Search results for "liquid"

Lignans from Torreya jackii identified by stopped-flow high-performance liquid chromatography–nuclear magnetic resonance spectroscopy

1999

Abstract Coupled reversed-phase HPLC–NMR spectroscopy has been applied to the rapid detection and identification of plant metabolites of Torreya jackii , a species of Taxaceae. Analysis consisted of gradient HPLC elution and directly coupled 1 H NMR (500 MHz) spectroscopic detection in a stopped-flow mode. Seven lignans were detected and their structures were elucidated, based on their HPLC– 1 H NMR spectra and MS data. The structures were confirmed by isolation of the single components followed by conventional NMR measurements.

Corrigendum to "Analysis of cannabinoids by liquid chromatography-mass spectrometry in milk, liver and hemp seed to ensure food safety" [Food Chem. 2…

2018

Prospects for Carbon as Packing Material in High-Performance Liquid Chromatography

1983

Abstract Early work on use of carbons for liquid chromatography shows that special carbons must be developed if carbon is to be useful in HPLC. The processes used to make carbons, the properties of such carbons and the requirements for HPLC carbons are discussed. The preparation of HPLC carbons is reviewed in detail and the results which have been obtained are assessed in terms of their kinetic and thermodynamic performance. Applications are reviewed.

High Submicellar Liquid Chromatography

2013

Surfactant addition above the critical micellar concentration (CMC), in reversed-phase liquid chromatography (RPLC), was proposed as a way to modify the selectivity and analysis time, giving rise to a chromatographic mode called micellar liquid chromatography (MLC). However, solutions containing only surfactant are too weak and yield poor peak shape. This was remediated by the addition of a small amount of organic solvent. To preserve the existence of micelles, in MLC high contents of organic solvent are avoided. Nevertheless, there is no reason to neglect the potentiality of mobile phases containing a surfactant above its CMC in water and a high organic solvent content (without micelles). …

Description of the Retention and Peak Profile for Chromolith Columns in Isocratic and Gradient Elution Using Mobile Phase Composition and Flow Rate a…

2014

The effect of the modifier concentration and flow rate on the chromatographic performance of a second generation Chromolith® RP-18e column, under isocratic and gradient elution with acetonitrile-water mixtures, was examined using four sulphonamides as probe compounds. The acetonitrile concentration was varied between 5 and 55% (v/v), and the flow rate between 0.1 and 5.0 mL/min, keeping the other factors constant. The changes in both retention and peak profile were modelled, and used to build simple plots, where the logarithm of the retention factor was represented against the modifier concentration (in gradient elution, against the initial modifier concentration), and the half-widths or wi…

Quantitative Bestimmung von Gelatine in Arzneizubereitungen durch HPLC mit fluorimetrischer Detektion

1986

Gelatine ist als pharmazeutischer Hilfsstoff fur Kapseln, Gele, Globuli und Tabletten sowie als Lebensmittelzusatzstoff unverandert wichtig. Aus Proteinen hoher Molekularmasse1 bestehend, ist Gelatine spezifischen quantitativen Bestimmungen relativ schwer zuganglich2-6.

Literature survey of the on-line preconcentration in flow-injection atomic spectrometric analysis

1992

The literature on the use of “on-line” preconcentration in flow injection atomic spectrometric analysis is reviewed, taking into account its application both in flame and electrothermal atomic absorption methods as well as in plasma emission spectrometry. The basis of the different preconcentration approaches, such as liquid-liquid extraction, column preconcentration and “on-line” precipitation are discussed. The literature survey reveals the analytical performance of the developed methodologies.

Comparative Study on the Determination of Cephalexin in its Dosage Forms by Spectrophotometry and HPLC with UV-vis Detection

1997

This paper discusses the spectrophotometric determination of cephalexin as the intact cephalexin or as its acid-induced degradation product. Cephalexin can be determined in the range 1 × 10−5−18 × 10−5M with relative standard deviations of 5-1%. The limits of quantitation and detection were 10−5 and 0.3 × 10−5M, respectively. These procedures were compared with reversed-phase HPLC determination. No interference was observed in the presence of common pharmaceutical adjuvants. The H-point standard additions method was applied in order to correct for the possible presence of the cephalexin precursor, 7-aminocephalosporanic acid; this improves the selectivity of the UV-vis spectrophotometric me…

Colorimetric method for the determination of vanadium with tannic acid in water and oils

1994

A new spectrophotometric method was developed to determine vanadium using tannic acid as a complexing reagent to form a coloured reaction product which can easily be extracted by 1-pentanol in the presence of cetylpyridinium. The developed method can successfully be applied to determine trace levels of 10 ng/ml of vanadium in natural waters without any preconcentration step. It can also determine less than 1 mg/kg of vanadium in edible oils and petroleum products.

A comparison of various calibration techniques applied to the ninhydrin-cefoxitin determination

1996

Abstract This report deals with spectrophotometric determination of cefoxitin from intact antibiotics or from its acid induced degradation product by means of their reaction with ninhydrin in a strong sulphuric acid medium. To obtain the calibration graphs four methods were used: absorbance of reacted cefoxitin against a reagent blank as an analytical signal, first-derivative signal of absorbance against a water blank as an analytical signal, first-derivative signal of absorbance against a reagent blank as an analytical signal and the H-Point Standard Additions Method (HPSAM) by using absorbance increment values as analytical signals. The HPSAM is applied to the determination of cefoxitin i…