Evidence map›Paper›PMID 39940856›Full record

ArticleInternational journal of molecular sciences2025

Preparation of Diosgenin-Functionalized Gold Nanoparticles: From Synthesis to Antitumor Activities.

Elżbieta U Stolarczyk, Weronika Strzempek, Magdalena Muszyńska, Marek Kubiszewski, Anna B Witkowska, Kinga Trzcińska, Piotr Wojdasiewicz, Krzysztof Stolarczyk

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
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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.

Elżbieta U StolarczykSpectrometric Methods Department, National Medicine Institute, 30/34 Chełmska Street, 00-725 Warsaw, Poland.ORCID 0000-0002-2880-0072
Weronika StrzempekFaculty of Chemistry, Jagiellonian University, 2 Gronostajowa Street, 30-387 Krakow, Poland.
Magdalena MuszyńskaFaculty of Chemistry, University of Warsaw, 1 Pasteura Street, 02-093 Warsaw, Poland.ORCID 0000-0003-3046-0924
Marek KubiszewskiAnalytical Research Section, Pharmaceutical Analysis Laboratory Łukasiewicz Research Network, Industrial Chemistry Institute, 8 Rydygiera Street, 01-793 Warsaw, Poland.
Anna B WitkowskaSpectrometric Methods Department, National Medicine Institute, 30/34 Chełmska Street, 00-725 Warsaw, Poland.ORCID 0000-0002-6641-0673
Kinga TrzcińskaAnalytical Research Section, Pharmaceutical Analysis Laboratory Łukasiewicz Research Network, Industrial Chemistry Institute, 8 Rydygiera Street, 01-793 Warsaw, Poland.
Piotr WojdasiewiczDepartment of Biophysics, Physiology and Pathophysiology, Faculty of Health Sciences, Medical University of Warsaw, Chałubińskiego 5, 02-004 Warsaw, Poland.ORCID 0000-0003-3309-996X
Krzysztof StolarczykFaculty of Chemistry, University of Warsaw, 1 Pasteura Street, 02-093 Warsaw, Poland.ORCID 0000-0002-1510-3454

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer ranks among the top causes of illness and death globally. Nanotechnology holds considerable promise for enhancing the effectiveness of therapeutic and diagnostic approaches in cancer treatment. Our study presents a promising strategy for applying thiocompound nanomedicine in cancer therapy. Our first study aimed to investigate the biological properties of a new compound thiodiosgenin (TDG)-a new derivative of diosgenin-a natural compound with known antioxidant and anticancer properties. Our current second study aimed to compare the therapeutic efficacy of a new diosgenin-functionalized gold nanoparticles-with its precursor on prostate cancer (DU-145) cell lines. Moreover, the safety of the new thio-derivative and new conjugates was tested against the human epithelial line PNT-2. New advanced analytical techniques were developed for the characterization of nanomaterials using methods such as SP-ICP-MS, UV-Vis, TEM, NMR, FT-IR ELS, and TGA. Our synthetic approach was based, on the one hand, on the ligand exchange of citrates to thiodiosgenin (TDG) on gold nanoparticles, and on the other hand, on the attachment of DG through an ester bond to the linker, which was 3-mercaptopropionic acid (MPA) on gold nanoparticles. Initial in vitro studies indicate that TDG shows greater cytotoxic effects on cancer cells but poses risks to normal prostate epithelial cells (PNT-2). It was demonstrated that all the conjugates produced exhibited significant cytotoxic effects against cancer cells while being less harmful to normal prostate epithelial cells (PNT-2) compared to TDG itself. All the obtained conjugates showed antitumor properties; however, for targeted transport, the system referred to as AuNPs-MPAm1-DG is promising, due to the size of the nanoparticles of 53 nm, zeta potential of -30 mV, and loading content of 27.6%. New methods for synthesizing conjugates with diosgenin were developed and optimized for medical applications. Advanced new analytical methodologies were developed to characterize new conjugates, particularly the use of SP-ICP-MS, to solve existing differences in the shape and morphology of the surface of new conjugates.

Indexed as

Antineoplastic AgentsDiosgeninGoldMetal NanoparticlesCell Line, TumorCell SurvivalHumansMaleProstatic NeoplasmsAntineoplastic AgentsDiosgeninGoldanticancer drugsbiological active compoundcancer cellscytotoxic studydiosgenindrug carriersnanoparticlesSP-ICP-MSthiol derivatives

Identifiers

PMID39940856
PMCPMC11817374

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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.