Toward an automated workflow for the study of plasma
protein-drug interactions based on capillary
electrophoresis-frontal analysis combined with in-capillary
mixing of interacting partners

J 2021

Toward an automated workflow for the study of plasma protein-drug interactions based on capillary electrophoresis-frontal analysis combined with in-capillary mixing of interacting partners

MICHALCOVÁ, Lenka; Hana NEVÍDALOVÁ a Zdeněk GLATZ

Základní údaje

Originální název

Toward an automated workflow for the study of plasma protein-drug interactions based on capillary electrophoresis-frontal analysis combined with in-capillary mixing of interacting partners

Autoři

MICHALCOVÁ, Lenka; Hana NEVÍDALOVÁ a Zdeněk GLATZ

Vydání

Journal of Chromatography A, Amsterdam, Elsevier, 2021, 0021-9673

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Obor

10600 1.6 Biological sciences

Stát vydavatele

Nizozemské království

Utajení

není předmětem státního či obchodního tajemství

Odkazy

URL

Impakt faktor

Impact factor: 4.601

Označené pro přenos do RIV

Ano

Kód RIV

RIV/00216224:14310/21:00118782

Organizační jednotka

Přírodovědecká fakulta

Klíčová slova anglicky

capillary electrophoresis-frontal analysis; on-line mixing; TDLFP; protein-drug interaction

Štítky

14313050, rivok

Příznaky

Mezinárodní význam, Recenzováno

Změněno: 19. 2. 2021 21:17, prof. RNDr. Zdeněk Glatz, CSc.

Anotace

V originále

Capillary electrophoresis-frontal analysis (CE-FA) together with mobility shift affinity CE is the most frequently used mode of affinity CE for a study of plasma protein-drug interactions, which is a substantial part of the early stage of drug discovery. Whereas in the classic CE-FA setup the sample is prepared by off-line mixing of the interaction partners in the sample vial outside the CE instrument and after a short incubation period loaded into the capillary and analysed, in this work a new methodological approach has been developed that combines CE-FA with the mixing of interacting partners directly inside the capillary. This combination gives rise to a fully automated and versatile methodology for the characterization of these binding interactions besides a substantial reduction in the amounts of sample compounds used. The minimization of possible experimental errors due to the full involving of sophisticated CE instrument in the injection procedure, mixing and separation instead of manual manipulation is another fundamental benefit. The in-capillary mixing is based on the transverse diffusion of laminar flow profile methodology introduced by Krylov et al. using its multi-zone injection modification presented by Řemínek at al.. Actually, after the method optimization, the alternate introduction of six plugs of drug and six plugs of bovine serum protein in BGE, each injected for 3 s at a pressure of -10 mbar (-1 kPa) into the capillary filled by BGE, was found to be the best injection procedure. The method repeatability calculated as RSDs of plateau highs of bovine serum albumin and propranolol as model sample compounds were better than 3.44 %. Its applicability was finally demonstrated on the determination of apparent binding parameters of bovine serum albumin for basic drugs propranolol and lidocaine and acid drug phenylbutazone. The values obtained by a new on-line CE-FA methodology are in agreement with values estimated by classic off-line CE-FA, as well as with literature data obtained using different techniques.

Návaznosti

GA19-08358S, projekt VaV

Název: Nové přístupy pro studium afinitních interakcí založené na kapilární elektroforéze

Investor: Grantová agentura ČR, Nove přístupy pro studium afinitních interakcí založené na kapilární elektroforéze

Citovat

MICHALCOVÁ, Lenka; Hana NEVÍDALOVÁ a Zdeněk GLATZ. Toward an automated workflow for the study of plasma protein-drug interactions based on capillary electrophoresis-frontal analysis combined with in-capillary mixing of interacting partners. Journal of Chromatography A. Amsterdam: Elsevier, 2021, roč. 1635, January 2021, s. 461734-461742. ISSN 0021-9673. Dostupné z: https://doi.org/10.1016/j.chroma.2020.461734.

@article{1696696,
   author = {Michalcová, Lenka and Nevídalová, Hana and Glatz, Zdeněk},
   article_location = {Amsterdam},
   article_number = {January 2021},
   doi = {https://doi.org/10.1016/j.chroma.2020.461734},
   keywords = {capillary electrophoresis-frontal analysis; on-line mixing; TDLFP; protein-drug interaction},
   language = {eng},
   issn = {0021-9673},
   journal = {Journal of Chromatography A},
   title = {Toward an automated workflow for the study of plasma protein-drug interactions based on capillary electrophoresis-frontal analysis combined with in-capillary mixing of interacting partners},
   url = {https://doi.org/10.1016/j.chroma.2020.461734},
   volume = {1635},
   year = {2021}
}

TY  - JOUR
ID  - 1696696
AU  - Michalcová, Lenka - Nevídalová, Hana - Glatz, Zdeněk
PY  - 2021
TI  - Toward an automated workflow for the study of plasma protein-drug interactions based on capillary electrophoresis-frontal analysis combined with in-capillary mixing of interacting partners
JF  - Journal of Chromatography A
VL  - 1635
IS  - January 2021
SP  - 461734
EP  - 461734
PB  - Elsevier
SN  - 00219673
KW  - capillary electrophoresis-frontal analysis
KW  - on-line mixing
KW  - TDLFP
KW  - protein-drug interaction
UR  - https://doi.org/10.1016/j.chroma.2020.461734
L2  - https://doi.org/10.1016/j.chroma.2020.461734
N2  - Capillary electrophoresis-frontal analysis (CE-FA) together with mobility shift affinity CE is the most frequently used mode of affinity CE for a study of plasma protein-drug interactions, which is a substantial part of the early stage of drug discovery. Whereas in the classic CE-FA setup the sample is prepared by off-line mixing of the interaction partners in the sample vial outside the CE instrument and after a short incubation period loaded into the capillary and analysed, in this work a new methodological approach has been developed that combines CE-FA with the mixing of interacting partners directly inside the capillary. This combination gives rise to a fully automated and versatile methodology for the characterization of these binding interactions besides a substantial reduction in the amounts of sample compounds used. The minimization of possible experimental errors due to the full involving of sophisticated CE instrument in the injection procedure, mixing and separation instead of manual manipulation is another fundamental benefit. The in-capillary mixing is based on the transverse diffusion of laminar flow profile methodology introduced by Krylov et al. using its multi-zone injection modification presented by Řemínek at al.. Actually, after the method optimization, the alternate introduction of six plugs of drug and six plugs of bovine serum protein in BGE, each injected for 3 s at a pressure of -10 mbar (-1 kPa) into the capillary filled by BGE, was found to be the best injection procedure. The method repeatability calculated as RSDs of plateau highs of bovine serum albumin and propranolol as model sample compounds were better than 3.44 %. Its applicability was finally demonstrated on the determination of apparent binding parameters of bovine serum albumin for basic drugs propranolol and lidocaine and acid drug phenylbutazone. The values obtained by a new on-line CE-FA methodology are in agreement with values estimated by classic off-line CE-FA, as well as with literature data obtained using different techniques.
ER  -

MICHALCOVÁ, Lenka; Hana NEVÍDALOVÁ a Zdeněk GLATZ. Toward an automated workflow for the study of plasma protein-drug interactions based on capillary electrophoresis-frontal analysis combined with in-capillary mixing of interacting partners. \textit{Journal of Chromatography A}. Amsterdam: Elsevier, 2021, roč.~1635, January 2021, s.~461734-461742. ISSN~0021-9673. Dostupné z: https://doi.org/10.1016/j.chroma.2020.461734.

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