Evidence map›Paper›PMID 40996472›Full record

ArticleNaunyn-Schmiedeberg's archives of pharmacology2026

Synthesis of CNP-SAR405 delivery system for improved therapeutics anticancer activity using A549 human lung cancer cell lines.

Ruqayyah A Bashirah, Nur Balqis Zamri, Noorjahan Banu Alitheen, Saila Ismail, Mas Jaffri Masarudin

Abstract read
In one paragraph

Article in Naunyn-Schmiedeberg's archives of pharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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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

5 authors.

Ruqayyah A BashirahDepartment of Cell and Molecular Biology, Faculty of Biotechnology and Biomolecular Sciences, Universiti Putra Malaysia, 43400, Serdang, Selangor, Malaysia.ORCID http://orcid.org/0009-0000-7775-2161
Nur Balqis ZamriDepartment of Cell and Molecular Biology, Faculty of Biotechnology and Biomolecular Sciences, Universiti Putra Malaysia, 43400, Serdang, Selangor, Malaysia.ORCID http://orcid.org/0009-0007-6810-9466
Noorjahan Banu AlitheenDepartment of Cell and Molecular Biology, Faculty of Biotechnology and Biomolecular Sciences, Universiti Putra Malaysia, 43400, Serdang, Selangor, Malaysia.ORCID http://orcid.org/0000-0003-1966-8580
Saila IsmailDepartment of Microbiology, Faculty of Biotechnology and Biomolecular Sciences, Universiti Putra Malaysia, 43400, Serdang, Selangor, Malaysia.
Mas Jaffri MasarudinDepartment of Cell and Molecular Biology, Faculty of Biotechnology and Biomolecular Sciences, Universiti Putra Malaysia, 43400, Serdang, Selangor, Malaysia. masjaffri@upm.edu.my.ORCID http://orcid.org/0000-0003-0695-2136

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autophagy, a critical homeostatic process, is increasingly implicated in cancer progression and therapy resistance. SAR405 is a potent inhibitor of the autophagy related PIK3C3/VPS34 complex, offering potential as an anticancer agent. This study reports the synthesis, characterization, and biological evaluation of SAR405-loaded chitosan nanoparticles (CNP-SAR405) designed to improve therapeutic delivery and efficacy in A549 human lung carcinoma cells. CNPs were prepared via ionic gelation using chitosan and sodium tripolyphosphate (TPP), yielding stable monodisperse nanoparticles ~ 77.4 nm, PDI ~ 0.2). Upon SAR405 encapsulation, nanoparticle size increased to ~ 110 nm while maintaining uniform distribution. Encapsulation efficiency reached 80% at 200 nM SAR405, confirmed by UV-Vis spectroscopy. Morphological analyses using FESEM and TEM verified spherical nanoparticle structures, while FTIR confirmed successful SAR405 incorporation. FITC-labelling enabled real-time tracking of intracellular uptake, revealing detectable internalization as early as 12 h post-treatment, with fluorescence intensity peaking at 72 h. In vitro cytotoxicity assays demonstrated enhanced anticancer efficacy of CNP-SAR405 compared to free SAR405, CNP-SAR405 achieved similar cytotoxic effects at 69 nM compared to 100 nM for free SAR405 in A549 cells. Furthermore, co-treatment with the autophagy inducer Torin-2 validated that CNP-SAR405 more effectively inhibited autophagosome formation than SAR405 alone, particularly at the 24-h mark. These findings underscore the potential of chitosan nanoparticle-mediated delivery to increase SAR405 bioavailability and anticancer potency while achieving comparable cytotoxic at a lower dose than free SAR405. The CNP-SAR405 formulation represents a promising nanotechnology-driven approach to targeted lung cancer therapy. All experiments were performed in triplicate biological replicates with technical triplicates, and data were analysed using one-way ANOVA followed by Tukey's multiple comparison post-hoc test (p < 0.05 considered significant).

Indexed as

Antineoplastic AgentsChitosanLung NeoplasmsNanoparticle Drug Delivery SystemNanoparticlesXanthenesA549 CellsAutophagyCell SurvivalHumansAntineoplastic AgentsChitosanNanoparticle Drug Delivery SystemXanthenesAnticancerAutophagyChitosan nanoparticlesNanomedicineSAR405

Identifiers

PMID40996472
PMCPMC12901243

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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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.