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Simple and efficient capture of EGFR-expressing tumor cells using magnetic nanoparticles
- Source :
- Sensors and Actuators B: Chemical. 201:144-152
- Publication Year :
- 2014
- Publisher :
- Elsevier BV, 2014.
-
Abstract
- Capturing tumor cells has attracted the attention because such cells can be used for diagnosing the occurrence and progression of cancers. Here we present a simple and efficient capturing of tumor cells using anti-EGFR antibody-conjugated magnetic nanoparticles. EGFR is a well-established epithelial cancer-specific marker that is over-expressed in many types of tumor cells. The conjugation of an anti-EGFR antibody with magnetic nanoparticles through a PEG-linker was shown to be highly efficient for preventing the non-specific binding of cells and improving the stability of the resulting nanoparticles even at a high salt concentration. The use of EGFR-targetable nanoparticles resulted in about 57% capture efficiency in 20 min for two cancer cell lines, PC9 (lung cancer) and HeLa (cervical cancer). The survival rate of the captured cells was approximately 85%, and most of the cells were retrievable, providing options for a further analysis of captured cells such as a mutational investigation of EGFR-related cancers. The present approach can be used for capturing circulating tumor cells (CTCs) expressing EGFR and the subsequent diagnostic analysis of the captured cells.
- Subjects :
- biology
Chemistry
Metals and Alloys
Nanotechnology
Condensed Matter Physics
medicine.disease
biology.organism_classification
Surfaces, Coatings and Films
Electronic, Optical and Magnetic Materials
HeLa
chemistry.chemical_compound
Circulating tumor cell
Growth factor receptor
Hepatocellular carcinoma
Materials Chemistry
medicine
Cancer research
biology.protein
Magnetic nanoparticles
Electrical and Electronic Engineering
Antibody
Lung cancer
Instrumentation
Iron oxide nanoparticles
Subjects
Details
- ISSN :
- 09254005
- Volume :
- 201
- Database :
- OpenAIRE
- Journal :
- Sensors and Actuators B: Chemical
- Accession number :
- edsair.doi...........a44710e874bd7859dd4a593612f43288
- Full Text :
- https://doi.org/10.1016/j.snb.2014.05.016