Appropriate Size of Fe 3 O 4 Nanoparticles for Cancer Therapy by Ferroptosis

Iron oxide nanoparticles can induce cell death due to the ferroptosis mechanism, showing a great potential for cancer therapy. Here, we synthesized different-sized iron oxide nanoparticles (2-100 nm) to investigate their antitumor effect and toxicity mechanism. It was found that ultrasmall nanoparti...

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Veröffentlicht in:ACS applied bio materials 2022-04, Vol.5 (4), p.1692-1699
Hauptverfasser: Tian, Xiangrong, Ruan, Li, Zhou, Shengwang, Wu, Lin, Cao, Jin, Qi, Xueyong, Zhang, Xin, Shen, Song
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container_issue 4
container_start_page 1692
container_title ACS applied bio materials
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creator Tian, Xiangrong
Ruan, Li
Zhou, Shengwang
Wu, Lin
Cao, Jin
Qi, Xueyong
Zhang, Xin
Shen, Song
description Iron oxide nanoparticles can induce cell death due to the ferroptosis mechanism, showing a great potential for cancer therapy. Here, we synthesized different-sized iron oxide nanoparticles (2-100 nm) to investigate their antitumor effect and toxicity mechanism. It was found that ultrasmall nanoparticles (< ∼5 nm) could accumulate in nucleus and were more efficient in triggering the generation of OH than larger nanoparticles due to the quicker release of Fe , thus exhibiting more remarkable cytotoxicity. Nevertheless, 10 nm iron oxide nanoparticles group displayed the best antitumor effect . We studied the and intratumoral biodistribution of the nanoparticles and found that the therapeutic effects were related to both the tumoral accumulation and intratumoral distribution of nanoparticles. This work indicates the appropriate size of Fe O NPs for cancer treatment and illustrates the possible factors that influence the therapeutic effect, suggesting the great potential of iron oxide in clinical application.
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Here, we synthesized different-sized iron oxide nanoparticles (2-100 nm) to investigate their antitumor effect and toxicity mechanism. It was found that ultrasmall nanoparticles (&lt; ∼5 nm) could accumulate in nucleus and were more efficient in triggering the generation of OH than larger nanoparticles due to the quicker release of Fe , thus exhibiting more remarkable cytotoxicity. Nevertheless, 10 nm iron oxide nanoparticles group displayed the best antitumor effect . We studied the and intratumoral biodistribution of the nanoparticles and found that the therapeutic effects were related to both the tumoral accumulation and intratumoral distribution of nanoparticles. 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subjects Cell Death
Ferroptosis
Humans
Nanoparticles - therapeutic use
Neoplasms - drug therapy
Tissue Distribution
title Appropriate Size of Fe 3 O 4 Nanoparticles for Cancer Therapy by Ferroptosis
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