolution and reproducibility were excellent for more than 50 compounds. By this method beverages could be analyzed directly, without solvent extraction, for flavoring compounds. 相似文献