Evidence map›Paper›PMID 42630516›Full record

ArticleFrontiers in pharmacology2026

Microphysiological modeling of the Blood-CSF barrier for biopharmaceutical transport and sequestration: evaluation of PEG-induced accumulation and vacuolation in the choroid plexus epithelium.

Jacquelyn Ann Brown, Monika G Judge, David K Schaffer, Dillon C Gavlock, Armando Irizarry Rovira, Steven K Engle, Thomas K Baker, John P Wikswo

Abstract read
In one paragraph

Article in Frontiers in pharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Jacquelyn Ann BrownOrgan Pathobiology and Therapeutics Institute, University of Pittsburgh, Pittsburgh, PA, United States.
Monika G JudgeDepartment of Physics and Astronomy, Vanderbilt University, Nashville, TN, United States.
David K SchafferDepartment of Physics and Astronomy, Vanderbilt University, Nashville, TN, United States.
Dillon C GavlockOrgan Pathobiology and Therapeutics Institute, University of Pittsburgh, Pittsburgh, PA, United States.
Armando Irizarry RoviraLilly Research Laboratories, A Division of Eli Lilly and Company, Indianapolis, IN, United States.
Steven K EngleLilly Research Laboratories, A Division of Eli Lilly and Company, Indianapolis, IN, United States.
Thomas K BakerLilly Research Laboratories, A Division of Eli Lilly and Company, Indianapolis, IN, United States.
John P WikswoDepartment of Physics and Astronomy, Vanderbilt University, Nashville, TN, United States.

Funding

Drug development for tuberous sclerosis complex and other pediatric epileptogenic diseases using neurovascular and cardiac microphysiological modelsUH3TR002097 · NCATS · VANDERBILT UNIVERSITY · PI ESS, KEVIN C, NEELY, MAJA DIANA · 2019 to 2021
$4.6M
Opera Phenix High-Content Imaging System for Drug DiscoveryS10OD028450 · OD · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI TAYLOR, D. LANSING · 2020 to 2020
$1.0M
NCATS NIH HHS UH3 TR002097NIH HHS S10 OD028450
6 · The paper itself

Abstract

Background: It has long been established that the central nervous system (CNS) is a highly privileged space, with the blood-brain barrier (BBB) acting as the gatekeeper that allows or denies access to the brain by nutrients, drugs, and toxins. The BBB, however, is not the only barrier at play. The barrier between blood and cerebrospinal fluid (CSF) also has a critical role in guarding and feeding the CNS, but despite its importance, the blood-CSF barrier (BCSFB) remains relatively unexplored compared to the BBB, particularly with regard to models that do not rely on animals. Methods: Given the lack of physiologically relevant Results: By leveraging advanced microfluidic organ chip design and gravity perfusion, we have generated a hBCSFB organ chip that recapitulates many of the physiologically relevant characteristics of this barrier, including junctional protein expression, permeability less than 1.55e-5 cm/s, transcytosis that showed dose-dependent accumulation of 10%-35%, and selective transport that was both statistically significant (p ≤ 0.05) and reproducible. Conclusion: Having achieved these benchmarks and validated their reproducibility, this work provides a useful

Indexed as

blood-brain barrier (BBB)blood-CSF barriercentral nervous system (CNS)microphysiological system (MPS)polyethylene glycols (PEG)

Identifiers

PMID42630516
PMCPMC13494263

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.