Evidence map›Paper›PMID 39992321›Full record

ArticleJournal of fluorescence2025

Novel Silicon-Based Fluorescent Nanocomposite Drug Carriers for Natural Compound Delivery in Melanoma Treatment.

Fei Gao, Lei Li, Linbo Liu, Guangshuai Li, Jianan Zhang, Wang Zhan, Wenjian You, Xia Lin, Yun Liu, Jiayao Wang and 1 more

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of fluorescence, 2025. 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

11 authors.

Fei GaoDepartment of Plastic Surgery, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Lei LiDepartment of Emergency, Hainan General Hospital, Haikou, Hainan, China.
Linbo LiuDepartment of Plastic Surgery, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China. liulinbo2021@yeah.net.
Guangshuai LiDepartment of Plastic Surgery, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Jianan ZhangDepartment of Plastic and Cosmetic Surgery, Hainan General Hospital, Haikou, Hainan, China.
Wang ZhanDepartment of Plastic and Cosmetic Surgery, Hainan General Hospital, Haikou, Hainan, China.
Wenjian YouDepartment of Plastic and Cosmetic Surgery, Hainan General Hospital, Haikou, Hainan, China.
Xia LinDepartment of Plastic and Cosmetic Surgery, Hainan General Hospital, Haikou, Hainan, China.
Yun LiuDepartment of Plastic and Cosmetic Surgery, Hainan General Hospital, Haikou, Hainan, China.
Jiayao WangDepartment of Plastic and Cosmetic Surgery, Hainan General Hospital, Haikou, Hainan, China.
Denglin ChenDepartment of Oncology, Hainan General Hospital, Haikou, Hainan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Melanoma, a highly aggressive cancer, is closely associated with an elevated tumor mutation burden (TMB) and an active tumor microenvironment (TME). Melanin synthesis, a key feature of melanoma progression, is primarily regulated by tyrosinase (TYR), the rate-limiting enzyme controlled by the microphthalmia-associated transcription factor (MITF). Resveratrol (Res), a natural polyphenol known for its antioxidant and anticancer properties, faces limitations including poor solubility, low bioavailability, and rapid metabolism. To overcome these challenges, a three-dimensional Co(II) coordination polymer {[Co(bpdado)(bpe)(H₂O)₂]·2DMF·2 H₂O}n (1) was synthesized and incorporated into a composite material, 1@CP1, for Res delivery (1@CP1@Res). The system exhibited enhanced solubility, pH-sensitive release, and improved biological activity. Fluorescence assays demonstrated significant quenching in the presence of Cu²⁺ ions, indicating a high sensitivity of 1@CP1@Res to metal ion interactions. The pH-responsive drug release profile was confirmed by in vitro studies showing accelerated release at lower pH values, mimicking the acidic tumor microenvironment. Cell viability assays revealed that 1@CP1@Res significantly inhibited the proliferation of murine B16-F10 melanoma cells, with cell survival rates of 72.4%, 58.2%, and 43.6% at 24, 48, and 72 h of incubation, respectively, at a concentration of 100 µM. Molecular docking studies further revealed multiple binding interactions between Res and the coordination polymer, suggesting a promising therapeutic strategy for melanoma treatment by integrating advanced materials with bioactive compounds.

Indexed as

Antineoplastic AgentsDrug CarriersFluorescent DyesMelanomaNanocompositesSiliconStilbenesAnimalsCell Line, TumorCell ProliferationCell SurvivalDrug LiberationHydrogen-Ion ConcentrationMiceMolecular Docking SimulationResveratrolAntineoplastic AgentsDrug CarriersFluorescent DyesResveratrolSiliconStilbenesMelanomaNanocompositeResSilicon

Identifiers

PMID39992321

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.