Evidence map›Paper›PMID 39829590›Full record

ArticleACS omega2025

Comparative Study of Functionalized Carbosilane Dendrimers for siRNA Delivery: Synthesis, Cytotoxicity, and Biophysical Properties.

Monika Müllerová, Piotr Tarach, Tomáš Strašák, Petra Cuřínová, Roman Petrickovic, Táňa Závodná, Jan Topinka, Anna Janaszewska, Barbara Klajnert-Maculewicz, Lucie Červenková Št'astná

Abstract read
In one paragraph

Article in ACS omega, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

10 authors.

Monika MüllerováInstitute of Chemical Process Fundamentals Czech Academy of Sciences, Rozvojová 135, Prague 165 02, Czech Republic.ORCID https://orcid.org/0000-0002-2505-5230
Piotr TarachFaculty of Biology and Environmental Protection, Department of General Biophysics, University of Lodz, Pomorska 141/143, Lodz 90-236, Poland.ORCID https://orcid.org/0000-0002-4751-3079
Tomáš StrašákInstitute of Chemical Process Fundamentals Czech Academy of Sciences, Rozvojová 135, Prague 165 02, Czech Republic.ORCID https://orcid.org/0000-0001-6413-0494
Petra CuřínováInstitute of Chemical Process Fundamentals Czech Academy of Sciences, Rozvojová 135, Prague 165 02, Czech Republic.ORCID https://orcid.org/0000-0001-8264-7032
Roman PetrickovicInstitute of Chemical Process Fundamentals Czech Academy of Sciences, Rozvojová 135, Prague 165 02, Czech Republic.
Táňa ZávodnáInstitute of Experimental Medicine, Czech Academy of Sciences, Vídeňská 1083, Prague 142 00, Czech Republic.ORCID https://orcid.org/0000-0002-1482-9341
Jan TopinkaInstitute of Experimental Medicine, Czech Academy of Sciences, Vídeňská 1083, Prague 142 00, Czech Republic.ORCID https://orcid.org/0000-0001-6860-7253
Anna JanaszewskaFaculty of Biology and Environmental Protection, Department of General Biophysics, University of Lodz, Pomorska 141/143, Lodz 90-236, Poland.
Barbara Klajnert-MaculewiczFaculty of Biology and Environmental Protection, Department of General Biophysics, University of Lodz, Pomorska 141/143, Lodz 90-236, Poland.ORCID https://orcid.org/0000-0003-3459-8947
Lucie Červenková Št'astnáInstitute of Chemical Process Fundamentals Czech Academy of Sciences, Rozvojová 135, Prague 165 02, Czech Republic.ORCID https://orcid.org/0000-0002-9968-1082

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Efficient and safe carriers of genetic material are crucial for advancing gene therapy. Three new series of cationic dendritic nanocarriers based on a carbosilane scaffold, differentiated by peripheral modifications: saccharide (CS-glyco), amine (CS-N), and phosphonium dendrimers (CS-P) were designed for binding, protecting, and releasing polyanionic compounds like therapeutic siRNA. Besides introducing synthetic methodology, this study brings a unique direct interstructural comparison of 16 dendritic nanovector's characteristics, addressing a gap in typical research that focuses on uniform structural types. The study evaluates the dendrimer's

Identifiers

PMID39829590
PMCPMC11740622

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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.