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111.
Three simple, sensitive, and reproducible spectrophotometric methods (A-C) for the determination of pipazethate hydrochloride (PiCl) in pure form and in pharmaceutical formulations are described. The first and second methods, A and B, are based on the oxidation of the drug by Fe3+ in the presence of o-phenanthroline (o-phen) or bipyridyl (bipy). The formation of tris-complex upon reactions with Fe3+-o-phen and/or Fe3+-bipy mixture in an acetate buffer solution of the optimum pH values was demonstrated at 510 and 522 nm, respectively, with o-phen and bipy. The third method, C, is based on the reduction of Fe(III) by PiCl in acid medium and subsequent interaction of Fe(II) with ferricyanide to form Prussian blue, which exhibits an absorption maximum at 750 nm. The concentration ranges are from 0.5 to 8, 2 to 16, and 3 to 15 microg/mL for Methods A-C, respectively. For more accurate analysis, Ringbom optimum concentration ranges were calculated. The molar absorptivity, Sandell sensitivity, and detection and quantitation limits were calculated. The developed methods were successfully applied to the determination of PiCl in bulk and pharmaceutical formulations without any interference from common excipients. The relative standard deviations were < or =0.83% with recoveries of 98.9-101.15%. 相似文献
112.
Amin AS El-Sheikh R Zahran F Gouda AA 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2007,67(3-4):1088-1093
A simple, accurate and highly sensitive spectrophotometric method is proposed for the rapid determination of pipazethate hydrochloride, dextromethorphan hydrobromide and drotaverine hydrochloride using chromotrope 2B (C2B) and chromotrope 2R (C2R). The method consists of extracting the formed ion-associates into chloroform in the case of pipazethate HCl and dextromethorphan HBr or into methylene chloride in the case of drotaverine HCl. The ion-associates exhibit absorption maxima at 528, 540 and 532 nm with C2B and at 526, 517 and 522 nm with C2R for pipazethate HCl, dextromethorphan HBr and drotaverine HCl, respectively. The calibration curves resulting from the measurements of absorbance-concentration relations (at the optimum reaction conditions) of the extracted ion-pairs are linear over the concentration range 4.36-52.32 microg mL(-1) for pipazethate, 3.7-48.15 microg mL(-1) for dextromethorphan and 4.34-60.76 microg mL(-1) for drotaverine, respectively. The effect of acidity, reagent concentration, time, solvent and stoichiometric ratio of the ion-associates were estimated. The molar absorptivity and Sandell sensitivity of the reaction products were calculated. Statistical treatment of the results reflects that the procedure is precise, accurate and easily applied for the determination of the drugs under investigation in pure form and in their pharmaceutical preparations. 相似文献
113.
114.
Wafaa S. Hamama Moustafa A. Gouda Marwa H. Abd El‐Wahab Hanafi H. Zoorob 《Journal of heterocyclic chemistry》2014,51(6):1558-1581
Amino‐1,3,4‐thiadiazoles, although scarce in nature, constitute a group of nitrogen and sulfur heterocyclic compounds that have shown significant biological activities. Their transformations into other biologically active compounds have been exploited. This review describes the work on the synthesis and reactions of amino‐1,3,4‐thiadiazoles as well as their biological evaluation. 相似文献
115.
Prakash Gouda Avaji Sangamesh A. Patil Prema S. Badami 《Transition Metal Chemistry》2008,33(3):275-283
A series of Co(II) complexes have been synthesized with Schiff bases derived from 3-substituted-4-amino-5-hydrazino-1,2,4-triazole
and substituted salicylaldehydes. These complexes are insoluble in water but more soluble in DMF and DMSO. The complexes have
been characterized by elemental analyses, spectral (IR, UV–Vis, 1H-NMR, FAB-mass, fluorescence), magnetic, thermal, solid-state DC electrical conductivity and molar conductance data. The
molar conductivity values indicate that they are non-electrolytes. The elemental analyses of the complexes suggest a stoichiometry
of the type Co · L1–L16 · 2H2O. The complexes have been considered as semiconductors on the basis of the solid-state DC electrical conductivity data.
Fluorescence spectra of one Schiff base and its complex were investigated in various solvents and some of the Schiff bases
and their complexes were evaluated for their antimicrobial activities. 相似文献
116.
Hassan WS El-Henawee MM Gouda AA 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2008,69(1):245-255
Two rapid, simple and sensitive extractive specrophotometric methods has been developed for the determination of three histamine H1-antagonists drugs, e.g., chlorphenoxamine hydrochloride (CPX), diphenhydramine hydrochloride (DPH) and clemastine (CMT) in bulk and in their pharmaceutical formulations. The first method depend upon the reaction of molybdenum(V) thiocyanate ions (Method A) with the cited drugs to form stable ion-pair complexes which extractable with methylene chloride, the orange red color complex was determined colorimetrically at lambda(max) 470nm. The second method is based on the formation of an ion-association complex with alizarin red S as chromogenic reagents in acidic medium (Method B), which is extracted into chloroform. The complexes have a maximum absorbance at 425 and 426nm for (DPH or CMT) and CPX, respectively. Regression analysis of Beer-Lambert plots showed a good correlation in the concentration ranges of 5.0-40 and 5-70microgmL(-1) for molybdenum(V) thiocyanate (Method A) and alizarin red S (Method B), respectively. For more accurate analysis, Ringbom optimum concentration ranges were calculated. The molar absorptivity, Sandell sensitivity, detection and quantification limits were calculated. Applications of the procedure to the analysis of various pharmaceutical preparations gave reproducible and accurate results. Further, the validity of the procedure was confirmed by applying the standard addition technique and the results obtained in good agreement well with those obtained by the official method. 相似文献
117.
Background
A routine method for the quantification of beryllium in biological fluids is essential for the development of a chelation therapy for Chronic Beryllium Disease (CBD). We describe a procedure for the direct determination of beryllium in undigested micro quantities of human blood and serum using graphite furnace atomic absorption spectrometry. Blood and serum samples are prepared respectively by a simple 8-fold and 5-fold dilution with a Nash Reagent. Three experimental setups are compared: using no modifier, using magnesium nitrate and using palladium/citric acid as chemical modifiers.Results
In serum, both modifiers did not improve the method sensitivity, the optimal pyrolysis and atomization temperatures are 1000°C and 2900°C, respectively. In blood, 6 μg of magnesium nitrate was found to improve the method sensitivity. The optimal pyrolysis and atomization temperatures were 800°C and 2800°C respectively.Conclusion
In serum, the method detection limit was 2 ng l-1, the characteristic mass was 0.22 (± 0.07) pg and the accuracy ranged from 95 to 100%. In blood, the detection limit was 7 ng l-1, the characteristic mass was 0.20 (± 0.02) pg and the accuracy ranged from 99 to 101%. 相似文献118.
Izzuddin Zaman Hsu‐Chiang Kuan Qingshi Meng Andrew Michelmore Nobuyuki Kawashima Terry Pitt Liqun Zhang Sherif Gouda Lee Luong Jun Ma 《Advanced functional materials》2012,22(13):2735-2743
A scalable approach for the mass production of chemically modified graphene has yet to be developed, which holds the key to the large‐scale production of stable graphene colloids for optical electronics, energy conversion, and storage materials, catalysis, sensors, composites, etc. Here, a facile approach to fabricating covalently modified graphene and its polymer nanocomposites is presented. The method involves: i) employing a common furnace, rather than a furnace installed with a quartz tube and operated in inert gas as required in previous studies, to treat a commercial graphite intercalation compound with thermal shocking and ultrasonication and fabricate graphene platelets (GnPs) with a thickness of 2.51 ± 0.39 nm that contain only 7 at% oxygen; ii) grafting these GnPs with a commercial, long‐chain surfactant, which is able to create molecular entanglement with polymer matrixes by taking advantage of the reactions between the epoxide groups of the platelets and the end amine groups of the surfactant, to produce chemically modified graphene platelets (m‐ GnPs); and iii) solution‐mixing m‐GnPs with a commonly used polymer to fabricate nanocomposites. These m‐GnPs are well dispersed in a polymer with highly improved mechanical properties and a low percolation threshold of electrical conductivity at 0.25 vol%. This novel approach could lead to the future scalable production of graphene and its nanocomposites. 相似文献
119.
V. K. Gouda G. I. Youssef N. A. Abdel Ghany 《Surface and interface analysis : SIA》2012,44(10):1338-1345
This paper presents the results of in situ non‐destructive X‐ray fluorescence determination of the chemical analysis of a collection of ten bronze statues that are on display at the Egyptian museum of Cairo. The statues are from the late period of the ancient Egyptian history. In addition, destructive technique X‐ray diffraction analysis was applied on 11 damaged archaeological objects to determine the corrosion products and the alloy compositions. Specimens of the latter objects were subjected to metallographic examinations to determine the microstructure of the alloy. Surprisingly, the results indicated that all ten statues and 10 of the 11 damaged objects were made of lead – bronze alloy; the percentage of the lead varied from 3.43 to 18.04, the tin varied from 2.53 to 10.67. The chemical composition of the patina on eight damaged objects is essentially composed of (Cu2O) cuprite for all objects in addition to other compounds such as (SnO2) cassiterite in two objects, (PbCO3) cerussite in three other objects and (Cu2(OH)3Cl) atacamite or (Cu(OH)3Cl) paratacamite in two other objects. The formation of chlorides and carbonate resulted from the interaction between surrounding environment and the alloy. The results of the metallographic examinations indicated a non‐homogenous structure and the increase of the lead content increases the globular lead particles. In spite of this condition, the galvanic corrosion tendency when the alloy is exposed to moist air or soil is not possible as lead compounds are electrically insulating. Another advantage for using leaded bronze in making statues is being heavy and thus leads to stability. Copyright © 2012 John Wiley & Sons, Ltd. 相似文献
120.
Gouda YG Abdel-Baky AM Mohamed KM Darwish FM Kasai R Yamasaki K 《Natural product research》2006,20(10):935-939
Further phytochemical investigation of the fruits of Kigelia pinnata DC. has yielded a new phenylpropanoid derivative identified as 6-p-coumaroyl-sucrose (1) together with ten known phenylpropanoid and phenylethanoid derivatives (2-11) and a flavonoid glycoside (12). The structures of the isolated compounds were elucidated using various techniques of NMR and MS spectral analysis. 相似文献