-
Je něco špatně v tomto záznamu ?
Insights into head-column field-amplified sample stacking: Part II. Study of the behavior of the electrophoretic system after electrokinetic injection of cationic compounds across a short water plug
J. Šesták, W. Thormann,
Jazyk angličtina Země Nizozemsko
Typ dokumentu časopisecké články
- MeSH
- elektroforéza kapilární přístrojové vybavení metody MeSH
- elektrolyty chemie MeSH
- elektroosmóza MeSH
- kationty chemie MeSH
- kyseliny fosforečné chemie MeSH
- počítačová simulace MeSH
- pufry MeSH
- voda chemie MeSH
- Publikační typ
- časopisecké články MeSH
Part I on head-column field-amplified sample stacking comprised a detailed study of the electrokinetic injection of a weak base across a short water plug into a phosphate buffer at low pH. The water plug is converted into a low conductive acidic zone and cationic analytes become stacked at the interface between this and a newly formed phosphoric acid zone. The fundamentals of electrokinetic processes occurring thereafter were studied experimentally and with computer simulation and are presented as part II. The configuration analyzed represents a discontinuous buffer system. Computer simulation revealed that the phosphoric acid zone at the plug-buffer interface becomes converted into a migrating phosphate buffer plug which corresponds to the cationically migrating system zone of the phosphate buffer system. Its mobility is higher than that of the analytes such that they migrate behind the system zone in a phosphate buffer comparable to the applied background electrolyte. The temporal behaviour of the current and the conductivity across the water plug were monitored and found to reflect the changes in the low conductivity plug. Determination of the buffer flow in the capillary revealed increased pumping caused by the mismatch of electroosmosis within the low conductivity plug and the buffer. This effect becomes elevated with increasing water plug length. For plug lengths up to 1% of the total column length the flow quickly drops to the electroosmotic flow of the buffer and simulations with experimentally determined current and flow values predict negligible band dispersion and no loss of resolution for both low and large molecular mass components.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc18016484
- 003
- CZ-PrNML
- 005
- 20180515103743.0
- 007
- ta
- 008
- 180515s2017 ne f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1016/j.chroma.2017.06.073 $2 doi
- 035 __
- $a (PubMed)28712552
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a ne
- 100 1_
- $a Šesták, Jozef $u Clinical Pharmacology Laboratory, Institute for Infectious Diseases, University of Bern, Bern, Switzerland; Institute of Analytical Chemistry of the Czech Academy of Sciences, v. v. i., Brno, Czechia.
- 245 10
- $a Insights into head-column field-amplified sample stacking: Part II. Study of the behavior of the electrophoretic system after electrokinetic injection of cationic compounds across a short water plug / $c J. Šesták, W. Thormann,
- 520 9_
- $a Part I on head-column field-amplified sample stacking comprised a detailed study of the electrokinetic injection of a weak base across a short water plug into a phosphate buffer at low pH. The water plug is converted into a low conductive acidic zone and cationic analytes become stacked at the interface between this and a newly formed phosphoric acid zone. The fundamentals of electrokinetic processes occurring thereafter were studied experimentally and with computer simulation and are presented as part II. The configuration analyzed represents a discontinuous buffer system. Computer simulation revealed that the phosphoric acid zone at the plug-buffer interface becomes converted into a migrating phosphate buffer plug which corresponds to the cationically migrating system zone of the phosphate buffer system. Its mobility is higher than that of the analytes such that they migrate behind the system zone in a phosphate buffer comparable to the applied background electrolyte. The temporal behaviour of the current and the conductivity across the water plug were monitored and found to reflect the changes in the low conductivity plug. Determination of the buffer flow in the capillary revealed increased pumping caused by the mismatch of electroosmosis within the low conductivity plug and the buffer. This effect becomes elevated with increasing water plug length. For plug lengths up to 1% of the total column length the flow quickly drops to the electroosmotic flow of the buffer and simulations with experimentally determined current and flow values predict negligible band dispersion and no loss of resolution for both low and large molecular mass components.
- 650 _2
- $a pufry $7 D002021
- 650 _2
- $a kationty $x chemie $7 D002412
- 650 _2
- $a počítačová simulace $7 D003198
- 650 _2
- $a elektrolyty $x chemie $7 D004573
- 650 _2
- $a elektroosmóza $7 D053841
- 650 _2
- $a elektroforéza kapilární $x přístrojové vybavení $x metody $7 D019075
- 650 _2
- $a kyseliny fosforečné $x chemie $7 D010756
- 650 _2
- $a voda $x chemie $7 D014867
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Thormann, Wolfgang $u Clinical Pharmacology Laboratory, Institute for Infectious Diseases, University of Bern, Bern, Switzerland. Electronic address: wolfgang.thormann@ifik.unibe.ch.
- 773 0_
- $w MED00004962 $t Journal of chromatography. A $x 1873-3778 $g Roč. 1512, č. - (2017), s. 124-132
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/28712552 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20180515 $b ABA008
- 991 __
- $a 20180515103917 $b ABA008
- 999 __
- $a ok $b bmc $g 1300108 $s 1013324
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2017 $b 1512 $c - $d 124-132 $e 20170630 $i 1873-3778 $m Journal of chromatography. A, Including electrophoresis and other separation methods $n J Chromatogr A $x MED00004962
- LZP __
- $a Pubmed-20180515