Evidence map›Paper›PMID 37513209›Full record

ArticleMolecules (Basel, Switzerland)2023

Dendritic Mesoporous Organosilica Nanoparticles with Photosensitizers for Cell Imaging, siRNA Delivery and Protein Loading.

Haneen Omar, Sara Jakimoska, Julia Guillot, Edreese Alsharaeh, Clarence Charnay, Frédérique Cunin, Aurélie Bessière, Jean-Olivier Durand, Laurence Raehm, Laure Lichon and 2 more

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

12 authors.

Haneen OmarChemistry Department, Collage of Science, Alfaisal University, Riyadh 11533, Saudi Arabia.ORCID 0000-0003-1036-0387
Sara JakimoskaIBMM, University Montpellier, CNRS, ENSCM, 34193 Montpellier, France.
Julia GuillotIBMM, University Montpellier, CNRS, ENSCM, 34193 Montpellier, France.
Edreese AlsharaehChemistry Department, Collage of Science, Alfaisal University, Riyadh 11533, Saudi Arabia.ORCID 0000-0002-6285-8083
Clarence CharnayICGM, University Montpellier, CNRS, ENSCM, 34193 Montpellier, France.ORCID 0000-0002-8796-3701
Frédérique CuninICGM, University Montpellier, CNRS, ENSCM, 34193 Montpellier, France.
Aurélie BessièreICGM, University Montpellier, CNRS, ENSCM, 34193 Montpellier, France.ORCID 0000-0003-0082-546X
Jean-Olivier DurandICGM, University Montpellier, CNRS, ENSCM, 34193 Montpellier, France.ORCID 0000-0003-4606-2576
Laurence RaehmICGM, University Montpellier, CNRS, ENSCM, 34193 Montpellier, France.
Laure LichonIBMM, University Montpellier, CNRS, ENSCM, 34193 Montpellier, France.
Mélanie OnofreIBMM, University Montpellier, CNRS, ENSCM, 34193 Montpellier, France.
Magali Gary-BoboIBMM, University Montpellier, CNRS, ENSCM, 34193 Montpellier, France.ORCID 0000-0001-9641-212X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dendritic mesoporous organosilica nanoparticles (DMON) are a new class of biodegradable nanoparticles suitable for biomolecule delivery. We studied the photochemical internalization (PCI) and photodynamic therapy (PDT) of DMON to investigate new ways for DMON to escape from the endosomes-lysosomes and deliver biomolecules into the cytoplasm of cells. We added photosensitizers in the framework of DMON and found that DMON were loaded with siRNA or FVIII factor protein. We made four formulations with four different photosensitizers. The photosensitizers allowed us to perform imaging of DMON in cancer cells, but the presence of the tetrasulfide bond in the framework of DMON quenched the formation of singlet oxygen. Fortunately, one formulation allowed us to efficiently deliver proapoptotic siRNA in MCF-7 cancer cells leading to 31% of cancer cell death, without irradiation. As for FVIII protein, it was loaded in two formulations with drug-loading capacities (DLC) up to 25%. In conclusion, DMON are versatile nanoparticles capable of loading siRNA and delivering it into cancer cells, and also loading FVIII protein with good DLC. Due to the presence of tetrasulfide, it was not possible to perform PDT or PCI.

Indexed as

NanoparticlesPhotochemotherapyCell Line, TumorHumansMCF-7 CellsPhotosensitizing AgentsRNA, Small InterferingPhotosensitizing AgentsRNA, Small Interferingdendritic mesoporous organosilica nanoparticlesFVIII factorsiRNA

Identifiers

PMID37513209
PMCPMC10385246

What OpenQuestion holds

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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.