Doxazosin Mesylate

Keyword(s):  
2009 ◽  
Vol 92 (1) ◽  
pp. 131-137 ◽  
Author(s):  
Zeynep Aydomu ◽  
Asli Barla

Abstract Two accurate, easy spectrophotometric methods for the determination of doxazosin mesylate were described. The first method was based on the formation of ion-pair complexes with the acidic sulfophthalein dyes bromocresol purple (BCP) and bromophenol blue (BPB) in pH 3.3 and 4.5 citratephosphate buffer, respectively. The formed complexes were extracted into dichloromethane, and their absorbance was measured at 403 and 410 nm for BCP and BPB, respectively. The second method was based on the charge transfer reaction of the drug as an n-electron donor with either 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) or 7,7,8,8-tetracyanoquinodimethane (TCNQ) as -acceptors, to give colored radical anions. The absorbances of products were measured at 457 nm in acetonitrile and 838 nm in methanol for DDQ and TCNQ, respectively. Under the optimum reaction conditions, Beer's law was obeyed with a good correlation coefficient (r = 0.99970.9999) in the concentration ranges 3.018.0, 3.020.0, 15.095.0, and 10.0100.0 g/mL for the BCP, BPB, DDQ, and TCNQ methods, respectively. Limits of detection of the BCP, BPB, DDQ, and TCNQ methods were 0.314, 0.408, 1.935, and 1.610 g/mL, respectively. The limits of quantification were 1.045, 1.360, 6.449, and 5.367 g/mL, respectively. The parameters molar absorptivity, precision, accuracy, recovery, robustness, and stability constant were studied. The proposed methods were successfully applied for determination of the drug in tablets with good accuracy and precision. Statistical comparison of the results with those obtained by a reported method showed good agreement and indicated no significant difference in accuracy and precision.


2012 ◽  
Vol 6 (4) ◽  
pp. 266
Author(s):  
ShilpaP Chaudhari ◽  
NeerajR Kotian ◽  
MaheshM Bhadgale ◽  
VardhmanC Bafna

2011 ◽  
Vol 33 (3) ◽  
pp. 209-213 ◽  
Author(s):  
Katiane Cella Gabriel ◽  
Rafael Rodrigues Dihl ◽  
Mauricio Lehmann ◽  
Maria Luiza Reguly ◽  
Marc François Richter ◽  
...  

2003 ◽  
Vol 59 (6) ◽  
pp. 787-793 ◽  
Author(s):  
Vladimir V. Chernyshev ◽  
Denis Machon ◽  
Andrew N. Fitch ◽  
Sergei A. Zaitsev ◽  
Alexandr V. Yatsenko ◽  
...  

The three-dimensional solid-state structures of two modifications of doxazosin mesylate C23H26N5O_5^+·CH3SO_3^-, 4-amino-2-[4-[(2,3-dihydro-1,4-benzodioxin-2-yl)carbonyl]piperazin-1-yl]-6,7-dimethoxyquinazoline methanesulfonate, a commonly used antihypertensive agent, have been determined by synchrotron X-ray powder diffraction. An anhydrous form (A) and a dihydrate form (d G) crystallize in monoclinic space groups. In both forms the doxazosin molecule is protonated at the N1 atom of the quinazoline bicycle. The N1 atom, and the amino H atoms and O atoms of the mesylate moieties are involved in three-dimensional hydrogen-bonding networks, while solvent water molecules and carboxamide O atoms are also incorporated in a hydrogen-bonding network in d G.


2005 ◽  
Vol 28 (6) ◽  
pp. 730-735 ◽  
Author(s):  
Young-Taek Sohn ◽  
Yoon-Hee Lee
Keyword(s):  

2017 ◽  
Vol 1 (1) ◽  
pp. 56-60
Author(s):  
Itamar Luís Gonçalves ◽  
Mariana Maier Gaelzer ◽  
Gabriel Oliveira de Azambuja ◽  
Christianne Gazzana Salbego ◽  
Vera Lucia Eifler-Lima

Doxazosin is an important drug used for treating hypertension and prostatic hyperplasia. An enantiomeric mixture (R)/(S) doxazosin mesylate was complete characterized by NMR and additionally FT-IR spectroscopy techniques. Were performed different NMR experiments, such as APT, HSQC, and HMBC in order to confirm the NMR signals assignments. All the hydrogens and the most of carbons atoms were assigned. 


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