Affinity of Antifungal Isoxazolo[3,4-<i>b</i>]pyridine-3(1<i>H</i>)-Ones to Phospholipids in Immobilized Artificial Membrane (IAM) Chromatography
Currently, rapid evaluation of the physicochemical parameters of drug candidates, such as lipophilicity, is in high demand owing to it enabling the approximation of the processes of absorption, distribution, metabolism, and elimination. Although the lipophilicity of drug candidates is determined usi...
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2020-10-01
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doaj-fe9601ce57504dbb9e82b9008fde9bc92020-11-25T03:44:29ZengMDPI AGMolecules1420-30492020-10-01254835483510.3390/molecules25204835Affinity of Antifungal Isoxazolo[3,4-<i>b</i>]pyridine-3(1<i>H</i>)-Ones to Phospholipids in Immobilized Artificial Membrane (IAM) ChromatographyKrzesimir Ciura0Joanna Fedorowicz1Petar Žuvela2Mario Lovrić3Hanna Kapica4Paweł Baranowski5Wiesław Sawicki6Ming Wah Wong7Jarosław Sączewski8Department of Physical Chemistry, Faculty of Pharmacy, Medical University of Gdańsk, Al. Gen. J. Hallera 107, 80-416, Gdańsk, PolandDepartment of Chemical Technology of Drugs, Faculty of Pharmacy, Medical University of Gdańsk, Al. Gen. J. Hallera 107, 80-416, Gdańsk, PolandDepartment of Chemistry, National University of Singapore, 3 Science Drive 3, Singapore 117543, SingaporeKnow-Center, Inffeldgasse 13, AT-8010 Graz, AustriaDepartment of Physical Chemistry, Faculty of Pharmacy, Medical University of Gdańsk, Al. Gen. J. Hallera 107, 80-416, Gdańsk, PolandDepartment of Physical Chemistry, Faculty of Pharmacy, Medical University of Gdańsk, Al. Gen. J. Hallera 107, 80-416, Gdańsk, PolandDepartment of Physical Chemistry, Faculty of Pharmacy, Medical University of Gdańsk, Al. Gen. J. Hallera 107, 80-416, Gdańsk, PolandDepartment of Chemistry, National University of Singapore, 3 Science Drive 3, Singapore 117543, SingaporeDepartment of Organic Chemistry, Faculty of Pharmacy, Medical University of Gdańsk, Al. Gen. J. Hallera 107, 80-416, Gdańsk, PolandCurrently, rapid evaluation of the physicochemical parameters of drug candidates, such as lipophilicity, is in high demand owing to it enabling the approximation of the processes of absorption, distribution, metabolism, and elimination. Although the lipophilicity of drug candidates is determined using the shake flash method (<i>n</i>-octanol/water system) or reversed phase liquid chromatography (RP-LC), more biosimilar alternatives to classical lipophilicity measurement are currently available. One of the alternatives is immobilized artificial membrane (IAM) chromatography. The present study is a continuation of our research focused on physiochemical characterization of biologically active derivatives of isoxazolo[3,4-<i>b</i>]pyridine-3(1<i>H</i>)-ones. The main goal of this study was to assess the affinity of isoxazolones to phospholipids using IAM chromatography and compare it with the lipophilicity parameters established by reversed phase chromatography. Quantitative structure–retention relationship (QSRR) modeling of IAM retention using differential evolution coupled with partial least squares (DE-PLS) regression was performed. The results indicate that in the studied group of structurally related isoxazolone derivatives, discrepancies occur between the retention under IAM and RP-LC conditions. Although some correlation between these two chromatographic methods can be found, lipophilicity does not fully explain the affinities of the investigated molecules to phospholipids. QSRR analysis also shows common factors that contribute to retention under IAM and RP-LC conditions. In this context, the significant influences of WHIM and GETAWAY descriptors in all the obtained models should be highlighted.https://www.mdpi.com/1420-3049/25/20/4835immobilized artificial membraneIAM-HPLCisoxazolo[3,4-<i>b</i>]pyridin-3(1<i>H</i>)-oneisoxazolone |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Krzesimir Ciura Joanna Fedorowicz Petar Žuvela Mario Lovrić Hanna Kapica Paweł Baranowski Wiesław Sawicki Ming Wah Wong Jarosław Sączewski |
spellingShingle |
Krzesimir Ciura Joanna Fedorowicz Petar Žuvela Mario Lovrić Hanna Kapica Paweł Baranowski Wiesław Sawicki Ming Wah Wong Jarosław Sączewski Affinity of Antifungal Isoxazolo[3,4-<i>b</i>]pyridine-3(1<i>H</i>)-Ones to Phospholipids in Immobilized Artificial Membrane (IAM) Chromatography Molecules immobilized artificial membrane IAM-HPLC isoxazolo[3,4-<i>b</i>]pyridin-3(1<i>H</i>)-one isoxazolone |
author_facet |
Krzesimir Ciura Joanna Fedorowicz Petar Žuvela Mario Lovrić Hanna Kapica Paweł Baranowski Wiesław Sawicki Ming Wah Wong Jarosław Sączewski |
author_sort |
Krzesimir Ciura |
title |
Affinity of Antifungal Isoxazolo[3,4-<i>b</i>]pyridine-3(1<i>H</i>)-Ones to Phospholipids in Immobilized Artificial Membrane (IAM) Chromatography |
title_short |
Affinity of Antifungal Isoxazolo[3,4-<i>b</i>]pyridine-3(1<i>H</i>)-Ones to Phospholipids in Immobilized Artificial Membrane (IAM) Chromatography |
title_full |
Affinity of Antifungal Isoxazolo[3,4-<i>b</i>]pyridine-3(1<i>H</i>)-Ones to Phospholipids in Immobilized Artificial Membrane (IAM) Chromatography |
title_fullStr |
Affinity of Antifungal Isoxazolo[3,4-<i>b</i>]pyridine-3(1<i>H</i>)-Ones to Phospholipids in Immobilized Artificial Membrane (IAM) Chromatography |
title_full_unstemmed |
Affinity of Antifungal Isoxazolo[3,4-<i>b</i>]pyridine-3(1<i>H</i>)-Ones to Phospholipids in Immobilized Artificial Membrane (IAM) Chromatography |
title_sort |
affinity of antifungal isoxazolo[3,4-<i>b</i>]pyridine-3(1<i>h</i>)-ones to phospholipids in immobilized artificial membrane (iam) chromatography |
publisher |
MDPI AG |
series |
Molecules |
issn |
1420-3049 |
publishDate |
2020-10-01 |
description |
Currently, rapid evaluation of the physicochemical parameters of drug candidates, such as lipophilicity, is in high demand owing to it enabling the approximation of the processes of absorption, distribution, metabolism, and elimination. Although the lipophilicity of drug candidates is determined using the shake flash method (<i>n</i>-octanol/water system) or reversed phase liquid chromatography (RP-LC), more biosimilar alternatives to classical lipophilicity measurement are currently available. One of the alternatives is immobilized artificial membrane (IAM) chromatography. The present study is a continuation of our research focused on physiochemical characterization of biologically active derivatives of isoxazolo[3,4-<i>b</i>]pyridine-3(1<i>H</i>)-ones. The main goal of this study was to assess the affinity of isoxazolones to phospholipids using IAM chromatography and compare it with the lipophilicity parameters established by reversed phase chromatography. Quantitative structure–retention relationship (QSRR) modeling of IAM retention using differential evolution coupled with partial least squares (DE-PLS) regression was performed. The results indicate that in the studied group of structurally related isoxazolone derivatives, discrepancies occur between the retention under IAM and RP-LC conditions. Although some correlation between these two chromatographic methods can be found, lipophilicity does not fully explain the affinities of the investigated molecules to phospholipids. QSRR analysis also shows common factors that contribute to retention under IAM and RP-LC conditions. In this context, the significant influences of WHIM and GETAWAY descriptors in all the obtained models should be highlighted. |
topic |
immobilized artificial membrane IAM-HPLC isoxazolo[3,4-<i>b</i>]pyridin-3(1<i>H</i>)-one isoxazolone |
url |
https://www.mdpi.com/1420-3049/25/20/4835 |
work_keys_str_mv |
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