High precision liquid chromatography

HPLC High-Precision Liquid Chromatography or High-Pressure Liquid Chromatography... 

HPLC-MS High-precision liquid chromatography None Mass spectrometry... 

The concentration profiles of the reactant and the products were monitored by means of high precision liquid chromatography (HPLC), equipped with a Biorad Aminex HPX-87C carbohydrate column according to the method described in [4]. 

R. J. Caimi and J. T. Brenna, High-precision liquid chromatography-combustion isotope ratio mass spectrometry. Anal Chem. 65, 3497-3500 (1993)... 

As a consequence of the previous considerations Kieber et al. [75] have developed an enzymic method to quantify formic acid in non-saline water samples at sub-micromolar concentrations. The method is based on the oxidation of formate by formate dehydrogenase with corresponding reduction of /3-nicotinamide adenine dinucleotide (j6-NAD+) to reduced -NAD+(/3-NADH) jS-NADH is quantified by reversed-phase high performance liquid chromatography with fluorimetric detection. An important feature of this method is that the enzymic reaction occurs directly in aqueous media, even seawater, and does not require sample pre-treatment other than simple filtration. The reaction proceeds at room temperature at a slightly alkaline pH (7.5-8.5), and is specific for formate with a detection limit of 0.5 im (SIN = 4) for a 200 xl injection. The precision of the method was 4.6% relative standard deviation (n = 6) for a 0.6 xM standard addition of formate to Sargasso seawater. Average re-... 

High-performance liquid chromatography is also called high-precision and high-pressure liquid chromatography. 

The isocratic system (Fig. 1.2 (a)) provides an economic first step into high-performance liquid chromatography techniques. The system is built around a high-performance, dual-piston, pulse-free pump providing precision flow from 0.01 to 5ml min-1. 

Lanina et al. 1992 Oishi 1990). These methods include gas chromatography (GC) combined with mass spectrometry (MS) and high-performance liquid chromatography (HPLC) combined with an ultraviolet detector (UV). No comparisons can be made between methods since no data were given regarding sensitivity, recovery, or precision. 

High-performance liquid chromatography (HPLC), followed by GC/MS, has been used to fractionate and then quantitate the aliphatic and aromatic hydrocarbons present in liquid fuel precursors in order to determine the fuel potential of the compounds. Kerosene had the advantage of not requiring any sample preparation. Other light fuel oils may require the use of methylene chloride as a solvent prior to HPLC analysis (Lamey et al. 1991). The sensitivity, precision, and recovery of this method were not reported. 

Capable of the same quantitative accuracy and precision as high-pressure liquid chromatography (HPLC), particularly when used in conjunction with an internal... 

The combination of high-pressure liquid chromatography (HPLC) with monitoring by UV/visible detection provides an accurate, precise and robust method for quantitative analysis of pharmaceutical products and is the industry standard method for this purpose. 

When seeking a tool which could be used to determine the biological activity of mixture components in a more precise way, researchers directed their attention towards high-performance liquid chromatography (HPLC). Its advantage over TLC is its higher resolution, which helps to avoid false results caused by the co-elution of different compounds. 

The application of atomic spectroscopic instruments as element-specific detectors in chromatography has been reviewed by van Loon More recently, Krull has extensively reviewed their use in high pressure liquid chromatography (HPLC). Atomic spectrometry has found wide acceptance in the field of liquid chromatography because, in most cases, the fractions can be directly analysed after elution from the column. However, it is possible to use the technique for the analysis of solid samples without first dissolving the matrix. This is particularly useful after electrophoresis, where the fractions are fixed either in a gel or on paper. Kamel et al. have shown that it is possible to cut the appropriate sections and insert them into the carbon furnace for analysis. The disadvantage of this approach is that the precision is usually poorer (about 10%) and it is difficult to calibrate the instrument. Nevertheless, this approach is very useful if it is used for qualitative speciation. 

A method for the determination of personal exposure to benzidine-based dyes has been developed. This procedure involved the reduction of benzidine-based dye filter samples to free benzidine with neutral buffered sodium hydrosulfite solution. The benzidine-containing reduction solution was then analyzed by high performance liquid chromatography. The reduction was found to be quantitative by visible-spectrum analysis. This reduction and analysis method was evaluated with four benzidine-based dyes over the range from 12 to 300 micrograms per sample. Precision for the reduction and analysis of the four dyes falls within % coefficient of variation. This method can differentiate between benzidine-and benzidine congener-based dyes. Results are reported in terms of free benzidine. 

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