The separation of cyclic diadenosine diphosphorothioate and the diastereomers of its difluorinated derivative and the estimation of the binding constants and ionic mobilities of their complexes with 2-hydroxypropyl-β-cyclodextrin by affinity capillary electrophoresis

0581779 - ÚOCHB 2025 RIV US eng J - Článek v odborném periodiku
Štěpánová, Sille - Břehová, Petra - Kašička, Václav
The separation of cyclic diadenosine diphosphorothioate and the diastereomers of its difluorinated derivative and the estimation of the binding constants and ionic mobilities of their complexes with 2-hydroxypropyl-β-cyclodextrin by affinity capillary electrophoresis.
Electrophoresis. (2024). ISSN 0173-0835. E-ISSN 1522-2683
Grant CEP: GA ČR(CZ) GA20-03899S
Institucionální podpora: RVO:61388963
Klíčová slova: affinity capillary electrophoresis * binding constant * chiral analysis * cyclic dinucleotides * cyclodextrins
Impakt faktor: 2.9, rok: 2022
Způsob publikování: Open access
https://doi.org/10.1002/elps.202300191

The incorporation of phosphorothioate linkages has recently been extensively employed in therapeutic oligonucleotides. For their separation and quality control, new high-efficient and high-sensitive analytical methods are needed. In this work, a new affinity capillary electrophoresis method has been developed and applied for the separation of a potential anticancer drug, 2 ',3 '-cyclic diadenosine diphosphorothioate (Rp, Rp) (ADU-S100), and three recently newly synthesized diastereomers of its difluorinated derivative, 3 ',3 '-cyclic di(2 '-fluoro, 2 '-deoxyadenosine phosphorothioate). The separation was performed in the various background electrolytes (BGEs) within a pH range 5-9 using several native and derivatized cyclodextrins (CDs) as chiral additives of the BGE. Relatively good separations were obtained with beta-, gamma-, and 2-hydroxypropyl-gamma-CDs in some of the BGEs tested. However, the best separation was achieved using the 2-hydroxypropyl-beta-CD chiral selector at 43.5 mM average concentration in the BGE composed of 40 mM Tris, 40 mM tricine, pH 8.1. Under these conditions, all the previous four cyclic dinucleotides (CDNs) were baseline separated within 4 min. Additionally, the average apparent binding constants and the average actual ionic mobilities of the complexes of all four CDNs with 2-hydroxypropyl-beta-CD in the above BGE were determined. The formed complexes were found to be relatively weak, with the average apparent binding constants in the range of 12.2-94.1 L mol-1 and with the actual ionic mobilities spanning the interval (-7.8 to12.7) x 10-9 m2 V-1 s-1. The developed method can be applied for the separation, analysis, and characterization of the above and similar CDNs.
Trvalý link: https://hdl.handle.net/11104/0349913