๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Colorimetric methods for the assay of nomifensine maleate

โœ Scribed by Mohammad A. Abounassif; Mohamed E. Mohamed; Hassan Y. Aboul-Enein


Publisher
Elsevier Science
Year
1989
Tongue
English
Weight
384 KB
Volume
7
Category
Article
ISSN
0731-7085

No coin nor oath required. For personal study only.

โœฆ Synopsis


Two colorimetric methods are reported for the assay of nomifensine maleate. The methods are based on coupling between the diazotised form of nomifensine maleate and (i) N-(1-naphthyl)-ethylene diamine dihydrochloride (Bratton-Marshall reagent) and (ii) p-aminosalicylic acid (PAS). The optimum conditions for the reactions were investigated. The coupled products exhibit maximum absorbance at 470 and 435 nm for the Bratton-Marshall and PAS reagents, respectively. With PAS, a linear relationship has been established between absorbance (Amax) and concentration of nomefensine maleate over the range 2-12 micrograms ml-1. Similarly, with the Bratton-Marshall reagent, a linear relationship exists in the concentration range 2-16 micrograms ml-1. The calculated mean percent recoveries for nomifensine maleate in the commercial capsules (Merital 25 mg) respectively. Similarly, for the added recoveries, the percentage obtained were 99.01 +/- 0.46 and 100.03 +/- 1.03, respectively.


๐Ÿ“œ SIMILAR VOLUMES


Modified colorimetric ninhydrin methods
โœ Etsushiro Doi; Daisuke Shibata; Teruyoshi Matoba ๐Ÿ“‚ Article ๐Ÿ“… 1981 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 999 KB

Four calorimetric procedures suitable for the determination of peptidase activity on peptides having a free (Y-or e-amino group are described. Two of the methods (A and B) are modifications of the conventional ninhydrin method described by S. Moore and W. H. Stein (( 1948) J. Viol. Chem. 176, 367-38

A novel colorimetric method for assaying
โœ Mahmoud Aminlari ๐Ÿ“‚ Article ๐Ÿ“… 1992 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 556 KB

Arginase catalyzes the conversion of arginine to urea and ornithine in the liver of ureotelic animals. Higher activity of this enzyme is found in tumors as well as in the sera of patients with hepatic diseases. We have developed a simple colorimetric method for its determination. This is based on th