Rapid growth in the use of LC-MS/MS for the analysis of drugs in biological matrices has been compelled by the need for timely and high-quality data at every stages in drug discovery and development process: from throughput screening of drug candidates and rapid data generation for pre-clinical studies to almost 'real-time' analysis of clinical samples. A well developed bioanalytical development and its validation plays a pivotal role in achieving the goals. .
The aim behind this review is to enlighten the need of validation which provide a practical approach for determining the different parameters like selectivity, specifity, limit of detection, lower limit of quantitation, linearity, range, accuracy, precision, recovery, stability, ruggedness, and robustness to help the perfect studies of pharmacokinetic, toxic kinetic, bioavailability and bioequivalence. Bio-analysis study is for the quantitative determination of drug and their metabolites in biological fluids. Accurate and robust methods for quantitative analysis of drug and their metabolites are important for the successful conduct of pre-clinical, bio-pharmaceutics and clinical pharmacology.
By Ashutosh Badola | Preeti Joshi | Preeti Kothiyal""A General Review on Bioanalytical Method Development & Validation for LC-MS/MS"" Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-2 | Issue-4 , June 2018,
URL: http://www.ijtsrd.com/papers/ijtsrd14203.pdf
Direct Link - http://www.ijtsrd.com/pharmacy/pharmaceutics/14203/a-general-review-on-bioanalytical-method-development-and-validation-for-lc-msms/ashutosh-badola
research publication, international peer reviewed journal, submit paper online
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