• Je něco špatně v tomto záznamu ?

A comprehensive LC/MS analysis of novel cyclopentenedione library

B. Papouskova, M. Bernard, J. Ottenschlager, J. Karban, P. Velisek, J. Hrbac, J. Sykora, J. Storch, J. Vacek,

. 2016 ; 128 (-) : 342-51. [pub] 20160602

Jazyk angličtina Země Anglie, Velká Británie

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/bmc17023896

Cyclopentenediones (CPDs) are compounds with a variety of applications ranging from the preparation of functional polymers to the development of antimicrobial agents, suggesting the potential use of CPDs as novel bioactive compounds or drugs. For this reason, a detailed characterization of CPDs and the development of robust analytical methods for their trace analysis are being sought. Here we focused on the design and synthesis of a library of novelized benzylidene CPD derivatives that were consequently characterized by ultra-high performance liquid chromatography (UHPLC) on-line connected with tandem mass spectrometry (MS/MS). The library design was based on a 2-benzylidene-4-cyclopentene-1,3-dione skeleton substituted with a variety of hydroxy, methoxy, halogen, linear aliphatic, heterocyclic and saccharide moieties, primarily modulating the skeleton's hydrophobicity. The prepared CPDs were effectively ionized by positive/negative atmospheric pressure photoionization (APPI) and atmospheric pressure chemical ionization (APCI). After careful optimization of the dopant composition and flow rate, positive-mode APPI proved to be more sensitive than APCI. In negative mode, both ionization techniques gave similar results. Further, a detailed MS fragmentation study was performed, confirming the structure of the compounds and enabling positional isomers of CPDs to be differentiated on the basis of their collision spectra analysis. Finally, an optimization of the composition of the mobile phase and reversed-phased separation mode were done, followed by a selection of the most suitable UHPLC stationary phases, i.e. C18, C8 and phenyl. The applicability of the method was evaluated by the inclusion of the other two substances in the study, i.e. monomeric and dimeric bioactive CPDs, compound TX-1123 and nostotrebin 6 with cytostatic and antimicrobial activities, respectively. The results presented here could be used in further investigations of the chromatographic retention and MS behavior of CPDs, which could be utilized for their isolation, detailed characterization and analysis in biological systems.

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc17023896
003      
CZ-PrNML
005      
20170720123608.0
007      
ta
008      
170720s2016 enk f 000 0|eng||
009      
AR
024    7_
$a 10.1016/j.jpba.2016.05.048 $2 doi
035    __
$a (PubMed)27328361
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a enk
100    1_
$a Papouskova, Barbora $u Department of Analytical Chemistry, Regional Centre of Advanced Technologies and Materials, Faculty of Science, Palacky University, 17 listopadu 12, Olomouc 771 46, Czech Republic.
245    12
$a A comprehensive LC/MS analysis of novel cyclopentenedione library / $c B. Papouskova, M. Bernard, J. Ottenschlager, J. Karban, P. Velisek, J. Hrbac, J. Sykora, J. Storch, J. Vacek,
520    9_
$a Cyclopentenediones (CPDs) are compounds with a variety of applications ranging from the preparation of functional polymers to the development of antimicrobial agents, suggesting the potential use of CPDs as novel bioactive compounds or drugs. For this reason, a detailed characterization of CPDs and the development of robust analytical methods for their trace analysis are being sought. Here we focused on the design and synthesis of a library of novelized benzylidene CPD derivatives that were consequently characterized by ultra-high performance liquid chromatography (UHPLC) on-line connected with tandem mass spectrometry (MS/MS). The library design was based on a 2-benzylidene-4-cyclopentene-1,3-dione skeleton substituted with a variety of hydroxy, methoxy, halogen, linear aliphatic, heterocyclic and saccharide moieties, primarily modulating the skeleton's hydrophobicity. The prepared CPDs were effectively ionized by positive/negative atmospheric pressure photoionization (APPI) and atmospheric pressure chemical ionization (APCI). After careful optimization of the dopant composition and flow rate, positive-mode APPI proved to be more sensitive than APCI. In negative mode, both ionization techniques gave similar results. Further, a detailed MS fragmentation study was performed, confirming the structure of the compounds and enabling positional isomers of CPDs to be differentiated on the basis of their collision spectra analysis. Finally, an optimization of the composition of the mobile phase and reversed-phased separation mode were done, followed by a selection of the most suitable UHPLC stationary phases, i.e. C18, C8 and phenyl. The applicability of the method was evaluated by the inclusion of the other two substances in the study, i.e. monomeric and dimeric bioactive CPDs, compound TX-1123 and nostotrebin 6 with cytostatic and antimicrobial activities, respectively. The results presented here could be used in further investigations of the chromatographic retention and MS behavior of CPDs, which could be utilized for their isolation, detailed characterization and analysis in biological systems.
650    _2
$a benzylidenové deriváty $x analýza $7 D001597
650    12
$a vysokoúčinná kapalinová chromatografie $7 D002851
650    _2
$a cyklopentany $x analýza $x chemická syntéza $7 D003517
650    _2
$a molekulární struktura $7 D015394
650    12
$a tandemová hmotnostní spektrometrie $7 D053719
655    _2
$a časopisecké články $7 D016428
700    1_
$a Bernard, Martin $u Institute of Chemical Process Fundamentals of the AS CR, v.v.i., Rozvojova 135/1, Praha 165 02, Czech Republic.
700    1_
$a Ottenschlager, Jakub $u Institute of Chemical Process Fundamentals of the AS CR, v.v.i., Rozvojova 135/1, Praha 165 02, Czech Republic.
700    1_
$a Karban, Jindrich $u Institute of Chemical Process Fundamentals of the AS CR, v.v.i., Rozvojova 135/1, Praha 165 02, Czech Republic.
700    1_
$a Velisek, Petr $u Institute of Chemical Process Fundamentals of the AS CR, v.v.i., Rozvojova 135/1, Praha 165 02, Czech Republic.
700    1_
$a Hrbac, Jan $u Department of Analytical Chemistry, Regional Centre of Advanced Technologies and Materials, Faculty of Science, Palacky University, 17 listopadu 12, Olomouc 771 46, Czech Republic.
700    1_
$a Sykora, Jan $u Institute of Chemical Process Fundamentals of the AS CR, v.v.i., Rozvojova 135/1, Praha 165 02, Czech Republic.
700    1_
$a Storch, Jan $u Institute of Chemical Process Fundamentals of the AS CR, v.v.i., Rozvojova 135/1, Praha 165 02, Czech Republic.
700    1_
$a Vacek, Jan $u Department of Medical Chemistry and Biochemistry, Faculty of Medicine and Dentistry, Palacky University, Hnevotinska 3, Olomouc 775 15, Czech Republic. Electronic address: jan.vacek@upol.cz.
773    0_
$w MED00002894 $t Journal of pharmaceutical and biomedical analysis $x 1873-264X $g Roč. 128, č. - (2016), s. 342-51
856    41
$u https://pubmed.ncbi.nlm.nih.gov/27328361 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20170720 $b ABA008
991    __
$a 20170720124101 $b ABA008
999    __
$a ok $b bmc $g 1239577 $s 984809
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2016 $b 128 $c - $d 342-51 $e 20160602 $i 1873-264X $m Journal of pharmaceutical and biomedical analysis $n J Pharm Biomed Anal $x MED00002894
LZP    __
$a Pubmed-20170720

Najít záznam

Citační ukazatele

Nahrávání dat ...

    Možnosti archivace