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61.
The partition coefficient (log P) for n-octanol/water system was calculated applying PACO program for various theoretically possible mono and dihalogenated IDA derivatives. Some of the synthesized ligands (SOLCOIODIDA, IODIDA and DIIODIDA) were labeled with the technetium-99m. The biodistribution and influence of bilirubin on their biokinetics were investigated in rats. The correlation between partition coefficients of ligands increase (log P) and better hepatobiliary properties of 99mTc-IDA derivatives was determined. The values of log P increase from 1.16 for SOLCOIODIDA, 3.11 for IODIDA to 3.47 for DIIODIDA. In correlation with these results, biliary excretion decreased for 59% for 99mTc-SOLCOIODIDA and 11% for 99mTc-IODIDA and 99mTc-DIIODIDA under hyperbilirubinemia (3.5 min after injection) and 45%, 11% and 0.38% respectively (15 min after injection). The highest biliary excretion had 99mTc-DIIODIDA (55.4% for 3.5 min). Considering the correlation between hepatobiliary properties and log P, the evaluation of biological properties for various trifluoromethyl mono and dihalogenated IDA derivatives was performed on the basis of the calculated log P in order to synthetize a new radiopharmaceutical for hepatobiliary scintigraphy.  相似文献   
62.
Preconcentration was effected using a 50 mm × 2 mm i.d. minicolumn packed with a spherical cellulose sorbent with chemically bound quinolin-8-ol function groups (Ostorb Oxin). The column was connected to the nebulizer of the atomic absorption spectrometer and the sample solution and eluent (2 M hydrochloric acid) were sucked through it at a flow-rate of 2–3 ml min?1 by utilizing the negative pressure of the nebulizer. The experimental design was tested with the determination of traces of copper. Peak-area and peak-height measurements were compared. Owing to the simple calibration, the former method was used for quantification. The dynamic range was from 0.3 ng ml?1 (detection limit) to 5 μg ml?1 (breakthrough). The reproducibility in the concentration range 25 ng ml?1-5 μg ml?1 was better than 5%. Water-soluble inorganic salts, ammonia and sodium hydroxide were analysed. The accuracy of the results was checked by anodic-stripping voltammetry and by electrothermal AAS.  相似文献   
63.
Summary The retention of benzene derivatives with nonpolar and polar substituents on a porous methacrylate copolymer containing epoxy groups using both nonpolar and polar eluents was investigated. When n-hexane is used as the eluent, the retention of n-alkylbenzenes and polymethylbenzenes is weaker than that of benzene. In the case of benzene derivatives containing polar functional groups their capacity ratios (k) on this porous polymer increases approximately linearly with the increase of the adsorbate molecules dipole moment. The retention characteristics of the methacrylate copolymer were compared with that of a styrene-divinylbenzene copolymer and silica gels with a hydroxylated surface and with a surface modified by chemically bonded alkylsilyl groups.  相似文献   
64.
The influence of the position of the CH3 group in picoline and lutidine ligands on the degree of chemical change of the NCS groups in coordination compounds of the type Cu(NCS)2L2 (whereL=2-, 3- and 4-picoline, and 2,3-, 2,4-, 2,5-, 2,6-, 3,4- and 3,5-lutidine) is dealt with. The most marked effect of the CH3 group is found to be exerted in position 4. This effect of the methyl group on the degree of chemical change points to the mutual influence of the ligands in coordination compounds of Cu(II).
Zusammenfassung Der Artikel befaßt sich mit dem Einfluß der Lage der CH3 Gruppe in Pikolinen und Lutidinen als Liganden auf den Grad der chemischen Änderungen der Gruppen NSC in Koordinationsverbindungen des Typs Cu(NCS)2L2 (L=2-, 3- und 4-Pikoline, 2,3-, 2,4-, 2,5-, 2,6-, 3,4- und 3,5-Lutidine). Der ausgeprägteste Effekt der CH3 Gruppe wurde in der Position 4 beobachtet. Dieser Einfluß der Methylgruppe auf das Ausmaß der chemischen Änderungen deutet auch auf die gegenseitige Wirkung der Liganden in Koordinationsverbindungen von Cu(II).

Résumé L'article a trait à l'influence de la position du groupe CH2 dans les picolines et lutidines, en tant que ligands, sur le degré des changements chimiques des groupes SCN dans les composés de coordination du type Cu(SCN)2L2 (L=2-, 3 et 4-picoline, 2,3-, 2,4-,2,5-, 2,6-, 3,4- et 3,6-lutidine). L'effet le plus prononcé du groupe CH3 s'observe en position 4. Cette influence du groupe méthyle sur le degré des changements chimiques indique aussi l'influence mutuelle des ligands dans les composés de coordination du Cu(II).

- , , NCS Cu(NCS)2,L2, L=2-, 3- 4- , 2.3-, 2.4-, 2.5-, 2.6-, 3.4- 3.5-. , 4. Cu(II).
  相似文献   
65.
The effect of carbon black with various particle sizes and specific surfaces on the thermal properties of the sulphur vulcanizates ofcis-1,4-polyisoprene was studied by means of thermal analysis. It was found that the addition of carbon black does not change the nature of the thermal processes in isoprene rubber vulcanizates essentially, but it distincly affects the positions of the peaks recorded in the DTA curves. The specific surface of carbon black affects the temperature of the first exothermic process and the temperature and rate of destruction of cross-linked polyisoprene. The presence of carbon black brings about a reduction in the flammability ofcis-1,4-polyisoprene vulcanizates. The specific surface of carbon black influences the value of the oxygen index OI.
Zusammenfassung Mittels Thermoanalyse wurde der Einfluß von Ruß mit unterschiedlicher Partikelgröße und unterschiedlicher spezifischer Oberfläche auf die thermischen Eigenschaften von Schwefelvulkanisaten von cis-1,4-Polyisopren untersucht. Es wurde festgestellt, daß die Zugabe von Ruß die thermischen Vorgänge in Isoprengummivulkanisaten nicht wesentlich verändert, daß jedoch die Lage der in den DTA-Kurven aufgezeichneten Peaks eindeutig beeinflußt wird. Die spezifische Oberfläche von Ruß beeinflußt die Temperatur des ersten exothermen Vorganges sowie Temperatur und Geschwindigkeit von Abbau des vernetzten Polyisoprenes. Die Gegenwart von Ruß führt eine Verminderung der Entflammbarkeit voncis-1,4-Polyisopren-Vulkanisaten herbei. Die spezifische Oberfläche von Ruß beeinflußt den Wert der Sauerstoffzahl.
  相似文献   
66.
Summary A flow-through two electrode wall-jet cell with a platinum measuring electrode and a cell volume of 20 nl has been designed and evaluated. It has been used to detect phenols by reversed phase liquid chromatography using short micro bore columns. The linear dynamic range between the measured current and the concentration is greater than 103 (1.5×10–7–5×10–4 mol/l) and the minimum analyzable amount was found to be 10 pg for pyrocatechol. A negligible broadening in the detector permits the use of micro columns down to 0.5 mm internal diameter, packed with 5 m particles, without any substantial distortion of eluted zones.Presented at the 14th International Symposium on Chromatography London, September, 1982  相似文献   
67.
Thermal degradation at 180° in air of PVC stabilized with an equimolar mixture of Ba and Cd stearates has been studied. The “unreacted” stearates were separated by filtering tetrahydrofuran solutions of samples. The filtration and thermal degradation were examined by means of infrared spectroscopy in the range 1400–1800 cm?1. It has been demonstrated that, during the thermal stress, CdCl2 is accumulated in the sample and that the presence of Ba stearate supports only the consumption of Cd stearate.  相似文献   
68.
The estimation scheme of uncertainty of determination of 1-hydroxypyrene (1-OHP) in urine was developed analysing the main stages of the analytical procedure: (1) preparation of 1-OHP standards, (2) creation of the calibration curve for the high performance liquid chromatography (HPLC) analysis method with the evaluation of recovery, (3) measuring procedure of aliquot of urine, (4) adjusting the pH of aliquot and hydrolysis with enzyme, (5) solid phase extraction, (6) concentration of the extract, (7) injection of the extract to chromatograph and analysing by the HPLC method, (8) calculation of 1-OHP mass from the calibration curve, (9) calculation of 1-OHP concentration in urine. The evaluation of the uncertainty is based on quantification of individual components. Combined uncertainty was calculated using the law of propagation of uncertainties according to the EURACHEM/CITAC guidelines. Level dependence of the uncertainty arises from the calibration curve. The limits of detection and quantification were found to be equal to 0.03 and 0.1 ng/mL, respectively. The calculated expanded level-dependent uncertainty covers 47–27–25% within the concentration range 0.03–0.1–0.4 ng/mL with the materials and equipment used. These parameters could easily be recalculated according to the proposed scheme if there are some changes in the analysis procedure.  相似文献   
69.
The polysaccharide (PSH) extracts from the edible mushroom species Coprinus comatus and Coprinellus truncorum were screened in liquid for their acetylcholinesterase inhibitory (AChE) activity. Both extracts were found to display inhibition of the aforementioned enzyme reaching similar IC50 values of 0.62 ± 0.07 and 0.61 ± 0.03 mg/mL, respectively. According to the means of FTIR spectroscopy, these PSH extracts mostly contained β-glucans. However, the presence of some proteins and polyphenolics as minor ingredients were also detected. Compared with existing literature data for anti-AChE activity of the sugar samples, the findings within this study may be treated as a profound bioactivity. Consequently, this study puts some light on the possible use of the screened macrofungi in the palliative treatment of Alzheimer’s disease.  相似文献   
70.
Substituted ]-(6-methoxy-2-benzothiazolyt)-2-pyridones were prepared from 2-amino-6-methoxybenzathiazate through N-(6-methoxy-2-benzothiazotyl) cyanvorearmileaznd-3-aryl-N-(6-methoxy-2-benzothiazolyt)-2-cyano-2-propenamides. The cyclization of the latter with malonodinitrile in the presence of piperidine gave the corresponding pyridones. The structures of the synthesized compounds were confirmed by1H NMR and mass spectral data.Department of Organic Chemistry, Mass Spectrometry Laboratory, Slovak Technical University, 812 37 Bratislava, Slovakia. Published in Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1402–1404, October, 1995. Original article submitted August 24, 1995.  相似文献   
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