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Drug Res (Stuttg) ; 68(11): 648-652, 2018 Nov.
Article in English | MEDLINE | ID: mdl-29895088

ABSTRACT

Sevelamer carbonate is a cross-linked polymeric amine; it is the active ingredient in Renvela® tablets. US FDA provides recommendation for demonstrating bioequivalence for the development of a generic product of sevelamer carbonte using in-vitro equilibrium binding study. A simple UV-vis spectrophotometry method was developed and validated for quantification of free phosphate to determine the binding parameter constant of sevelamer. The method validation demonstrated the specificity, limit of quantification, accuracy and precision of measurements. The validated method has been successfully used to analyze samples in in-vitro equilibrium binding study for demonstrating bioequivalence.


Subject(s)
Chelating Agents/pharmacology , Chemistry, Pharmaceutical/methods , Drugs, Generic/pharmacology , Phosphates/antagonists & inhibitors , Sevelamer/pharmacology , Calcium Carbonate/chemistry , Chemistry, Pharmaceutical/instrumentation , Sensitivity and Specificity , Spectrophotometry/instrumentation , Spectrophotometry/methods , Tablets , Therapeutic Equivalency
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