PUBLICATION

Ultrabright fluorescent silica nanoparticles for in vivo targeting of xenografted human tumors and cancer cells in zebrafish

Authors
Peerzade, S.A.M.A., Qin, X., Laroche, F.J.F., Palantavida, S., Dokukin, M., Peng, B., Feng, H., Sokolov, I.
ID
ZDB-PUB-191115-5
Date
2019
Source
Nanoscale   11(46): 22316-22327 (Journal)
Registered Authors
Feng, Hui
Keywords
none
MeSH Terms
  • Animals
  • Female
  • Folic Acid/chemistry
  • HeLa Cells
  • Humans
  • Nanoparticles/chemistry*
  • Neoplasms/diagnostic imaging*
  • Optical Imaging
  • Particle Size
  • Polyethylene Glycols/chemistry
  • Porosity
  • Silicon Dioxide/chemistry*
  • Transplantation, Heterologous
  • Zebrafish
PubMed
31724677 Full text @ Nanoscale
Abstract
New ultrabright fluorescent silica nanoparticles capable of the fast targeting of epithelial tumors in vivo are presented. The as-synthesized folate-functionalized ultrabright particles of 30-40 nm are 230 times brighter than quantum dots (QD450) and 50% brighter than the polymer dots with similar spectra (excitation 365 nm and emission 486 nm). To decrease non-specific targeting, particles are coated with polyethylene glycol (PEG). We demonstrate the in vivo targeting of xenographic human cervical epithelial tumors (HeLa cells) using zebrafish as a model system. The particles target tumors (and probably even individual HeLa cells) as small as 10-20 microns within 20-30 minutes after blood injection. To demonstrate the advantages of ultrabrightness, we repeated the experiments with similar but 200× less bright particles. Compared to those, ultrabright particles showed ∼3× faster tumor detection and ∼2× higher relative fluorescent contrast of tumors/cancer cells.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping