Number of found documents: 472
Published from to

Comparison of the Covalent Laccase Immobilization at Amino- and Carboxylfunctionalized Mesoporous Silica, Glassy Carbon, and Graphite Powders using Different Coupling Agents for Optimal Biosensor Preparation
Tvorynska, Sofiia; Barek, J.; Josypčuk, Bohdan
2021 - English
In order to find the most suitable immobilization protocol, a comparison of three strategies\nbased on the application of –NH2 and –COOH functionalized supports with the different\nactivation agents (glutaraldehyde and carbodiimide) have been conducted for the covalent\nenzyme (laccase) attachment. Two kinds of the supports, namely mesoporous silica (SBA−15,\nMCM−41) and carbonaceous (glassy carbon, graphite) powders, have been used. It was found\nthat a biosensor consisted of tubular detector of silver solid amalgam as a working electrode\nand the enzymatic mini-reactor with laccase covalently attached to glutaraldehyde activated\n–NH2 functionalized MCM−41 shows the best results regarding sensitivity and stability for\ndopamine detection. Keywords: Covalent enzyme immobilization; Support surface functionalization; Laccase Available on request at various institutes of the ASCR
Comparison of the Covalent Laccase Immobilization at Amino- and Carboxylfunctionalized Mesoporous Silica, Glassy Carbon, and Graphite Powders using Different Coupling Agents for Optimal Biosensor Preparation

In order to find the most suitable immobilization protocol, a comparison of three strategies\nbased on the application of –NH2 and –COOH functionalized supports with the different\nactivation agents ...

Tvorynska, Sofiia; Barek, J.; Josypčuk, Bohdan
Ústav fyzikální chemie J. Heyrovského, 2021

EPR/UV-VIS-NIR Spectroelectrochemical Examination of the Association Properties of Thienoacene-Bridged Tetrathiafulvalenes Supported by DFT Calculations
Lušpai, Karol; Rapta, P.; Zalibera, M.; Darvasiová, D.; Lukeš, V.
2021 - English
This work was focused on the EPR/UV-VIS-NIR spectroelectrochemical examination of\nassociation properties of radical cations electrochemically produced from tetrathiafulvalene\n(TTF) derivatives, in relation to the molecular structure, mainly the number and orientation of\nthiophene rings in the spacer between fulvalene redox centers. Results from EPR/UV-VIS-NIR\nspectroelectrochemistry were supported by DFT calculations. Keywords: Tetrathiafulvalene; EPR/UV-VIS-NIR spectroelectrochemistry; Cyclic voltammetry Available on request at various institutes of the ASCR
EPR/UV-VIS-NIR Spectroelectrochemical Examination of the Association Properties of Thienoacene-Bridged Tetrathiafulvalenes Supported by DFT Calculations

This work was focused on the EPR/UV-VIS-NIR spectroelectrochemical examination of\nassociation properties of radical cations electrochemically produced from tetrathiafulvalene\n(TTF) derivatives, in ...

Lušpai, Karol; Rapta, P.; Zalibera, M.; Darvasiová, D.; Lukeš, V.
Ústav fyzikální chemie J. Heyrovského, 2021

UV-Vis and IR Spectroelectrocbemistry of Copper Complexes and Bioactive Compounds
Sokolová, Romana; Obluková, Michaela; Sýs, M.; Mikysek, T.; Wantulok, J.; Nycz, J. E.; Degano, I.
2021 - English
The interpretation of the change of absorption spectrum of an oxidized and reduced molecule\nrecorded during the electron transfer is an efficient tool for the determination of oxidation or\nreduction mechanism. This technique provides the information about the electroactive\nchromophore and is performed in two regimes of electrochemical measurement, cyclic\nvoltammetry and chronoamperometry, respectively. This approach was successfully applied to\nstudy the fundamental electrochemical behavior of recently synthesized copper complexes\nproviding biomimetic activity, ofpolyphenolic bioactive compounds, and also for the reduction\nof halogenated phenanthrolines. The identification of redox products was done by\nchromatographic techniques as HPLC-DAD and HPLC-ESI-MS/MS. Keywords: Copper complexes; Catechol; spectroelectrochemistry Available on request at various institutes of the ASCR
UV-Vis and IR Spectroelectrocbemistry of Copper Complexes and Bioactive Compounds

The interpretation of the change of absorption spectrum of an oxidized and reduced molecule\nrecorded during the electron transfer is an efficient tool for the determination of oxidation or\nreduction ...

Sokolová, Romana; Obluková, Michaela; Sýs, M.; Mikysek, T.; Wantulok, J.; Nycz, J. E.; Degano, I.
Ústav fyzikální chemie J. Heyrovského, 2021

Ion Transfer Voltammetry across the Polarized Ionic Liquid/Water Interface: Base for Electrochemical Sensors
Langmaier, Jan; Samec, Zdeněk
2021 - English
Some electrochemical techniques such as voltammetry at the polarized interfaces between two\nimmiscible electrolyte solutions (ITIES) represent interesting alternatives to classical\nelectrochemistry. The benefit of the ion transfer voltammetry lies in the possibility of detection\nof ionic species which are not otherwise redox active. The methodology enables apart of direct\ndetermination of ionic samples (including pharmaceutical and clinical ones) also to monitor\nreaction processes (acido-basic, enzymatic, etc.), determination of reaction substrates and\nproducts in one experimental step, evaluation of reaction and transport kinetics, and estimation\nof lipophilicity of involved species. Keywords: ion transfer voltammetry; electrochemical detection; ionic liquid Available on request at various institutes of the ASCR
Ion Transfer Voltammetry across the Polarized Ionic Liquid/Water Interface: Base for Electrochemical Sensors

Some electrochemical techniques such as voltammetry at the polarized interfaces between two\nimmiscible electrolyte solutions (ITIES) represent interesting alternatives to classical\nelectrochemistry. ...

Langmaier, Jan; Samec, Zdeněk
Ústav fyzikální chemie J. Heyrovského, 2021

The use of Boron Doped Diamond Electrode for Determination of 5-hydroxyindoleacetic Acid
Hrdlička, Vojtěch; Navrátil, Tomáš
2021 - English
A new method for voltammetric determination of clinical biomarker 5-hydroxyindoleacetic\nacid (HIAA) at the boron-doped diamond electrode (BDDE) was developed. Anodically and\ncathodically pretreated BDDEs were tested in the pH ranges from 1 to 12, pre-treatment at\n+2.0V/60 s, and pH 3 was found to be the optimum.\nThe optimum square wave voltammetry (SWV) parameters were: f = 12 Hz, amplitude 60\nmV, and potential step 4 mV. SWV concentration dependency was constructed in the range\nfrom 0.1 to 100 μmol L−1, limits of determination and detection were 0.3 and 0.1 μmol L−1,\nrespectively. HIAA oxidation electrode process at BDDE was diffusion-controlled, as\nuncovered by cyclic voltammetry. Interestingly, HIAA peak potential was constant in various\nranges of pH, indicating a non-Nernstian behavior at the BDDE, in contrast to a previously\npublished electrooxidation mechanism consisting of a coupled H+/e− transfer. Keywords: boron-doped diamond electrode; 5-hydroxyindoleacetic acid; square wave voltammetry Available on request at various institutes of the ASCR
The use of Boron Doped Diamond Electrode for Determination of 5-hydroxyindoleacetic Acid

A new method for voltammetric determination of clinical biomarker 5-hydroxyindoleacetic\nacid (HIAA) at the boron-doped diamond electrode (BDDE) was developed. Anodically and\ncathodically pretreated ...

Hrdlička, Vojtěch; Navrátil, Tomáš
Ústav fyzikální chemie J. Heyrovského, 2021

Determination of Selected Drugs using 3D Printed Electrodes
Choińska-Mlynarczyk, Marta; Hrdlička, Vojtěch; Navrátil, Tomáš
2021 - English
The main aim of this research was to develop a new method for voltammetric determination of\npopular antidepressants, analgesics, and illicit drugs using a laboratory-made 3D printed\nelectrode and to compare the achieved results with those registered using a commercially\navailable glassy carbon electrode. These experiments represent the first step in the development\nof a method applicable in clinical and forensic praxis for the rapid and inexpensive\ndetermination of commonly misused groups of biologically active compounds. Keywords: analgesics; antidepressants; biologically active compounds Available on request at various institutes of the ASCR
Determination of Selected Drugs using 3D Printed Electrodes

The main aim of this research was to develop a new method for voltammetric determination of\npopular antidepressants, analgesics, and illicit drugs using a laboratory-made 3D printed\nelectrode and to ...

Choińska-Mlynarczyk, Marta; Hrdlička, Vojtěch; Navrátil, Tomáš
Ústav fyzikální chemie J. Heyrovského, 2021

Rozdíly v elektrochemické redukci jedno- a vícejaderných acylgermanů
Liška, Alan; Frühwirt, P.; Haas, M.; Ludvík, Jiří; Gescheidt-Demmer, G.
2021 - Czech
Acylgermany představují pestrou třídu organoprvkových sloučenin, které se vyznacuJI\npozoruhodnými fotochemickými vlastnostmi, laditelnými zavedením různých typů periferních\nsubstituentů, jejich počtem, polohou, případně způsobem přemostění. Většina známých\nderivátů podléhá vlivem DV-záření nebo dokonce krátkovlnějšího viditelného světla\nhomolytickému štěpení vazby C-Ge za vzniku radikálů. Některé (např. Ivocerin®) se proto již\ndelší dobu používají v zubní medicíně jako fotoiniciátory polymerizace při přípravě bílých\nnetoxických zubních výplní. Příslušné mechanismy reakcí uplatňujících se v praxi jsou v\nliteratuře dobře dokumentovány. Vzhledem k tomu, že penetrační hloubka\nelektromagnetického záření je nepřímo úměrná jeho energii, existuje snaha nalézt další\nderiváty, které budou efektivně štěpeny světlem o co největší vlnové délce. Kromě absorpčních\nspekter a teoretických výpočtů molekulových vlastností (ionizační energie, elektronové\nafinity) se při hledání nových látek s výhodou uplatňují elektrochemické metody, protože\npoloha prvního redukčního potenciálu (resp. rozdíl mezi prvním redukčním a prvním\noxidačním potenciálem) koreluje se schopností molekuly absorbovat světlo a zaujímat vyšší\nexcitované stavy, což se projeví jako poloha dlouhovlnného pásu UV-vis spekter. Ail the studied compounds accept first electron under formation a stable anion radical. The\ncorresponding reduction potentials in aprotic media depend on electronic (inductive,\nmesomeric) properties of the substituents, their number, and position. Here, aromatic acyl group\n(benzoyl group with various substitution on aromatic ring) is the principal substituent. The\nredox properties of presented organoelement compounds with central heteroatom Ge (Si, Sn)\nare controlled by peripheral carbonyl groups (in role of redox centers), their number, and\naromatic ring substitution. The measured first reduction potentials E1 values are found in wide\nrange (> 900 mV) due to the fact that the redox centers are carbony 1 groups connected through\nheteroatom in case of acylgermanes, while for di- and trinuclear derivatives (which are\nmolecules with multiple redox centers) the easiest reducible center is the bridging aromatic unit\ninfluenced by the closest carbonyl groups. Thus, it is possible to distinguish both groups ofnonequivalent\ncarbonyl substituents. Keywords: Acylgermanes; Electrochemistry; Voltammetry Available on request at various institutes of the ASCR
Rozdíly v elektrochemické redukci jedno- a vícejaderných acylgermanů

Acylgermany představují pestrou třídu organoprvkových sloučenin, které se vyznacuJI\npozoruhodnými fotochemickými vlastnostmi, laditelnými zavedením různých typů periferních\nsubstituentů, jejich ...

Liška, Alan; Frühwirt, P.; Haas, M.; Ludvík, Jiří; Gescheidt-Demmer, G.
Ústav fyzikální chemie J. Heyrovského, 2021

Determination of heavy metal poisoning antidote 2,3-dimercapto-1-propanesulfonic acid using silver solid amalgam electrode
Choińska-Mlynarczyk, Marta; Hrdlička, Vojtěch; Redondo, B. R.; Barek, J.; Navrátil, Tomáš
2020 - English
2,3-Dimercapto-1-propane-sulfonic acid (DMPS) was investigated using direct current voltammetry (DCV), differential pulse cathodic stripping voltammetry (DPCSV), differential pulse anodic stripping voltammetry (DPASV), and elimination voltammetry with linear scan (EVLS) at a polished (p-AgSAE)and at a meniscus modified silver solid amalgam electrode (m-AgSAE). EVLS confirmed two consecutive reductions with coupled proton/electron transfer. Voltammetric titrations of DMPS with Pb2+ proved complex formation, with limits of quantification (LOQs) and detection (LODs) 0.3 and 0.1 mu mol L-1 at m-AgSAE and 0.8 and 0.3 mu mol L-1 at p-AgSAE, respectively. Determination of DMPS in commercial drug Dimaval and human urine samples confirmed practical applicability of the developed method. Keywords: cathodic stripping voltammetry; 2,3-dimercapto-1-pro-panesulfonic acid; elimination voltammetry with linear scan Available on request at various institutes of the ASCR
Determination of heavy metal poisoning antidote 2,3-dimercapto-1-propanesulfonic acid using silver solid amalgam electrode

2,3-Dimercapto-1-propane-sulfonic acid (DMPS) was investigated using direct current voltammetry (DCV), differential pulse cathodic stripping voltammetry (DPCSV), differential pulse anodic stripping ...

Choińska-Mlynarczyk, Marta; Hrdlička, Vojtěch; Redondo, B. R.; Barek, J.; Navrátil, Tomáš
Ústav fyzikální chemie J. Heyrovského, 2020

Voltametrické stanovení pálivosti chilli paprik na elektrodě ze skelného uhlíku modifikované fosfolipidy
Skopalová, J.; Rajcová, A.; Vokounová, D.; Navrátil, Tomáš
2019 - Czech
Kapsaicin je přírodní alkaloid vyskytující se v plodech chilli paprik, které patří k nejdůležitějším a nejrozšířenějším kořením. Za jejich popularitou stojí významné organoleptické vlastnosti (typická pálivá chuť), antioxidační či antimikrobiální účinky. Pálivost chilli paprik je hlavním důvodem jejich konzumace a z pohledu konzumenta představuje jednu z jejich nejdůležitějších charakteristik. Od toho se proto odvozuje potřeba tuto charakteristiku kvantifikovat. Míra pálivosti přímo souvisí s obsahem kapsaicinu a jemu podobných látek (kapsaicinoidů) v paprikách. Kromě potravinářství nachází kapsaicin své užití i v lesnictví (zemědělství) jako ochrana před okusem stromů zvěří. The aim of this study was to develop a simple method for evaluation of the pungency in chili peppers with a glassy carbon electrode modified using phospholipid membrane prepared from asolectin. For these purposes cyclic voltammetry (CV) and differential pulse voltammetry (DPV) have been used. A few different methods have been tested: direct method, transfer method on unmodified and modified electrode, using standard addition method as well as calibration curve method. A statistically significant correlations with the results of the reference HPLC method have been found in case of voltammetric methods, especially in DPV with asolectin modified electrode. Keywords: capsaicin; voltammetry; glassy carbon electrode Available on request at various institutes of the ASCR
Voltametrické stanovení pálivosti chilli paprik na elektrodě ze skelného uhlíku modifikované fosfolipidy

Kapsaicin je přírodní alkaloid vyskytující se v plodech chilli paprik, které patří k nejdůležitějším a nejrozšířenějším kořením. Za jejich popularitou stojí významné organoleptické vlastnosti (typická ...

Skopalová, J.; Rajcová, A.; Vokounová, D.; Navrátil, Tomáš
Ústav fyzikální chemie J. Heyrovského, 2019

Charge Transport in Single Oligophenylene Molecular Wires with Different Anchoring Groups
Hromadová, Magdaléna; Kolivoška, Viliam; Šebera, Jakub; Sebechlebská, Táňa; Gasior, Jindřich; Nováková Lachmanová, Štěpánka; Mészáros, G.; Lindner, M.; Mayor, M.; Valášek, M.
2019 - English
This work compares single molecule conductance measurements of selected organic systems containing identical oligophenylene molecular wires and different tripodal anchoring groups. Single molecule conductance G was obtained by a scanning tunneling microscopy break junction technique complemented by theoretical calculations based on the density functional theory and non-equilibrium Green’s function formalism. Two molecules were compared where the same oligophenylene wire is connected to one of the electrodes via a tripod substituted on each leg by a thiol group either in the meta or para position. By combined experimental and theoretical analysis it was possible to confirm that single molecule conductance in the metal-molecule-metal junction of both molecules corresponds to a fully extended molecular wire, which is attached to one of the electrodes by all three thiolate bonds of the tripod. Experimental results confirmed that G value of meta-connected molecules is lower than that of para, whereas junction formation probability was higher for meta functionalization. Keywords: STM break junction; Tetraphenylmethane Tripodal anchor; Single molecule conductance Available at various institutes of the ASCR
Charge Transport in Single Oligophenylene Molecular Wires with Different Anchoring Groups

This work compares single molecule conductance measurements of selected organic systems containing identical oligophenylene molecular wires and different tripodal anchoring groups. Single molecule ...

Hromadová, Magdaléna; Kolivoška, Viliam; Šebera, Jakub; Sebechlebská, Táňa; Gasior, Jindřich; Nováková Lachmanová, Štěpánka; Mészáros, G.; Lindner, M.; Mayor, M.; Valášek, M.
Ústav fyzikální chemie J. Heyrovského, 2019

About project

NRGL provides central access to information on grey literature produced in the Czech Republic in the fields of science, research and education. You can find more information about grey literature and NRGL at service web

Send your suggestions and comments to nusl@techlib.cz

Provider

http://www.techlib.cz

Facebook

Other bases