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用于MRI引导热疗的近红外仿生混合磁性纳米载体

Near Infrared Biomimetic Hybrid Magnetic Nanocarrier for MRI-Guided Thermal Therapy.

作者信息

Rocha João Victor Ribeiro, Krause Rafael Freire, Ribeiro Carlos Eduardo, Oliveira Nathália Corrêa de Almeida, Ribeiro de Sousa Lucas, Leandro Santos Juracy, Castro Samuel de Melo, Valadares Marize Campos, Cunha Xavier Pinto Mauro, Pavam Marcilia Viana, Lima Eliana Martins, Antônio Mendanha Sebastião, Bakuzis Andris Figueiroa

机构信息

Institute of Physics, Federal University of Goiás, Goianiâ, Goiás 74690-900, Brazil.

FarmaTec - Laboratory of Pharmaceutical Technology, Federal University of Goiás, Goianiâ, Goiás 74690-631, Brazil.

出版信息

ACS Appl Mater Interfaces. 2025 Mar 5;17(9):13094-13110. doi: 10.1021/acsami.4c03434. Epub 2024 Jul 8.

DOI:10.1021/acsami.4c03434
PMID:38973727
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11891835/
Abstract

Cell-membrane hybrid nanoparticles (NPs) are designed to improve drug delivery, thermal therapy, and immunotherapy for several diseases. Here, we report the development of distinct biomimetic magnetic nanocarriers containing magnetic nanoparticles encapsulated in vesicles and IR780 near-infrared dyes incorporated in the membranes. Distinct cell membranes are investigated, red blood cell (RBC), melanoma (B16F10), and glioblastoma (GL261). Hybrid nanocarriers containing synthetic lipids and a cell membrane are designed. The biomedical applications of several systems are compared. The inorganic nanoparticle consisted of Mn-ferrite nanoparticles with a core diameter of 15 ± 4 nm. TEM images show many multicore nanostructures (∼40 nm), which correlate with the hydrodynamic size. Ultrahigh transverse relaxivity values are reported for the magnetic NPs, 746 mMs, decreasing respectively to 445 mMs and 278 mMs for the B16F10 and GL261 hybrid vesicles. The ratio of relaxivities / decreased with the higher encapsulation of NPs and increased for the biomimetic liposomes. Therapeutic temperatures are achieved by both, magnetic nanoparticle hyperthermia and photothermal therapy. Photothermal conversion efficiency ∼25-30% are reported. Cell culture revealed lower wrapping times for the biomimetic vesicles. experiments with distinct routes of nanoparticle administration were investigated. Intratumoral injection proved the nanoparticle-mediated PTT efficiency. MRI and near-infrared images showed that the nanoparticles accumulate in the tumor after intravenous or intraperitoneal administration. Both routes benefit from MRI-guided PTT and demonstrate the multimodal theranostic applications for cancer therapy.

摘要

细胞膜杂化纳米颗粒(NPs)旨在改善多种疾病的药物递送、热疗和免疫治疗。在此,我们报告了一种独特的仿生磁性纳米载体的研发,该载体包含包裹在囊泡中的磁性纳米颗粒以及掺入膜中的IR780近红外染料。我们研究了不同的细胞膜,包括红细胞(RBC)、黑色素瘤(B16F10)和胶质母细胞瘤(GL261)。设计了包含合成脂质和细胞膜的杂化纳米载体。比较了几种系统的生物医学应用。无机纳米颗粒由核心直径为15±4 nm的锰铁氧体纳米颗粒组成。透射电子显微镜(TEM)图像显示许多多核纳米结构(约40 nm),这与流体动力学尺寸相关。据报道,磁性纳米颗粒的横向弛豫率极高,为746 mM s⁻¹,对于B16F10和GL261杂化囊泡分别降至445 mM s⁻¹和278 mM s⁻¹。弛豫率之比随着纳米颗粒更高的包封率而降低,而对于仿生脂质体则增加。通过磁性纳米颗粒热疗和光热疗法均可达到治疗温度。据报道光热转换效率约为25 - 30%。细胞培养显示仿生囊泡具有更短的包裹时间。研究了纳米颗粒不同给药途径的实验。瘤内注射证明了纳米颗粒介导的光热疗法(PTT)效率。磁共振成像(MRI)和近红外图像显示,纳米颗粒在静脉内或腹腔内给药后在肿瘤中积累。这两种途径都受益于MRI引导的PTT,并展示了癌症治疗的多模态诊疗应用。

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