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H Vuorela

Publications and source records attributed to H Vuorela.

30 records · Page 2Linked to original sources
PubMed1996

Structure-retention relationships of steroid hormones in reversed-phase liquid chromatography and micellar electrokinetic capillary chromatography.

Quantitative structure-retention relationship (QSRR) studies are useful in retention prediction, finding the relevant structural descriptors for analytes and estimating the relative biological activities of a series of analytes. Most of the studies have been conducted by RP-HPLC and a few by micellar electrokinetic capillary chromatography (MECC). The aim of this work was to find structural parameters and characteristics related to the RP retention and electrophoretic migration of steroids in order to predict the retention/migration of steroid hormones on the basis of their molecular structure. Retention data were obtained with an ODS column using a mobile phases aqueous methanol-acetonitrile (mobile phase A) and methanol-tetrahydrofuran (mobile phase B). MECC was conducted with a sodium dodecyl sulfate (SDS)-borate system and with a mixed micellar solution of SDS and sodium cholate. Several topological indices, such as the connectivity indices, chi, were used as structural parameters. Steric factors seem to have a great effect on the retention of steroid hormones, especially with the MeCN-containing mobile phase. Retention in mobile phase B could be predicted more accurately. Topological indices can be used in the modelling and prediction of the retention/migration of steroid hormones when the solutes form a congeneric series and stereochemical properties do not govern the separation process.

Chromatography↗
PubMed1994

Bioactivity of certain Egyptian Ficus species.

The fruit extracts of Ficus sycomorus L., F. benjamina L., F. bengalensis L. and F. religiosa L. were screened for bioactivity. F. bengalensis and F. religiosa demonstrated activity in the brine shrimp test (Artemia salina) which indicates toxicity, whereas F. sycomorus and F. benjamina showed no activity. All the fruit extracts exhibited antitumor activity in the potato disc bioassay. None of the tested extracts showed any marked inhibition on the uptake of calcium into rat pituitary cells GH4C1. The extracts of the four tested Ficus species had significant antibacterial activity, but no antifungal activity. The results of this preliminary investigation support the traditional use of these plants in folk medicine for respiratory disorders and certain skin diseases.

Animals↗
PubMed1994

Statistical evaluation of molecular descriptors and quantitative structure-property relationship studies of retinoids.

Various molecular descriptors, including connectivity indices, sums of the intrinsic state values, electrotopological state indices, topological equivalence indices, kappa indices, normalized Bonchev-Trinajstic and Shannon information indices, Wiener and Platt's F numbers and molecular weight, were calculated for 73 retinoids, whose structures and properties were taken from the literature. A novel methodology using statistical analyses (cluster, factor and stepwise regression) in selecting relevant molecular descriptors for quantitative structure-property relationship (QSPR) studies has been developed. The analyses were used in correlating molecular structure with affinity, pharmacokinetic properties and reversed-phase retention of retinoids.

Molecular Weight↗
PubMed1993

Effects of organic mobile phase modifiers on elution and separation of beta-blockers in micellar electrokinetic capillary chromatography.

A study was made of the effect of organic modifiers (acetone, acetonitrile, ethanol, ethylene glycol, methanol and 2-propanol) in phosphate buffer (0.08 M) containing 15 mM cetyltrimethylammonium bromide as surfactant on the elution and separation of eleven common beta-adrenergic blocking agents. The amount of the modifier was varied from 0.1 to 10.0% (v/v). At maximum addition, the organic solvents increased the viscosity of the buffer solution as follows: acetone 16%, acetonitrile 9%, ethanol 26%, ethylene glycol 27%, methanol 20% and 2-propanol 29%. In contrast to the migration time of the other beta-blockers, that of labetalol was not increased by the addition of organic solvent to the buffer solution. Rather, labetalol eluted more quickly with increase in the amount of modifier, and thereby effected changes in the elution order of the beta-blockers. The addition of modifiers also affected the resolution, and the best resolution values were achieved with the following amounts of organic solvent in MEKC buffer: acetone 0.1%, acetonitrile 0.1-0.5%, ethanol 5.0-7.5%, ethylene glycol 1.0-2.5%, methanol 5.0% and 2-propanol 1.0-2.5% (v/v). No significant relationship was found between the elution order and separation and the structure of the beta-blockers in micellar electrokinetic capillary chromatography with an organic modifier in buffer solutions.

Adrenergic beta-Antagonists↗
PubMed1993

Effect of buffer solution pH on the elution and separation of beta-blockers by micellar electrokinetic capillary chromatography.

Study was made of the effect of the pH of phosphate buffer (0.08 M) containing 15 mM cetyltrimethylammonium bromide as surfactant on the elution order of eleven widely used beta-adrenergic blocking agents. In the pH range 6.0-7.8 the elution order of six of the beta-blockers remained the same, while the order of five of them changed. Sotalol eluted as the sixth compound at pH 6.8 and migrated more quickly with increasing pH. Below pH 7.0 labetalol eluted before propranolol and above pH 7.0 afterwards. Likewise, the order of elution of atenolol and timolol was reversed at pH 7.0. The pH also affected the resolution; the best resolution values were achieved between pH 6.6 and 7.0 and between pH 7.4 and 7.8. The relationship between the structure of the beta-blockers described by molecular and molecular connectivity indices and the elution order and separation of the beta-blockers in micellar electrokinetic capillary chromatography at varying pH of the buffer solution is discussed.

Adrenergic beta-Antagonists↗
PubMed1993

Differential inhibition of coumarin 7-hydroxylase activity in mouse and human liver microsomes.

Coumarin is 7-hydroxylated by the P450 isoform Cyp2a-5 in mice and CYP2A6 in humans. Various drugs, endogenous substances, plant substances and carcinogens, altogether about 90 chemicals, were evaluated as possible inhibitors of coumarin 7-hydroxylase (COH) activity in mouse microsomes. The effects of selected compounds on COH activity in human liver microsomes were also tested. The furanocoumarin derivatives methoxsalen (8-methoxypsoralen) and psoralen proved to be the most potent inhibitors of mouse COH activity (IC50 values 1.0 and 3.1 microM, respectively). The furanocoumarins bergapten (5-methoxypsoralen), isopimpinellin (5,8-dimethoxypsoralen), imperatorin and sphondin also effectively inhibited mouse COH activity (IC50 values 19-40 microM). Methoxsalen, isopimpinellin and metyrapone were also inhibitors in mice in vivo. Methoxsalen was a potent inhibitor of COH activity also in human liver microsomes, (IC50 value 5.4 microM), whereas bergapten, isopimpinellin and imperatorin had no effect. The imidazole antimycotic miconazole was a potent but non-specific inhibitor of COH activity. Several known substrates and inhibitors of members in the CYP1A, CYP2B, CYP2C, CYP2D and CYP3A subfamilies were poor inhibitors of COH activity. These results suggest that (i) the coumarin-type compounds in particular interact with the active sites of Cyp2a-5 and CYP2A6, and (ii) the active sites of Cyp2a-5 and CYP2A6 are structurally different, since a number of compounds inhibited mouse, but not human COH activity.

Animals↗
PubMed1992

Choice of solvent in the extraction of Angelica archangelica roots with reference to calcium blocking activity.

Twenty solvents were tested in the extraction of compounds from the roots of Angelica archangelica L. (Apiaceae), and the calcium-antagonistic activity of the extracts was investigated. Special attention was paid to the physical and chemical properties of the solvents and their extraction abilities. The calcium antagonistic effect of the extracts was investigated by measuring the inhibition of depolarization-induced Ca2+ uptake in rat pituitary GH4C1 cells. The criteria used in determining the best solvents for the extraction were the yield and the biological activity of the extract, as well as the amount of nonpolar compounds in the extract. The final criterion used in selecting the solvent was its usability with reference to boiling point, chemical interactions (e.g. methylation), etc. Chloroform was found to be the best solvent for the extraction of nonpolar, biologically active compounds from the roots of A. archangelica.

Animals↗
PubMed1989

Rapid determination of tyramine in fish feed and slaughter offal by HPLC using coulometric detection.

Fish feed and slaughter offal products may contain decomposition compounds such as biogenic amines. Owing to their harmful effects on animals fed with such products, there is a need for determining the amine content. In the work a simple and fast HPLC method, based on coulometric detection (EC) measuring only tyramine, was developed for routine quality screening. The samples were extracted with 0.4 mol/L perchloric acid and analysed directly by HPLC using a mobile phase of 0.2 mol/L potassium dihydrogen phosphate in water at pH 3. Tyramine was detected using a coulometric detector consisting of two analytical cells, the first one at 0.4 V and the second at 0.7 V. The calibration was linear over the range 4.52 to 452 ng/ml. The minimum detectable quantity was 10 pg/20 microliters. The reproducibility and the recoveries were high. Comparison of the tyramine content measured by EC or derivatization followed by ultraviolet detection showed that both methods gave similar results. HPLC using EC is a fast and sensitive method for analysing tyramine reliably in fish feed and slaughter offal samples without any time-consuming derivatization steps.

Animal Feed↗
PubMedDate not supplied

Characterization of the polyphenolic composition of purple loosestrife (Lythrum salicaria).

Phenolic compounds of purple loosestrife (Lythrum salicaria L.) were analysed by the use of liquid chromatography-mass spectrometry (LC/MS) equipped with atmospheric pressure chemical ionisation (APCI) and electrospray ionisation (ESI). The presence of vitexin and orientin as well as their isomers, isovitexin and isoorientin, were confirmed using ion trap multiple stage LC/MS3 analysis. Several phenolic acids and tannins were also detected. Ellagitannins, vescalagin and pedunculagin, are reported from the plant for the first time.

Chromatography, High Pressure Liquid↗