文献检索文档翻译深度研究
Suppr Zotero 插件Zotero 插件
邀请有礼套餐&价格历史记录

新学期,新优惠

限时优惠:9月1日-9月22日

30天高级会员仅需29元

1天体验卡首发特惠仅需5.99元

了解详情
不再提醒
插件&应用
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
高级版
套餐订阅购买积分包
AI 工具
文献检索文档翻译深度研究
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2025

用于体内肺肿瘤 T2 加权磁共振成像的磁性、生物相容的 FeCO 纳米颗粒。

Magnetic, biocompatible FeCO nanoparticles for T2-weighted magnetic resonance imaging of in vivo lung tumors.

机构信息

Institute for Translational Research in Biomedicine, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung, 833, Taiwan.

Department of Biomedical Imaging and Radiological Sciences, National Yang Ming Chiao Tung University, Taipei, 112, Taiwan.

出版信息

J Nanobiotechnology. 2022 Mar 25;20(1):157. doi: 10.1186/s12951-022-01355-3.


DOI:10.1186/s12951-022-01355-3
PMID:35337331
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8952886/
Abstract

BACKGROUND: Late diagnosis of lung cancer is one of the leading causes of higher mortality in lung cancer patients worldwide. Significant research attention has focused on the use of magnetic resonance imaging (MRI) based nano contrast agents to efficiently locate cancer tumors for surgical removal or disease diagnostics. Although contrast agents offer significant advantages, further clinical applications require improvements in biocompatibility, biosafety and efficacy. RESULTS: To address these challenges, we fabricated ultra-fine Iron Carbonate Nanoparticles (FeCO NPs) for the first time via modified literature method. Synthesized NPs exhibit ultra-fine size (~ 17 nm), good dispersibility and excellent stability in both aqueous and biological media. We evaluated the MR contrast abilities of FeCO NPs and observed remarkable T2 weighted MRI contrast in a concentration dependent manner, with a transverse relaxivity (r2) value of 730.9 ± 4.8 mM Sat 9.4 T. Moreover, the r2 values of present FeCO NPs are respectively 1.95 and 2.3 times higher than the clinically approved contrast agents Resovist and Friedx at same 9.4 T MR scanner. FeCO NPs demonstrate an enhanced T2 weighted contrast for in vivo lung tumors within 5 h of post intravenous administration with no apparent systemic toxicity or induction of inflammation observed in in vivo mice models. CONCLUSION: The excellent biocompatibility and T2 weighted contrast abilities of FeCO NPs suggest potential for future clinical use in early diagnosis of lung tumors.

摘要

背景:肺癌的晚期诊断是导致全球肺癌患者死亡率较高的主要原因之一。大量研究关注于使用基于磁共振成像(MRI)的纳米对比剂来高效定位癌症肿瘤,以进行手术切除或疾病诊断。尽管对比剂具有显著优势,但进一步的临床应用需要提高生物相容性、生物安全性和疗效。

结果:为了解决这些挑战,我们首次通过改良文献法制备了超精细的碳酸亚铁纳米粒子(FeCO NPs)。合成的 NPs 具有超小的尺寸(约 17nm)、良好的分散性和在水相和生物介质中的优异稳定性。我们评估了 FeCO NPs 的磁共振对比能力,观察到其在浓度依赖性方式下具有显著的 T2 加权 MRI 对比,横向弛豫率(r2)值在 9.4T 下为 730.9±4.8mM Sat。此外,在相同的 9.4T MRI 扫描仪下,本研究中 FeCO NPs 的 r2 值分别比临床批准的对比剂 Resovist 和 Feridex 高 1.95 倍和 2.3 倍。FeCO NPs 在静脉注射后 5 小时内对体内肺肿瘤具有增强的 T2 加权对比,在体内小鼠模型中未观察到明显的全身毒性或炎症诱导。

结论:FeCO NPs 的优异生物相容性和 T2 加权对比能力表明其在肺部肿瘤的早期诊断中具有潜在的临床应用前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d284/8952886/cc9a64003938/12951_2022_1355_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d284/8952886/95da3e6cb29a/12951_2022_1355_Sch1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d284/8952886/551479c73ef0/12951_2022_1355_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d284/8952886/f1050f100b99/12951_2022_1355_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d284/8952886/ad62deea1e2c/12951_2022_1355_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d284/8952886/cc9a64003938/12951_2022_1355_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d284/8952886/95da3e6cb29a/12951_2022_1355_Sch1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d284/8952886/551479c73ef0/12951_2022_1355_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d284/8952886/f1050f100b99/12951_2022_1355_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d284/8952886/ad62deea1e2c/12951_2022_1355_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d284/8952886/cc9a64003938/12951_2022_1355_Fig4_HTML.jpg

相似文献

[1]
Magnetic, biocompatible FeCO nanoparticles for T2-weighted magnetic resonance imaging of in vivo lung tumors.

J Nanobiotechnology. 2022-3-25

[2]
Ligand free FeSn alloy nanoparticles for safe -weighted MR imaging of lung tumors.

Biomater Sci. 2023-3-14

[3]
Facile synthesis of superparamagnetic nickel-doped iron oxide nanoparticles as high-performance contrast agents for magnetic resonance imaging.

J Mater Chem B. 2022-3-9

[4]
Magnetic PEGylated Pt3Co nanoparticles as a novel MR contrast agent: in vivo MR imaging and long-term toxicity study.

Nanoscale. 2013-12-21

[5]
Biodegradable and biocompatible exceedingly small magnetic iron oxide nanoparticles for T-weighted magnetic resonance imaging of tumors.

J Nanobiotechnology. 2022-7-30

[6]
One-step, room-temperature synthesis of glutathione-capped iron-oxide nanoparticles and their application in in vivo T1-weighted magnetic resonance imaging.

Small. 2014-7-9

[7]
LAPONITE®-stabilized iron oxide nanoparticles for in vivo MR imaging of tumors.

Biomater Sci. 2016-3

[8]
Targeted MR Imaging Adopting T1-Weighted Ultra-Small Iron Oxide Nanoparticles for Early Hepatocellular Carcinoma: An and Study.

Chin Med Sci J. 2020-6-30

[9]
Casein-Coated Fe5C2 Nanoparticles with Superior r2 Relaxivity for Liver-Specific Magnetic Resonance Imaging.

Theranostics. 2015-8-9

[10]
Targeted dual-contrast T1- and T2-weighted magnetic resonance imaging of tumors using multifunctional gadolinium-labeled superparamagnetic iron oxide nanoparticles.

Biomaterials. 2011-3-31

引用本文的文献

[1]
Ferrocene-Functionalized Black Phosphorus Nanoplatform Enables Targeted and Prolonged MRI Visualization of Atherosclerotic Plaques.

Adv Sci (Weinh). 2025-8

[2]
Applications of Matrix Metalloproteinase-9-Related Nanomedicines in Tumors and Vascular Diseases.

Pharmaceutics. 2025-4-7

[3]
Iodinated gadolinium-gold nanomaterial as a multimodal contrast agent for cartilage tissue imaging.

APL Bioeng. 2024-8-19

[4]
Magneto-optical nanosystems for tumor multimodal imaging and therapy .

Mater Today Bio. 2024-3-16

[5]
EP300 regulates the SLC16A1-AS1-AS1/TCF3 axis to promote lung cancer malignancies through the Wnt signaling pathway.

Heliyon. 2024-3-7

[6]
Identification of the novel biomarkers involved in the mitochondrial metabolism-related reactive oxygen species and their role in lung cancer T-cell exhaustion and immunotherapy.

Heliyon. 2024-2-29

[7]
Advances in nanotechnology-based targeted-contrast agents for computed tomography and magnetic resonance.

Sci Prog. 2024

[8]
Recent advances in melittin-based nanoparticles for antitumor treatment: from mechanisms to targeted delivery strategies.

J Nanobiotechnology. 2023-11-28

[9]
Modified gefitinib conjugated FeO NPs for improved delivery of chemo drugs following an image-guided mechanistic study of inner vs. outer tumor uptake for the treatment of non-small cell lung cancer.

Front Bioeng Biotechnol. 2023-10-9

[10]
-Acetylcysteine-Loaded Magnetic Nanoparticles for Magnetic Resonance Imaging.

Int J Mol Sci. 2023-7-13

本文引用的文献

[1]
A pH-Activatable MnCO Nanoparticle for Improved Magnetic Resonance Imaging of Tumor Malignancy and Metastasis.

ACS Appl Mater Interfaces. 2021-4-28

[2]
Application of multiparametric MR imaging to predict the diversification of renal function in miR29a-mediated diabetic nephropathy.

Sci Rep. 2021-1-21

[3]
Advancements in the Blood-Brain Barrier Penetrating Nanoplatforms for Brain Related Disease Diagnostics and Therapeutic Applications.

Polymers (Basel). 2020-12-20

[4]
Nanomotor-based adsorbent for blood Lead(II) removal and in pig models.

Bioact Mater. 2020-10-23

[5]
Biodegradable pH-responsive amorphous calcium carbonate nanoparticles as immunoadjuvants for multimodal imaging and enhanced photoimmunotherapy.

J Mater Chem B. 2020-9-23

[6]
Hyaluronic Acid-Functionalized Gadolinium Oxide Nanoparticles for Magnetic Resonance Imaging-Guided Radiotherapy of Tumors.

Nanoscale Res Lett. 2020-4-25

[7]
Toxicological profile of calcium carbonate nanoparticles for industrial applications.

Colloids Surf B Biointerfaces. 2020-6

[8]
Size- and cell type-dependent cellular uptake, cytotoxicity and in vivo distribution of gold nanoparticles.

Int J Nanomedicine. 2019-8-28

[9]
Alliance with EPR Effect: Combined Strategies to Improve the EPR Effect in the Tumor Microenvironment.

Theranostics. 2019-10-17

[10]
Amino acid secretion influences the size and composition of copper carbonate nanoparticles synthesized by ureolytic fungi.

Appl Microbiol Biotechnol. 2019-7-9

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

推荐工具

医学文档翻译智能文献检索