Development of a new methodology to determine size differences of nanoparticles with nanoparticle tracking analysis

被引:0
作者
Yann Pellequer
Gilbert Zanetta
Jean-Michel Rebibou
Isabelle Severin
Marie-Christine Chagnon
Gernot Zissel
Fabrice Neiers
Renaud Seigneuric
机构
[1] Université de Bourgogne Franche-Comté,PEPITE EA4267
[2] Centre Hospitalier Universitaire,Service de Néphrologie
[3] Université de Bourgogne Franche-Comté,Faculty of Health Sciences
[4] INSERM UMR1098,INCREASE
[5] Fédération Hospitalo-Universitaire,Équipe NUTOX, UMR 1231 AgroSup
[6] Université de Bourgogne Franche-Comté,Department of Pneumology, Faculty of Medicine
[7] Derttech “Packtox”,Centre des Sciences du Goût et de l’Alimentation (CSGA)
[8] INSERM,UMR 1231 LNC
[9] University Medical Centre,LipSTIC LabEx
[10] Université Bourgogne Franche-Comté,undefined
[11] CNRS,undefined
[12] INRA,undefined
[13] INSERM,undefined
[14] Fondation de Coopération Scientifique Bourgogne-Franche Comté,undefined
[15] TranslationR,undefined
[16] Maison Régionale de l’Innovation,undefined
[17] Biomedical and Health Informatics,undefined
[18] IBioLab,undefined
[19] Computer Science Department,undefined
[20] State University of New York,undefined
来源
Applied Nanoscience | 2021年 / 11卷
关键词
Nanoscience; Extracellular vesicle; Drug delivery system; Liposome; Nanoparticle tracking analysis;
D O I
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中图分类号
学科分类号
摘要
The current frontiers in Biology thus in Medicine and Pharmacy are at the nanoscale. Indeed, this is the relevant scale for extracting or synthetizing, visualizing, counting, characterizing and/or modifying nanoparticles. Nanoparticles are highly diverse including: extracellular vesicles (e.g.: exosomes), proteins, viruses and nanovectors or drug delivery systems for instance. To quantify the concentration of nano-sized objects, a growing number of size-tracking instruments is being developed. However, to date, the generated data is only used to provide a concentration measurement. The objective of this study was to determine which sizes of nanoparticles are statistically significant between 2 groups of samples. Using different samples (in silico data; calibrated beads; various biological samples), an approach that statistically compares 2 groups of samples was developed and validated. The proof of concept of the proposed approach was illustrated with applications in the field of Biology, Medicine and Pharmacy using liposomes and extracellular vesicles. For the first time to our knowledge, our results suggest that the presented approach enables comparing different groups of biological samples. It may be extended to situations such as batch 1 versus batch 2; healthy versus disease or non-treated versus treated.
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页码:2129 / 2141
页数:12
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