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941.
von Euler H Olsson JM Hultenby K Thörne A Lagerstedt AS 《Bioelectrochemistry (Amsterdam, Netherlands)》2003,59(1-2):89-98
INTRODUCTION: Electrochemical treatment (EChT) has been taken under serious consideration as being one of several techniques for local treatment of malignancies. The advantage of EChT is the minimal invasive approach and the absence of serious side effects. Macroscopic, histopathological and ultra-structural findings in liver following a four-electrode configuration (dog) and a two-electrode EChT design (dog and rat) were studied. MATERIALS AND METHODS: 30 female Sprague-Dawley rats and four female beagle dogs were studied with EChT using Platinum:Iridium electrodes and the delivered dose was 5, 10 or 90 C (As). After EChT, the animals were euthanized. RESULTS: The distribution of the lesions was predictable, irrespective of dose and electrode configuration. Destruction volumes were found to fit into a logarithmic curve (dose-response). Histopathological examination confirmed a spherical (rat) and cylindrical/ellipsoidal (dog) lesion. The type of necrosis differed due to electrode polarity. Ultra-structural analysis showed distinct features of cell damage depending on the distance from the electrode. Histopathological and ultra-structural examination demonstrated that the liver tissue close to the border of the lesion displayed a normal morphology. CONCLUSIONS: The in vivo dose-planning model is reliable, even in species with larger tissue mass such as dogs. A multi-electrode EChT-design could obtain predictable lesions. The cellular toxicity following EChT is clearly identified and varies with the distance from the electrode and polarity. The distinct border between the lesion and normal tissue suggests that EChT in a clinical setting for the treatment of liver tumours can give a reliable destruction margin. 相似文献
942.
Two novel bidentate Schiff base ligands, 2-(2-hydroxy-3,5-dichloro/diboromo) benzaldehyde-[4-(3-methyl-3-mesitylcyclobutyl)-1,3-thiazol-2-yl]hydrazone,
L1H, L2H and their transition metal complexes are reported. The new ligands and their complexes have been characterized by elemental
analyses, ΛM, infrared, u.v.–vis, 1H- and 13C-n.m.r. spectroscopy, and magnetic susceptibility measurements. The thermal properties of all complexes have been investigated
by TG technique. The complexes contain two monoanionic, bidentate NO ligands. It was found that all the complexes are mononuclear.
Antimicrobial activities of the ligands and their complexes have been tested against five different microorganisms, and some
of the complexes were found to be active against some of the microorganisms studied. 相似文献
943.
《Tetrahedron: Asymmetry》2006,17(16):2386-2392
An l-phenylalanine derived oxadiazinanone bearing an isopropyl group at the N4-position was prepared and acylated with either hydrocinnamoyl or propanoyl chloride. These oxadiazinanones were utilized in titanium-mediated asymmetric aldol reactions with aromatic and aliphatic aldehydes. The diastereoselectivities observed from these reactions ranged from fair to very good and suggested that the N4-isopropyl-l-phenylalanine based oxadiazinanones are conformationally and configurationally stable at the N4-nitrogen. 相似文献
944.
Yoshitsugu Arai Shū-ichi Kuwayama Yoshio Takeuchi Toru Koizumi 《Tetrahedron letters》1985,26(50):6205-6208
The Diels-Alder reaction of a novel chiral dienophile, alkyl ()-2--tolylsulfinylacrylates 1 with anthracene and cyclopentadiene showed high diastereoselectivity under the chelation controlled condition. 相似文献
945.
Dušan J. Radanović Zoran D. Matović Gustavo Ponticelli Paola Scano Inessa A. Efimenko 《Transition Metal Chemistry》1994,19(6):646-650
Summary The synthesis and characterization of AuIII complexes with several heterocyclic ligands are reported. The compounds have general formula [AuX3(L)], where L =N-methylimidazole (N-MeIz),N-ethylimidazole (N-EtIz),N-propylimidazole (N-PrIz), benzoxazole (BO), 2-methylbenzoxazole (2-MeBO), 2,5-dimethylbenzoxazole (2,5-diMeBO), 2-amino-pyrimidine (2-APm), 4(6) -hydroxy-pyrimidine [4(6)-hydrPm] or hypoxanthine (Hypox) and X = Cl or Br. Elemental analysis, conductivity measurements and spectral studies were used for the characterization of the complexes. A square-planar geometry withN-bonded heterocyclic ligands is suggested. 相似文献
946.
Summary The cephalosporin derivatives moxalactam, cefazolin, cefuroxime, ceftriaxone and cefotaxime were studied by direct current, sampled direct current, differential pulse polarography and cyclic voltammetry. While moxalactam and cefazolin give rise to one reduction wave, cefuroxime, ceftriaxone and cefotaxime exhibit two reduction waves. The characteristics of corresponding electrode reactions and their analytical parameters are presented and discussed. Optimum pH-ranges for the determination of the five cephalosporins are given. Linear concentration ranges varied from 0.1 to 200 g/ml and limits of determination were of the order of 0.01 to 0.04 g/ml depending on the compound of interest. The precision of the proposed method is excellent with relative standard deviation around 1.3% at a concentration of 0.5 g/ml for all investigated cephalosporins.
Polarographische Analyse einiger Cephalosporin-Antibiotica相似文献
947.
Y. BallesterosM.J. Gonzalez de la Huebra M.C. QuintanaP. Hernandez L. Hernandez 《Microchemical Journal》2003,74(2):193-202
The electrochemical behaviour of kinetin (6-furfurylaminopurine) on a carbon paste modified with OV-17 silicone electrode, is studied. The determination of kinetin is possible working in square wave voltammetric techniques, reaching limits of determination of 38.7 ng ml−1. The proposed method was successfully applied to determine the cytokinin in extracts of apples (previously spiked with kinetin) and the obtained results were in accordance with the results obtained with HPLC-UV. 相似文献
948.
On the basis of a better analytical exploitation of acid-induced cloud point approach, a systematic study on the phase behaviour of acid aqueous solutions of anionic surfactants and factors affecting anionic surfactant-mediated extractions was performed. The anionic surfactants investigated were alkylsulphonates (ASS) with alkylchain lengths comprised between 8 and 16 carbon atoms. The critical hydrochloric acid concentration (minimal acid concentration required to separation in two liquid phases) was found to increase as alkylchain length of the anionic surfactant increased from 10 to 14. Non-acid-induced liquid-liquid phase separation was observed for sodium octanesulphonate (SOS) or sodium hexadecyl sulphonate (SHS) in the hydrochloric concentration range 0-10 M. Acid aqueous solutions of sodium decylsulphonate (SDeS) and sodium dodecylsulphonate (SDoS) separated into two liquid phases at temperatures ranging between 10 and 80 °C, while temperatures >35 °C were required for sodium tetradecylsulphonate. The influence on extraction efficiency and concentrating ability of experimental variables such as hydrophobicity and concentration of surfactant, nature and concentration of analyte, hydrochloric acid concentration, time and temperature of extraction and time of equilibration and centrifugation was examined. Advantages provided by anionic surfactant-mediated extractions over the use of non-ionic surfactants (cloud point extractions) are discussed. 相似文献
949.
Andrés Izquierdo Pilar Linares M. D. Luque de Castro Miguel Valcarcel 《Fresenius' Journal of Analytical Chemistry》1990,336(6):490-493
Summary Two fluorimetric methods are proposed for the simultaneous determination of ammonia and urea based on the reaction of the former with o-phthalaldehyde/2-mercaptoethanol and on the use of a dual injection system in which the valves are coupled in series or in parallel. An enzymatic reactor converts urea into ammonia which is determined by the same reaction. These configurations provide very similar results with a linear determination range between 0.5 and 10.0 g ml–1 and a sampling frequency of 60 h–1. The proposed methods are very tolerant to foreign species commonly found in water, as shown by applying them to samples of different origins. 相似文献
950.
A. Segura Carretero C. Cruces Blanco R. Estrada Fernández A. Fernández Gutiérrez 《Analytical and bioanalytical chemistry》1998,360(5):605-608
A method for the determination of the fungicide thiabendazole (TBZ) by micellar-stabilized room-temperature phosphorescence is described. It does not require any separation step and allows the direct determination of the fungicide in canned pineapple samples. The effect of various experimental conditions is discussed in detail. The analytical curve of thiabendazole gives a linear dynamic range of 23.8–500.0 ng mL–1 and a detection limit of 23.8 ng mL–1. Recoveries of 103.9 and 89.2% for syrup and canned pineapple pulp, respectively, were obtained for 250 ng mL–1 thiabendazole. 相似文献