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利用荧光共振能量转移(FRET)技术捕捉基于碳菁荧光团的脂质纳米颗粒的动态完整性。

Capturing the dynamic integrity of carbocyanine fluorophore-based lipid nanoparticles using the FRET technique.

作者信息

Long Siyu, Turner David A, Hamill Kevin J, Natrajan Louise S, McDonald Tom O

机构信息

Department of Chemistry, University of Manchester, Oxford Road, Manchester, M13 9PL, UK.

Henry Royce Institute, The University of Manchester, Oxford Road, Manchester, UK.

出版信息

J Mater Chem B. 2025 Feb 12;13(7):2295-2305. doi: 10.1039/d4tb02653e.

Abstract

Nanoparticles capable of dynamically reporting their structural integrity in real-time are a powerful tool to guide the design of drug delivery technologies. Lipid nanoparticles (LNPs) offer multiple important advantages for drug delivery, including stability, protection of active substances, and sustained release capabilities. However, tracking their structural integrity and dynamic behaviour in complex biological environments remains challenging. Here, we report the development of a Förster resonance energy transfer (FRET)-enabled LNP platform that achieves unprecedented sensitivity and precision in monitoring nanoparticle disintegration. The FRET-based LNPs were prepared using nanoprecipitation, encapsulating high levels of 3,3'-dioctadecyloxacarbocyanine perchlorate (DiO) and 1,1'-dioctadecyl-3,3,3',3'-tetramethylindocarbocyanine perchlorate (DiI) fluorophores as the donor and acceptors, respectively. The resulting LNPs had a mean diameter of 114 ± 19 nm with a distinct FRET signal. An optimal energy transfer efficiency of 0.98 and an emission quantum yield of 0.13 were achieved at 11.1% fluorophore loading in the LNPs, balancing efficient energy transfer and minimal aggregation-induced quenching. Using the FRET reporting, three dissociation stages of FRET LNPs were observed: solvation, indicated by an increased emission intensity; swelling and partial dissolution, evidenced by changes in emission maxima and mean size; and complete dissociation, confirmed by emission solely from DiO and the absence of particles. Testing the nanoparticles in live cells (telomerase-immortalised human corneal epithelial cells, hTCEpi cells) revealed a direct link to the disappearance of the FRET signal with the dissociation of FRET NPs. The nanoparticles initially exhibited a strong extracellular FRET signal, which diminished after cellular internalisation. This suggests that the LNPs disintegrate after entering the cells. These findings establish FRET-based LNPs as a robust tool for real-time nanoparticle tracking, offering insights into their integrity and release mechanisms, with potential applications in advanced drug delivery and diagnostics.

摘要

能够实时动态报告其结构完整性的纳米颗粒是指导药物递送技术设计的有力工具。脂质纳米颗粒(LNPs)在药物递送方面具有多种重要优势,包括稳定性、对活性物质的保护以及缓释能力。然而,在复杂的生物环境中追踪它们的结构完整性和动态行为仍然具有挑战性。在此,我们报告了一种基于Förster共振能量转移(FRET)的LNP平台的开发,该平台在监测纳米颗粒解体方面实现了前所未有的灵敏度和精度。基于FRET的LNPs采用纳米沉淀法制备,分别封装了高含量的高氯酸3,3'-二辛基氧杂碳菁(DiO)和高氯酸1,1'-二辛基-3,3,3',3'-四甲基吲哚碳菁(DiI)荧光团作为供体和受体。所得LNPs的平均直径为114±19 nm,具有明显的FRET信号。在LNPs中荧光团负载量为11.1%时,实现了0.98的最佳能量转移效率和0.13的发射量子产率,平衡了高效的能量转移和最小的聚集诱导猝灭。利用FRET报告,观察到FRET LNPs的三个解离阶段:溶剂化,表现为发射强度增加;膨胀和部分溶解,由发射最大值和平均尺寸的变化证明;以及完全解离,通过仅来自DiO的发射和颗粒的消失得到证实。在活细胞(端粒酶永生化的人角膜上皮细胞,hTCEpi细胞)中测试纳米颗粒发现,FRET信号的消失与FRET NPs的解离直接相关。纳米颗粒最初表现出强烈的细胞外FRET信号,在细胞内化后减弱。这表明LNPs在进入细胞后解体。这些发现确立了基于FRET的LNPs作为实时纳米颗粒追踪的强大工具,为其完整性和释放机制提供了见解,在先进药物递送和诊断中具有潜在应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e59/11783621/5a5d8fe5eff9/d4tb02653e-f1.jpg

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