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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Main Authors: Krzesimir Ciura, Joanna Fedorowicz, Petar Žuvela, Mario Lovrić, Hanna Kapica, Paweł Baranowski, Wiesław Sawicki, Ming Wah Wong, Jarosław Sączewski
Format: Article
Language:English
Published: MDPI AG 2020-10-01
Series:Molecules
Subjects:
Online Access:https://www.mdpi.com/1420-3049/25/20/4835
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spelling 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
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