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PubMed2000

Improving lipase enantioselectivity in organic solvents by forming substrate salts with chiral agents.

We recently demonstrated (J Am Chem Soc 121:3334-3340, 1999) that enzymatic enantioselectivity in organic solvents can be markedly enhanced by temporarily enlarging the substrate via salt formation. In the present study, this approach was expanded by finding that, in addition to its size, the stereochemistry of the counterion can greatly affect the enantioselectivity enhancement. For example, the enantioselectivity [E = (k(cat)/K(M))(S)/(k(cat)/K(M))(R)] of crystalline Pseudomonas cepacia lipase in the propanolysis of phenylalanine methyl ester (PheOMe) in anhydrous acetonitrile was found to be 5.8 +/- 0.6; the E value doubled when PheOMe's salt with S mandelic acid was used as a substrate instead of the free ester, and rose sevenfold with R mandelic acid as a Bronsted-Lowry acid. Similar effects were observed with other bulky, but not petite, counterions. The greatest enantioselectivity enhancement was afforded by 10-camphorsulfonic acid: the E value increased to 18 +/- 2 for a salt with its R enantiomer and jumped to 53 +/- 4 for the S. These effects, also observed in other organic solvents, were explained by means of structure-based molecular modeling of the lipase-bound transition states of the substrate enantiomers and their diastereomeric salts.

Biotechnology↗
PubMed1994

Intervention study on the influence of reduction of occupational exposure to styrene on sister chromatid exchanges in lymphocytes.

An intervention study was performed on 28 workers exposed by inhalation to styrene in the reinforced plastics industry and 20 controls not occupationally exposed to the compound. The workers involved were 14 laminators exposed to a time-weighted average of approximately 40 ppm styrene and 14 formers exposed to an average of about 10 ppm styrene. Ambient air monitoring data and the concentration of mandelic acid in the urine were used for the assessment of exposure. From each subject, peripheral blood lymphocytes were analysed for sister chromatid exchanges (SCEs). In the laminators, the mean SCE frequency was significantly higher than in the controls in both the group of smokers (9.59 +/- 0.77 SCEs/cell vs 7.23 +/- 1.00 SCEs/cell) and the group of non-smokers (10.25 +/- 1.08 SCEs/cell vs 5.98 +/- 0.60 SCEs/cell). The mean SCE frequency of the formers (7.42 +/- 128 SCEs/cell in smokers) did not differ statistically from the controls (7.23 +/- 1.00 SCEs/cell in smokers). No evaluation was made for non-smoking formers since all but one worker in this group were smokers. In order to comply with a lowering of the occupational exposure limit (MAK value) for occupational exposure to styrene in the Federal Republic of Germany from 100 ppm to 20 ppm, considerable technical and hygienic improvements were made at the work site of the laminators. This intervention led to a reduction of average exposure of these workers by inhalation from 40 ppm to approximately 20 ppm. One year after these improvements were made, a second investigation was performed. In all but one of the laminators, the concentration of mandelic acid in urine had dropped considerably. The SCE frequency in blood lymphocytes of the laminators had likewise dropped significantly to 7.74 +/- 0.59 SCEs/cell in the non-smokers. In the smokers, it was also lower than on the first occasion (9.02 +/- 1.19), yet statistical evaluation was not possible due to insufficient numbers. Overall, the results of the intervention study show that the lowering of the occupational exposure limit for styrene to 20 ppm in Germany was justified and that a reduction of occupational exposure to the chemical has led to a prevention of adverse cytogenetic effects.

Adult↗
PubMed1995

Further study on the use of uncharged beta-cyclodextrin polymer in capillary electrophoresis: enantiomeric separation of some alpha-hydroxy acids.

Uncharged beta-cyclodextrin polymer was used as chiral selector for the enantiomeric separation of some alpha-hydroxy acids by capillary electrophoresis. Complexation and enantiomeric resolution of mandelic acid, m-hydroxy and p-hydroxymandelic acid, 3,4-dihydroxymandelic acid, as well as 2- and 3-phenyllactic acid were studied, changing the concentration of the beta-cyclodextrin polymer added to the background electrolyte at different pH in the range of 4.5-7. Furthermore, the effects of the concentration of the background electrolyte, column temperature, and applied voltage on chiral resolution were also examined. The best enantiomeric separations were obtained using a background electrolyte at pH 6 containing 100 mg/mL of beta-cyclodextrin polymer.

Cyclodextrins↗
PubMed1986

Effects of some monocyclic aromatic solvents and their metabolites on brain dopamine in rabbits.

Adult male rabbits were exposed to high concentrations (750 ppm, 12 hours daily for 7 days) of toluene, xylenes, styrene, ethylbenzene, vinyltoluene (3-methylstyrene), and 7-methyl-styrene vapours or were dosed with 4 mM/kg/day i.p. of hippuric, methylhippuric, mandelic, phenylglyoxylic, and 7-methyl-mandelic acids. Styrene, vinyltoluene and ethylbenzene caused a marked depletion of striatal and tuberoinfundibular dopamine. Such an effect was also caused by treatment with phenylglyoxylic and mandelic acids. Dopamine depletion was associated with an increase in homovanillic acid concentration in the same regions. These results indicate that dopamine metabolism is a target for the neurotoxic effects of some monocyclic aromatic hydrocarbons and their metabolites, a lateral vinyl- or ethyl-chain being crucial for the structure/activity relationship of such compounds.

Animals↗
PubMed1981

Microsurgical urology: a silicone cover to protect the ureter from induced retroperitoneal fibrosis in rats.

Retroperitoneal fibrosis was induced in 30 rats by placing a paraffin pellet containing 5 mg of phenol-mandelic acid behind the left ureter. In an additional 15 rats, the left urinary tract was transposed into a silicone sheath before the pellet of phenol-mandelic acid was placed behind the ureter in an attempt to protect the urinary tract from retroperitoneal fibrosis. In all 30 animals without the sheath, hydronephrosis of the left side occurred, and in the 15 animals with the sheath, lateral and anterior displacement of the left tract occurred, but function was not impaired. It is concluded that the silicone-sheath technique may represent a new therapeutic approach to retroperitoneal fibrosis.

Animals↗
PubMed1981

Study of infective (secondary) renal calculus formation in vitro.

The factors of infective calculus formation and the conditions favoring their prevention were studied by examining in vitro the role of the most common representative of urease-producing bacteria, Proteus mirabilis. The stream of Proteus-containing urine was found to form deposits of magnesium ammonium phosphate, carbonate apatite and ammonium-urate on the glass surfaces. Application either of mandelic acid or of Gentamycin was found to reduce the production of these deposits, and their joint application proved fully preventive to their formation. Gentamycin applied in saline acidified with mandelic acid was capable of dissolving previously formed crystals. A medication of this composition is advocated for preventive use after surgery for staghorn calculi. The necessity for continuing peroral medication and specific antibacterial therapy for months is emphasized.

Crystallization↗
PubMed2004

Enantiomeric and mesomeric mandelate complexes of molybdenum -- on their stereospecific formations and absolute configurations.

The stereospecific formation and absolute configuration of R-homocitrate coordinated FeMo-co in nitrogenase was mimicked through the structural analyses of a collection of enantiomeric and mesomeric mandelato molybdenum complexes, i.e., (NH(4))(2)[Mo(Delta)O(2)(R-mand)(2)]x3H(2)O (1a), (NH(4))(2)[Mo(Lambda)O(2)(S-mand)(2)]x3H(2)O (1b), (NH(4))(4)[Mo(Delta)O(2)(RS-mand)(2)][Mo(Lambda)O(2)(RS-mand)(2)]x8H(2)O (2), (NH(4))(2)[W(Delta)O(2)(R-mand)(2)]x2H(2)O (3a), (NH(4))(2)[W(Lambda)O(2)(S-mand)(2)]x2H(2)O (3b) (H(2)mand=mandelic acid, C(8)H(8)O(3)), which have been characterized by elemental analyses, optical rotation, circular dichroism, IR, NMR spectroscopes and X-ray single crystal studies. The R and S chiral mandelic acids induce the formations of the enantiomeric pair of chiral complexes, which are supported by the characterizations of optical rotation and circular dichroism. The configuration of the resulted metal center could be assigned as Delta or Lambda. While the RS racemic reagent yields only mesomeric compound. The Delta(R,R)-complexes 1a and 3a are enantiomers of Lambda(S,S)-1b and 3b, respectively. Of the five complexes, Mo and W atoms are all hexa-coordinated by two cis-oxo groups and two bidentate mandelate ligands through the deprotonated alpha-alkoxyl and alpha-carboxyl groups, forming a stable five-membered chelated rings. The average Mo(VI)-O bond distances with alpha-alkoxyl and alpha-carboxyl are 1.944 and 2.210 A, respectively. Further comparison indicates that bonds of alpha-alkoxyl groups in the hydroxycarboxylato molybdenum complexes are much sensitive to the change in the oxidation state of molybdenum, which support the possible Mo activation model in FeMo-co through the protonation and cleavage of alpha-alkoxyl group in homocitrate ligand.

Journal Article↗
PubMed1993

Monitoring occupational exposure to styrene from hemoglobin adducts and metabolites in blood.

Monitoring occupational exposure to styrene was achieved through quantification of adducts of styrene 7,8-oxide to N-terminal valine in hemoglobin (Hb) on the basis of the enrichment of adducted globin chains by ion-exchange chromatography and gas chromatographic-mass spectrometric analysis by the use of the N-alkyl Edman method. Application to blood samples from reinforced plastics workers exposed to styrene and from referents showed Hb adduct levels correlating with the blood styrene glycol and urinary mandelic acid concentrations. The blood styrene glycol and styrene 7,8-oxide levels of the exposed workers averaged 2.5 mumol.l-1 (17 subjects) and 0.09 mumol.l-1 (7 subjects), respectively. The blood styrene glycol and urinary mandelic acid content (mean 9.5 mmol.l-1, 17 subjects) suggested a styrene concentration of about 300 mg.m-3 (75 ppm) in the workplace air. The Hb adduct levels were low (mean 28 pmol.g-1), indicating rapid detoxification of styrene 7,8-oxide in humans.

Adult↗
PubMed1993

Dose-dependent kinetics of inhaled styrene in man.

One female and one male volunteer were exposed to styrene vapour (2 h; 50 W) at four different concentrations (26, 77, 201 and 386 ppm). Styrene levels were measured in arterialized capillary blood during and after exposure by head-space gas chromatography, and the levels of mandelic acid in urine were analysed by high-performance liquid chromatography. Non-linear relationships between the level of exposure to styrene and the concentration of styrene in arterial blood and 0-5 h cumulative excretion of mandelic acid indicated metabolic saturation. A physiologically based pharmacokinetic model was used to estimate the maximum metabolic rate (Vmax) of styrene from data on blood styrene. According to the model, the Vmax is 2.9 mmol/h, and metabolic saturation occurs at concentrations of 100-200 ppm styrene, depending on the level of physical activity. To our knowledge, this is the first time that dose-dependent kinetics of styrene has been shown in humans.

Administration, Inhalation↗
PubMedDate not supplied

Disposition of oral [14C]cefcanel daloxate hydrochloride in healthy male subjects.

The pharmacokinetics of the main metabolites of cefcanel daloxate hydrochloride, a new oral cephalosporin diester prodrug, was investigated. Cefcanel is antimicrobially active. After oral administration of a single dose of [14C]cefcanel daloxate hydrochloride to 7 healthy male volunteers (group A), plasma concentrations (t1/2 approximately 1 hr) and excretion of radioactivity, cefcanel (Aer = 38.2 +/- 3.8%, t1/2 approximately 1 hr), mandelic acid glycine conjugate (Aer = 3.7 +/- 0.5%, t1/2 approximately 15 hr) and N-mandelyl-2-aminoethanol (Aer = 7.5 +/- 3.0%) were evaluated. The absolute oral bioavailability of cefcanel was approximately 40% after administration of cefcanel daloxate hydrochloride and the extent of urinary excretion of cefcanel, mandelic acid glycine conjugate, and N-mandelyl-2-aminoethanol after an equimolar intravenous administration of cefcanel, were determined in a separate, similar group of volunteers (N = 12, group B). Total plasma clearance of cefcanel was 179.1 +/- 22.4 ml/min/1.73 m2 after intravenous administration. Renal clearances of cefcanel were 173.9 +/- 95.6 (po, group B), 166.6 +/- 31.9 (i.v., group B), and 136.3 +/- 16.1 ml/min/1.73 m2 (po, group A). Cefcanel was almost completely (92.6 +/- 7.3%) excreted in the urine as unmetabolized drug after intravenous administration (group B). However, when cefcanel daloxate hydrochloride was administered orally, more than 30% of the total urinary excretion was due to metabolites other than cefcanel. A large proportion of these metabolites were formed at a late stage, in the absence of systemic cefcanel. It is probable that biotransformed materials, distinct from cefcanel, were formed in the gastrointestinal tract and slowly absorbed rather than being systemic products of metabolic degradation of cefcanel.(ABSTRACT TRUNCATED AT 250 WORDS)

Administration, Oral↗
PubMed1989

[A thin-layer chromatography method for determining the styrene metabolites mandelic and phenylglyoxylic acid in urine].

A thin-layer chromatographic method is described for the determination of mandelic and phenyglyoxillic acid on silicagel (Silufol UV 254) after extraction from urine of styrene exposed workers. The quantitative determination was performed after eluting the spots. Phenylglyoxilic acid was measured at 255 nm and mandelic acid by derivative spectroscopically estimation of the .CH(OH).COOH -chromophore at 217 nm or by a three-wavelength mode, respectively. The recovery in urine was 80-104% for phenylglyoxilic acid and 99-105% for mandelic acid.

Chromatography, Thin Layer↗
PubMed1991

Styrene revisited--exposure assessment and risk estimation in reinforced plastics industry.

A survey performed in 32 workshops in reinforced plastics industry showed the mean TWA 8 h concentration of styrene in personal air to be 43 ppm (range 5-182 ppm) among laminators and 11 ppm (range 1-133 ppm) among other workers. The biological measurement of urinary mandelic acid + phenylglyoxylic acid showed mean values of 2.4 mmol/l among laminators without respirators and 1.3 mmol/l when respirators were used. No effects of work related exposure were detected in the cytogenetic parameters, chromosome aberrations, sister chromatid exchanges or micronuclei analyzed in peripheral blood lymphocytes. Grading of the exposure on the basis of lamination method, years of exposure, daily laminating time, air styrene concentration and urinary mandelic acid among laminators, neither revealed any dose dependency.

Air Pollutants, Occupational↗
PubMed1995

Development of a combined NMR paramagnetic ion-induced line-broadening/dynamic light scattering method for permeability measurements across lipid bilayer membranes.

A combined method using NMR line-broadening for permeant lifetime determination and dynamic light scattering for vesicle size determination has been developed for the measurement of permeability coefficients of ionizable permeants across phospholipid:cholesterol large unilamellar vesicles. The method has been validated by examining its reproducibility and the influence of various factors that might affect the permeability measurements. The vesicle hydrodynamic diameter was varied between 0.1 and 0.2 micron by extruding multilamellar vesicles through polycarbonate membranes with different pore sizes (0.03-0.2 microns). For these large unilamellar vesicles, the normalized size distributions analyzed by the CONTIN method had standard deviations < 0.36, which led to errors in permeability coefficients < 10% as predicted from a theoretical model developed here. The permeability coefficient for acetic acid is independent of its concentration, vesicle hydrodynamic diameter, the concentration of Pr3+, and ionic strength over the ranges 0.01-0.2 M, 0.1-0.2 microns, 0.004-0.04 M, and 0.03-0.3, respectively. Membrane/water and decane/water partition coefficient measurements of acetic acid indicate that the effects of permeant binding onto the bilayer membrane and self-association are negligible within the permeant concentration range 0.01-0.2 M. The addition of Pr3+ ions induces vesicle fusion with rates increasing with temperature and decreasing with cholesterol concentration in the membranes. While the intravesicular resonance intensity for acetic acid decreases continuously with time due to vesicle fusion under certain conditions, the corresponding line width and chemical shift remain constant over the same period, highlighting an important advantage of this NMR method over those based on detecting net flux in response to a concentration gradient as there is no means in the latter experiments of discerning vesicle leakiness from passive diffusion rates. The effective chemical nature of a dimristoylphosphatidylcholine:cholesterol bilayer barrier microenvironment was explored by comparing the transport of two permeants, D-(-)-mandelic acid and phenylacetic acid, to their relative bulk solvent/water partition coefficients using three reference solvents (n-decane, 1,9-decadiene, and isoamyl alcohol). Using the NMR line-broadening method, the permeability coefficients for these two permeants were determined to be (2.9 +/- 0.4) x 10(-4) cm/s and (3.9 +/- 0.7) x 10(-2) cm/s, respectively, at 294 K and Xchol = 0.3. The incremental free energy of transport for the additional OH group in D-(-)-mandelic acid, delta delta G0 = +2.9 kcal/mol, resembles most closely that for the transfer of this group from water to 1,9-decadiene, suggesting that the barrier domain resides in the acyl chain region and is slightly more polar/polarizable than a saturated hydrocarbon, possibly due to the presence of a double bond in cholesterol and/or the proximity of the barrier domain to the hydrophilic interface.

Acetates↗
PubMed2006

Synthesis and characterization of (S)-amino alcohol modified M41S as effective material for the enantioseparation of racemic compounds.

A new chiral stationary phase (CSP) was synthesized based on (S)-1-anilino-3-propyl-2-propanol covalently bonded to the mesoporous semi-crystalline material M41S. Direct semipreparative enantioseparation of mandelic acid could be achieved using medium pressure chromatography. Partly separated could also be the enantiomers of 2,2'-dihydroxy-1,1'-binaphthalene, cyanochromene oxide, diethyl tartrate and 2-phenyl propionic acid. The characterization of CSP was accomplished by microanalysis, cross polarized magic angle spinning (CP-MAS) 13C NMR, powder X-ray diffraction (XRD), FTIR, thermo-gravimetric analysis (TGA), N2 adsorption-desorption isotherm, scanning electron microscopy (SEM) and solid reflectance UV-vis spectroscopy. Furthermore the stability of CSP was satisfactory as it could withstand three washing and reuse experiments of enantioseparation of mandelic acid without loss in its performance.

Amino Alcohols↗
PubMed2000

alpha-t-butyl- and alpha-i-propyl-ortho-hydroxybenzylamines: racemic synthesis/resolution and asymmetric synthesis.

Efficient routes to alpha-tert-butyl- and alpha-iso-propyl-ortho-hydroxybenzylamines 1a and 1b are described. Highly enantioenriched 1a and 1b were obtained by resolution of the methoxy derivatives 2 by recrystallization of the salts formed with mandelic acid followed by Lewis acid mediated demethylation. The chiral 1,3-amino alcohol 1a has also been obtained in an asymmetric synthesis with the key step a diastereoselective alkylation of the imine obtained by condensation of o-anisaldehyde with phenyl glycinol. The absolute stereochemistry of these 1,3-aminophenols was determined by CD spectroscopy of the salicylideneamines 12 and by an X-ray structure analysis of the salt formed between (R)-mandelic acid and (S)-alpha-tert-butyl-ortho-methoxybenzylamine ((S)-2a).

Journal Article↗
PubMed1994

Review of the metabolic fate of styrene.

Styrene and styrene oxide have been implicated as reproductive toxicants, neurotoxicants, or carcinogens in vivo or in vitro. The use of these chemicals in the manufacture of plastics and polymers and in the boat-building industry has raised concerns related to the risk associated with human exposure. This review describes the literature to date on the metabolic fate of styrene and styrene oxide in laboratory animals and in humans. Many studies have been conducted to assess the metabolic fate of styrene in rats, and investigations on the metabolism of styrene in humans have been of considerable interest. Limited research has been done to assess metabolism in the mouse. The metabolism of styrene to styrene oxide and further conversion to styrene glycol (via epoxide hydrolase), mandelic acid, and phenylglyoxylic acid has been given considerable attention, and is considered to be the major pathway of activation and detoxication for humans. While the hydrolysis of styrene oxide to styrene glycol historically has been the favored pathway for the rat, studies in more recent years have indicated that glutathione conjugation also is a viable and significant pathway for both the rat and the mouse. This pathway has not been established in humans. Mandelic acid and phenylglyoxylic acid have been used as urinary markers of exposure in humans exposed to styrene. Extensive investigations have been conducted on the kinetics of styrene and styrene oxide in rodents. In people, the kinetics of styrene and styrene oxide in the blood of occupationally exposed workers and volunteers have been determined. Pharmacokinetic models developed in the last decade have become increasingly complex, with the most recent physiologically based model describing the kinetics of styrene and styrene oxide. This model shows pronounced species differences in sensitivity coefficients for styrene or styrene oxide between mice, rats, and humans, where mice are the more sensitive species to the Vmax for both epoxide hydrolase and monooxygenase. This result is particularly interesting in light of the recent findings of extensive mortality and hepatotoxicity for mice exposed to relatively low levels of styrene (250 to 500 ppm), while rats and humans exhibit only nasal and eye irritations at exposure concentrations well above 500 ppm.

Animals↗
PubMed1995

Assessment of long-term styrene exposure: a comparative study of a logbook method and biological monitoring.

In a recent joint European research project "Biomonitoring of human populations exposed to genotoxic environmental chemicals: biomonitoring of styrene exposed individuals", a logbook method for assessment of long-term styrene exposure was applied in two Danish factories manufacturing glass fibre-reinforced polyester. The method was based on work process identification, assignment of work process concentrations and logbook keeping. Measures of exposure calculated by this method were compared with results from simultaneous measurements of styrene in blood and the metabolites mandelic acid and phenylglyoxylic acid in urine. Correlations were comparable with those obtained by use of personal samplers as published in the literature. Styrene in blood, however, only correlated with logbook concentrations at the time of sampling. Exposures were moderate to low. Mean personal 8-h time-weighted average concentration (8hTWAC) was 76 mg/m3 styrene (SD 54 mg/m3, range 2-230 mg/m3). The Danish 8hTWAC threshold limit value for styrene in air, 105 mg/m3 (25 ppm), was exceeded on 17% of personal days. The summed urinary metabolites, mandelic acid and phenylglyoxylic acid, had a mean personal value of 138 mg/g creatinine (SD 84 mg/g creatinine) on the day of sampling. Blood styrene mean value was 129 micrograms/l (SD 74 micrograms/l, range 66-358 micrograms/l). It is concluded that the logbook method offers a technique for testing whether measurements are performed on representative days and may be recommended as a tool supplementary to biological monitoring in the assessment of long-term exposure.

Adult↗
PubMed2001

Simultaneous high-performance liquid chromatographic determination of urinary mandelic and phenylglyoxylic acids as indirect evaluation of styrene exposure.

Styrene is rapidly metabolised to mandelic acid (MA) and phenylglyoxylic acid (PGA), which are excreted in urine. In this work, we have developed a simple, sensitive and specific high-performance liquid chromatographic method with minor sample preparation procedures for the simultaneous determination of MA and PGA in urine of workers exposed to styrene. Moreover, urine samples from workers of two plastic factories were analysed, styrene exposure levels of the workers were estimated and data obtained from the two factories were compared.

Chromatography, High Pressure Liquid↗