scholarly journals Second and First-Derivative Spectrophotometry for Efficient Simultaneous and Individual Determination of Palladium and Cobalt Using 1-(2-Pyridylazo)-2-naphthol in Sodium Dodecylsulfate Micellar Media

2003 ◽  
Vol 19 (11) ◽  
pp. 1513-1518 ◽  
Author(s):  
Habibollah ESKANDARI ◽  
Ali GHANBARI SAGHSELOO
2012 ◽  
Vol 9 (3) ◽  
pp. 1357-1363 ◽  
Author(s):  
Rajni Rohilla ◽  
Usha Gupta

A first-derivative spectrophotometry method for the simultaneous determination of Co (II) and Ni (II) with Alizarin Red S in presence of Triton X-100 is described. Measurements were made at the zero-crossing wavelengths at 549.0 nm for Co (II) and 546.0 nm for Ni (II). The linearity is obtained in the range of 0.291- 4.676 μg/ml of Ni (II) and 0.293- 4.124 μg/ml of Co (II) in the presence of each other by using first derivative spectrophotometric method. The possible interfering effects of various ions were studied. The validity of the method was examined by using synthetic mixtures of Co (II) and Ni (II). The developed derivative procedure, using the zero crossing technique, has been successfully applied for the simultaneous analysis of Co (II) and Ni (II) in spiked water samples.


2011 ◽  
Vol 94 (1) ◽  
pp. 128-135 ◽  
Author(s):  
Elif Karacan ◽  
Mehmet Gokhan Çaġlayan ◽  
İsmail Murat Palabiyik ◽  
Feyyaz Onur

Abstract A new RP-LC method and two new spectrophotometric methods, principal component regression (PCR) and first derivative spectrophotometry, are proposed for simultaneous determination of diflucortolone valerate (DIF) and isoconazole nitrate (ISO) in cream formulations. An isocratic system consisting of an ACE® C18 column and a mobile phase composed of methanol–water (95+5, v/v) was used for the optimal chromatographic separation. In PCR, the concentration data matrix was prepared by using synthetic mixtures containing these drugs in methanol–water (3+1, v/v). The absorbance data matrix corresponding to the concentration data matrix was obtained by measuring the absorbances at 29 wavelengths in the range of 242–298 nm for DIF and ISO in the zero-order spectra of their combinations. In first derivative spectrophotometry, dA/dλ values were measured at 247.8 nm for DIF and at 240.2 nm for ISO in first derivative spectra of the solution of DIF and ISO in methanol–water (3+1, v/v). The linear ranges were 4.00–48.0 μg/mL for DIF and 50.0–400 μg/mL for ISO in the LC method, and 2.40–40.0 μg/mL for DIF and 60.0–260 μg/mL for ISO in the PCR and first derivative spectrophotometric methods. These methods were validated by analyzing synthetic mixtures. These three methods were successfully applied to two pharmaceutical cream preparations.


2006 ◽  
Vol 89 (6) ◽  
pp. 1524-1531 ◽  
Author(s):  
Samah S Abbas ◽  
Lories I Bebawy ◽  
Laila A Fattah ◽  
Heba H Refaat

Abstract Five simple and sensitive methods were developed for the determination of leflunomide (I) in the presence of its degradates 4-trifluoromethyl aniline (II) and 3-methyl-4-carboxy isoxazole (III). Method A was based on differential derivative spectrophotometry by measuring the △1D value at 279.5 nm. Beer's law was obeyed in the concentration range of 2.0020.00 μg/mL with mean percentage accuracy of 100.07 1.32. Method B depended on first-derivative spectrophotometry and measuring the amplitude at 253.4 nm. Beer's law was obeyed in the concentration range of 2.0016.00 μg/mL with mean percentage accuracy of 98.42 1.61. Method C was based on the reaction of degradate (II) with 2,6-dichloroquinone-4-chloroimide (Gibbs reagent). The colored product was measured at 469 nm. Method D depended on the reaction of degradate (II) with para-dimethyl aminocinnamaldehyde (p-DAC). The absorbance of the colored product was measured at 533.4 nm. Method E utilized 3-methyl-2-benzothiazolinone hydrazone in the presence of cerric ammonium sulfate with degradate (II). The green colored product was measured at 605.5 nm. The linearity range was 40.00-280.00, 2.40-24.00, and 30-250 μg/mL with mean percentage accuracy of 100.75 1.21, 100.13 1.45, and 99.74 1.39 for Methods CE, respectively. All variables were studied to optimize the reaction conditions. The proposed methods have been successfully applied to the analysis of leflunomide in pharmaceutical dosage forms and the results were statistically compared with that previously reported.


1996 ◽  
Vol 29 (15) ◽  
pp. 2679-2689 ◽  
Author(s):  
M. Inés Toral ◽  
Pablo Richter ◽  
Eyleen Araya ◽  
Sandra Fuentes

1997 ◽  
Vol 126 (1-2) ◽  
pp. 153-157 ◽  
Author(s):  
Luis Fermín Capitán-Vallvey ◽  
Natalia Navas Iglesias ◽  
Ignacio de Orbe Payá ◽  
Ramiro Avidad Castaneda

2007 ◽  
Vol 95 (1) ◽  
Author(s):  
A. A. El-Sayed ◽  
Mostafa M. Hamed ◽  
H. A. Hmmad ◽  
S. El-Reefy

The need exists for preconcentration of trace and ultratrace amounts of uranium from environmental, geological and biological samples. The adsorption of uranium on various solids is important from the purification, environmental, and radioactivity waste disposal points of view. A method is described for the determination of traces of uranium using first-derivative spectrophotometry after adsorptive preconcentration of uranium on activated carbon. Various parameters that influence the adsorptive preconcentration of uranium on activated carbon,


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