Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add filters








Language
Year range
1.
Bulletin of Faculty of Pharmacy-Cairo University. 1998; 36 (1): 1-9
in English | IMEMR | ID: emr-47766

ABSTRACT

Three fluorimetric methods have been developed for the determination of some cardiovascular drugs. Amiodarone hydrochloride in 0.1 N sulphuric acid showed native fluorescence with excitation at 270 nm and emission at 540 nm. Methanolic solution of amlodipine besylate exhibits maximum excitation and emission at 365 nm and 450 nm, respectively. Propafenone hydrochloride forms fluorescent ion-pair with eosine at pH 5, which is extractable in chloroform, the excitation and emission at 318 nm and 550 nm, respectively. Linearity is obtained upon determining authentic samples in concentration range of 40 - 200 mug/ml, 0.4-2.8 mug/ml and 7-24.5 mug/ml for amiodarone, amlodipine and propafenone, respectively. The precision of the proposed method is checked by analyzing different samples of bulk powder and mean percentage recoveries are 100.26 +/- 1, 99.83 +/- 1.03 and 100.2 +/- 0.91 for amiodarone, amlodipine and propafenone, respectively. The pharmaceutical formulations are also estimated applying the proposed fluorimetric methods using st and ard addition technique, showing accurate results having great agreement with those of the reference methods


Subject(s)
Amiodarone/analysis , Amlodipine/analysis , Propafenone/analysis , Fluorometry/methods , Spectrometry, Fluorescence/methods
2.
Bulletin of Faculty of Pharmacy-Cairo University. 1998; 36 (3): 1-12
in English | IMEMR | ID: emr-47793

ABSTRACT

Amiodarone and propafenone reacted with copper acetate forming drug- copper complexes and the copper content in the complexes was determined either titrimetrically or by atomic absorption spectrophotometry at 324.7 nm. Amiodarone was also estimated via its reaction with mercuric acetate and titration with lead nitrate in the presence of xylenol orange as indicator. On the other h and, propafenone was determined in the base form by precipitating its silver complex and the excess silver was titrated with ammonium thiocyanate solution. The validity of the methods were assessed by applying the st and ard addition technique and the results were compared with those obtained by the reference methods showing a great agreement


Subject(s)
Propafenone/analysis , Chelating Agents , Spectrophotometry , Acetates , Copper , Silver Nitrate , Mercury Compounds
SELECTION OF CITATIONS
SEARCH DETAIL