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Macrophage-Laden Gold Nanoflowers Embedded with Ultrasmall Iron Oxide Nanoparticles for Enhanced Dual-Mode CT/MR Imaging of Tumors
The design of multimodal imaging nanoplatforms with improved tumor accumulation represents a major trend in the current development of precision nanomedicine. To this end, we report herein the preparation of macrophage (MA)-laden gold nanoflowers (NFs) embedded with ultrasmall iron oxide nanoparticl...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8308993/ https://www.ncbi.nlm.nih.gov/pubmed/34209296 http://dx.doi.org/10.3390/pharmaceutics13070995 |
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author | Peng, Yucheng Wang, Xiaomeng Wang, Yue Gao, Yue Guo, Rui Shi, Xiangyang Cao, Xueyan |
author_facet | Peng, Yucheng Wang, Xiaomeng Wang, Yue Gao, Yue Guo, Rui Shi, Xiangyang Cao, Xueyan |
author_sort | Peng, Yucheng |
collection | PubMed |
description | The design of multimodal imaging nanoplatforms with improved tumor accumulation represents a major trend in the current development of precision nanomedicine. To this end, we report herein the preparation of macrophage (MA)-laden gold nanoflowers (NFs) embedded with ultrasmall iron oxide nanoparticles (USIO NPs) for enhanced dual-mode computed tomography (CT) and magnetic resonance (MR) imaging of tumors. In this work, generation 5 poly(amidoamine) (G5 PAMAM) dendrimer-stabilized gold (Au) NPs were conjugated with sodium citrate-stabilized USIO NPs to form hybrid seed particles for the subsequent growth of Au nanoflowers (NFs). Afterwards, the remaining terminal amines of dendrimers were acetylated to form the dendrimer-stabilized Fe(3)O(4)/Au NFs (for short, Fe(3)O(4)/Au DSNFs). The acquired Fe(3)O(4)/Au DSNFs possess an average size around 90 nm, display a high r(1) relaxivity (1.22 mM(−1) s(−1)), and exhibit good colloidal stability and cytocompatibility. The created hybrid DSNFs can be loaded within MAs without producing any toxicity to the cells. Through the mediation of MAs with a tumor homing and immune evasion property, the Fe(3)O(4)/Au DSNFs can be delivered to tumors more efficiently than those without MAs after intravenous injection, thus significantly improving the MR/CT imaging performance of tumors. The developed MA-mediated delivery system may hold great promise for enhanced tumor delivery of other contrast agents or nanomedicines for precision cancer nanomedicine applications. |
format | Online Article Text |
id | pubmed-8308993 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-83089932021-07-25 Macrophage-Laden Gold Nanoflowers Embedded with Ultrasmall Iron Oxide Nanoparticles for Enhanced Dual-Mode CT/MR Imaging of Tumors Peng, Yucheng Wang, Xiaomeng Wang, Yue Gao, Yue Guo, Rui Shi, Xiangyang Cao, Xueyan Pharmaceutics Article The design of multimodal imaging nanoplatforms with improved tumor accumulation represents a major trend in the current development of precision nanomedicine. To this end, we report herein the preparation of macrophage (MA)-laden gold nanoflowers (NFs) embedded with ultrasmall iron oxide nanoparticles (USIO NPs) for enhanced dual-mode computed tomography (CT) and magnetic resonance (MR) imaging of tumors. In this work, generation 5 poly(amidoamine) (G5 PAMAM) dendrimer-stabilized gold (Au) NPs were conjugated with sodium citrate-stabilized USIO NPs to form hybrid seed particles for the subsequent growth of Au nanoflowers (NFs). Afterwards, the remaining terminal amines of dendrimers were acetylated to form the dendrimer-stabilized Fe(3)O(4)/Au NFs (for short, Fe(3)O(4)/Au DSNFs). The acquired Fe(3)O(4)/Au DSNFs possess an average size around 90 nm, display a high r(1) relaxivity (1.22 mM(−1) s(−1)), and exhibit good colloidal stability and cytocompatibility. The created hybrid DSNFs can be loaded within MAs without producing any toxicity to the cells. Through the mediation of MAs with a tumor homing and immune evasion property, the Fe(3)O(4)/Au DSNFs can be delivered to tumors more efficiently than those without MAs after intravenous injection, thus significantly improving the MR/CT imaging performance of tumors. The developed MA-mediated delivery system may hold great promise for enhanced tumor delivery of other contrast agents or nanomedicines for precision cancer nanomedicine applications. MDPI 2021-06-30 /pmc/articles/PMC8308993/ /pubmed/34209296 http://dx.doi.org/10.3390/pharmaceutics13070995 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Peng, Yucheng Wang, Xiaomeng Wang, Yue Gao, Yue Guo, Rui Shi, Xiangyang Cao, Xueyan Macrophage-Laden Gold Nanoflowers Embedded with Ultrasmall Iron Oxide Nanoparticles for Enhanced Dual-Mode CT/MR Imaging of Tumors |
title | Macrophage-Laden Gold Nanoflowers Embedded with Ultrasmall Iron Oxide Nanoparticles for Enhanced Dual-Mode CT/MR Imaging of Tumors |
title_full | Macrophage-Laden Gold Nanoflowers Embedded with Ultrasmall Iron Oxide Nanoparticles for Enhanced Dual-Mode CT/MR Imaging of Tumors |
title_fullStr | Macrophage-Laden Gold Nanoflowers Embedded with Ultrasmall Iron Oxide Nanoparticles for Enhanced Dual-Mode CT/MR Imaging of Tumors |
title_full_unstemmed | Macrophage-Laden Gold Nanoflowers Embedded with Ultrasmall Iron Oxide Nanoparticles for Enhanced Dual-Mode CT/MR Imaging of Tumors |
title_short | Macrophage-Laden Gold Nanoflowers Embedded with Ultrasmall Iron Oxide Nanoparticles for Enhanced Dual-Mode CT/MR Imaging of Tumors |
title_sort | macrophage-laden gold nanoflowers embedded with ultrasmall iron oxide nanoparticles for enhanced dual-mode ct/mr imaging of tumors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8308993/ https://www.ncbi.nlm.nih.gov/pubmed/34209296 http://dx.doi.org/10.3390/pharmaceutics13070995 |
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