• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
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
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
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 @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

不同荧光染料负载纳米颗粒的定量比较。

Quantitative comparison of different fluorescent dye-loaded nanoparticles.

机构信息

Australian Institute for Bioengineering and Nanotechnology, University of Queensland, St. Lucia, Queensland, Australia.

Australian Institute for Bioengineering and Nanotechnology, University of Queensland, St. Lucia, Queensland, Australia.

出版信息

Colloids Surf B Biointerfaces. 2021 Oct;206:111923. doi: 10.1016/j.colsurfb.2021.111923. Epub 2021 Jun 15.

DOI:10.1016/j.colsurfb.2021.111923
PMID:34146992
Abstract

Labeling nanoparticles with fluorescent dyes is a common approach to investigate their cell uptake and biodistribution, providing valuable information for the preclinical assessment of nanoparticles for drug delivery. However, the underlying assumption that the fluorescence intensity of dye-labeled nanoparticles correlates positively with the amount of nanoparticles taken up by cells might not be valid under some conditions, as it can be affected by many factors including dye dispersion, dye quenching, and material shading. Here we demonstrated that both nanoparticles with hydrophobic dyes encapsulated inside and nanoparticles with hydrophilic dyes conjugated on the particle surface suffer from different degrees of dye quenching, making it challenging for quantitative comparison of cell uptake of different nanoparticles. To address this challenge, we proposed a possible solution for direct comparative studies of dye-labeled nanoparticles. This work provides valuable information for designing and evaluating different nanoparticles for drug delivery applications.

摘要

用荧光染料标记纳米颗粒是研究其细胞摄取和生物分布的常用方法,为纳米颗粒用于药物输送的临床前评估提供了有价值的信息。然而,荧光强度与细胞摄取的纳米颗粒数量呈正相关的假设在某些情况下可能并不成立,因为它会受到许多因素的影响,包括染料分散、染料猝灭和材料遮蔽。在这里,我们证明了内部封装疏水性染料的纳米颗粒和表面连接亲水性染料的纳米颗粒都受到不同程度的染料猝灭,这使得定量比较不同纳米颗粒的细胞摄取变得具有挑战性。为了解决这个挑战,我们提出了一种用于直接比较染料标记纳米颗粒的可能方法。这项工作为设计和评估用于药物输送应用的不同纳米颗粒提供了有价值的信息。

相似文献

1
Quantitative comparison of different fluorescent dye-loaded nanoparticles.不同荧光染料负载纳米颗粒的定量比较。
Colloids Surf B Biointerfaces. 2021 Oct;206:111923. doi: 10.1016/j.colsurfb.2021.111923. Epub 2021 Jun 15.
2
Self-Assembled Supramolecular Bilayer Nanoparticles Composed of Near-Infrared Dye as a Theranostic Nanoplatform To Encapsulate Hydrophilic Drugs Effectively.自组装超分子双层纳米粒子由近红外染料组成,作为治疗诊断纳米平台有效包裹亲水性药物。
ACS Biomater Sci Eng. 2020 Jan 13;6(1):474-484. doi: 10.1021/acsbiomaterials.9b01587. Epub 2019 Dec 3.
3
Comparative biodistribution in mice of cyanine dyes loaded in lipid nanoparticles.脂质纳米颗粒中负载的花青染料在小鼠体内的比较生物分布。
Eur J Pharm Biopharm. 2015 Jun;93:1-10. doi: 10.1016/j.ejpb.2015.03.019. Epub 2015 Mar 21.
4
Composite fluorescent nanoparticles for biomedical imaging.用于生物医学成像的复合荧光纳米颗粒。
Mol Imaging Biol. 2014 Apr;16(2):180-8. doi: 10.1007/s11307-013-0689-9.
5
Labeling nanoparticles: Dye leakage and altered cellular uptake.纳米颗粒标记:染料泄漏与细胞摄取改变。
Cytometry A. 2017 Aug;91(8):760-766. doi: 10.1002/cyto.a.22853. Epub 2016 Apr 14.
6
Core-shell polymeric nanoparticles co-loaded with photosensitizer and organic dye for photodynamic therapy guided by fluorescence imaging in near and short-wave infrared spectral regions.载光敏剂和有机染料的核壳聚合物纳米粒子,用于近红外和短波近红外荧光成像引导的光动力学治疗。
J Nanobiotechnology. 2020 Jan 23;18(1):19. doi: 10.1186/s12951-020-0572-1.
7
Fighting Aggregation-Caused Quenching and Leakage of Dyes in Fluorescent Polymer Nanoparticles: Universal Role of Counterion.对抗聚集引起的荧光聚合物纳米粒子的染料猝灭和泄漏:抗衡离子的普遍作用。
Chem Asian J. 2019 Mar 15;14(6):836-846. doi: 10.1002/asia.201801592. Epub 2019 Jan 23.
8
FRET Sensor for Erythrosine Dye Based on Organic Nanoparticles: Application to Analysis of Food Stuff.基于有机纳米颗粒的赤藓红染料荧光共振能量转移传感器:在食品分析中的应用
J Fluoresc. 2016 Jul;26(4):1467-78. doi: 10.1007/s10895-016-1839-7. Epub 2016 May 31.
9
Quantitative Assessment of Nanoparticle Biodistribution by Fluorescence Imaging, Revisited.荧光成像技术定量评估纳米颗粒生物分布的再研究。
ACS Nano. 2018 Jul 24;12(7):6458-6468. doi: 10.1021/acsnano.8b02881. Epub 2018 Jul 2.
10
Dye labeling for optical imaging biases drug carriers' biodistribution and tumor uptake.染料标记会影响光学成像药物载体的生物分布和肿瘤摄取。
Nanomedicine. 2023 Feb;48:102650. doi: 10.1016/j.nano.2023.102650. Epub 2023 Jan 7.

引用本文的文献

1
Oxymatrine and astragaloside IV co-loaded liposomes: Scale-up purposes and their enhancement of anti-PD-1 efficacy against breast cancer.氧化苦参碱和黄芪甲苷IV共载脂质体:放大生产目的及其对乳腺癌抗PD-1疗效的增强作用
Mater Today Bio. 2025 Mar 4;32:101634. doi: 10.1016/j.mtbio.2025.101634. eCollection 2025 Jun.
2
Advanced bioanalytical techniques for pharmacokinetic studies of nanocarrier drug delivery systems.用于纳米载体药物递送系统药代动力学研究的先进生物分析技术。
J Pharm Anal. 2025 Jan;15(1):101070. doi: 10.1016/j.jpha.2024.101070. Epub 2024 Aug 14.
3
Rational nanoparticle design: Optimization using insights from experiments and mathematical models.
理性纳米粒子设计:从实验和数学模型中获得的见解进行优化。
J Control Release. 2023 Aug;360:772-783. doi: 10.1016/j.jconrel.2023.07.018. Epub 2023 Jul 22.
4
Assessing the interactions between nanoparticles and biological barriers in vitro: a new challenge for microscopy techniques in nanomedicine.评估纳米粒子与生物屏障在体外的相互作用:纳米医学中显微镜技术的新挑战。
Eur J Histochem. 2022 Nov 24;66(4):3603. doi: 10.4081/ejh.2022.3603.
5
Immunophenotyping: Analytical approaches and role in preclinical development of nanomedicines.免疫表型分析:在纳米药物临床前开发中的分析方法和作用。
Adv Drug Deliv Rev. 2022 Jun;185:114281. doi: 10.1016/j.addr.2022.114281. Epub 2022 Apr 9.
6
FRET Ratiometric Nanoprobes for Nanoparticle Monitoring.用于纳米颗粒监测的荧光共振能量转移(FRET)比率型纳米探针。
Biosensors (Basel). 2021 Dec 9;11(12):505. doi: 10.3390/bios11120505.