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
Link To Document :
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