Abstract
The application of radioimmunoassay (RIA) for quantitation of pharmaceutical drug concentration in biological matrices has increased in recent years due to several factors. The first reason has been the development of more efficacious drugs, resulting in lower effective doses and subsequent lower concentrations in matrices such as plasma or urine. Although traditional chromatographic analytical procedures such as high-performance liquid chromatography (HPLC) or gas chromatography (GC) have demonstrated improved sensitivity, compounds continue to be developed that cannot be measured by HPLC or GC. A second factor involved in the increased use of RIA is an enhanced awareness and willingness to develop the complex synthetic chemistry necessary to produce the requisite immunological and radiochemical reagents for RIA. Lastly, with the advent of radioactivity counters that can rapidly count large numbers of assay samples and perform the required data reduction, RIA has become more time efficient than chromatographic methods.
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Nordblom, G.D., Barksdale, C.M. (1994). Contemporary Aspects of Radioimmunoassay Development for Drug Analysis. In: Welling, P.G., Balant, L.P. (eds) Pharmacokinetics of Drugs. Handbook of Experimental Pharmacology, vol 110. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-78680-8_2
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DOI: https://doi.org/10.1007/978-3-642-78680-8_2
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