Determination of the thermodynamic dissociation constant of p-nitrophenol in {NaCl+EtOH+H2O} mixture by ultra-violet spectrophotometry

2010 ◽  
Vol 10 (3) ◽  
pp. 206-212 ◽  
Author(s):  
Jia-Zhen Yang ◽  
Dian-Yuan Men ◽  
Xiu-Dan Guan
1883 ◽  
Vol 36 (228-231) ◽  
pp. 137-138

M. Fievez has recently sent me a map of the solar spectrum from C to A* inclusive, and as part of this region is one which I have been measuring, I have examined the new publication with great interest. Photography and eye measurements do not exactly coincide in the detail of the grouping of the little a group as far as A, and A itself is shown by M. Fievez’s map as wanting some details which appear in the photographs. Thus in the photographs there are some seventeen lines, whilst in M. Fievez’s map there are but thirteen. Between A and a there are several lines of marked intensity in the photograph which are not shown in the new map. The wave-lengths of the different lines from above “ a ” to A are not the same as those given by Fievez, when they are taken from comparison photo-graphs of the 1st order of the red and 2nd of the ultra-violet on the same plate, or when checked by photographs of the 2nd order of the red with the 3rd order of the green taken in a similar manner. In my paper, “Phil. Trans.,” Part II, 1880, I gave a method of using mirrors by which this could be effected, but since Professor Rowland introduced his concave gratings this is much more readily carried out. He has kindly furnished me with gratings for the purpose, having about 14,400 lines to the inch, with focal distances of 7 feet 6 inches and 12 feet 6 inches respectively. These have been employed in determining the wave-lengths of this part of the spectrum. Cornu’s map was used as a reference for the ultra-violet wave-lengths, and Ångström’s map for those in the blue and green. The two maps may be taken as equally exact. The determination of A has been made by Maseart, Smyth, and others, besides Ångström and Langley, with discordant results. I think the above may be taken as accurate as are Cornu’s and Ångström maps.


2002 ◽  
Vol 770 (1-2) ◽  
pp. 145-154 ◽  
Author(s):  
Dušan Koval ◽  
Václav Kašička ◽  
Jiřı́ Jiráček ◽  
Michaela Collinsová ◽  
Timothy A. Garrow

2021 ◽  
Vol 33 (7) ◽  
pp. 1692-1698
Author(s):  
S.S. Jadiya ◽  
N. Upmanyu ◽  
S. Arulmozhi ◽  
V. Jain ◽  
S. Sankaran ◽  
...  

In present study, an advanced, simple and a rapid reverse phase high performance liquid chromatography (RP-HPLC) method was developed for the quantitative determination of sulfasalazine in rabbit plasma. Sulfasalazine was separated using Chromatopak C-18 basic peerless (250 mm × 4.6 mm, 5μ) column in an isocratic mode using mobile phase consisting of the mixture of 10mM Ammonium acetate pH adjusted to 4.5 and acetonitrile (70:30 v/v) with a flow rate of about 1.0 mL/min at ambient temperature. An ultra-violet detection of sulfasalazine and the internal standard was carried out at 362 nm. Both sulfasalazine and internal standard (IS, 4-hydroxy benzoate) were extracted from plasma matrices with high efficiency using a simple protein precipitation method. The method was found to be highly selective with no carryover effects. Linearity of sulfasalazine was found with the range of 2.5-100 μg/mL with the value of r2 > 0.995 a correlation coefficient. At all three quality control levels, developed bioanalytical method was found as repeatable and reproducible as well. The average recoveries of sulfasalazine from plasma were in the range of 95.59-97.16%. The bioanalytical samples showed good and acceptable stability of sulfasalazine solution at different storage, packaging and handling conditions. Hence, in conclusion, the validated and developed HPLC-UV method could be effectively utilized for determination of sulfasalazine in pharmacokinetic studies involving novel formulations.


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