# Integrative Profiling for BBB Permeability Using Capillary Electrochromatography, Experimental Physicochemical Parameters, and Ensemble Machine Learning

**Authors:** Justyna Godyń, Jakub Jończyk, Anna Więckowska, Marek Bajda

PMC · DOI: 10.3390/ijms27010328 · International Journal of Molecular Sciences · 2025-12-28

## TL;DR

This paper introduces a new in vitro method combining capillary electrochromatography and machine learning to predict how well drugs can cross the blood-brain barrier.

## Contribution

The novel contribution is an integrative high-throughput method for predicting BBB permeability using CEC data and machine learning models.

## Key findings

- A regression model with R2 = 0.64 was developed to predict log BB values using CEC retention factor, pKa, and log D7.4.
- Machine learning classification of CEC electropherograms achieved an accuracy of 0.81 and F1weighted score of 0.8.

## Abstract

Profiling the blood–brain barrier (BBB) permeability of bioactive molecules during early drug development is critical for optimizing their pharmacokinetic profile. The in vivo ability of a compound to cross the BBB is measured by the log BB parameter; however, its determination requires costly and time-consuming animal experiments. This study aimed to develop a novel in vitro method for high-throughput prediction of log BB values. The approach combines experimental data from open-tubular capillary electrochromatography (CEC) and automated potentiometric titrations, including the CEC retention factor (k′), electropherograms, and physicochemical parameters pKa and log D7.4. The k′ parameter reflects BBB permeability using a capillary internally coated with liposomes that mimic a biological membrane. Preliminary CEC analyses were conducted for 25 neutral drugs at pH 7.4, revealing a promising correlation between the permeability parameters log k and log BB. The validation was extended to 57 ionized drugs, with additional determination of pKa and log D7.4. A regression model was developed: log BB = −2.45 + 0.1k′ + 0.3logD7.4 + 0.27pKa (R2 = 0.64). Furthermore, the analysis of CEC electropherograms enabled the machine learning-based rapid classification of compounds using Dynamic Time Warping, k-Nearest Neighbors, and the Bag-of-SFA-Symbols in Vector Space model, yielding an accuracy of 0.81 and an F1weighted score of 0.8.

## Full-text entities

- **Genes:** ABCB1 (ATP binding cassette subfamily B member 1) [NCBI Gene 403879] {aka MDR1, p-gp}
- **Diseases:** injury to (MESH:D014947)
- **Chemicals:** diclofenac sodium (MESH:D004008), bromperidol (MESH:C006820), chlorpromazine hydrochloride (MESH:D002746), octanol (MESH:D000442), venlafaxine hydrochloride (MESH:D000069470), acetylsalicylic acid (MESH:D001241), fluphenazine dihydrochloride (MESH:D005476), water (MESH:D014867), phospholipid (MESH:D010743), galanthamine hydrobromide (MESH:D005702), buspirone hydrochloride (MESH:D002065), loperamide (MESH:D008139), thioridazine hydrochloride (MESH:D013881), KOH (MESH:C029943), levofloxacin (MESH:D064704), physostigmine salicylate (MESH:C026718), atropine sulfate (MESH:D001285), trazodone hydrochloride (MESH:D014196), dodecane (MESH:C007548), chloroform (MESH:D002725), amitriptyline hydrochloride (MESH:D000639), lipids (MESH:D008055), betahistine dihydrochloride (MESH:D001621), nortriptyline hydrochloride (MESH:D009661), 2-propanol (MESH:D019840), verapamil (MESH:D014700), ranitidine hydrochloride (MESH:D011899), HCl (MESH:D006851), metoprolol tartrate (MESH:D008790), KCl (MESH:D011189), desipramine hydrochloride (MESH:D003891), metoclopramide hydrochloride (MESH:D008787), risperidone (MESH:D018967), NaOH (MESH:D012972), DMSO (MESH:D004121), pindolol (MESH:D010869), trifluoperazine dihydrochloride (MESH:D014268), methanol (MESH:D000432), phenylbutazone (MESH:D010653), donepezil hydrochloride (MESH:D000077265), naproxen (MESH:D009288), ibuprofen (MESH:D007052), 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (MESH:C028694), clonidine hydrochloride (MESH:D003000), 1,2-diacyl-sn-glycero-3-phospho-L-serine (-), haloperidol (MESH:D006220), rivastigmine tartrate (MESH:D000068836), clozapine (MESH:D003024), imipramine (MESH:D007099), 1-Octanol (MESH:D020003), potassium hydrogen phthalate (MESH:C032279), HEPES (MESH:D006531), albuterol sulfate (MESH:D000420), dipotassium hydrogen orthophosphate (MESH:C013216), indomethacin (MESH:D007213), atenolol (MESH:D001262), Nitrogen (MESH:D009584), chlorambucil (MESH:D002699), ropinirole hydrochloride (MESH:C046649), triprolidine hydrochloride (MESH:D014311)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** Caco-2 — Homo sapiens (Human), Colon adenocarcinoma, Cancer cell line (CVCL_0025), MDCK — Canis lupus familiaris (Dog), Spontaneously immortalized cell line (CVCL_0422)

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12785511/full.md

## References

60 references — full list in the complete paper: https://tomesphere.com/paper/PMC12785511/full.md

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Source: https://tomesphere.com/paper/PMC12785511