Computational Approach to Drug Penetration across the Blood-Brain and Blood-Milk Barrier Using Chromatographic Descriptors.
Karolina WanatRojek AgataBrzezińska ElżbietaPublished in: Cells (2023)
Drug penetration through biological barriers is an important aspect of pharmacokinetics. Although the structure of the blood-brain and blood-milk barriers is different, a connection can be found in the literature between drugs entering the central nervous system (CNS) and breast milk. This study was created to reveal such a relationship with the use of statistical modelling. The basic physicochemical properties of 37 active pharmaceutical compounds (APIs) and their chromatographic retention data (TLC and HPLC) were incorporated into calculations as molecular descriptors (MDs). Chromatography was performed in a thin layer format (TLC), where the plates were impregnated with bovine serum albumin to mimic plasma protein binding. Two columns were used in high performance liquid chromatography (HPLC): one with immobilized human serum albumin (HSA), and the other containing an immobilized artificial membrane (IAM). Statistical methods including multiple linear regression (MLR), cluster analysis (CA) and random forest regression (RF) were performed with satisfactory results: the MLR model explains 83% of the independent variable variability related to CNS bioavailability; while the RF model explains up to 87%. In both cases, the parameter related to breast milk penetration was included in the created models. A significant share of reversed-phase TLC retention values was also noticed in the RF model.
Keyphrases
- high performance liquid chromatography
- simultaneous determination
- tandem mass spectrometry
- mass spectrometry
- solid phase extraction
- liquid chromatography
- ms ms
- human serum albumin
- white matter
- blood brain barrier
- climate change
- systematic review
- molecular dynamics
- emergency department
- high resolution
- small molecule
- single cell
- single molecule
- cerebrospinal fluid
- deep learning
- neural network
- protein protein