Behavior of circulating tumor cells detected by EGF tagged SERS nanoparticles in head and neck cancer patients.

2012 ◽  
Vol 30 (15_suppl) ◽  
pp. e21161-e21161 ◽  
Author(s):  
Jonathan Jay Beitler ◽  
Xu Wang ◽  
Ximei Qian ◽  
Hong Wang ◽  
Zhuo Georgia Chen ◽  
...  

e21161 Background: Quantification of circulating tumor cells(CTCs) is becoming central to the management of metastatic breast, colorectal and prostate cancers and the potential to improve management of head and neck squamous cell cancer (HNSCC) patients is very high. Our group has published our experience with nanotechnology, highly specific, surface-enhanced Raman spectroscopy(SERS) and Epidermal Growth Factor Receptor(EGFR) ligands to identify 7-720 CTCs/ml in 19 samples from HNSCC patients[1]. Our goal here is to understand the clinical behavior of CTCs in HNSCC for selected patients whom we believe our single channel assay has been accurate. Methods: Our methods for detection of CTCs using EGFR ligands have been previously described[1]. After comparing CTCs in 116 patient samples with and without gross disease, we examined 8 patients with decreasing sequential single channel assays of CTCs and no evidence of disease at last follow-up. Results: For 56 samples from patients with no gross disease, the mean CTC was 94/ml. For 61 samples from patients with gross disease the mean CTC was 193/ml (p=0.002). Among our 4 samples where we had initial disease and a non-zero, no evidence of disease, second sample, the absolute and percentage decrease per month in CTC was 121/ml/month(range 43-160) and 17%/month(range 11-25%). The decrease of 121 CTC/ml/month correlated well with 5 out of 6 other data sets. Conclusions: Targeting of EGFR for detection of CTCs in HNSCC patients appears very promising. Among +EGFR HNSCC patients who appear cured, the average decrease in CTC per ml was 121 per month and 17% per month. To further enhance the sensitivity and specificity of detection of CTCs, we are developing 3 SERS nanoparticles (multiplexed SERS) to target specific and distinct targets on the CTC surface while still maintaining a single tube assay system. 1. Wang, X., et al., Detection of circulating tumor cells in human peripheral blood using surface-enhanced Raman scattering nanoparticles. Cancer Research, 2011. 71(5): p. 1526-32.

1996 ◽  
Vol 50 (12) ◽  
pp. 1569-1577 ◽  
Author(s):  
Z. Q. Tian ◽  
W. H. Li ◽  
B. W. Mao ◽  
S. Z. Zou ◽  
J. S. Gao

This paper describes a novel technique called potential-averaged surface-enhanced Raman spectroscopy (PASERS) which has several advantages over SERS. A PASERS spectrum is acquired when the electrode is rapidly modulated between two potentials by applying a square-wave voltage. The potential-averaged SERS spectrum contains all the information on the surface species at the two modulated potentials, and each individual SERS spectrum can then be extracted by deconvolution. By properly choosing the two modulating potentials, one can obtain SERS spectra of surface species at electrode potentials where SERS-active sites are normally unstable. PASERS also leads to a unique way of studying complex interfacial kinetic processes by controlling the voltage pulse height, frequency, and shape. Moreover, the measurement of time-resolved spectra in the very low vibrational frequency region can be achieved by PASERS with the use of a conventional scanning spectrometer with a single-channel detector. In this paper, the main advantages of PASERS are illustrated by studying two typical SERS systems, i.e., thiocyanate ion and thiourea adsorbed at silver electrodes, respectively. It is shown that the potential-averaging method can be applied as a common method to many other existing spectroelectrochemical techniques.


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