Barbora Papoušková

Email: barborapapouskova@seznam.cz

Location: 17. listopadu 12, Olomouc

Phone: (+420) 58563 4447

Fax: (+420) 585 63 4433

Oblast výzkumu:

kapalinová chromatografie (capLC, UHPLC, konvenč. LC)

hmotnostní spektrometrie (ESI, MALDI, IT, QqTOF) malých molekul

spojené techniky

analýza metabolitů léčiv

analýza rostlinných materiálů se zaměřením na sekundární rostlinné metabolity

charakterizace vybraných prekurzorů chemických bojových látek

Kvalifikace:

Mgr.: analytická chemie, PřF UP Olomouc

Ph.D.: analytická chemie, PřF UP Olomouc

Show publications

Publications

2011

  • [DOI] B. Papouskova, P. Bednar, K. Hron, J. Stavek, J. Balik, R. Myjavcova, P. Bartak, E. Tomankova, and K. Lemr, “Advanced liquid chromatography/mass spectrometry profiling of
    anthocyanins in relation to set of red wine varieties certified in Czech
    Republic,” JOURNAL OF CHROMATOGRAPHY A, vol. 1218, iss. 42, pp. 7581-7591, 2011.
    [Bibtex]
    @article ISI:000296037900020,
    Author = Papouskova, Barbora and Bednar, Petr and Hron, Karel and Stavek, Jan and
       Balik, Josef and Myjavcova, Renata and Bartak, Petr and Tomankova, Eva
       and Lemr, Karel,
    Title = Advanced liquid chromatography/mass spectrometry profiling of
       anthocyanins in relation to set of red wine varieties certified in Czech
       Republic,
    Journal = JOURNAL OF CHROMATOGRAPHY A,
    Year = 2011,
    Volume = 1218,
    Number = 42,
    Pages = 7581-7591,
    Month = OCT 21,
    Abstract = Hyphenation of micro-liquid and ultra-performance liquid chromatography
       with a hybrid (QqTOF) tandem mass spectrometry was studied from the
       viewpoint of their applicability for monitoring of anthocyanin dyes in
       various cultivars and different vintages of red wine. After appropriate
       optimization both techniques proved to be suitable for this task. UHPLC
       system provided lower LOD and LOQ values as well as higher productivity
       and precision of retention parameters and peak areas with respect to
       micro-LC method. On the other hand, micro-LC method offers significant
       savings of mobile phase, less contamination of ion source of mass
       spectrometer and makes the nebulization process in electrospray much
       easier. In combination with principal component analysis (PCA), the
       method allows to elucidate long-term relations in a complete set of
       certified red wine cultivars grown in South Moravia (certified in Czech
       Republic until year 2005). Among the studied varieties Rubinet exhibit a
       specific anthocyanin profile. Especially interesting is a high content
       of 3-coumaroylglucoside-5-glucosides of malvidin and peonidin. Those
       dyes can be used as markers of artificial color enhancement. Principal
       component analysis applied to data processed with regard to enzymatic
       activity markedly facilitate classification among varieties. This
       approach allows resolution of teinturiers. variety Blaufrankish and
       partial classification of other varieties. (C) 2011 Elsevier B.V. All
       rights reserved.,
    DOI = 10.1016/j.chroma.2011.07.027,
    ISSN = 0021-9673,
    Unique-ID = ISI:000296037900020,
    
  • [DOI] P. Kosina, J. Vacek, B. Papouskova, M. Stiborova, J. Styskala, P. Cankar, E. Vrublova, J. Vostalova, V. Simanek, and J. Ulrichova, “Identification of benzo[c]phenanthridine metabolites in human
    hepatocytes by liquid chromatography with electrospray ion-trap and
    quadrupole time-of-flight mass spectrometry,” JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL
    AND LIFE SCIENCES
    , vol. 879, iss. 15-16, pp. 1077-1085, 2011.
    [Bibtex]
    @article ISI:000290645400008,
    Author = Kosina, Pavel and Vacek, Jan and Papouskova, Barbora and Stiborova,
       Marie and Styskala, Jakub and Cankar, Petr and Vrublova, Eva and
       Vostalova, Jitka and Simanek, Vilim and Ulrichova, Jitka,
    Title = Identification of benzo[c]phenanthridine metabolites in human
       hepatocytes by liquid chromatography with electrospray ion-trap and
       quadrupole time-of-flight mass spectrometry,
    Journal = JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL
       AND LIFE SCIENCES,
    Year = 2011,
    Volume = 879,
    Number = 15-16,
    Pages = 1077-1085,
    Month = MAY 1,
    Abstract = The metabolism of the benzo[c]phenanthridine alkaloids was studied
       using human hepatocytes which are an excellent model system for
       biotransformation studies. For analysis of the alkaloids and their
       metabolites, an electrospray quadrupole ion-trap mass spectrometry (ESI
       ion-trap MS) connected to a reversed phase chromatographic system based
       on cyanopropyl modified silica was used. The optimized experimental
       protocol allowed simultaneous analysis of the alkaloids and their
       metabolites and enabled study of their uptake into and interconversion
       in human hepatocytes. The results show that formation of the dihydro
       metabolite which may be followed by specific
       O-demethylenation/O-demethylation processes, is probably the main route
       of biotransformation (detoxification) of the benzo[c]phenanthridines
       in human hepatocytes. The structure of the main O-demethyl metabolite
       (2-methoxy-12-methyl-12,13-dihydro[1,3]dioxolo[4',5':4,5]benzo[1,2
       -c]phenanthridin-1-ol; 336.1 m/z,) was proposed by the multi-stage MS
       and quadrupole time-of-flight MS methods using chemically synthesized
       standard. (C) 2011 Elsevier B.V. All rights reserved.,
    DOI = 10.1016/j.jchromb.2011.03.023,
    ISSN = 1570-0232,
    Unique-ID = ISI:000290645400008,
    

2010

  • [DOI] R. Myjavcova, P. Marhol, V. Kren, V. Simanek, J. Ulrichova, I. Palikova, B. Papouskova, K. Lemr, and P. Bednar, “Analysis of anthocyanin pigments in Lonicera (Caerulea) extracts using
    chromatographic fractionation followed by microcolumn liquid
    chromatography-mass spectrometry,” JOURNAL OF CHROMATOGRAPHY A, vol. 1217, iss. 51, pp. 7932-7941, 2010.
    [Bibtex]
    @article ISI:000285429700002,
    Author = Myjavcova, Renata and Marhol, Petr and Kren, Vladimir and Simanek, Vilim
       and Ulrichova, Jitka and Palikova, Irena and Papouskova, Barbora and
       Lemr, Karel and Bednar, Petr,
    Title = Analysis of anthocyanin pigments in Lonicera (Caerulea) extracts using
       chromatographic fractionation followed by microcolumn liquid
       chromatography-mass spectrometry,
    Journal = JOURNAL OF CHROMATOGRAPHY A,
    Year = 2010,
    Volume = 1217,
    Number = 51,
    Pages = 7932-7941,
    Month = DEC 17,
    Note = 25th International Symposium on Microscale BioSeparations (MSB 2010),
       Prague, CZECH REPUBLIC, MAR 21-25, 2010,
    Abstract = Anthocyanins from the fruit Lonicera caerulea L var. kamtschatica
       (blueberry honeysuckle, Caprifoliaceae) were studied via
       (semi)preparative chromatographic fractionation followed by MS and mu
       LC/MS analysis. The extraction procedure was optimized with respect to
       analytical purposes as well as its potential use for the preparation of
       nutraceuticals. The highest yield of anthocyanins was obtained using
       acidified methanol as the extraction medium. A comparable total
       anthocyanin content was obtained using a mixture of methanol and
       acetone. However, when Lonicera anthocyanins were in contact with
       acetone, a condensation reaction occurred to a large extent and related
       5-methylpyranoanthocyanins were found. The effect of other extraction
       media, including ethanol as a ``green'' solvent, is also discussed.
       The potential of two fractionation procedures for extract purification
       differing in their chromatographic selectivity and scale was studied
       (i.e. using a Sephadex LH-20 gel column and a reversed phase). Fractions
       obtained by both procedures were used for a detailed analysis. MS and mu
       LC/MS(2) methods were used for monitoring anthocyanin and
       5-methylpyranoderivatives content as well as identifying less common and
       more complex dyes (dimer of cyanidin-3-hexoside,
       cyanidin-ethyl-catechin-hexosides, etc.). These more complex dyes are
       most likely formed during fruit treatment. (C) 2010 Elsevier B.V. All
       rights reserved.,
    DOI = 10.1016/j.chroma.2010.05.058,
    ISSN = 0021-9673,
    Unique-ID = ISI:000285429700002,
    
  • [DOI] L. Hartmanova, V. Ranc, B. Papouskova, P. Bednar, V. Havlicek, and K. Lemr, “Fast profiling of anthocyanins in wine by desorption nano-electrospray
    ionization mass spectrometry,” JOURNAL OF CHROMATOGRAPHY A, vol. 1217, iss. 25, SI, pp. 4223-4228, 2010.
    [Bibtex]
    @article ISI:000278779000031,
    Author = Hartmanova, Lucie and Ranc, Vaclav and Papouskova, Barbora and Bednar,
       Petr and Havlicek, Vladimir and Lemr, Karel,
    Title = Fast profiling of anthocyanins in wine by desorption nano-electrospray
       ionization mass spectrometry,
    Journal = JOURNAL OF CHROMATOGRAPHY A,
    Year = 2010,
    Volume = 1217,
    Number = 25, SI,
    Pages = 4223-4228,
    Month = JUN 18,
    Abstract = Desorption electrospray ionization (DESI) mass spectrometry appears to
       be a useful technique applicable in different areas (e.g. analysis of
       pharmaceuticals, identification of biologically active compounds in
       tissues, imaging mass spectrometry). Its modification termed desorption
       nano-electrospray (nano-DESI) was tested for analysis of anthocyanins.
       Acidifying of samples and acidic spray liquid (methanol:water = 75:25
       with 0.2\% HCOOH) were essential for obtaining good quality spectra.
       Profiles of main anthocyanins in wine samples, two vintages (2005 and
       2007) of three cultivars (Alibernet, Neronet and Rubinet), were
       successfully acquired. They were in agreement with results of LC/MS
       experiments (anthocyanins isolated by solid phase extraction were
       separated by mu-HPLC with gradient elution and detected by ESI-MS).
       Nano-DESI-MS data also allowed to determine ratio of two cultivars
       (Neronet and Rubinet) in their mixture and to detect coloring of wine by
       tenturier or elderberry extract. Detection of main anthocyanins in
       slices of wine grape, chokeberries and elderberries or in a wine stain
       on cotton fabric is also presented. (C) 2010 Elsevier B.V. All rights
       reserved.,
    DOI = 10.1016/j.chroma.2010.03.018,
    ISSN = 0021-9673,
    Unique-ID = ISI:000278779000031,
    
  • [DOI] S. Pirildar, N. Sutlupmar, B. Atasever, S. Erdem-Kuruca, B. Papouskova, and V. Simanek, “Chemical constituents of the different parts of Colchicum baytopiorum
    and their cytotoxic activities on K562 and HL60 cell lines,” PHARMACEUTICAL BIOLOGY, vol. 48, iss. 1, pp. 32-39, 2010.
    [Bibtex]
    @article ISI:000273992300005,
    Author = Pirildar, S. and Sutlupmar, N. and Atasever, B. and Erdem-Kuruca, S. and
       Papouskova, B. and Simanek, V.,
    Title = Chemical constituents of the different parts of Colchicum baytopiorum
       and their cytotoxic activities on K562 and HL60 cell lines,
    Journal = PHARMACEUTICAL BIOLOGY,
    Year = 2010,
    Volume = 48,
    Number = 1,
    Pages = 32-39,
    Month = JAN,
    Abstract = The plant chemistry and cytotoxic activity of Colchicum baytopiorum CD
       Brickell (Liliaceae/Colchicaceae), an endemic species growing in Turkey,
       has been studied for the first time. Nine known alkaloids were isolated
       and their structures were identified by spectral methods (UV, IR,
       (1)H-NMR, and ESI/MS), and the presence of three alkaloids, which could
       not be isolated from the plant, was also detected by LC/MS/MS
       spectrometry. Phenolic acids were elaborated using LC/MS and 11 phenolic
       acids were identified. The presence of two flavonoids appeared to be
       valuable for chemotaxonomic purposes. Guided by the brine shrimp
       lethality test (BSLT), methanol extracts were tested for cytotoxic
       activity by colorimetric MTT test on K562 and HL60 cells. Except the
       seed extract, all methanol extracts showed more cytotoxic activity on
       HL60 cells (IC(50) : 6.5-< 0.1 mu g/mL) than on K562 cells (IC(50) : >
       500-44 mu g/mL).,
    DOI = 10.3109/13880200903029373,
    ISSN = 1388-0209,
    Unique-ID = ISI:000273992300005,
    

2009

  • [DOI] B. Papouskova, P. Bednar, J. Styskala, J. Hlavac, P. Bartak, and K. Lemr, “Mass spectrometry as a tool for characterization of
    N,N-dialkylaminoethane-2-thiols – precursors and degradation products of
    chemical warfare agents,” JOURNAL OF MASS SPECTROMETRY, vol. 44, iss. 11, pp. 1604-1612, 2009.
    [Bibtex]
    @article ISI:000272150300008,
    Author = Papouskova, Barbora and Bednar, Petr and Styskala, Jakub and Hlavac, Jan
       and Bartak, Petr and Lemr, Karel,
    Title = Mass spectrometry as a tool for characterization of
       N,N-dialkylaminoethane-2-thiols - precursors and degradation products of
       chemical warfare agents,
    Journal = JOURNAL OF MASS SPECTROMETRY,
    Year = 2009,
    Volume = 44,
    Number = 11,
    Pages = 1604-1612,
    Month = NOV,
    Abstract = N,N-dialkylaminoethane-2-thiols belong to the group of precursors and
       degradation products of chemical warfare agents (CWAs). These compounds
       were analyzed by means of electrospray ionization-multiple stage mass
       spectrometry (ion trap) and proposed fragments were confirmed by
       accurate mass measurement using a QqTOF system. The fragmentation
       pathways of studied compounds and the products of oxidation (formation
       of -S-S- linkage) were described. Some minor interesting processes, such
       as rearrangement of SH group, were observed and proved. A new mu LC/MS
       method, based on ion-pairing chromatography, was developed.
       Trifluoroacetic acid was employed as an ion-pairing agent to increase
       the low retention of compounds of interest in the reverse-phase system.
       The technique was compared with the UPLC/MS method, allowing fast
       analysis of all the studied thiols as well as an explorative control of
       originated disulfides. Copyright (C) 2009 John Wiley \& Sons, Ltd.,
    DOI = 10.1002/jms.1674,
    ISSN = 1076-5174,
    Unique-ID = ISI:000272150300008,
    
  • [DOI] B. Uhnakova, A. Petrickova, D. Biedermann, L. Homolka, V. Vejvoda, P. Bednar, B. Papouskova, M. Sulc, and L. Martinkova, “Biodegradation of brominated aromatics by cultures and laccase of
    Trametes versicolor,” CHEMOSPHERE, vol. 76, iss. 6, pp. 826-832, 2009.
    [Bibtex]
    @article ISI:000269243900015,
    Author = Uhnakova, B. and Petrickova, A. and Biedermann, D. and Homolka, L. and
       Vejvoda, V. and Bednar, P. and Papouskova, B. and Sulc, M. and
       Martinkova, L.,
    Title = Biodegradation of brominated aromatics by cultures and laccase of
       Trametes versicolor,
    Journal = CHEMOSPHERE,
    Year = 2009,
    Volume = 76,
    Number = 6,
    Pages = 826-832,
    Month = AUG,
    Abstract = 2-Bromophenol (1), 4-bromophenol (2), 2,4-dibromophenol (3),
       2,6-dibromophenol (4), 2,4,6-tribromophenol (5) and tetrabromobis phenol
       A (6) (1 mM each) added to growing submerged cultures of Trametes
       versicolor CCBAS 612 were eliminated by 65-85\% from the culture medium
       within 4 d. Extracellular laccase activity in the culture medium was
       influenced by the type of brominated compound added. Maximum level of
       laccase (63 U L(-1)) was found in the culture with 2-bromophenol.
       Tetrabromobisphenol A was degraded by a commercial laccase from Trametes
       versicolor in absence of any oxidation mediator, hydroxylated
       dibrominated compounds being detected as soluble reaction products by
       LC/MS. A significant degradation of brominated phenols by laccase was
       achieved only in the presence of ABTS structural characterization of
       major products suggesting reaction between bromophenol and ABTS
       radicals. (C) 2009 Elsevier Ltd. All rights reserved.,
    DOI = 10.1016/j.chemosphere.2009.04.016,
    ISSN = 0045-6535,
    Unique-ID = ISI:000269243900015,
    

2008

  • [DOI] P. Henklova, R. Vrzal, B. Papouskova, P. Bednar, P. Jancova, E. Anzenbacherova, J. Ulrichova, P. Maurel, P. Pavek, and Z. Dvorak, “SB203580, a pharmacological inhibitor of p38 MAP kinase transduction
    pathway activates ERK and JNK MAP kinases in primary cultures of human
    hepatocytes,” EUROPEAN JOURNAL OF PHARMACOLOGY, vol. 593, iss. 1-3, pp. 16-23, 2008.
    [Bibtex]
    @article ISI:000259508100003,
    Author = Henklova, Pavla and Vrzal, Radim and Papouskova, Barbora and Bednar,
       Petr and Jancova, Petra and Anzenbacherova, Eva and Ulrichova, Jitka and
       Maurel, Patrick and Pavek, Petr and Dvorak, Zdenek,
    Title = SB203580, a pharmacological inhibitor of p38 MAP kinase transduction
       pathway activates ERK and JNK MAP kinases in primary cultures of human
       hepatocytes,
    Journal = EUROPEAN JOURNAL OF PHARMACOLOGY,
    Year = 2008,
    Volume = 593,
    Number = 1-3,
    Pages = 16-23,
    Month = SEP 28,
    Abstract = Mitogen-activated protein kinases (MAPKs) were extensively studied in
       cancer-derived cell lines; however, studies in non-transformed human
       cells are scarce. In the current paper, we studied the effect of
       SB203580, a pharmacological inhibitor of p38 MAPK, on activation and
       inhibition of p38 MAPK transduction partway in primary human hepatocytes
       (in vitro model of differentiated cells) in comparison with several
       tumor cell lines (proliferating non-differentiated in vitro model). In
       addition, we analyzed the effect of SB203580 on extracellular-regulated
       protein kinase (ERK) and c-jun-N-terminal kinase (JNK) pathways both in
       primary human hepatocytes and tumor cell lines employing primary
       antibodies detecting phosphorylated kinases. We show that SB203580
       activates ERK and JNK in primary cultures of human hepatocytes. The
       levels of ERK-P(Thr202/Tyr204),JNK-P(Thr183/Tyr185) and
       c-Jun-P(Ser63/73), a target down-stream protein of JNK, were increased
       by SB203580. In contrast, SB203580 activated ERK but not JNK in HepG2,
       HL-60, Saos-2 and HaCaT human cancer cell lines. We tested, whether the
       effects of SB203580 are due to metabolism. Using liquid
       chromatography/mass spectrometry, we found one minor metabolite in human
       liver microsomes but not in HepG2 cells. These data imply that
       biotransformation could be responsible for the effects of SB203580 in
       human hepatocytes. This study is the first report on the effects of MAPK
       activators (sorbitol, anisomycin, EGF) and MAPK inhibitors in primary
       human hepatocytes. We observed differential effects of these compounds
       in primary human hepatocytes and in cancer cells, implying the cell-type
       specificity and the essential differences between the role and function
       of MAPKs in normal and cancer cells. (C) 2008 Elsevier B.V. All rights
       reserved.,
    DOI = 10.1016/j.ejphar.2008.07.007,
    ISSN = 0014-2999,
    Unique-ID = ISI:000259508100003,
    

2007

  • [DOI] B. Papouskova, P. Bednar, L. Frysova, J. Styskala, J. Hlavac, P. Bartak, J. Ulrichova, J. Jirkovsky, and K. Lemr, “Mass spectrometric study of selected precursors and degradation products
    of chemical warfare agents,” JOURNAL OF MASS SPECTROMETRY, vol. 42, iss. 12, pp. 1550-1561, 2007.
    [Bibtex]
    @article ISI:000252511900003,
    Author = Papouskova, Barbora and Bednar, Petr and Frysova, Lveta and Styskala,
       Jakub and Hlavac, Jan and Bartak, Petr and Ulrichova, Jitka and
       Jirkovsky, Jaromir and Lemr, Karel,
    Title = Mass spectrometric study of selected precursors and degradation products
       of chemical warfare agents,
    Journal = JOURNAL OF MASS SPECTROMETRY,
    Year = 2007,
    Volume = 42,
    Number = 12,
    Pages = 1550-1561,
    Month = DEC,
    Note = 25th Informal Meeting on Mass Spectrometry (IMMS), Nyiregyhaza-Sosto,
       HUNGARY, MAY 06-10, 2007,
    Organization = Natl Sci Council, Taiwan; Natl Sun Tat-Sen Univ; Org Prohibition Chem
       Weapons; State Off Nucl Safety; Minist Educ, Youth \& Sports,
    Abstract = Selected precursors and degradation products of chemical warfare agents
       namely N,N-dialkylaminoethane-2-ols, N,N-dialkylaminoethyl-2-chlorides
       and some of related N-quaternary salts were studied by means of
       electrospray ionization-multiple tandem mass spectrometry (ESI-MSn).
       Proposed structures were confirmed with accurate mass measurement.
       General fragmentation patterns of these compounds are discussed in
       detail and suggested processes are confirmed using deuterated standards.
       The typical processes are elimination of alkene, hydrogen chloride, or
       water, respectively. Besides, elimination of ethene from propyl chain
       under specific conditions was observed and unambiguously confirmed using
       exact mass measurement and labelled standard. The potential of mass
       spectrometry to distinguish the positional isomers occurring among the
       studied compounds is reviewed in detail using two different MS
       instruments (i.e. ion trap and hybrid quadrupole-time of flight (Q-TOF)
       analyzer). A new microcolumn liquid chromatography (mu LC)/MSn method
       was designed for the cases where the resolution based solely on
       differences in fragmentation is not sufficient. Low retention of the
       derivatives on reversed phase (RP) was overcome by using addition of
       less typical ion pairing agent (1 mm/l, 3,5-dinitrobenzoic acid) to the
       mobile phase (mixture water: acetonitrile). Copyright (C) 2007 John
       Wiley \& Sons, Ltd.,
    DOI = 10.1002/jms.1319,
    ISSN = 1076-5174,
    Unique-ID = ISI:000252511900003,
    
  • [DOI] P. Jancova, E. Anzenbacherova, B. Papouskova, K. Lemr, P. Luzna, A. Veinlichova, P. Anzenbacher, and V. Simanek, “Silybin is metabolized by cytochrome P4502C8 in vitro,” DRUG METABOLISM AND DISPOSITION, vol. 35, iss. 11, pp. 2035-2039, 2007.
    [Bibtex]
    @article ISI:000250282400008,
    Author = Jancova, Petra and Anzenbacherova, Eva and Papouskova, Barbora and Lemr,
       Karel and Luzna, Pavla and Veinlichova, Alena and Anzenbacher, Pavel and
       Simanek, Vilim,
    Title = Silybin is metabolized by cytochrome P4502C8 in vitro,
    Journal = DRUG METABOLISM AND DISPOSITION,
    Year = 2007,
    Volume = 35,
    Number = 11,
    Pages = 2035-2039,
    Month = NOV,
    Abstract = Silybin (a flavonolignan, the main component of silymarin, an extract
       from the seeds of Silybum marianum) has been used to date mostly as a
       hepatoprotectant. However, it also has other interesting activities, e.
       g., anticancer and hypocholesterolemic effects. It is also known that
       silybin can inhibit the activities of the cytochrome P450 (P450)
       enzymes. In this study, a weak interaction of silybin with human
       microsomal CYP2E1, 2A6, 2B6, 2C19, and 2D6 (IC50 >= 250 mu M) was found;
       a moderate inhibition was observed for CYP1A2 and 2C8. The most
       prominent inhibition effect was found with CYP3A4 and CYP2C9 (IC50 <= 50
       mu M). Using mass spectometry detection, production of O-demethylated
       (the main metabolite) as well as hydroxylated derivatives of silybin
       formed by P450 enzymes was detected. The effect of different P450
       inhibitors on the formation of O-demethylated product was also studied.
       In particular, a relatively specific inhibitor of CYP2C8 (quercetin)
       markedly inhibited the formation of this metabolite. With the help of
       recombinant enzymes (bactosomes), it was confirmed that the CYP2C8
       enzyme is responsible for the reaction leading to O-demethylated
       silybin.,
    DOI = 10.1124/dmd.107.016410,
    ISSN = 0090-9556,
    Unique-ID = ISI:000250282400008,
    

2006

  • [DOI] B. Papouskova, P. Bednar, P. Bartak, P. Frycak, J. Sevcik, Z. Stransky, and K. Lemr, "Utilisation of separation methods in the analysis of chemical warfare
    agents," JOURNAL OF SEPARATION SCIENCE, vol. 29, iss. 11, pp. 1531-1538, 2006.
    [Bibtex]
    @article ISI:000239574100001,
    Author = Papouskova, Barbora and Bednar, Petr and Bartak, Petr and Frycak, Petr
       and Sevcik, Juraj and Stransky, Zdenek and Lemr, Karel,
    Title = Utilisation of separation methods in the analysis of chemical warfare
       agents,
    Journal = JOURNAL OF SEPARATION SCIENCE,
    Year = 2006,
    Volume = 29,
    Number = 11,
    Pages = 1531-1538,
    Month = JUL,
    Abstract = Chemical warfare agents and their degradation products represent a broad
       group of compounds with different chemical properties (polarity,
       volatility, thermostability, etc.). These chemicals often have to be
       detected and determined in complex matrices and therefore highly
       efficient separation techniques hyphenated to selective and sensitive
       detectors play an indispensable role. This review offers an overview of
       selected papers devoted to the title subject. It cannot be considered as
       a comprehensive literature compilation but should allow the reader to
       obtain an insight into the application of separation techniques in the
       important area of human protection and control of chemical weapons.,
    DOI = 10.1002/jssc.200500432,
    ISSN = 1615-9306,
    Unique-ID = ISI:000239574100001,
    

2005

  • [DOI] P. Bednar, B. Papouskova, L. Muller, P. Bartak, J. Stavek, P. Pavlousek, and K. Lemr, "Utilization of capillary electrophoresis/mass spectrometry (CE/MSn) for
    the study of anthocyanin dyes," JOURNAL OF SEPARATION SCIENCE, vol. 28, iss. 12, pp. 1291-1299, 2005.
    [Bibtex]
    @article ISI:000231513900006,
    Author = Bednar, P and Papouskova, B and Muller, L and Bartak, P and Stavek, J
       and Pavlousek, P and Lemr, K,
    Title = Utilization of capillary electrophoresis/mass spectrometry (CE/MSn) for
       the study of anthocyanin dyes,
    Journal = JOURNAL OF SEPARATION SCIENCE,
    Year = 2005,
    Volume = 28,
    Number = 12,
    Pages = 1291-1299,
    Month = AUG,
    Note = Symposium on Advances in Chromatography and Electrophoresis and
       Chiranal, Palacky Univ, Fac Phys Culture, Olomouc, CZECH REPUBLIC, FEB
       07-10, 2005,
    Organization = Palacky Univ, Fac Sci Dept Analyt Chem; Czech Chem Soc, Chromatog \&
       Electrophoresis Grp,
    Abstract = Hyphenation of capillary electrophoresis with electrospray ionization
       mass spectrometry was utilized for the monitoring of anthocyanins in
       wine and wine musts. CE/MS was performed in two electrolytes: 1) an
       acidic one (chloroacetate-ammonium, pH 2) and 2) a basic one with high
       selectivity towards derivatives containing vicinal hydroxy groups
       (borate-ammonium, pH 9). The setup of MS was optimized and the
       fragmentation of common anthocyanins was studied in detail. Attention
       was also focused on the fragmentation of anthocyanidin skeleton. The
       anthocyanidins substituted with hydroxy groups fragment via a cascade of
       neutral losses of water and carbon monoxide. Fragmentation of
       anthocyanidins containing a methoxy group on their B-ring starts with
       the cleavage of methane and/or methyl radical. The optimized method was
       utilized for the monitoring of changes in anthocyanin profile in red
       wines as well as the process of release of anthocyanins to wine must.,
    DOI = 10.1002/jssc.200500071,
    ISSN = 1615-9306,
    Unique-ID = ISI:000231513900006,