Size and surface charge characterization of nanoparticles with a salt gradient

被引:340
作者
Rasmussen, Martin K. [1 ]
Pedersen, Jonas N. [1 ]
Marie, Rodolphe [1 ]
机构
[1] Tech Univ Denmark, Dept Hlth Technol, Oersteds Plads Bldg 345c, DK-2800 Kongens Lyngby, Denmark
关键词
DRUG-DELIVERY; COLLOID TRANSPORT; EXOSOMES; NANOCARRIERS; SEPARATION; LIPOSOMES; PROGRESS;
D O I
10.1038/s41467-020-15889-3
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Exosomes are nanometer-sized lipid vesicles present in liquid biopsies and used as biomarkers for several diseases including cancer, Alzheimer's, and central nervous system diseases. Purification and subsequent size and surface characterization are essential to exosome-based diagnostics. Sample purification is, however, time consuming and potentially damaging, and no current method gives the size and zeta potential from a single measurement. Here, we concentrate exosomes from a dilute solution and measure their size and zeta potential in a one-step measurement with a salt gradient in a capillary channel. The salt gradient causes oppositely directed particle and fluid transport that trap particles. Within minutes, the particle concentration increases more than two orders of magnitude. A fit to the spatial distribution of a single or an ensemble of exosomes returns both their size and surface charge. Our method is applicable for other types of nanoparticles. The capillary is fabricated in a low-cost polymer device. Exosomes are used as disease biomarkers, but their characterization in biological samples is challenging. Here the authors achieve simultaneous characterization of size and zeta potential of individual nanoparticles and particle mixtures at physiological salinity conditions, exploiting a salt gradient in a capillary channel.
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页数:8
相关论文
共 40 条
[1]   Liposomes: From a Clinically Established Drug Delivery System to a Nanoparticle Platform for Theranostic Nanomedicine [J].
Al-Jamal, Wafa' T. ;
Kostarelos, Kostas .
ACCOUNTS OF CHEMICAL RESEARCH, 2011, 44 (10) :1094-1104
[2]  
ANDERSON JL, 1989, ANNU REV FLUID MECH, V21, P61
[3]   Using exosomes, naturally-equipped nanocarriers, for drug delivery [J].
Batrakova, Elena V. ;
Kim, Myung Soo .
JOURNAL OF CONTROLLED RELEASE, 2015, 219 :396-405
[4]   Particle entrainment in dead-end pores by diffusiophoresis [J].
Battat, Sarah ;
Ault, Jesse T. ;
Shin, Sangwoo ;
Khodaparast, Sepideh ;
Stone, Howard A. .
SOFT MATTER, 2019, 15 (19) :3879-3885
[5]   Principles of nanoparticle design for overcoming biological barriers to drug delivery [J].
Blanco, Elvin ;
Shen, Haifa ;
Ferrari, Mauro .
NATURE BIOTECHNOLOGY, 2015, 33 (09) :941-951
[6]  
Cho EC, 2011, NAT NANOTECHNOL, V6, P385, DOI [10.1038/nnano.2011.58, 10.1038/NNANO.2011.58]
[7]   Impact of Nanotechnology on Drug Delivery [J].
Farokhzad, Omid C. ;
Langer, Robert .
ACS NANO, 2009, 3 (01) :16-20
[8]   pH-Triggered copolymer micelles as drug nanocarriers for intracellular delivery [J].
Hao, Weiju ;
Liu, Danyang ;
Shang, Yazhuo ;
Zhang, Junqi ;
Xu, Shouhong ;
Liu, Honglai .
RSC ADVANCES, 2016, 6 (35) :29149-29158
[9]  
Happel J., 1965, Low Reynolds number hydrodynamics: with special applications to particulate media
[10]   Effect of Zeta Potential on the Properties of Nano-Drug Delivery Systems - A Review (Part 1) [J].
Honary, Soheyla ;
Zahir, Foruhe .
TROPICAL JOURNAL OF PHARMACEUTICAL RESEARCH, 2013, 12 (02) :255-264