SPECTROPHOTOMETRIC DETERMINATION OF CEFPROZIL IN PHARMACEUTICAL DOSAGE FORMS, IN URINE AND IN THE PRESENCE OF ITS ALKALINE INDUCED DEGRADATION PRODUCTS

2001 ◽  
Vol 34 (10) ◽  
pp. 1639-1655 ◽  
Author(s):  
H. G. Daabees ◽  
M. S. Mahrous ◽  
M. M. Abdel-Khalek ◽  
Y. A. Beltagy ◽  
K. N. Emil
2010 ◽  
Vol 60 (2) ◽  
pp. 217-227 ◽  
Author(s):  
Padmarajaiah Nagaraja ◽  
Ashwinee Shrestha ◽  
Anantharaman Shivakumar ◽  
Avinash Gowda

Use ofN, N-diethyl-p-phenylenediamine sulphate for the spectrophotometric determination of some phenolic and amine drugsSpectrophotometric methods are proposed for the determination of drugs containing a phenol group [salbutamol sulphate (SLB), ritodrine hydrochloride (RTD), isoxsuprine hydrochloride (IXP)] and drugs containing an aromatic amine group [dapsone hydrochloride (DAP), sulfamethoxazole (SFM), and sulfadiazine (SFD)] in pharmaceutical dosage forms. The methods are based on coupling ofN, N-diethyl-p-phenylenediamine sulphate with the drugs in the presence of KIO4to give a green colored product (λmaxat 670 nm) and a red colored product (λmaxat 550 nm), respectively. Linear relationships with good correlation coefficients (0.9986-0.9996) were found between absorbance and the corresponding concentration of drugs in the range 1-7, 2-22, 1-17, 1.5-12, 2-25, and 2-21 μg mL-1for SLB, RTD, IXP, DAP, SFM and SFD, respectively. Variable parameters such as temperature, reaction time and concentration of the reactants have been analyzed and optimized. The RSD of intra-day and inter-day studies was in the range of 0.2-1.0 and 0.4-1.0%, respectively. No interference was observed from common pharmaceutical adjuvants. The reliability and performance of the proposed methods was validated statistically; the percentage recovery ranged from 99.5 ± 0.1 to 99.9 ± 0.3%. Limits of detection were 0.14, 0.21, 0.51, 0.44, 0.33 and 0.37 μg mL-1for SLB, RTD, IXP, DAP, SFM, and SFD, respectively.


The Analyst ◽  
1982 ◽  
Vol 107 (1276) ◽  
pp. 776 ◽  
Author(s):  
G. Ramana Rao ◽  
Y. Pulla Rao ◽  
I. R. K. Raju

2012 ◽  
Vol 1 (11) ◽  
pp. 336-341 ◽  
Author(s):  
Napa Delhi Raj ◽  
Sockalingam Anbazhagan ◽  
Kunapareddy Anudeep Babu ◽  
Sunkara Narendra Babu ◽  
Chusena Narasimharaju Bhimanadhuni

A rapid and precise RP-HPLC method for determination of Olmesartan medoxomil and Hydrochlorothiazide in bulk and pharmaceutical dosage forms. Olmesartan medoxomil & Hydrochlorothiazide are found to be degraded together under different set of conditions as followed according to ICH guidelines and the degradants so formed along with olmesartan & hydrochlorothiazide are separated by using INERTSIL ODS C18 3V (150 x 4.6, 5µ) using mobile phase 1ml triethanolamine in one litre water and the pH was adjusted to 2.5 with orthophosphoric acid and acetonitrile using a gradient program with a flow rate of 1ml/min, throughout the gradient program with a detection wavelength of 225nm for both the compounds with a injection volume of 10µl. The method was validated for selectivity, linearity, accuracy, robustness, precision and specificity. The results were indicating the method was selective in analysis of both olmesartan medoxomil and hydrochlorothiazide in the presence of degradation products formed under various stress conditions.DOI: http://dx.doi.org/10.3329/icpj.v1i11.12058 International Current Pharmaceutical Journal 2012, 1(11): 336-341


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