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Heiningen, P.N.M., Hartorp, V., Nielsen, K.K., Hansen, K.T., Lier, J.J., Merbel, N.C., Oosterhuis, B. and Jonkman, J.H.G. (1999) Absorption, Metabolism and Excretion of a Single Oral Dose of 14C-Repaglinide during Repaglinide Multiple Dosing. European Journal of Clinical Pharmacology, 55, 521-525.
http://dx.doi.org/10.1007/s002280050667

has been cited by the following article:

• TITLE: Liquid Chromatography Tandem Mass Spectrometry Method for Determination of Anti-Diabetic Drug Repaglinide in Human Plasma

  AUTHORS: Manar K. Fayyad, Ezzeldeen H. Ghanem

  KEYWORDS: Repaglinide; LC-MS/MS; Human Plasma; Bioequivalence

  JOURNAL NAME: American Journal of Analytical Chemistry, Vol.5 No.4, March 21, 2014

  ABSTRACT: A highly sensitive, accurate and rapid analytical method based on reversed-phase liquid chromatography/electrospray ionization tandem mass spectrometry (RP-LC-ESI-MS/MS) has been developed and validated for the determination of repaglinide in human plasma using cetirizine as an internal standard (IS). The method was validated over a linear range of 0.5 - 100 ng/ml. After addition of IS, analytes were extracted from the plasma samples by liquid-liquid extraction using tert-butyl methyl ether as. The dried residue was reconstituted with 500 μL of mobile phase consisting of water/methanol/acetonitrile (62.5:20:17.5, v/v/v) and 0.2% formic acid. Chromatographic separations were achieved on a C18 analytical column. The analytes were detected with a triple quadrupole mass spectrometer using turbo V? ion spray source with positive ionization in multiple reaction monitoring (MRM) mode using MRM transitions m/z 453.3 > 162.2 and m/z 389.0 > 201.1 for the drug and IS, respectively. The proposed method was fully validated in terms of linearity, accuracy, precision, specificity, sensitivity, recovery and stability, giving results within the acceptable range. This method was successfully applied for a large number of authentic human plasma samples from a bioequivalence study.