DocumentCode
1195583
Title
Tumor-Targeted Quantum Dots Can Help Surgeons Find Tumor Boundaries
Author
Arndt-Jovin, Donna J. ; Kantelhardt, Sven R. ; Caarls, Wouter ; De Vries, Anthony H B ; Giese, Alf ; Jovin, Thomas M.
Author_Institution
Lab. of Cellular Dynamics, Max Planck Inst. for Biophys. Chem., Goettingen
Volume
8
Issue
1
fYear
2009
fDate
3/1/2009 12:00:00 AM
Firstpage
65
Lastpage
71
Abstract
Despite surgical advances and recent progress in adjuvant therapies, the prognosis for patients with malignant brain tumors such as glioblastoma multiforme has remained poor, and the neurological deterioration suffered by most patients as a consequence of tumor progression is dramatic and severe. In addition, malignant brain tumors have > 95% recurrence close to the primary site of initial resection. Unfortunately, standard imaging techniques do not permit the intraoperative identification of individual or small clusters of residual tumor cells, precluding their selective removal while sparing the surrounding normal brain tissue. In this report, we show that quantum dots (QDs) coupled to epidermal growth factor (EGF) or anti-EGF receptor (EGFR, Her1) specifically and sensitively label glial tumor cells in cell culture, glioma mouse models, and human brain-tumor biopsies. A clear demarcation between brain and tumor tissue at the macroscopic as well as the cellular level is provided by the fluorescence emission of the QDs.
Keywords
biomedical optical imaging; brain; cancer; cellular biophysics; neurophysiology; semiconductor quantum dots; surgery; tumours; adjuvant therapy; anti-EGF receptor; epidermal growth factor; fluorescence microscopy; glioblastoma multiforme; glioma mouse model; human brain-tumor biopsy; image-guided neuronavigation; malignant brain tumor cell; neurological deterioration; tumor-targeted quantum dots; Cellular imaging; confocal microscopy; epidermal growth factor (EGF); epidermal growth factor receptor (EGFR); experimental intraoperative imaging; extent of resection; glioma; programmable array microscope (PAM) microscopy; Animals; Antibodies, Monoclonal; Brain Neoplasms; Cell Line, Tumor; Epidermal Growth Factor; Glioma; Humans; Image Enhancement; Mice; Microscopy, Fluorescence; Molecular Probe Techniques; Quantum Dots; Sensitivity and Specificity;
fLanguage
English
Journal_Title
NanoBioscience, IEEE Transactions on
Publisher
ieee
ISSN
1536-1241
Type
jour
DOI
10.1109/TNB.2009.2016548
Filename
4801981
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