DEVELOPMENT AND VALIDATION OF UV METHOD OF TEMOZOLOMIDE IN BULK AND CAPSULE FORMULATION
AbstractAn UV spectrophotometric method for the quantitative determination of Temozolomide (TMZ) in bulk and capsule was developed in present work. The parameters linearity, precision, accuracy, limit of detection and limit of quantitation were studied according to International Conference on Harmonization guidelines. UV spectroscopic determination was carried out at an absorption maximum of 328 nm using 0.1N Hydrochloric acid as solvent. In the UV spectroscopic method linearity over the concentration range of TMZ was found to be 2-18 µg/ml with a correlation coefficient 0.999. The limit of detection and limit of quantification were found to be 0.5271 and 1.6454 mg/ml respectively. Results of the analysis were validated statistically and by recovery studies. The proposed method is simple, rapid, precise, accurate and reliable and can be used for the routine quantitative analysis of TMZ in bulk and pharmaceutical formulation.
Article Information
22
1419-1423
268KB
1679
English
IJPSR
A. Abdul Razak*, Sk. Masthanamma, B. Omshanthi, V. Suresh and P. Obulamma
Department of Pharmaceutical Analysis, Sree Vidyanikethan College of Pharmacy, Tirupati, Andhra Pradesh, India
razakabdul20@gmail.com
17 December, 2012
25 January, 2013
21 March, 2013
http://dx.doi.org/10.13040/IJPSR.0975-8232.4(4).1419-23
01 April, 2013
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