uv-spectrophotometric method for the simultaneous estimation of carisoprodol, paracetamol and caffeine: validation and application for marketed tablet analysis

نویسندگان

khanage shantaram gajanan

dharam prachi gangadhar

mohite popat baban

deshmukh vinayak kashinath

چکیده

a simple, sensitive, accurate and precise simultaneous uv spectrophotometric method has been developed for the estimation of carisoprodol, paracetamol and caffeine in tablet dosage form. the absorption maxima of the drugs were found to be 221, 248 and 273 nm for carisoprodol, paracetamol and caffeine respectively, in methanol, using a double beam uv/visible spectrophotometer. carisoprodol, paracetamol and caffeine obeyed beer’s law in the concentration range of 0.4-2 μg/ml, 2-10 μg/ml and 2-10 μg/ml, respectively. the correlation coefficient was found to be 0.9922, 0.9917 and 0.9943 for carisoprodol, paracetamol and caffeine, respectively. the method was validated for various parameters according to international conference on harmonization guidelines. the low relative standard deviation values indicate a good precision and high recovery values indicate the accuracy of the proposed method.

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Validation of UV-Spectrophotometric and RP-HPLC methods for the simultaneous analysis of Paracetamol and Aceclofenac in marketed tablets

The aim of the study was to develop UV-spectrophotometric and RP-HPLC methods for the simultaneous analysis of paracetamol and aceclofenac in marketed tablets. The methods were validated in terms of linearity, accuracy (% Recovery), precision (inter day, intraday and reproducibility) and robustness. Both the methods were linear (R = 0.997-0.999 for UV method and 0.999 for RP-HPLC method) and ac...

متن کامل

Simultaneous Spectrophotometric Estimation of Valdecoxib and Paracetamol in Tablet Formulations

The validated method was applied for determination of residual solvents in certain film-coated marketed antibiotic formulation of ciprofloxacin, norfloxacin, pefloxacin, and ofloxacin. Twenty tablets each containing 500 mg, 400 mg, 400 mg, and 200 mg of ciprofloxacin, norfloxacin, pefloxacin, and ofloxacin, respectively were accurately weighed separately. The tablets were crushed in a separate ...

متن کامل

The Simultaneous Estimation of Paracetamol and Tolperisone Hydrochloride in Tablet by UV Spectrophotometric Methods

Two methods for simultaneous estimation of Paracetamol and Tolperisone Hydrochloride in combined tablet dosage form have been developed using Water as a solvent. The first UV spectrophotometric method was a determination using the simultaneous equation method at 242.5 nm and 260 nm. The second UV spectrophotometric method is the Q – analysis (absorption ratio) method, which involves the formati...

متن کامل

Development of a Uv-spectrophotometric Method for the Simultaneous Determination of Tramadol Hydrochloride and Paracetamol in Bulk and Marketed Product

A specific, rapid and simple UV spectrophotometric method with good sensitivity was developed and validated for the simultaneous quantification of tramadol HCl and paracetamol in bulk and marketed product by simultaneous equation method. From the optical characteristics of the proposed methods, it was found that the λmax of tramadol·HCl and paracetamol was found to 271 nm and 248 nm respectivel...

متن کامل

UV-Visible Spectrophotometric Method Development and Validation of Assay of Paracetamol Tablet Formulation

It is the branch of science dealing with the study of interaction between Electromagnetic radiation and matter. It is a most powerful tool available for the study of atomic and molecular structure/s and is used in the analysis of wide range of samples. Optical spectroscopy includes the region on electromagnetic spectrum between 100 Å and 400 μm. The regions of electromagnetic spectrum are shown...

متن کامل

Development and Validation of Uv Spectrophotometric Method for Quantitative Estimation of Lafutidine from Tablet Formulation

One simple and sensitive spectrophotometric method has been developed for the quantitative estimation of Lafutidine from tablet. The method was developed and based on the solubility of Lafutidine in 0.1 N HCl (pH 1.2). The drug showed maximum absorbance at 286 nm and linearity (Lambert Beer’s Range) was found in concentration range of 10-60 μg/ml and the standard curve equation was found to be ...

متن کامل

منابع من

با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید


عنوان ژورنال:
iranian journal of analytical chemistry

ناشر: payame noor university, iran

ISSN 2383-2207

دوره 2

شماره 2 2015

میزبانی شده توسط پلتفرم ابری doprax.com

copyright © 2015-2023