Evidence map›Paper›PMID 40504477›Full record

ArticlePhotochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology2025

In silico study of active delivery of a photodynamic therapy drug targeting the folate receptor.

Basak Koca Fındık, Elise Lognon, Saron Catak, Antonio Monari

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Article in Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

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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

4 authors.

Basak Koca FındıkUniversité Paris Cité and CNRS, ITODYS, 75006, Paris, France.
Elise LognonUniversité Paris Cité and CNRS, ITODYS, 75006, Paris, France.
Saron CatakDepartment of Chemistry, Bogazici University, Bebek, 34342, Istanbul, Turkey.
Antonio MonariUniversité Paris Cité and CNRS, ITODYS, 75006, Paris, France. antonio.monari@u-paris.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Photodynamic Therapy (PDT), which involves the combined action of a drug and its activation by suitable light, is a particularly attractive novel cancer therapy method due to less systemic side effects. However, the delivery and accumulation of the PDT drug into cancer cells is still problematic. Here, by using μ-scale molecular dynamic simulations combined with quantum mechanics/molecular mechanics approaches, we examine the behavior of a PDT drug functionalized with a folic acid unit targeting the folate receptor α (FR-α), which is overexpressed in ovarian cancer cells. We show that the PDT drug forms a stable complex with the folate receptor, albeit slightly disrupting the main interaction patterns as compared to the parent folate ligand. Furthermore, we also show that the optical properties of the PDT drug are not altered by its interaction with the protein. Our results confirm that coupling with folate is an attractive strategy for selective active delivery of PDT agents.

Indexed as

Drug Delivery SystemsFolate Receptor 1Folic AcidPhotochemotherapyPhotosensitizing AgentsHumansMolecular Dynamics SimulationFolate Receptor 1Folic AcidPhotosensitizing AgentsDrug deliveryFolate receptorMolecular dynamics simulationsPhotodynamic therapyQuantum mechanics/molecular mechanics

Identifiers

What Socratic holds

Textmetadata
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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 Socratic graph.