用于乳腺肿瘤靶向MRI和SPECT成像的肽偶联固体脂质纳米颗粒的设计和表征。

IF 4.3 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
ACS Omega Pub Date : 2025-04-22 eCollection Date: 2025-05-06 DOI:10.1021/acsomega.4c10153
Tahereh Rahdari, Hossein Ghafouri, Sorour Ramezanpour, Mehdi Shafiee Ardestani, S Mohsen Asghari
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引用次数: 0

摘要

三阴性乳腺癌(TNBC)由于其侵袭性行为和缺乏靶向治疗而面临重大挑战。高分辨率成像技术和靶向纳米颗粒为TNBC的早期检测和监测提供了潜在的解决方案。在这项研究中,我们开发并表征了固体脂质纳米颗粒(sln)与内皮抑素衍生的c肽结合,靶向TNBC中过表达的整合素αvβ3。这些sln装载了超顺磁性氧化铁纳米粒子(SPIONs),用于增强磁共振成像(MRI),并用锝-99m (99mTc)进行放射性标记,用于单光子发射计算机断层扫描(SPECT),从而实现双模成像。利用各种先进技术对纳米颗粒进行了广泛的表征,包括动态光散射(DLS)、差示扫描量热法(DSC)、热重分析(TGA)、x射线衍射(XRD)、振动样品磁强计(VSM)、场发射扫描电子显微镜(FE-SEM)和原子力显微镜(AFM)。这项综合分析验证了纳米颗粒的成功合成和功能化,以及它们卓越的磁性能,同时也揭示了它们独特的球形形态、最佳尺寸、均匀分布和胶体稳定性。利用流式细胞术和MRI对4T1细胞进行MTT和受体结合实验,证明c肽的结合显著提高了体外靶向效率。使用4T1小鼠模型的体内研究表明,肽结合的sln在肿瘤组织中积累,在MRI中提供了优越的对比,并在SPECT成像中增强了肿瘤特异性定位。生物分布分析证实,与非靶向制剂相比,脱靶积累减少,特别是在肝脏中。总的来说,c肽共轭sln为TNBC提供了一个有前途的双模成像平台,提高了诊断准确性和肿瘤靶向性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Design and Characterization of Peptide-Conjugated Solid Lipid Nanoparticles for Targeted MRI and SPECT Imaging of Breast Tumors.

Triple-negative breast cancer (TNBC) presents significant challenges due to its aggressive behavior and lack of targeted treatments. High-resolution imaging techniques and targeted nanoparticles offer potential solutions for early detection and monitoring of TNBC. In this study, we developed and characterized solid lipid nanoparticles (SLNs) conjugated with a C-peptide derived from endostatin to target integrin αvβ3, overexpressed in TNBC. These SLNs were loaded with superparamagnetic iron oxide nanoparticles (SPIONs) for enhanced magnetic resonance imaging (MRI) and radiolabeled with technetium-99m (99mTc) for single-photon emission computed tomography (SPECT), enabling dual-modality imaging. Extensive characterization of the nanoparticles was performed utilizing a variety of advanced techniques, including dynamic light scattering (DLS), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), X-ray diffraction (XRD), vibrating sample magnetometry (VSM), field-emission scanning electron microscopy (FE-SEM), and atomic force microscopy (AFM). This comprehensive analysis validated the successful synthesis and functionalization of the nanoparticles, along with their remarkable magnetic properties, while also revealing their distinct spherical morphology, optimal size, uniform distribution, and colloidal stability. The conjugation of C-peptide significantly enhanced the targeting efficiency in vitro, as evidenced by the MTT and receptor-binding assays in 4T1 cells using flow cytometry and MRI. In vivo studies using a 4T1 murine model demonstrated that peptide-conjugated SLNs accumulated in tumor tissues, providing superior contrast in MRI and enhanced tumor-specific localization in SPECT imaging. Biodistribution analysis confirmed reduced off-target accumulation, particularly in the liver, compared to nontargeted formulations. Collectively, C-peptide-conjugated SLNs provide a promising dual-modality imaging platform for TNBC, offering improved diagnostic accuracy and tumor targeting.

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来源期刊
ACS Omega
ACS Omega Chemical Engineering-General Chemical Engineering
CiteScore
6.60
自引率
4.90%
发文量
3945
审稿时长
2.4 months
期刊介绍: ACS Omega is an open-access global publication for scientific articles that describe new findings in chemistry and interfacing areas of science, without any perceived evaluation of immediate impact.
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