-
Je něco špatně v tomto záznamu ?
Meta-Analysis of Permeability Literature Data Shows Possibilities and Limitations of Popular Methods
K. Storchmannová, M. Balouch, J. Juračka, F. Štěpánek, K. Berka
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, metaanalýza
- MeSH
- buňky MDCK MeSH
- Caco-2 buňky MeSH
- hematoencefalická bariéra metabolismus MeSH
- lidé MeSH
- liposomy * chemie MeSH
- membrány umělé MeSH
- permeabilita buněčné membrány fyziologie MeSH
- permeabilita * MeSH
- psi MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- psi MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- metaanalýza MeSH
Permeability is an important molecular property in drug discovery, as it co-determines pharmacokinetics whenever a drug crosses the phospholipid bilayer, e.g., into the cell, in the gastrointestinal tract, or across the blood-brain barrier. Many methods for the determination of permeability have been developed, including cell line assays (CACO-2 and MDCK), cell-free model systems like parallel artificial membrane permeability assay (PAMPA) mimicking, e.g., gastrointestinal epithelia or the skin, as well as the black lipid membrane (BLM) and submicrometer liposomes. Furthermore, many in silico approaches have been developed for permeability prediction: meta-analysis of publicly available databases for permeability data (MolMeDB and ChEMBL) was performed to establish their usability. Four experimental and two computational methods were evaluated. It was shown that repeatability of the reported permeability measurement is not great even for the same method. For the PAMPA method, two different permeabilities are reported: intrinsic and apparent. They can vary in degrees of magnitude; thus, we suggest being extra cautious using literature data on permeability. When we compared data for the same molecules using different methods, the best agreement was between cell-based methods and between BLM and computational methods. Existence of unstirred water layer (UWL) permeability limits the data agreement between cell-based methods (and apparent PAMPA) with data that are not limited by UWL permeability (computational methods, BLM, intrinsic PAMPA). Therefore, different methods have different limitations. Cell-based methods provide results only in a small range of permeabilities (-8 to -4 in cm/s), and computational methods can predict a wider range of permeabilities beyond physical limitations, but their precision is therefore limited. BLM with liposomes can be used for both fast and slow permeating molecules, but its usage is more complicated than standard transwell techniques. To sum up, when working with in-house measured or published permeability data, we recommend caution in interpreting and combining them.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc25009580
- 003
- CZ-PrNML
- 005
- 20250429135000.0
- 007
- ta
- 008
- 250415s2025 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1021/acs.molpharmaceut.4c00975 $2 doi
- 035 __
- $a (PubMed)39977255
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Storchmannová, Kateřina $u Department of Physical Chemistry, Faculty of Science, Palacký University Olomouc, 17. listopadu 12, 771 46 Olomouc, Czech Republic
- 245 10
- $a Meta-Analysis of Permeability Literature Data Shows Possibilities and Limitations of Popular Methods / $c K. Storchmannová, M. Balouch, J. Juračka, F. Štěpánek, K. Berka
- 520 9_
- $a Permeability is an important molecular property in drug discovery, as it co-determines pharmacokinetics whenever a drug crosses the phospholipid bilayer, e.g., into the cell, in the gastrointestinal tract, or across the blood-brain barrier. Many methods for the determination of permeability have been developed, including cell line assays (CACO-2 and MDCK), cell-free model systems like parallel artificial membrane permeability assay (PAMPA) mimicking, e.g., gastrointestinal epithelia or the skin, as well as the black lipid membrane (BLM) and submicrometer liposomes. Furthermore, many in silico approaches have been developed for permeability prediction: meta-analysis of publicly available databases for permeability data (MolMeDB and ChEMBL) was performed to establish their usability. Four experimental and two computational methods were evaluated. It was shown that repeatability of the reported permeability measurement is not great even for the same method. For the PAMPA method, two different permeabilities are reported: intrinsic and apparent. They can vary in degrees of magnitude; thus, we suggest being extra cautious using literature data on permeability. When we compared data for the same molecules using different methods, the best agreement was between cell-based methods and between BLM and computational methods. Existence of unstirred water layer (UWL) permeability limits the data agreement between cell-based methods (and apparent PAMPA) with data that are not limited by UWL permeability (computational methods, BLM, intrinsic PAMPA). Therefore, different methods have different limitations. Cell-based methods provide results only in a small range of permeabilities (-8 to -4 in cm/s), and computational methods can predict a wider range of permeabilities beyond physical limitations, but their precision is therefore limited. BLM with liposomes can be used for both fast and slow permeating molecules, but its usage is more complicated than standard transwell techniques. To sum up, when working with in-house measured or published permeability data, we recommend caution in interpreting and combining them.
- 650 _2
- $a lidé $7 D006801
- 650 12
- $a permeabilita $7 D010539
- 650 _2
- $a Caco-2 buňky $7 D018938
- 650 12
- $a liposomy $x chemie $7 D008081
- 650 _2
- $a psi $7 D004285
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a permeabilita buněčné membrány $x fyziologie $7 D002463
- 650 _2
- $a buňky MDCK $7 D061985
- 650 _2
- $a hematoencefalická bariéra $x metabolismus $7 D001812
- 650 _2
- $a membrány umělé $7 D008567
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a metaanalýza $7 D017418
- 700 1_
- $a Balouch, Martin $u Department of Chemical Engineering, University of Chemistry and Technology, Technická 3, Prague 6, 166 28 Prague, Czech Republic $u Zentiva, k.s., U. Kabelovny 130, Prague 10, 102 00 Prague, Czech Republic
- 700 1_
- $a Juračka, Jakub $u Department of Physical Chemistry, Faculty of Science, Palacký University Olomouc, 17. listopadu 12, 771 46 Olomouc, Czech Republic $u Department of Computer Science, Faculty of Science, Palacký University Olomouc, 17. listopadu 12, 771 46 Olomouc, Czech Republic
- 700 1_
- $a Štěpánek, František $u Department of Chemical Engineering, University of Chemistry and Technology, Technická 3, Prague 6, 166 28 Prague, Czech Republic $1 https://orcid.org/0000000192884568 $7 mzk2012703367
- 700 1_
- $a Berka, Karel $u Department of Physical Chemistry, Faculty of Science, Palacký University Olomouc, 17. listopadu 12, 771 46 Olomouc, Czech Republic $1 https://orcid.org/0000000194722589 $7 ola2015878473
- 773 0_
- $w MED00008279 $t Molecular pharmaceutics $x 1543-8392 $g Roč. 22, č. 3 (2025), s. 1293-1304
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/39977255 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y - $z 0
- 990 __
- $a 20250415 $b ABA008
- 991 __
- $a 20250429134955 $b ABA008
- 999 __
- $a ok $b bmc $g 2311141 $s 1246661
- BAS __
- $a 3
- BAS __
- $a PreBMC-MEDLINE
- BMC __
- $a 2025 $b 22 $c 3 $d 1293-1304 $e 20250220 $i 1543-8392 $m Molecular pharmaceutics $n Mol Pharm $x MED00008279
- LZP __
- $a Pubmed-20250415