Drug Res (Stuttg) 2018; 68(11): 648-652
DOI: 10.1055/a-0635-8246
Original Article
© Georg Thieme Verlag KG Stuttgart · New York

In-vitro Equilibrium Phosphate Binding Study of Sevelamer Carbonate by UV-Vis Spectrophotometry

Budi Prasaja
1   PT. Clinisindo Laboratories, Jakarta, Indonesia
,
M. Maulana Syabani
2   Division of Product Development, PT. Novell Pharmaceutical Laboratories, Jakarta, Indonesia
,
Endah Sari
2   Division of Product Development, PT. Novell Pharmaceutical Laboratories, Jakarta, Indonesia
,
Uci Chilmi
2   Division of Product Development, PT. Novell Pharmaceutical Laboratories, Jakarta, Indonesia
,
Prawitasari Cahyaningsih
2   Division of Product Development, PT. Novell Pharmaceutical Laboratories, Jakarta, Indonesia
,
Theresia Weliana Kosasih
2   Division of Product Development, PT. Novell Pharmaceutical Laboratories, Jakarta, Indonesia
› Author Affiliations
Further Information

Publication History

received 22 March 2018

accepted 22 May 2018

Publication Date:
12 June 2018 (online)

Preview

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.

Supporting Information