AN APPROACH TO BIOANALYTICAL METHOD DEVELOPMENT AND VALIDATION: A REVIEW
AbstractBioanalytical method development is the process of creating a procedure to enable a compound of interest to be identified and quantified in a biological matrix. A compound can often be measured by several methods and the choice of analytical method involves many considerations. Analysis of drugs and their metabolites in a biological matrix is carried out using different extraction techniques like liquid-liquid extraction, solid phase extraction (SPE) and protein precipitation from these extraction methods samples are spiked with calibration (reference) standards and using quality control (QC) samples. These methods and choice of analytical method describes the process of method development and includes sampling, sample preparation, separation, detection and evaluation of the results. The developed process is then validated. These bioanalytical validations play a significant role in evaluation and interpretation of bioavailability, bioequivalence, pharmacokinetic, and toxicokinetic studies. In which different parameters like accuracy, precision, selectivity, sensitivity, reproducibility, and stability are performed.
Article Information
4
2291-01
459
4040
English
IJPSR
Komal Arora and H.V. Gangadharappa *
Department of Pharmaceutics (Pharmaceutical Quality Assurance), JSS College of Pharmacy, JSS University, Sri Shivarathreeswara Nagara, Mysuru, Karnataka, India
gangujss@gmail.com
10 January, 2016
22 February, 2016
14 March, 2016
10.13040/IJPSR.0975-8232.7(6).2291-01
01 June 2016
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