High temporal resolution delayed analysis of clinical microdialysate streams.

This paper presents the use of tubing to store clinical microdialysis samples for delayed analysis with high temporal resolution, offering an alternative to traditional discrete offline microdialysis sampling. Samples stored in this way were found to be stable for up to 72 days at -80 °C. Examples of how this methodology can be applied to glucose and lactate measurement in a wide range of in vivo monitoring experiments are presented. This paper presents a general model, which allows for an informed choice of tubing parameters for a given storage time and flow rate avoiding high back pressure, which would otherwise cause the microdialysis probe to leak, while maximising temporal resolution.

Bicarbonate-sensitive cysteine induced elevation of extracellular aspartate and glutamate in rat hippocampus in vitro.

The effect of different concentrations of cysteine (0.125, 0.25, 0.5 and 1 mM) on the net efflux of endogenous amino acids was studied by the incubation of rat hippocampal slices. Addition of cysteine (1 mM) in bicarbonate containing low K+ medium (5 min) selectively increased the basal net efflux of glutamate and aspartate by 370% and 396%, respectively. High K+ media (50 mM) containing cysteine (1 mM) evoked the net efflux of glutamate and aspartate by 1454% and 1019%, respectively. The corresponding effects in control slices without cysteine were 669% and 404%, respectively. No changes were observed on the concentrations of GABA, glutamine and taurine. The cysteine oxidation products, cysteine sulfinate (0.5 microM) and cystine (0.25 mM) were without effects. The effect of cysteine (0.5 mM) was dramatically reduced in media with no added bicarbonate/CO2. Thus, cysteine in a bicarbonate-sensitive manner selectively increases the extracellular concentration of excitotoxic amino acids in adult rat brain in vitro, possibly by interfering with the carrier-mediated glutamate uptake/release.

Tris(2,2'-bipyridine)ruthenium (II) as a peroxide-producing replacement for enzymes as chemical labels.

The concentration of the ruthenium-based label is determined from the rate of hydrogen peroxide production elicited by photolysis. Electron transfer quenching of the photoexcited label by methyl viologen (1,1'-dimethyl-4,4'bipyridinium dication, MV2+) and/or oxygen in the presence of EDTA generates hydrogen peroxide. Both flow injection and direct photolysis techniques were tested, with the latter showing better results. Direct photolysis is more sensitive, faster, requires only a 20 microliters sample volume, uses only 30 mW laser power and shows a smaller background. The presence of 5% normal human serum in the sample did not interfere with the measurements. Linear calibration curves were obtained in the nanomolar concentration range for goat antimouse antibody labeled with the ruthenium complex. The determination of membrane-surface-bound labeled IgG is accomplished by direct photolysis of a membrane that covers a platinum microelectrode.

Net efflux of cysteine, glutathione and related metabolites from rat hippocampal slices during oxygen/glucose deprivation: dependence on gamma-glutamyl transpeptidase.

Extracellular metabolism of the protective substance glutathione (gamma-glutamyl-cysteinyl-glycine) may generate cysteine, glycine, several gamma-glutamyl-containing dipeptides and possibly free glutamate, all of which could participate in neurotoxicity. In the present study, we have examined how blockage of gamma-glutamyl transpeptidase, the key enzyme in glutathione degradation, influences the extracellular concentrations of glutathione, cysteine and related metabolites during anoxia/aglycemia of rat hippocampal slices. The net efflux, i.e., the increase in extracellular concentration due to changes in release and/or uptake, of cysteine, cysteine sulfinate, gamma-glutamyl-glutamate, gamma-glutamyl-glutamine, glutathione, gamma-glutamyl-cysteine and glutamate increased as a result of anoxia/aglycemia. These increases in net efflux of cysteine, cysteine sulfinate, gamma-glutamyl-glutamate and gamma-glutamyl-glutamine were reduced or blocked by acivicin, an inhibitor of gamma-glutamyl transpeptidase. In contrast, acivicin caused an increase in both basal and anoxia/aglycemia-induced net efflux of glutathione whereas the basal and anoxia/aglycemia-induced efflux of glutamate was unchanged by acivicin treatment. The effect of acivicin on the efflux of gamma-glutamyl-cysteine was similar to that of glutathione although less pronounced. Addition of beta-mercaptoethanol to the incubation medium during and after 30 min of anoxia/aglycemia decreased the net efflux of cysteine sulfinate specifically, indicating that the increase in cysteine sulfinate during anoxia/aglycemia may be partly derived from the spontaneous oxidation of cysteine. The results suggest that gamma-glutamyl transpeptidase may be involved in the regulation of the extracellular concentrations of cysteine, several gamma-glutamyl-containing dipeptides and glutathione but not glutamate during ischemia.

Alterations in glutathione and amino acid concentrations after hypoxia-ischemia in the immature rat brain.

Hypoxic-ischemic brain injury involves an increased formation of reactive oxygen species. Key factors in the cellular protection against such agents are the GSH-associated reactions. In the present study we examined alterations in total glutathione and GSSG concentrations in mitochondria-enriched fractions and tissue homogenates from the cerebral cortex of 7-day-old rats at 0, 1, 3, 8, 14, 24 and 72 h after hypoxia-ischemia. The concentration of total glutathione was transiently decreased immediately after hypoxia-ischemia in the mitochondrial fraction, but not in the tissue, recovered, and then decreased both in mitochondrial fraction and homogenate after 14 h, reaching a minimum at 24 h after hypoxia-ischemia. The level of GSSG was approximately 4% of total glutathione and increased selectively in the mitochondrial fraction immediately after hypoxia-ischemia. The decrease in glutathione may be important in the development of cell death via impaired free radical inactivation and/or redox related changes. The effects of hypoxia-ischemia on the concentrations of selected amino acids varied. The levels of phosphoethanolamine, an amine previously reported to be released in ischemia, mirrored the changes in glutathione. GABA concentrations initially increased (0-3 h) followed by a decrease at 72 h. Glutamine levels increased, whereas glutamate and aspartate were unchanged up to 24 h after the insult. The results on total glutathione and GSSG are discussed in relation to changes in mitochondrial respiration and microtubule associated protein-2 (MAP2) which are reported on in accompanying paper [64].

Molecular recognition of phenobarbital in plasticizers equilibrium investigations on the solubility of the barbiturate artificial receptor and its binding to phenobarbital in plasticizers.

Environmental concern is renewing interest in selective, waste-free extractions. A recent report demonstrated an improved extraction of phenobarbital by means of a specifically designed molecular receptor. In that work, the solvent was CHCl3. The current work is the first step in extending extractions based on molecular recognition to reusable solvents, namely plasticizers. Phenobarbital aqueous/organic partition coefficients, receptor solubility, and phenobarbital-receptor-formation constants in several plasticizers and in their CHCl3 solutions are reported. In addition, by a thermodynamic cycle, the free energy for transfer of the barbiturate-receptor complex from CHCl3 to plasticizers has been calculated. Finally, the data have been displayed in coordinate systems representing extraction efficiency and selectivity. The most selective extraction medium yielding useful extraction efficiency is dioctyl phthalate.

Sensitivity and selectivity of the electrochemical detection of the copper(II) complexes of bioactive peptides, and comparison to model studies by rotating ring-disc electrode.

Post-column reaction of peptides with Cu(II) can be used for the electrochemical detection of peptides as their biuret complexes. Understanding of the behavior (sensitivity at the anode and cathode in the dual-series electrochemical detector) of the system is facilitated through the observation of the rotating ring disc voltammetry of some model compounds. In operation, the anodic signal from the oxidation of the Cu(II)-peptide to the Cu(III) form can be used to detect peptides, or the downstream cathode can be used to detect the Cu(III) form. The signals appear at about 0.4 V (anode) for tetra- and longer peptides, 0.65 V for tripeptides. The anode signal is augmented by tyrosine (oxidation at 0.4-0.5 V) and tryptophan (0.5-0.6 V). If the cathode is used as the detector in a two working electrode cell, the sensitivity depends on the stability of the Cu(III) product. This is peptide dependent, but the signal is significant and useful analytically. Twenty-three bioactive peptides in two groups, naturally electrochemically active and naturally electrochemically silent, and several model compounds have been studied. Both naturally electrochemically active peptides (contain tyrosine and/or tryptophan) and naturally electrochemically silent peptides have been studied. Chromatography with an acetonitrile gradient has been used to separate the peptides in each group. Detection limits are for non-electroactive peptides in the range of 16-100 fmol (10- microliters injection 1.6-10 nM, 100 microliters injection 0.16-1.0 nM), and for electroactive peptides in the range of 6-40 fmol (0.6-4.0 nM for a 10- microliters injection and 60-400 pM for a 100- microliters injection). A tryptic digest of bovine cytochrome c is easily seen at 100 nM.

Optimization of a modified electrode for the sensitive and selective detection of alpha-dipeptides.

Sensitive and selective detection of dipeptides is important in neurochemistry. We have developed a flexible detection scheme for dipeptides based on a modified carbon electrode. The modification arises from the anodic treatment of the carbon electrode in alkaline solution. The flexibility of the detection scheme arises from the different conditions used in both the modification and the detection. It is shown that the modification step requires the presence of cupric ion, while the detection step does not. On the other hand, it is shown that the presence of copper in the detection eluent, as well as the pH of the environment, can be used in controlling the selectivity of the modified electrode. For example, the modified electrode is more selective for alpha-dipeptides over beta- and gamma-dipeptides as well as amino acids at pH 9.8, whereas it is selective for all dipeptides over amino acids at pH 8.0. Detection limits of dipeptides on the order of 10 nM were achieved at pH 8.0 by flow-injection analysis with a knotted Teflon tubing connecting the injector and the detector that gave a typical peak volume of about 0.50 ml at 1.0 ml/min. From surface analysis it is shown that the oxygenation of the glassy carbon electrode gives rise to the selectivity. The oxidation of dipeptides at the modified electrode is completely inhibited by 10 mM Mg2+ in the eluent.

Fluorescence, photodestruction, photoionization and thermal degradation of o-phthalaldehyde/beta-mercaptoethanol-labelled aliphatic alpha-oligopeptides.

Photophysical and photochemical properties of o-phthalaldehyde/beta-mercaptoethanol-labelled aliphatic alpha-peptides were investigated. It is found that alpha-peptide derivatives have lower fluorescence quantum yields, higher photodestruction quantum yields and lower yields for formation of solvated electrons as compared to amino acid and simple alkylamine derivatives in aqueous alkaline solution. These properties of the alpha-peptide derivatives sets narrow limits for their utilization in laser-based (high light intensity) detector systems. In contrast, the thermal stability of the peptide derivatives was found to be severalfold higher than for the parent amino acid derivatives. The differential rates of thermal derivative degradation could be utilized in a new approach towards selective determination of peptides. determination of peptides. determination of peptides.

Theoretical and experimental studies of electrostatic effects in reversed-phase liquid chromatography.

Electrostatic effects are important in many reversed-phase liquid chromatographic separations involving surfactants and ion-pair reagents. To give better understanding of such systems the Poisson-Boltzmann equation has been solved for two cases. The first is that of an infinitely long cylinder with charge density on the inner wall, and two phases in the interior, one in the center and the other around it. Salts with ions of various solubilities in each phase may be present. The solution is obtained for the low-potential case (Deltapsie / kT 1). The second case is that of a planar sandwich, wall/phase 1/phase 2/phase 1/wall, with the same chemistry as case 1 but without the low-potential restriction. In case 2, there is also a Langmuir adsorption isotherm for each ion. The theory shows that the information gained from the Stern-Gouy-Chapman theory, which is mathematically semi-infinite, only applies when the diffuse layer thickness is much smaller than the pore radius, an unlikely circumstance in chromatography. The volume-averaged electrostatic potential difference can be measured experimentally with the solutes ø(4)Si, ø(4)As(+), ø(4)B(-) (ø = phenyl). The results are in agreement with theory. They show that the electrostatics of the system is dominated by fixed charges on the silica when the salt present is insoluble in the stationary phase, but when ions with some solubility in the stationary phase are used, mixed effects are obtained.

Development of a liquid chromatographic method for picomole determination of S-sulfocysteine in trifluoroacetic acid extracts of neonatal rat brain.

Neonatal Sprague Dawley rat brain tissue was extracted with methanol, acetonitrile, acetic acid and trifluoroacetic acids (TFA). Among the extractants tested, 0.1 M TFA gave the highest recovery, 73.4 +/- 5.2% (slope of regression of 'added' vs. 'found' and standard error of the slope) of S-sulfocysteine (SSC). The poorest recovery of SSC was found with acetonitrile and 90% methanol extractions (less than 10%). Possible reasons for the low recoveries have been explored. The recovery of SSC from aqueous standards in 0.1 M TFA is 92 +/- 5%. Detection of picomole quantities of SSC has been demonstrated with a combination of the optimized extraction procedures and our previously developed detection system. Supernatant of rat brain homogenate (0.10 M TFA as extractant) was evaporated to dryness in a vacuum centrifuge. Residues were reconstituted with deionized water. Samples were separated on a reversed phase column. The mobile phase was 20 mM aqueous acetate buffer (pH 5.2) containing 0.40 mM cetyl trimethylammonium p-toluene sulfonate and 2 vol.% methanol. Electrochemical detection used dual series gold-mercury amalgam electrodes. For the first time, S-sulfocysteine was detected in normal neonatal rat brain. Its concentration is 0.99 +/- 0.25 pmol/mg brain tissue. The results indicate that TFA, rarely reported an an extractant, efficiently recovers SSC from rat brain tissues.

Determination of the pharmaceutical peptide TP9201 by post-column reaction with copper(II) followed by electrochemical detection.

An electrochemical detection method was applied to the determination of the synthetic peptide TP9201 (Telios Pharmaceuticals). The method utilizes reversed-phase HPLC, followed by post-column formation of Cu(II)-peptide complexes to render peptides electrochemically active via the Cu(III/II) couple. TP9201 is cyclic and N-amidated; the lack of a free amine precludes the use of typical fluorescent labeling reagents. Neither the cyclic structure nor the N-amidation prevented the copper complexation reaction, however. The detection limit in bovine serum was 20 nM, limited by interfering sample peaks, and the detector response was linear in a range 10-400 nM.

Selectivity in micellar chromatography using a zwitterionic surfactant.

This work discusses the effects of neutral zwitterionic micelles composed of N-dodecyl-N,N-dimethylammonium-3-propane-1-sulfonate (C12DAPS) on the retention of several substituted benzene compounds. The correlation of molecular properties and retention demonstrates that negative charge, hydrophobicity, and polarizability are important in governing a solute's distribution in the micelles. The selectivity of the micelles differs from that of the native reversed-phase stationary phase, especially for nitrophenol isomers and halobenzenes.

Electroosmotic push-pull perfusion: description and application to qualitative analysis of the hydrolysis of exogenous galanin in organotypic hippocampal slice cultures.

We demonstrate here a method that perfuses a small region of an organotypic hippocampal culture with a solution containing an enzyme substrate, a neuropeptide. Perfusate containing hydrolysis products is continually collected and subsequently analyzed for the products of the enzymatic degradation of the peptide substrate. The driving force for perfusion is an electric field. The fused silica capillaries used as "push" and "pull" or "source" and "collection" capillaries have a ζ-potential that is negative and greater in magnitude than the tissue's ζ-potential. Thus, depending on the magnitudes of particular dimensions, the electroosmotic flow in the capillaries augments the fluid velocity in the tissue. The flow rate is not directly measured; however, we determine it using a finite-element approach. We have determined the collection efficiency of the system using an all d-amino acid internal standard. The flow rates are low, in the nL/min range, and adjustable by controlling the current or voltage in the system. The collection efficiency of the d-amino acid peptide internal standard is variable, increasing with increased current and thus electroosmotic flow rate. The collection efficiency can be rationalized in the context of a Peclet number. Electroosmotic push-pull perfusion of the neuropeptide galanin (gal1-29) through the extracellular space of an organotypic hippocampal culture results in its hydrolysis by ectopeptidase reactions occurring in the extracellular space. The products of hydrolysis were identified by MALDI-MS. Experiments at two levels of current (8-12 µA and 19-40 µA) show that the probability of seeing hydrolysis products (apparently from aminopeptidases) is greater in the Cornu Ammonis area 3 (CA3) than in the Cornu Ammonis area 1 (CA1) in the higher current experiments. In the lower current experiments, shorter peptide products of aminopeptidases (gal13-29 to gal20-19) are seen with greater frequency in CA3 than in CA1 but there is no statistically significant difference for longer peptides (gal3-29 to gal12-29).

Assessment of tissue viability following electroosmotic push-pull perfusion from organotypic hippocampal slice cultures.

We have developed a novel sampling technique that allows both introduction and removal of fluid from the extracellular space of living tissue. This method is based on the fluidics of push-pull perfusion but flow is driven by electroosmosis. We have applied this method to organotypic hippocampal cultures. A source capillary is inserted into the tissue and a collection capillary is in contact with the tissue surface through a thin layer of fluid. A voltage is applied across the proximal ends of source and collection capillary. In the applied field, fluid will move from source, into the tissue, and then be collected. In this process, damage to cells may occur. To understand better what sampling conditions influence damage most, we tested various sampling geometries and applied voltages, quantifying damage 16-24 h later using propidium iodide as a cell death marker. We found that damage correlates with both voltage drop and power dissipated in the tissue, but that voltage drop is a better indicator of damage when comparing models in which capillary arrangement and length are different.

Signal-to-noise ratio in microelectrode-array-based electrochemical detectors.

The signal-to-noise ratio at an electrode array depends on the electrode area, the perimeter-to-area ratio of the electroactive portion of the surface, the mass transfer coefficient of the analyte-electrode combination, the measurement bandwidth, and the sources and magnitudes of the noises. Simple models for chronoamperometry with an array in quiescent solution and for hydrodynamic current at an array in one wall of a rectangular conduit through which analyte-containing solution is following are given. Noises from seven sources, including environmental noises, are considered in a noise model. The signal and noise models are combined to yield a model for signal-to-noise ratio at array-based electrochemical detectors. There exists an optimum array density for a given area that depends on the noise power, noise resistance, the current density at a sparse array, and the current density at a solid electrode of the same area. Approximations that lead to simple expressions for the optimum electroactive area fraction and noise resistance lead to results that are in good agreement with more complex and less approximate calculations. Electrodes of millimeter dimensions consisting of about 1% active surface with electroactive "pieces" of micrometer dimensions are anticipated to yield detection limits of about 1 fmol injected into a typical packed-column liquid chromatograph. This corresponds to about 10(-10) M analyte in the detector and about an order of magnitude improvement over solid electrodes.

Electrochemical detection of oligopeptides through the precolumn formation of biuret complexes.

The relatively slow kinetics of formation of the electroactive Cu(II)-peptide complexes from larger (greater than 6 amino acids) peptides requires relatively high temperature and long reaction times for a postcolumn reactor. The precolumn incubation of bradykinin, Tyr8-bradykinin and insulin A chain with biuret reagent for 20 min at 60 degrees C leads to the formation of biuret complexes which can be subjected to chromatography in acidic or basic eluents. These complexes are detected electrochemically with a sensitivity similar to the Cu(II)-(ala)3 complex (1 nC/pmol at 1.0 ml/min). The influence of the column-packing material on the electrochemical detector response of the Cu-peptide complexes has also been studied.

Polar bonded phase with the zwitterionic sulfobetaine functional group. Comparison to silica.

A new bonded phase has been prepared by the reaction of n-propylsultone with dimethylaminopropylsilane-modified silica. The resulting functional group is the zwitterionic ammonium propane sulfonate. Chromatographic solvents based on three strong solvents, methylene chloride, diisopropyl ether and acetonitrile, were prepared in hexane. Solutes, including substituted benzenes, polycyclic aromatic hydrocarbons and low-molecular-weight species commonly used as solvents, were chromatographed on the zwitterionic phase and on silica from the same supplier of the dimethylamino phase. The zwitterionic phase is a weaker adsorbent than silica and retentions are less influenced by the type of strong solvent employed, compared to silica. The retention (log k') of solutes on the zwitterionic phase is highly correlated with the free energy of transfer of solute from the vapor phase to water.