Background: High-performance liquid chromatography (HPLC) is the fastest-growing analytical technique for the analysis of drugs. Its simplicity, high specificity and wide range of sensitivity make it ideal for the analysis of many drugs in both dosage forms and biological fluids.
Objective: A simple, accurate, precise method was developed, for
the simultaneous estimation of the Chlorzoxazone, Pantoprazole, and Diclofenac
in solid dosage form.
Method: The chemicals used were Water-HPLC grade, Acetonitrile,
Triethylamine, Potassium dihydrogen orthophosphate, and Orthophosphoric acid.
Chromatogram was run through BDS C18150×4.6mm, 5m. Mobile phase containing 0.01
% KH2PO4 and Acetonitrile in the ratio of 52:48 v/v was
pumped through column at a flow rate of 1.0ml/min. The buffer used in this
method was 0.01% KH2PO4, Temperature was maintained at
30°C. The optimized wavelength for Phar Chlorzoxazone, Pantoprazole, and
Diclofenac was 229.0 nm.
Results: In the estimation of
the three drugs, four trials were conducted using various solvent systems,
columns, and experimental conditions. The retention time of Chlorzoxazone,
Pantoprazole, and Diclofenac were found to be 2.229 min, 2.958 min, and 3.568
min. The percent RSD of system precision for Chlorzoxazone, Pantoprazole and
Diclofenac were 0.9,0.6 And 0.6, respectively. The percent RSD of the method,
Pantoprazole and Diclofenac were found to be 0.6, 1.0 and 0.7 respectively. The
percent recovery was obtained as 99.86%, 100.07% and 99.70% for Chlorzoxazone,
Pantoprazole, and Diclofenac respectively. LOD values obtained from regression
equations of Chlorzoxazone, Pantoprazole and Diclofenac were 0.14 ppm, 0.24
ppm, and 1.83 pm, and LOQ values obtained from regression equations of
Chlorzoxazone, Pantoprazole and Diclofenac were 0.42 ppm, 0.72 pm, 5.53 ppm
respectively. The regression equation of Chlorzoxazone was y = 8321.9.x +
1397.8 Pantoprazole was y = 9806.1x +6071.7 and of Diclofenac was y = 2575x +
4338.4.
Conclusion: Sensitive detectors have transformed liquid column
chromatography into high speed, efficient, accurate and highly resolved methods
of separation. Retention times were decreased so that the method developed was
simple and economical hence it can be used in regular Quality control tests in
industries.
Author
(s) Details
Padmavathi
Sakinala
Department of Pharmaceutical Chemistry & Phytochemistry,
Pharmaceutical Analysis, Nirmala College of Pharmacy, Atmakur, Mangalagiri,
Guntur, AP- 522503, India.
Harini
Vahika
Department of Analysis, Nirmala College of Pharmacy, Atmakur,
Mangalagiri, Guntur, AP, India.
Ramu
Bhadrama Raju
Department of Chemistry, Madhira Institute of Technology and
Science, India.
Yeellanki
Krishnaveni
Department of Pharmacognosy, Madhira Institure of Science &
Technology, India.
K. Santhosh
Department of Analysis, Nirmala College of Pharmacy, Atmakur,
Mangalagiri, Guntur, AP, India.
Sandeep
Attinti
Department of Analysis, Nirmala College of Pharmacy, Atmakur,
Mangalagiri, Guntur, AP, India.
Please see the book here:- https://doi.org/10.9734/bpi/psnid/v1/3081
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