Colorimetric Determination of Propofol in Bulk form, Dosage Form and Biological Fluids

2000 ◽  
Vol 33 (12) ◽  
pp. 2515-2531 ◽  
Author(s):  
E.A. Gad-Kariem ◽  
M.A. Abounassif
RSC Advances ◽  
2016 ◽  
Vol 6 (57) ◽  
pp. 52026-52033
Author(s):  
Bahram Hemmateenejad ◽  
Arezoo Shahrivar-kevishahi ◽  
Fatemeh Shakerizadeh-Shirazi ◽  
Shohre Rouhani ◽  
Fereshteh Mohamadi-Gharaghani

A newly synthesized cyanine dye was used for sensitive colorimetric determination of total protein in biological fluids.


1997 ◽  
Vol 20 (1) ◽  
pp. 18-23 ◽  
Author(s):  
Vu Khue Nguyen ◽  
L. Ehret-Sabatier ◽  
M. Goeldner ◽  
C. Boudier ◽  
G. Jamet ◽  
...  

1972 ◽  
Vol 18 (9) ◽  
pp. 996-1000 ◽  
Author(s):  
A R Pettigrew ◽  
G S Fell

Abstract A colorimetric procedure for determination of small amounts of cyanide and thiocyanate, involving the synthesis of a pyridine dyestuff by the reaction of pyridine and an aromatic amine, has been simplified for the estimation of thiocyanate alone in biological fluids. Replacement of benzidine with p-phenylenediamine in the colorimetric reaction has both improved the precision of the analytical procedure and avoided a carcinogenic hazard. This method has been used to follow the decrease in plasma thiocyanate associated with abstinence from cigarette smoking, and its subsequent increase upon resumption. It has also been used to measure the plasma and urinary thiocyanate concentrations of patients suffering from the particular toxic amblyopias—tobacco amblyopia and Leber’s hereditary optic atrophy— believed to be associated with cyanide toxicity, and to follow the increased thiocyanate concentrations that accompany significant improvements in the patients’ vision brought about by various treatments.


Talanta ◽  
1985 ◽  
Vol 32 (8) ◽  
pp. 651-653 ◽  
Author(s):  
Mohamed S. Mahrous ◽  
Magdi M. Abdel-Khalek ◽  
Mohamed E. Abdel-Hamid

1972 ◽  
Vol 18 (9) ◽  
pp. 943-950 ◽  
Author(s):  
Nathan Gochman ◽  
Joan M Schmitz

Abstract We describe an automated, colorimetric determination of glucose in biological fluids that combines the specificity of glucose oxidase and of a new peroxide indicator reaction. In the presence of peroxidase, 3-methyl-2-benzothiazolinone hydrazone oxidatively couples with N,N-dimethylaniline to form a stable, intensely colored, water-soluble indamine dye, the concentration of which is proportional to that of the third reactant, hydrogen peroxide. This reaction, used earlier to determine uric acid [Clin. Chem. 17, 1154 (1971)], is substantially less affected by negative interference of reducing substances than are previously described peroxide indicators. Results from use of AutoAnalyzers I and II and this method were compared with those from a manual spectrophotometric hexokinase/glucose-6-phosphate dehydrogenase procedure, and showed good correlation for specimens from patients. The automated methods are suitable for measuring glucose in serum, plasma from fluoride-or iodoacetate-preserved blood, urine (without ion-exchange pretreatment), or cerebrospinal fluid. They eliminate the problem of falsely high results caused by medication or reducing metabolites associated with uremia, in methods in which alkaline ferricyanide or copper—neocuproine is used.


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