Retention mechanisms of imidazolin and piperazine-related compounds in non-aqueous hydrophilic interaction and supercritical fluid chromatography based on chemometric design and analysis
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2022
Authors
Obradović, Darija
Komsta, Lukasz
Stavrianidi Nikolaevič, Andrey
Shpigun Aleksejevič, Oleg
Pokrovskiy Igorevič, Oleg
Vujić, Zorica

Article (Published version)

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Show full item recordAbstract
The experimental design methodology based on central composite design of experiments was applied
to compare the retention mechanisms in supercritical fluid chromatography (SFC) and non-aqueous hy-
drophilic interaction liquid chromatography (NA-HILIC). The selected set consists of 26 compounds that
belong to imidazoline and serotonin receptor ligands. The different chemometric tools (multiple linear
regression, principal component analysis, parallel factor analysis) were used to examine the retention, as
well as to identify the most significant retention mechanisms. The retention mechanism was investigated
on two different stationary phases (diol, and mixed-mode diol). In NA-HILIC, the mobile phase contains
acetonitrile as a main component, and methanolic solution of ammonium formate (+ 0.1% of formic acid)
as a modifier. The same mobile phase modifier was used in SFC, with a difference in the main component
of the mobile phase which was CO2.
The retention behaviour differs s...ignificantly between HILIC and SFC conditions. The retention pattern
in HILIC mode was more partition-like, while in SFC the solute-sorbent interactions allowed retention.
The retention mechanism between mixed-mode diol and the diol phases varies depending on the applied
chromatographic mode, e.g., in HILIC the type of stationary phase significantly affects the elution order,
while in SFC this was not the case. The HILIC retention behaviour was influenced by the number of
tertiary amines-aliphatic, and N atom-centred fragments in tested compounds. On the other hand, the
number of pyrrole and pyridine rings in the structure of the compound showed correlation with their
SFC retention, simultaneously increasing the molecular weight and rapid elution of larger compounds. It
was found that temperature surprisingly plays a major role in SFC mode. The increase in temperature
reduces the relative contribution of enthalpy factors to total retention, so the separation in SFC was more
entropy-controlled. For further pharmaceutical research and optimization, the SFC would be considered
more beneficial compared to HILIC since it gives good selectivity in separation of chosen impurities.
Keywords:
Chemometric design / Chemometric design / Supercritical fluid chromatography / Hydrophilic interaction chromatographySource:
Journal of Chromatography A, 2022, 1678Publisher:
- Elsevier B.V.
Funding / projects:
- info:eu-repo/grantAgreement/MESTD/inst-2020/200161/RS// (RS-200161) (RS-200161)
- The Russian Science Foundation (Grant No. 22-13-00266)
- The Ministry of Science and Higher Education of the Russian Federation as part of the State Assignment of the Kurnakov Institute of General and In- organic Chemistry of the Russian Academy of Sciences.
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Institution/Community
PharmacyTY - JOUR AU - Obradović, Darija AU - Komsta, Lukasz AU - Stavrianidi Nikolaevič, Andrey AU - Shpigun Aleksejevič, Oleg AU - Pokrovskiy Igorevič, Oleg AU - Vujić, Zorica PY - 2022 UR - https://farfar.pharmacy.bg.ac.rs/handle/123456789/4250 AB - The experimental design methodology based on central composite design of experiments was applied to compare the retention mechanisms in supercritical fluid chromatography (SFC) and non-aqueous hy- drophilic interaction liquid chromatography (NA-HILIC). The selected set consists of 26 compounds that belong to imidazoline and serotonin receptor ligands. The different chemometric tools (multiple linear regression, principal component analysis, parallel factor analysis) were used to examine the retention, as well as to identify the most significant retention mechanisms. The retention mechanism was investigated on two different stationary phases (diol, and mixed-mode diol). In NA-HILIC, the mobile phase contains acetonitrile as a main component, and methanolic solution of ammonium formate (+ 0.1% of formic acid) as a modifier. The same mobile phase modifier was used in SFC, with a difference in the main component of the mobile phase which was CO2. The retention behaviour differs significantly between HILIC and SFC conditions. The retention pattern in HILIC mode was more partition-like, while in SFC the solute-sorbent interactions allowed retention. The retention mechanism between mixed-mode diol and the diol phases varies depending on the applied chromatographic mode, e.g., in HILIC the type of stationary phase significantly affects the elution order, while in SFC this was not the case. The HILIC retention behaviour was influenced by the number of tertiary amines-aliphatic, and N atom-centred fragments in tested compounds. On the other hand, the number of pyrrole and pyridine rings in the structure of the compound showed correlation with their SFC retention, simultaneously increasing the molecular weight and rapid elution of larger compounds. It was found that temperature surprisingly plays a major role in SFC mode. The increase in temperature reduces the relative contribution of enthalpy factors to total retention, so the separation in SFC was more entropy-controlled. For further pharmaceutical research and optimization, the SFC would be considered more beneficial compared to HILIC since it gives good selectivity in separation of chosen impurities. PB - Elsevier B.V. T2 - Journal of Chromatography A T1 - Retention mechanisms of imidazolin and piperazine-related compounds in non-aqueous hydrophilic interaction and supercritical fluid chromatography based on chemometric design and analysis VL - 1678 DO - 10.1016/j.chroma.2022.463340 ER -
@article{ author = "Obradović, Darija and Komsta, Lukasz and Stavrianidi Nikolaevič, Andrey and Shpigun Aleksejevič, Oleg and Pokrovskiy Igorevič, Oleg and Vujić, Zorica", year = "2022", abstract = "The experimental design methodology based on central composite design of experiments was applied to compare the retention mechanisms in supercritical fluid chromatography (SFC) and non-aqueous hy- drophilic interaction liquid chromatography (NA-HILIC). The selected set consists of 26 compounds that belong to imidazoline and serotonin receptor ligands. The different chemometric tools (multiple linear regression, principal component analysis, parallel factor analysis) were used to examine the retention, as well as to identify the most significant retention mechanisms. The retention mechanism was investigated on two different stationary phases (diol, and mixed-mode diol). In NA-HILIC, the mobile phase contains acetonitrile as a main component, and methanolic solution of ammonium formate (+ 0.1% of formic acid) as a modifier. The same mobile phase modifier was used in SFC, with a difference in the main component of the mobile phase which was CO2. The retention behaviour differs significantly between HILIC and SFC conditions. The retention pattern in HILIC mode was more partition-like, while in SFC the solute-sorbent interactions allowed retention. The retention mechanism between mixed-mode diol and the diol phases varies depending on the applied chromatographic mode, e.g., in HILIC the type of stationary phase significantly affects the elution order, while in SFC this was not the case. The HILIC retention behaviour was influenced by the number of tertiary amines-aliphatic, and N atom-centred fragments in tested compounds. On the other hand, the number of pyrrole and pyridine rings in the structure of the compound showed correlation with their SFC retention, simultaneously increasing the molecular weight and rapid elution of larger compounds. It was found that temperature surprisingly plays a major role in SFC mode. The increase in temperature reduces the relative contribution of enthalpy factors to total retention, so the separation in SFC was more entropy-controlled. For further pharmaceutical research and optimization, the SFC would be considered more beneficial compared to HILIC since it gives good selectivity in separation of chosen impurities.", publisher = "Elsevier B.V.", journal = "Journal of Chromatography A", title = "Retention mechanisms of imidazolin and piperazine-related compounds in non-aqueous hydrophilic interaction and supercritical fluid chromatography based on chemometric design and analysis", volume = "1678", doi = "10.1016/j.chroma.2022.463340" }
Obradović, D., Komsta, L., Stavrianidi Nikolaevič, A., Shpigun Aleksejevič, O., Pokrovskiy Igorevič, O.,& Vujić, Z.. (2022). Retention mechanisms of imidazolin and piperazine-related compounds in non-aqueous hydrophilic interaction and supercritical fluid chromatography based on chemometric design and analysis. in Journal of Chromatography A Elsevier B.V.., 1678. https://doi.org/10.1016/j.chroma.2022.463340
Obradović D, Komsta L, Stavrianidi Nikolaevič A, Shpigun Aleksejevič O, Pokrovskiy Igorevič O, Vujić Z. Retention mechanisms of imidazolin and piperazine-related compounds in non-aqueous hydrophilic interaction and supercritical fluid chromatography based on chemometric design and analysis. in Journal of Chromatography A. 2022;1678. doi:10.1016/j.chroma.2022.463340 .
Obradović, Darija, Komsta, Lukasz, Stavrianidi Nikolaevič, Andrey, Shpigun Aleksejevič, Oleg, Pokrovskiy Igorevič, Oleg, Vujić, Zorica, "Retention mechanisms of imidazolin and piperazine-related compounds in non-aqueous hydrophilic interaction and supercritical fluid chromatography based on chemometric design and analysis" in Journal of Chromatography A, 1678 (2022), https://doi.org/10.1016/j.chroma.2022.463340 . .