Evidence map›Paper›PMID 33519171›Full record

ArticleIEEE journal of selected topics in quantum electronics : a publication of the IEEE Lasers and Electro-optics Society

Photodynamic Priming Modulates Endothelial Cell-Cell Junction Phenotype for Light-activated Remote Control of Drug Delivery.

Collin T Inglut, Kelsey M Gray, Shruti Vig, Jae W Jung, Jillian Stabile, Yuji Zhang, Kimberly M Stroka, Huang-Chiao Huang

Open access · greenAbstract read
In one paragraph

Article in IEEE journal of selected topics in quantum electronics : a publication of the IEEE Lasers and Electro-optics Society. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.5field-weighted citation impact, top 14% of its field
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

14 citing papers in PubMed, 19 citations in OpenAlex.

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  9. Critical PDT theory II: Current concepts and indications.Photodiagnosis and photodynamic therapy · 2022
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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 at 2 institutions in 1 country.

Collin T InglutFischell Department of Bioengineering, University of Maryland, College Park, MD 20742, USA.
Kelsey M GrayFischell Department of Bioengineering, University of Maryland, College Park, MD 20742, USA.
Shruti VigFischell Department of Bioengineering, University of Maryland, College Park, MD 20742, USA.
Jae W JungFischell Department of Bioengineering, University of Maryland, College Park, MD 20742, USA.
Jillian StabileFischell Department of Bioengineering, University of Maryland, College Park, MD 20742, USA.
Yuji ZhangMarlene and Stewart Greenebaum Comprehensive Cancer Center, University of Maryland, Baltimore, MD 21201, USA.
Kimberly M StrokaFischell Department of Bioengineering, University of Maryland, College Park, MD 20742, USA.
Huang-Chiao HuangFischell Department of Bioengineering, University of Maryland, College Park, MD 20742, USA.
University of Maryland, College Park · USUniversity of Maryland, Baltimore · US

Funding

Multifunctional, GBM-Activatable Nanocarriers For Image-Guided PhotochemotherapyR00CA194269 · NCI · UNIV OF MARYLAND, COLLEGE PARK · PI HUANG, HUANG CHIAO · 2018 to 2020
$701k
Photodynamic Priming for Bidirectional Modulation of Drug Transport Across the Blood-Brain Tumor BarrierR21EB028508 · NIBIB · UNIV OF MARYLAND, COLLEGE PARK · PI HUANG, HUANG CHIAO · 2020 to 2022
$621k
NCI NIH HHS R00 CA194269NIBIB NIH HHS R21 EB028508
6 · The paper itself

Abstract

The blood-brain barrier (BBB) remains a major obstacle for drug delivery to the central nervous system. In particular, the tight and adherens junctions that join the brain capillary endothelial cells limit the diffusion of various molecules from the bloodstream into the brain. Photodynamic priming (PDP) is a non-cytotoxic modality that involves light activation of photosensitizers to photochemically modulate nearby molecules without killing the cells. Here we investigate the effects of sub-lethal photochemistry on junction phenotype (i.e., continuous, punctate, or perpendicular), as well as the BBB permeability in a transwell model of human brain microvascular endothelial cells (HBMECs). We showed that PDP decreases the continuous junction architecture by ~20%, increases the perpendicular junction architecture by ~40%, and has minimal impact on cell morphology in HBMECs. Furthermore, transwell permeability assay revealed that PDP improves the HBMEC permeability to dextran or nanoliposomes by up to 30-fold for 6-9 days. These results suggest that PDP could safely reverse the mature brain endothelial junctions without killing the HBMECs. This study not only emphasizes the critical roles of PDP in the modulation junction phenotype, but also highlights the opportunity to further develop PDP-based combinations that opens the cerebrum endothelium for enhanced drug transporter across the BBB.

Indexed as

Benzoporphyrin derivativesblood-brain barrierlight-controlled drug releasephotochemistryphotodynamic priming

Identifiers

PMID33519171
PMCPMC7839980
OpenAlexW3091358902

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.