ArticleMaterials today. Bio2025
Prodrug nanosystem equipped with a sonosensitizer for combined chemotherapy and sonodynamic therapy of melanoma.
Article in Materials today. Bio, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled 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.
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.
Who cites it
2 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Advances in ultrasound-activated nano-sonosensitizers for cancer treatment: a systematic review and meta-analysis.Ultrasonics sonochemistry · 2026Pooled it
- aHSCs-targeted bimetallic nanozymes and luteolin-loaded liposomes: Synergistic reversal of liver fibrosis via antioxidant, cellular senescence, and cellular apoptotic mechanisms.Materials today. Bio · 2025Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Melanoma is a severe eruptive disease caused by melanocyte lesions and characterized by aggressive tumors, which has become one of the fastest evolving cancers worldwide, and its incidence and mortality rates have shown larger increases than other types of cancers. Finding effective medicines has become an important topic in collaborative research. Many compounds have been removed from clinical application because of poor physicochemical properties, especially low solubility, a high clearance rate and toxic side effects. In this study, a reactive oxygen species (ROS)-responsive camptothecin (CPT) prodrug delivery system (CTS-S-CPT@IR 780 NPs) in which CPT was conjugated to chitosan was developed. The synthesized CTS-S-CPT conjugate self-assembled to form NPs loading IR 780 in solution. Sonodynamic therapy (SDT) at the tumor site can activate the sonosensitizer IR 780 to release large amounts of ROS and heat, inducing apoptosis. ROS can also cleave carbon‒sulfur bonds and release the chemotherapeutic drug CPT. ROS-responsive CTS-S-CPT@IR 780 NPs activated by combination chemotherapy/SDT were successfully prepared for tumor-targeted drug delivery and can effectively inhibit tumor growth in vivo and in vitro with lower toxic side effects, and localized, controllable, and on-demand release drug. This prodrug approach has spawned hope for overcoming such treatment dilemmas.
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Registered trials
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.