[PDF.31jy] Method development and validation of anti-histaminic drug in plasma: Determination of fexofenadine in human plasma using Ultra Performance Liquid Chromatography
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Method development and validation of anti-histaminic drug in plasma: Determination of fexofenadine in human plasma using Ultra Performance Liquid Chromatography
Mr.Maulikkumar Amin, Dr.Deepti Jain, Dr.M.M.Patel
[PDF.us94] Method development and validation of anti-histaminic drug in plasma: Determination of fexofenadine in human plasma using Ultra Performance Liquid Chromatography
Method development and validation Mr.Maulikkumar Amin, Dr.Deepti Jain, Dr.M.M.Patel epub Method development and validation Mr.Maulikkumar Amin, Dr.Deepti Jain, Dr.M.M.Patel pdf download Method development and validation Mr.Maulikkumar Amin, Dr.Deepti Jain, Dr.M.M.Patel pdf file Method development and validation Mr.Maulikkumar Amin, Dr.Deepti Jain, Dr.M.M.Patel audiobook Method development and validation Mr.Maulikkumar Amin, Dr.Deepti Jain, Dr.M.M.Patel book review Method development and validation Mr.Maulikkumar Amin, Dr.Deepti Jain, Dr.M.M.Patel summary
| 2011-08-18 | Original language:English | PDF # 1 | 8.66 x.18 x5.91l,.27 | File type: PDF | 76 pages|
A selective, rapid and sensitive reverse phase ultra- performance liquid chromatography method was developed for the quantitative determination of fexofenadine in human plasma. With carbamazepine as internal standard, sample pretreatment involved a one-step extraction with ethyl acetate from 980µl plasma. The sample was analyzed using 10mM KH2PO4 buffer pH 2.5 and acetonitrile (70:30 v/v) as mobile phase. Chromatographic separation was achieved on an ACQUI...
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