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Hi all,
I would be grateful if anyone can send by e-mail (or post on the web)
details of a recent (2002/2003) HPLC/UV method for assay in plasma of
Simvastatin and Lovastatin. We don't have use of an
HPLC/MS, but need to carry out bioequivalance studies on newer
formulations. Details of sample preparation, extraction, column
details etc would be highly appreciated.
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hi Jimmy,
Following are some of the references u may be interested in,
1. Determination of simvastatin in human plasma by high performance
liquid chromatography. Se Pu. 2000 May;18(3):232-4
2.Simultaneous determination of simvastatin and its hydroxy acid form
in human plasma by high-performance liquid chromatography with UV
detection.J Pharm Biomed Anal. 1992 Sep;10(9):693-7
3.Determination of lovastatin in human plasma using reverse-phase
high-performance liquid chromatography with UV detection. Ther Drug
Monit. 2000 Dec;22(6):737-41.
But the major concern to me is that I was not able to reproduce any of
these methods, specially recovery point of view.
Any suggestions in this regrad are welcome.
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