Evidence map›Paper›PMID 39205867›Full record

ArticleInternational journal of nanomedicine2024

S-Doped Hollow Multi-Metallic Prussian Blue Analogue (PBA) Nanoplatform for Enhanced Anticancer for Cervical Cancer.

Lu Xu, Jing Liu, Suli Li, Xingchen Lu, Wenjie Gu, Shunhua Zhu, Meng Wang, Xiaojin Wu, Qingli Huang

Abstract read
In one paragraph

Article in International journal of nanomedicine, 2024. 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. 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

9 authors.

Lu Xu *Public Experimental Research Center of Xuzhou Medical University, Xuzhou, Jiangsu Province, 221004, People's Republic of China.
Jing Liu *Department of Neurology, the Affiliated Xuzhou Municipal Hospital of Xuzhou Medical University, Xuzhou No. 1 People's Hospital, Xuzhou, Jiangsu Province, 221100, People's Republic of China.
Suli LiPublic Experimental Research Center of Xuzhou Medical University, Xuzhou, Jiangsu Province, 221004, People's Republic of China.
Xingchen LuPublic Experimental Research Center of Xuzhou Medical University, Xuzhou, Jiangsu Province, 221004, People's Republic of China.
Wenjie GuPublic Experimental Research Center of Xuzhou Medical University, Xuzhou, Jiangsu Province, 221004, People's Republic of China.
Shunhua ZhuPublic Experimental Research Center of Xuzhou Medical University, Xuzhou, Jiangsu Province, 221004, People's Republic of China.
Meng WangPublic Experimental Research Center of Xuzhou Medical University, Xuzhou, Jiangsu Province, 221004, People's Republic of China.
Xiaojin WuDepartment of radiotherapy, the affiliated Xuzhou Municipal Hospital of Xuzhou Medical University, Xuzhou No. 1 People's Hospital, Xuzhou, Jiangsu Province, 221100, People's Republic of China.
Qingli HuangPublic Experimental Research Center of Xuzhou Medical University, Xuzhou, Jiangsu Province, 221004, People's Republic of China.ORCID 0000-0001-6706-6053

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Developing novel multimodal nanomaterials-based anticancer agents to meet complex clinical demands is an urgent challenge. This study presents a novel uniform hollow S-doped NiCuFe Prussian blue analogue (NiCuFe-S) with satisfactory size and properties as anticancer agents for efficient cervical cancer therapy using a simple and environmentally friendly procedure. Methods: The formation mechanism and the reason for enhanced performance of NiCuFe-S were characterized and discussed by diverse spectroscopic and microscopic methods. Moreover, to demonstrate the anti-cancer ability of NiCuFe-S, in vitro and in vivo experiments were carried out. Results: Compared to the non-doped NiCuFe, the NiCuFe-S exhibited significantly enhanced photothermal and catalytic activity attributed to the electronic bandgap-narrowing effect and the increased electron circuit paths resulting from S doping. The hollow structure of NiCuFe-S facilitated the loading of small-molecule drugs, such as doxorubicin (DOX), transforming it into a multimodal nanoplatform for cervical cancer treatment. In vitro and in vivo experiments proved the potential of the NiCuFe-S nanotheranostic agent for chemodynamic therapy (CDT), photothermal therapy (PTT), and chemotherapy for cervical cancer. Conclusion: This research not only overcomes inherent limitations but also significantly broadens the applications of Prussian blue analogues in biomedicine.

Indexed as

Antineoplastic AgentsDoxorubicinFerrocyanidesUterine Cervical NeoplasmsAnimalsCell Line, TumorFemaleHeLa CellsHumansMiceMice, Inbred BALB CPhotothermal TherapyTheranostic NanomedicineAntineoplastic AgentsDoxorubicinferric ferrocyanideFerrocyanidesanticancercatalyticnanomaterialsphotothermal therapyPrussian blue analogue

Identifiers

PMID39205867
PMCPMC11353314

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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.