Issue 1, 2010

Enantioanalysis of S-Ibuprofen using [5–6] fullerene-C70 and diethyl (1,2-methanofullerene C70)-71-71-dicarboxylate

Abstract

[5–6] Fullerene-C70 and diethyl (1,2-methanofullerene C70)-71-71-dicarboxylate are used as chiral selectors for the construction of enantioselective, potentiometric membrane electrodes used in the enantioanalysis of S-Ibuprofen. The sensitivities (slopes) of the electrodes were 55.70 mV/pS-ibuprofen for [5–6] fullerene-C70 based electrode and 56.10 mV/pS-ibuprofen for diethyl (1,2-methanofullerene C70)-71-71-dicarboxylate based electrodes and the linear concentration ranges were between 10−10 and 10−3 mol L−1 (limit of detection 1 × 10−11 mol L−1), and between 10−10 and 10−4 mol L−1 (limit of detection 5.4 × 10−11 mol L−1), respectively. The recovery tests proved that these electrodes can be reliable used for the enantioanalysis of S-ibuprofen raw material (recovery higher than 99.00%) and from its pharmaceutical formulations (recovery higher than 98.40%).

Graphical abstract: Enantioanalysis of S-Ibuprofen using [5–6] fullerene-C70 and diethyl (1,2-methanofullerene C70)-71-71-dicarboxylate

Article information

Article type
Paper
Submitted
11 Mar 2009
Accepted
28 Oct 2009
First published
17 Nov 2009

Anal. Methods, 2010,2, 37-40

Enantioanalysis of S-Ibuprofen using [5–6] fullerene-C70 and diethyl (1,2-methanofullerene C70)-71-71-dicarboxylate

R. Stefan-van Staden, Anal. Methods, 2010, 2, 37 DOI: 10.1039/B9AY00086K

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