Bullock, S. (2007): Effective determination of glutamic acid by HPLC with ELSD . Varian Application Note SI-01214/TB1046. Daniels, D.H., Joe, F
, including micellar electrokinetic chromatography [ 6 – 7 ], mass spectrophotometry [ 8 – 9 ], high-performance liquid chromatography (HPLC) [ 10 – 12 ], FT–Raman spectroscopy [ 13 ], and thin-layer chromatography densitometry [ 14 ]. To the best of our
best glucose control in blood and for better compliance to therapy [ 6 ]. To the best of our knowledge, it is revealed that several reversed-phase high-performance liquid chromatography (RP-HPLC) methods are available for the determination of MTF and
compounds in red wine is high-performance liquid chromatography (HPLC). It can be coupled with ultraviolet/diode array detection (UV/DAD) [ 3 , 7 ], fluorescence [ 8 , 9 ], and MS detection [ 10 ]. Some recently published methods include also gas
Di Pietra, A.M., Cavrini, V., Bonazzi, D. & Benfenati, L. (1990): HPLC analysis of aspartame and saccharin in pharmaceutical and dietary formulations. Chromatographia , 30 , 215–219. Benfenati L
–mass spectrometry [ 8 ], liquid chromatography–tandem mass spectrometry [ 9 ], high-performance liquid chromatography (HPLC) [ 10 , 11 ], and fluorimetry [ 12 ] have been used for the determination of quercetin in natural samples. However, due to the complex matrix
GD18 gestation day of 18 HPLC high-performance liquid chromatography i
(HPTLC), high-performance liquid chromatography (HPLC), and capillary electrophoresis (CE). Among these methods, HPLC is the most popular method for quantitative analysis of drugs and impurities, due to its selectivity, precision, and accuracy [ 12 , 13
. Rossomando , E. F. ( 1998 ) HPLC in enzymatic analysis . In: Methods of Biochemical Anaysis , John Wiley & Sons, pp. 1 – 24 . 21. Salehi , P. , Asghari , B
l-Deprenyl and its major metabolites were subjected to reversed-phase high-performance liquid chromatography (HPLC). The separation was monitored using both ultraviolet (UV) and electrochemical detectors. Ultraviolet absorbance detected l-deprenyl, l-nordeprenyl, l-methamphetamine, and l-amphetamine. Amperometric detection was specific and sensitive to the parent compound (l-deprenyl, a tertiary amine) only. Peaks of the major L-deprenyl metabolites did not give any comparable signal using amperometric monitoring.
