Evidence map›Paper›PMID 39329032›Full record

ArticleInternational journal of nanomedicine2024

Ion Doped Hollow Silica Nanoparticles as Promising Oligonucleotide Delivery Systems to Mesenchymal Stem Cells.

Chloe Trayford, Dina M Ibrahim, Sabine van Rijt

Abstract read
In one paragraph

Article in International journal of nanomedicine, 2024. 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. Review
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

3 authors.

Chloe TrayfordMERLN Institute for Technology-Inspired Regenerative Medicine, Maastricht University, Maastricht, MD, 6200, the Netherlands.
Dina M IbrahimMERLN Institute for Technology-Inspired Regenerative Medicine, Maastricht University, Maastricht, MD, 6200, the Netherlands.
Sabine van RijtMERLN Institute for Technology-Inspired Regenerative Medicine, Maastricht University, Maastricht, MD, 6200, the Netherlands.ORCID 0000-0003-4102-4626

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Oligonucleotide (ON) therapy is a promising treatment for a wide range of complex genetic disorders, but inefficient intracellular ON delivery has hindered clinical translation. Hollow silica nanoparticles (HSN) hold potential as effective ON delivery vehicles since ON can be encapsulated in the hollow core in situ where they are protected from degradation by eg nucleases. However, HSN must be modified to allow degradation and subsequent (sub)cellular ON release. In this report, we investigated the use of ion and fluorescent dye co-doping in the HSN silica matrix to enable HSN degradability and in vitro visualization. Methods: HSN were core encapsulated with ON, doped with Ca Results: We successfully doped HSN with RITC and Ca Conclusion: We report a straightforward one-pot procedure to create ion and fluorescent dye co-doped HSN that can efficiently incorporate ON, as promising new gene vectors.

Indexed as

Mesenchymal Stem CellsNanoparticlesRhodaminesSilicon DioxideCalciumCell SurvivalFluorescent DyesHumansIonsOligonucleotidesZincCalciumFluorescent DyesIonsOligonucleotidesrhodamine isothiocyanateRhodaminesSilicon DioxideZinccontrolled deliveryhollow silica nanoparticlesintracellular specific degradationion-dopingoligonucleotide therapy

Identifiers

PMID39329032
PMCPMC11424689

What OpenQuestion holds

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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.