Evidence map›Paper›PMID 40736884›Full record

ArticleMedical oncology (Northwood, London, England)2025

Bioengineered and biodegradable 3D scaffold for controlled drug delivery of 5-fluorouracil-loaded nanoparticle for bone tumor treatment.

Huanzhi Ma, Jun Shi, Wei Zhang

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Article in Medical oncology (Northwood, London, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Huanzhi MaDepartment of Orthopedic Surgery, Shandong Provincial Hospital Affiliated to Shandong First Medical University, East Hospital District, Provincial Hospital, 9677 Jingshi Road, Jinan, 250021, China. mahuanzhi353@126.com.
Jun ShiDepartment of Orthopedic Surgery, Shandong Provincial Hospital Affiliated to Shandong First Medical University, East Hospital District, Provincial Hospital, 9677 Jingshi Road, Jinan, 250021, China.
Wei ZhangDepartment of Orthopedic Surgery, Shandong Provincial Hospital Affiliated to Shandong First Medical University, East Hospital District, Provincial Hospital, 9677 Jingshi Road, Jinan, 250021, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The main goal of the present was to develop an anticancer scaffold based on chitosan nanoparticles (CsNPs) loaded with 5-FU against bone tumor. The synthesized Cs/5-FU NPs were incorporated into an alginate hydrogel to obtain a functional scaffold. The results showed that the Cs/5-FU NPs have spherical morphology with a 112.3 ± 34.1 nm diameter and have a hydrodynamic size of around 321.0 ± 11.2 nm and the zeta potential of NPs was 31.4 ± 8.1 mV. SEM imaging showed that both hydrogels have a porous micro structure and the pores are interconnected and were biodegradable (lost around 70-85% of their initial weight during 28 days). The MTT assay showed that the Nanocomposite suppressed the cells growth and significantly induced anticancer cells effects, and significantly suppressed the migration/invasion potential of the cells. The intracellular Reactive Oxygen Species (ROS) measurement and mitochondrial membrane potential (ΔΨm) measurement assay showed that the Nanocomposite elevated the intracellular ROS and disrupted the ΔΨm, and subsequently induced apoptosis. The results indicate that the fabricated anticancer scaffold can be applied as an implantable scaffold for controlled and localized drug delivery of chemotherapeutic agents to bone tumor cells.

Indexed as

Antimetabolites, AntineoplasticBone NeoplasmsDrug Delivery SystemsFluorouracilNanoparticlesTissue ScaffoldsApoptosisBioengineeringCell Line, TumorChitosanHumansMembrane Potential, MitochondrialNanocompositesReactive Oxygen SpeciesAntimetabolites, AntineoplasticChitosanFluorouracilReactive Oxygen SpeciesBiodegradable scaffoldBone tumorChemotherapeutic agentControlled drug delivery

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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.