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Interaction of nanoparticles with endotoxin Importance in nanosafety testing and exploitation for endotoxin binding
- Source :
- Nanotoxicology.
- Publication Year :
- 2021
- Publisher :
- John Wiley & Sons, 2021.
-
Abstract
- The interaction between engineered nanoparticles and the bacterial lipopolysaccharide, or endotoxin, is an event that warrants attention. Endotoxin is one of the most potent stimulators of inflammation and immune reactions in human beings, and is a very common contaminant in research labs. In nanotoxicology and nanomedicine, the presence of endotoxin on the nanoparticle surface affects their biological properties leading to misinterpretation of results. This review discusses the importance of detecting the endotoxin contamination on nanoparticles, focusing on the current method of endotoxin detection and their suitability for nanoparticulate materials. Conversely, the capacity of nanoparticles to bind endotoxin can be enhanced by functionalization with endotoxin-capturing molecules, opening the way to the development of novel endotoxin detection assays.<br />The authors were supported by the EU H2020 grants ENDONANO [GA 812661] and PANDORA [GA 671881], the IG grant [21420] of the Associazione Italiana Ricerca sul Cancro (AIRC), the project NeON [ARS01_00769] of the Program PRIN, and the projects CIRO- Campania Infrastructure for Research in Oncology and PLATT of the Programma Operativo Regionale of Regione Campania [POR FERS 2014/2020].
- Subjects :
- Inflammation
Lipopolysaccharide
LPSsensors
SERS
Biomedical Engineering
Nanoparticle
02 engineering and technology
010501 environmental sciences
021001 nanoscience & nanotechnology
Toxicology
01 natural sciences
Engineered nanoparticles
Endotoxin binding
Microbiology
chemistry.chemical_compound
LPS sensors
chemistry
Endotoxin
medicine
Nanoparticles
medicine.symptom
0210 nano-technology
0105 earth and related environmental sciences
Subjects
Details
- ISSN :
- 17435404
- Database :
- OpenAIRE
- Journal :
- Nanotoxicology
- Accession number :
- edsair.doi.dedup.....55c781555ecbf1a4dbb3005c8b8fe8bb