scholarly journals Methods for direct determination of mitomycin C in aqueous solutions and in urine

10.1251/bpo12 ◽  
1998 ◽  
Vol 1 (2) ◽  
pp. 100-106 ◽  
Author(s):  
Dolores Marín ◽  
Pedro Pérez ◽  
Carmen Teijeiro ◽  
Emil Paleček
1956 ◽  
Vol 34 (2) ◽  
pp. 151-159 ◽  
Author(s):  
A. N. Campbell ◽  
J. B. Fishman ◽  
G. Rutherford ◽  
T. P. Schaefer ◽  
L. Ross

This paper is devoted to the direct determination of the vapor pressures of solutions of the nitrates of silver, of ammonium, and of lithium, at temperatures varying from 30 °C. to 105 °C. and at concentrations varying from 10 to 85 weight % (for lithium nitrate, the limited solubility precluded measurements beyond 65%). From the vapor pressures, the enthalpies of evaporation of water (by a modification of the Clapeyron–Clausius equation), the differential heats of dilution, and the activities of water (as compared with the mole fractions of the solvent) have been calculated. From the results we conclude that the water of hydration of the ammonium and silver ions (if, indeed, these ions are hydrated at all) is very loosely attached, while that of the lithium ion is strongly bound.


1973 ◽  
Vol 51 (17) ◽  
pp. 3006-3009 ◽  
Author(s):  
A. N. Campbell

The direct determination of the limiting conductance of 1/3In3+ ion is not possible because of hydrolysis. This figure has been obtained by a method which may be open to criticism as 56.3 mhos, at 25°. If anything, this figure is too high.


2012 ◽  
Vol 67 (5) ◽  
pp. 236-240
Author(s):  
A. V. Pirogov ◽  
E. B. Pashkova ◽  
A. A. Bendryshev ◽  
R. V. Ul’yanov ◽  
O. A. Shpigun

2005 ◽  
Vol 70 (2) ◽  
pp. 178-187 ◽  
Author(s):  
Wanyun Qu ◽  
Hong Wang ◽  
Kangbing Wu

An electrochemical method for the direct determination of mitomycin c (MMC), based on a multi wall carbon nanotube (MWNT)-modified electrode, has been developed. A well-shaped and highly sensitive oxidation peak at 0.79 V was observed on the MWNT-modified electrode for MMC. Further studies show strong evidence that MWNT-modified electrode significantly enhances the sensitivity of determination of MMC since the oxidation peak current of MMC increases remarkably, compared with that with a bare glassy carbon electrode. All the experimental parameters such as pH, scan rate, accumulation conditions, have been examined. A sensitive linear voltammetric response for MMC was obtained over the concentration range of 2.5 × 10-7-1.0 × 10-4 mol/l; the detection limit is 8 × 10-8 mol/l. Compared with other methods, this new-proposed method possesses advantages such as high sensitivity, fast response, low cost and simplicity. Eventually, the proposed method has been successfully employed to detect MMC in urine samples.


1989 ◽  
Vol 220 ◽  
pp. 235-241 ◽  
Author(s):  
T. Berthoud ◽  
P. Decambox ◽  
B. Kirsch ◽  
P. Mauchien ◽  
C. Moulin

1961 ◽  
Vol 41 (4) ◽  
pp. 380-384 ◽  
Author(s):  
Arthur F. Dratz ◽  
James C. Coberly
Keyword(s):  

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