High-performance liquid chromatographic detection and quantitation of synthetic acid fast dyes with a diode array detector

1986 ◽  
Vol 354 ◽  
pp. 486-489 ◽  
Author(s):  
K.M. Weaver ◽  
M.E. Neale
INDIAN DRUGS ◽  
2019 ◽  
Vol 56 (08) ◽  
pp. 61-68
Author(s):  
V. V Gawande ◽  
A. V. Chandewar ◽  

The proposed work involves High Performance Liquid Chromatographic – Diode Array Detector method for estimation of escitalopram oxalate and flupentixol dihydrochloride in combination. The analytes were resolved on Waters C18 Xterra column (50 × 4.6 mm id, particle size 3.5 μm) with mobile phase composition of water (containing 0.2 % triethylamine pH adjusted to 2.5 with orthophosphoric acid): acetonitrile: methanol (62:28:10 % v/v/v). The flow rate kept was 1.0 mL/min opting isocratic mode and eluents were tracked down at 230 nm. The retention times for both the drugs were 1.38±0.21 and 2.98±0.41, respectively. Standard addition method was employed for the analysis of flupentixol dihydrochloride. ICH guidelines were followed to validate the method. The method assured linearity in concentration range of 50-150 μg/mL and 2.5-7.5 μg/mL for ESC and FLU, respectively. The method assured high degree of precision and accuracy. The method was proved to be robust by assessing robustness parameters.


2009 ◽  
Vol 92 (2) ◽  
pp. 680-688 ◽  
Author(s):  
Pei Chen ◽  
Renata Atkinson ◽  
Wayne R Wolf

Abstract The purpose of this study was to develop a single-laboratory validated (SLV) method using high-performance liquid chromatography with different detectors diode array detector (DAD); fluorescence detector (FLD); and mass spectrometry (MS) for determination of 7 B-complex vitamins (B1-thiamin, B2-riboflavin, B3-nicotinamide, B6-pyridoxine, B9-folic acid, pantothenic acid, and biotin) and vitamin C in multivitamin/multimineral dietary supplements. The method involves the use of a reversed-phase octadecylsilyl column (4 m, 250 2.0 mm id) and a gradient mobile phase profile. Gradient elution was performed at a flow rate of 0.25 mL/min. After a 5 min isocratic elution at 100 A (0.1 formic acid in water), a linear gradient to 50 A and 50 B (0.1 formic acid in acetonitrile) at 15 min was employed. Detection was performed with a DAD as well as either an FLD or a triple-quadrupole MS detector in the multiple reaction monitoring mode. SLV was performed using Standard Reference Material (SRM) 3280 Multivitamin/Multimineral Tablets, being developed by the National Institute of Standards and Technology, with support by the Office of Dietary Supplements of the National Institutes of Health. Phosphate buffer (10 mM, pH 2.0) extracts of the NIST SRM 3280 were analyzed by the liquid chromatographic (LC)-DAD-FLD/MS method. Following extraction, the method does not require any sample cleanup/preconcentration steps except centrifugation and filtration.


2020 ◽  
Vol 11 (3) ◽  
pp. 4660-4664
Author(s):  
Ridhi Joshi ◽  
Rishikesh Meena ◽  
Preeti Mishra ◽  
Vidya Patni

Medicinal plants produce various useful metabolites such as alkaloids, flavonoids, tannins etc those are widely used for the preparation of various pharmaceutical products, or as food additives. A simple and precise reverse phase high performance liquid chromatographic (RP-HPLC) seperation method has been developed for determination and quantification of the flavonoids, quercetin and luteolin simultaneously, from methanolic extracts of Merremia aegyptia and Merremia dissecta after optimization of extracting solvent and chromatographic conditions through HPLC coupled to a Diode Array Detector(DAD). HPLC analysis estimated contents of the quercetin to be 20 ng/µl in M. aegyptia stem and 13.2 ng/ µl in M. dissecta callus whereas luteolin was found to be 0.4 mg/ml in M. dissecta callus. From the previous published literature, it appears that this is the first report of quantification of these flavonoid compounds as they have not been reported earlier in both the species under study.


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