Improved method for the determination of the cortisol production rate using high-performance liquid chromatography and liquid scintillation counting

Two new methods for the determination of the cortisol production rate using reversed-phase high-performance liquid chromatography are described. One uses ultraviolet detection at 205 nm, the other on-line post-column derivatization with benzamidine, followed by fluorimetric detection. The specific activity of tetrahydrocortisol and tetrahydrocortisone in urine from patients who had received tritium-labelled cortisol was determined by the indicated methods, followed by fraction collection and liquid scintillation counting. The post-column reaction detection procedure was superior to ultraviolet detection, both in selectivity and analysis time. Intra- and inter-assay variance of the post-column reaction detection procedure were 3.7 and 4.7%, respectively. A good correlation (r = 0.99) was obtained between values determined by this procedure and by a thin-layer chromatographic procedure.     

Determination of cisplatin and related platinum complexes in plasma ultrafiltrate and urine by high-performance liquid chromatography with on-line radioactivity detection

A reversed-phase ion-pair chromatographic method with on-line radioactivity detection for the simultaneous determination of 195mPt-labelled cisplatin and related platinum complexes has been developed. With this system a good resolution of various radiolabelled platinum complexes can be achieved. The detection limit of the radioactivity detector is 10 ng of cisplatin (specific activity of 15 MBq/mg cisplatin) per millilitre of urine or plasma ultrafiltrate. The detector response is independent of both the chemical structure of the platinum complexes and the matrix composition of the samples. This method may serve as a reference system for other high-performance liquid chromatographic systems with less specific and sensitive detectors.     

Approaches to enhancing the sensitivity of capillary electrophoresis methods for the determination of inorganic and small organic anions

One of the major problems facing the development of capillary electrophoresis (CE) is the relatively high limits of detection when compared to traditional high-performance liquid chromatographic (HPLC) methods. While the use of an alternative detector can offer better sensitivity, a more universal approach is sample preconcentration. Numerous on-line methods have been developed to improve the sensitivity of CE, and are based on electrophoretic principles, chromatographic principles, or a combination of both. This review will discuss all forms of on-line preconcentration methods for CE, with emphasis given to those that have shown particular merit when applied to inorganic and small organic anions.     

Analysis of Dehydroabietic Acid in Kraft Mill Effluents by High-Performance Liquid Chromatography

Abstract

A rapid high-performance liquid chromatographic method for the determination of dehydroabietic acid in kraft mill effluent is described. Selective solvent extraction of the samples with dichloromethane was performed. The samples were isocratically analysed on a Rad-Pak C18 column using 75% acetonitrile in water (0.1% acetic acid added). Detection was carried out at 220 nm and 267 nm on a variable wavelength detector with a detection limit of 0.01 mg/L.     

Determination of urinary normetanephrine, metanephrine and 3-methoxytyramine by high-performance liquid chromatography with electrochemical detection: comparison between automated column-switching and manual dual-column sample purification methods.

This report describes a high-performance liquid chromatographic method with electrochemical detection for the simultaneous quantitation of urinary metanephrine, normetanephrine and 3-methoxytyramine. This method, which involves manual dual-column purification steps for the routine determination of urinary metanephrines, is compared with the previously used spectrophotometric Pisano method and an on-line sample preparation procedure, where the automated sequential trace enrichment (ASTED) apparatus is used for the column-switching procedure. In order to automate the metanephrine assay, the enrichment technique was evaluated against the reference chromatographic method. Bio-Rad urine controls gave coefficients of variation of less than 9% at all levels for the reference method. Values of less than 19% were found in the reference range with the enrichment method, and the recovery of 3-methoxytyramine was also too poor to be measured in normal concentrations. The linearity of both methods is sufficient to determine pathological levels of these biogenic amines. Future developments should be focused on decreasing the variation of between-day assays in an on-line, automated procedure.     

Gas chromatographic assay for oxcarbazepine and its main metabolites in plasma

The new anti-epileptic drug oxcarbazepine is temperature-labile and decomposes under the conditions of gas chromatography, even when injected into a cooled, inert, fused-silica capillary column. In contrast, the trimethylsilyl derivative of oxcarbazepine is stable. The bis-trimethylsilyl derivatives of the enol of oxcarbazepine and of its active metabolite, 10-hydroxycarbazepine, and the tris-trimethylsilyl derivative of carbazepine-10,11-trans-diol can be synthesized easily at room temperature. Using the readily available carbamazepine as internal standard, a simple gas chromatographic assay was developed for the simultaneous routine measurement of these three compounds at therapeutic levels. This assay is ten times more sensitive to oxcarbazepine than the previously described high-performance liquid chromatographic assays. It involves a single-step solvent extraction, uses a fused-silica capillary column and a flame ionization detector. On processing 0.5 ml of plasma, limits of detection of 10 ng/ml were obtained for oxcarbazepine and 10-hydroxycarbazepine and a limit of detection of 25 ng/ml for carbazepine-10,11-trans-diol.     

Analysis of Norethindrone In Plasma by High-Performance Liquid Chromatography

Abstract

A sensitive specific high-performance liquid chromatographic procedure for the determination of norethindrone in plasma is described. The organic solvent extract from plasma is chromatographed on a reversed phase column using a high-performance liquid chromatograph fitted with an ultraviolet detector (254 nm); quantitation from plasma samples containing 2 ng/ml norethindrone is reported. Metabolites and endogenous substances do not interfere with the assay. The determination of norethindrone concentrations in plasma following administration of single oral dose to a mini-pig is described.     

Characterization of a poly(ethersulphone) by on-line coupling of size exclusion chromatography with NMR and FTIR spectroscopy

An on-line detection „on the flow”︁ during the size exclusion chromatography run using FTIR and NMR spectrometers was applied to investigate the liquid chromatographic separation process of oligomers and to identify the separated chromatographic compounds. The FTIR and NMR detectors give real-time information about the chemical structure and functional groups of the eluated species. The preferences and limits of the on-line coupling were discussed using an oligomeric hydroxyl terminated poly(ethersulphone) as an example. Molecular weights could be calculated from the ¹H-NMR spectra of the separated species using the intensities of end-group and main-chain signals. Residues of N-methylpyrrolidone which was used as solvent in the oligomer synthesis were identified by the FTIR detector.     

Measurement of penicillamine and N-acetylcysteine in human blood by high-performance liquid chromatography and electrochemical detection

A rapid and precise high-performance liquid chromatographic assay for both N-acetylcysteine and penicillamine in blood samples is described using selective reductive electrochemical detection and a high-efficiency C18 reversed-phase column. The use of an internal standard compensated for changes in detector responses during a run and for variable sample recovery. The detection limits for N-acetylcysteine and penicillamine were 25 and 10 ng/ml, respectively, using 500-microliters blood samples. Reproducibility of measurement for both thiols was excellent. This method allows routine monitoring of blood levels and pharmacokinetic studies with N-acetylcysteine and penicillamine.     

High-performance liquid chromatography applications of optical rotation detection with compensation for scattering and absorbance at the laser wavelength.

Use of instrumentation developed to enable simultaneous monitoring of optical rotation (OR) and transmittance allows OR measurements to be made in the presence of high levels of absorbance, scattering or other effects that change the intensity of the plane-polarised light at the photodiode detector. This extends the application of OR detection to areas where it was previously difficult. Examples of the application of high-performance liquid chromatography (HPLC) with the improved OR detector include (i) the analytical scale separation of fructose and sucrose and (ii) the semi-preparative separation of enantiomers of warfarin and Tr?gers base. A signal-to-noise improvement of up to 150% is found when comparing signals with and without correction for transmittance changes. The improved OR detector has been used in series with a UV detector and the system shown to be suitable for on-line measurement of peak purity in separations using a chiral column under overload conditions.     

Determination of plasma tranexamic acid using cation-exchange high-performance liquid chromatography with fluorescence detection

A procedure is described for the determination of plasma tranexamic acid concentrations using cation exchange high-performance liquid chromatography with fluorescence detection following post-column derivatisation with omicron-phthalaldehyde. The chromatographic conditions were optimised with respect to detector performance and the method applied to measuring the plasma tranexamic acid levels of patients in a double-blind trial.     

Urinary Uric Acid Determination by Reversed-Phase High-Performance Liquid Chromatography with Electrochemical Detection

Abstract

Determination of urinary uric acid has been attempted by reversed-phase high-performance liquid chromatography with electrochemical detection. We have found that the electrochemical detection method is suitable for monitoring eluate from reversed-phase column and also that the minimum detectable quantity of uric acid using en electrochemical detector is about 10 pg. Complete separation of uric acid was achieved in about 8 min under the present chromatographic conditions.     

High-performance liquid chromatographic separation of femtomolar quantities of endogenous carboxylic acids, including arachidonic acid metabolites, as 4-bromomethyl-7-acetoxycoumarin derivatives

A major limitation of high-performance liquid chromatographic techniques for measuring biologically active eicosanoids has been the inadequate sensitivity of most on-line detection systems. In addition, the availability of a technique suitable for measuring small quantities of non-esterified fatty acids (NEFAs) in plasma would allow longitudinal studies of plasma levels of these lipids in small animals. To improve the sensitivity of detection, the compounds with acyl groups containing carboxylic acids were derivatized with the highly fluorescent compound, 4-bromomethyl-7-acetoxycoumarin. All classes of NEFA and arachidonic acid metabolites, including the cyclooxygenase and lipoxygenase products, and hydroxy acid compounds could be derivatized with this reagent. The derivatized metabolites were separated with a reversed-phase high-performance liquid chromatographic system using a radial compression column and a gradient elution technique. Reproducible measurements of plasma NEFAs from as little as 5 microliters of plasma, and femtomolar concentrations of eicosanoids, could be detected using an on-line fluorescent spectrometer. This improvement in sensitivity should permit the quantification of all eicosanoids, including the leukotrienes, in biologic fluids and the longitudinal measurement of changes in plasma NEFA levels in small animals.     

Urinary selenium speciation by high-performance liquid chromatography-inductively coupled plasma mass spectrometry: advantages of detection with a double-focusing mass analyser with a hydride generation interface

A detailed comparison of the performance of inductively coupled plasma mass spectrometry (ICP-MS), with quadrupole and double-focusing instruments for the speciation of selenium in urine has been carried out. Selenium sensitivity about 23-59 times higher with double-focusing ICP-MS detection was observed, but limits of detection were only 1-8.7 times better because of background noise. Selenium species separation has been carried out by both reversed-phase and vesicle-mediated high-performance liquid chromatography (HPLC), coupled on-line with the detector via conventional nebulization and via on-line focused microwave digestion-hydride generation. A remarkable improvement in sensitivity (28-110 times better for (77)Se depending on the chromatographic system) and elimination of interference problems from the urinary matrix or the components of the mobile phases were achieved when an on-line microwave digestion-hydride generation interface was used, but the background noise was much higher than with conventional nebulization. Therefore, the limits of detection were not as low as expected from such improvement in the sensitivity. More selenocompounds can be separated, and a slight improvement in the sensitivity and limits of detection was obtained when the vesicle-mediated HPLC system was used as compared with reverse-phase chromatography. However, the use of several complementary chromatographic systems, such as reverse-phase HPLC, is recommended to bring some light on the selenocompounds present in basal human urine. Comparative data of rat urine speciation are also given.     

Analysis of terbutaline in human plasma by high-performance liquid chromatography with electrochemical detection using a micro-electrochemical flow cell.

A high-performance liquid chromatographic method is described for the determination of terbutaline in human plasma in the range 1-35 ng/ml. Detection was achieved using a carbon fibre micro-electrochemical detector and a column-switching system. The microelectrode cell has advantages over conventional glassy carbon electrode-based detection systems in that it is easy to prepare, flexible in its operation and suffers less trouble from problems such as air bubbles and leaks. Furthermore, it has a better detection limit for terbutaline (0.8 ng/ml) to that obtained using a conventional glassy carbon electrode flow detector (2 ng/ml). Sample clean-up was by on-line solid-phase extraction with column switching, providing a method which was sensitive and reproducible, where the mean overall coefficient of variation was 5.60% and drug recovery in excess of 86% at the concentration levels studied.     

Metabolic studies of explosives. II. High-performance liquid chromatography-mass spectrometry of metabolites of 2,4,6-trinitrotoluene

A series of metabolites of 2,4,6-trinitrotoluene were studied by combined high-performance liquid chromatography-mass spectrometry. These metabolites are formed mainly by oxidation and reduction processes. Separations were done on a C8 reversed-phase column, using acetonitrile-water at various relative concentrations as mobile phases, followed by ultraviolet and on-line mass spectrometry with a direct liquid insertion probe liquid chromatograph-mass spectrometer interface. The mass spectra obtained were chemical-ionization spectra with the mobile phase as reagent. Mass spectra obtained included mainly reduced ions, adduct ions and typical fragment ions. The combination of high-performance liquid chromatographic separation with on-line mass spectrometry was found to be a suitable method for the identification of the investigated metabolites.     

Coupled LC-GC-MS for on-line clean-up,separation, and identification of chlorinated polycyclic aromatic hydrocarbons at picogram levels in urban air

Coupled liquid chromatography – gas chromatography – mass spectrometry (LC-GC-MS) has been applied for on-line clean up, separation, and identification of chlorinated polycyclic aromatic hydrocarbons (CI-PAHs). A loop-type interface was used to couple the liquid chromatograph on-line with the GC-MS, and concurrent solvent evaporation was used for sample transfer. A back-flush technique was used in conjunction with a two-dimensional column system for isolation of CI-PAHs and polycyclic aromatic hydrocarbons (PAHs). This fraction was transferred on-line to the GC and separated on a capillary column. Selective and sensitive detection of CI-PAHs in the GC eluate was obtained by negative ion chemical ionization (NICI) mass spectrometry and selected ion monitoring (SIM). The combined on-line system for isolation, separation, and identification showed high precision and accuracy, and demonstrated a linear response from 1 to 1000 pg for chlorinated PAHs. The estimated detection limit was 250 fg for 1-chloropyrene and 1,6-dichloropyrene. The technique was demonstrated by analysis of urban air samples. The low detection limit made it possible to use the technique for analysis of personally carried monitoring equipment for measurement of exposure to CI-PAHs in the work environment.     

Sensitive method for the determination of vincristine in human serum by high-performance liquid chromatography after on-line column-extraction.

A column-switching high-performance liquid chromatographic method was developed for the determination of vincristine in serum. Sample preparation was carried out by means of on-line column-extraction, using a C18 reversed-phase preconcentration column. This technique is simple (minimizing manual sampling errors), rapid (reduction of time and costs) and can be easily automated. Both ultraviolet and electrochemical detection are possible, but the latter shows a cleaner chromatogram and is, by the use of a new electrochemical detector, far more sensitive (detection limit 0.3 microgram/l at a signal-to-noise ratio of 3). A matrix study was carried out (using human serum and urine and two kinds of calf's serum). Although it appeared that the system was matrix-dependent, no difference in matrix effects could be found in the serum or plasma of different patients. Controls for human serum analysis should be prepared in human serum. With the method described, pharmacokinetic studies of vincristine in children can be performed.     

The effects of eluent mixing on TLS detection in gradient elution HPLC

The effects of changing solvent composition on the LOD of TLS detection in gradient elution HPLC have been studied from the perspective of thermo-optical properties of the solvent. Hyphenated gradient high-performance liquid chromatography (HPLC)-thermal lens spectrometry (TLS), was used to separate and detect 13 carotenoid compounds and two chlorophylls. Utilization of mixing coils into the system reduces the inhomogeneities during eluent changes and therefore enables the application of thermal lens detection in the gradient HPLC method. For gradient chromatographic conditions in which the thermo-optical properties and related enhancement factor change as much as 50% over 10 min, the LODs for the TLS detector were enhanced by as much as three times in comparison with UV-Vis detection. For the isocratic part of the chromatogram, up to a tenfold improvement of LODs was achieved with TLS detection.     

On-line high-performance liquid chromatographic diode array spectrophotometric analysis of steroidal hormones in illegal preparations

An on-line high-performance liquid chromatographic diode array spectroscopic analytical method for the identification of more than 60 different steroidal compounds is described. For the chromatographic separation, a gradient elution that could distinguish the esterified and non-esterified steroids in the same run on a reversed-phase C18 column, using methanol as modifier, was developed. For both types of compound an internal standard was chosen to establish reproducible relative retention times that could be used as one element of the identification; the second element is the UV spectrum, which is recorded on-line during the separation. The combination of chromatographic and UV spectroscopic recordings selects only a few probable steroids, which could be the unknown. This approach has been applied to forensic analysis of illicit preparations used in cattle-breeding, some examples of which are shown. For those steroids that are very difficult to distinguish using this procedure, because of their chromatographic and spectroscopic similarity on this system, other solvent mixtures are used in place of methanol as modifier, namely acetonitrile or tetrahydrofuran, or both, with the same solvent strength, as proposed by Snyder. In this way totally different elution patterns and separations are obtained, providing complementary information for identification, as shown by the systematic analysis on two other isoeluotropic solvent systems.