Affinity capillary electrophoresis: the theory of electromigration
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F16%3A10332106" target="_blank" >RIV/00216208:11310/16:10332106 - isvavai.cz</a>
Výsledek na webu
<a href="http://dx.doi.org/10.1007/s00216-016-9799-y" target="_blank" >http://dx.doi.org/10.1007/s00216-016-9799-y</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1007/s00216-016-9799-y" target="_blank" >10.1007/s00216-016-9799-y</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Affinity capillary electrophoresis: the theory of electromigration
Popis výsledku v původním jazyce
We focus on the state-of-the-art theory of electromigration under single and multiple complexation equilibrium. Only 1:1 complexation stoichiometry is discussed because of its unique status in the field of affinity capillary electrophoresis (ACE). First, we summarize the formulas for the effective mobility in various ACE systems as they appeared since the pioneering days in 1992 up to the most recent theories till 2015. Disturbing phenomena that do not alter the mobility of the analyte directly but cause an unexpected peak broadening have been studied only recently and are also discussed in this paper. Second, we turn our attention to the viscosity effects in ACE. Change in the background electrolyte viscosity is unavoidable in ACE but numerous observations scattered throughout the literature have not been reviewed previously. This leads to an uncritical employment of correction factors that may or may not be appropriate in practice. Finally, we consider the ionic strength effects in ACE, too. Limitations of the current theories are also discussed and the tasks identified where open problems still prevail.
Název v anglickém jazyce
Affinity capillary electrophoresis: the theory of electromigration
Popis výsledku anglicky
We focus on the state-of-the-art theory of electromigration under single and multiple complexation equilibrium. Only 1:1 complexation stoichiometry is discussed because of its unique status in the field of affinity capillary electrophoresis (ACE). First, we summarize the formulas for the effective mobility in various ACE systems as they appeared since the pioneering days in 1992 up to the most recent theories till 2015. Disturbing phenomena that do not alter the mobility of the analyte directly but cause an unexpected peak broadening have been studied only recently and are also discussed in this paper. Second, we turn our attention to the viscosity effects in ACE. Change in the background electrolyte viscosity is unavoidable in ACE but numerous observations scattered throughout the literature have not been reviewed previously. This leads to an uncritical employment of correction factors that may or may not be appropriate in practice. Finally, we consider the ionic strength effects in ACE, too. Limitations of the current theories are also discussed and the tasks identified where open problems still prevail.
Klasifikace
Druh
J<sub>x</sub> - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)
CEP obor
CB - Analytická chemie, separace
OECD FORD obor
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Návaznosti výsledku
Projekt
<a href="/cs/project/GJ15-18424Y" target="_blank" >GJ15-18424Y: Vývoj nové generace software a pokročilé teorie elektromigrace v metodách elektrokinetické chromatografie</a><br>
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Ostatní
Rok uplatnění
2016
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Analytical and Bioanalytical Chemistry
ISSN
1618-2642
e-ISSN
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Svazek periodika
408
Číslo periodika v rámci svazku
30
Stát vydavatele periodika
DE - Spolková republika Německo
Počet stran výsledku
19
Strana od-do
8623-8641
Kód UT WoS článku
000389605400007
EID výsledku v databázi Scopus
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