Abstract
The detection of circulating tumor cells (CTCs) plays a very important role in the prevention and treatment of cancer. However, because of the low content of tumor cells in peripheral blood, these cells have always been difficult to detect. An efficient and accurate imaging method, the dark-field scanning imaging method, was innovatively proposed for the detection of CTCs in filtered and colored peripheral blood specimens. Here, the original dark-field scanning system was improved. By introducing an ellipsoidal mirror system, the noise in the sampling process is greatly reduced, and the sampling accuracy is significantly improved. Meanwhile, an automatic identification algorithm was developed to identify and screen CTCs in a large number of blood samples. Comparing with the other CTC detection methods, this method does not require a complex biological enrichment process, which may cause loss and destruction of CTCs.
Similar content being viewed by others
References
P. Paterlinibrechot, N.L. Benali, Cancer Lett. 253, 180 (2007)
M. Alunnifabbroni, M.T. Sandri, Methods 50, 289 (2010)
S. Maheswaran, D.A. Haber, Curr. Opin. Genet. Dev. 20, 96 (2010)
F. Tanaka, K.N. Yoneda, Clin. Cancer Res. 15, 6980 (2009)
V. Hofman, M.I. Ilie, E. Long, E. Selva, C. Bonnetaud, T. Molina, N. Vénissac, J. Mouroux, P. Vielh, P. Hofman, Int. J. Cancer 129, 1651 (2011)
M. LS Lim, M.C. Hu, W.C. Huang, A.T. Cheong, Gan, X.L. Looi et al., Lab Chip 12(21), 4388–4396 (2012)
S. Carroll, M. Alrubeai, J. Immunol. Methods 296(1), 171 (2005)
T.G. Ntouroupi, S.Q. Ashraf, S.B. McGregor, B.W. Turney, A. Seppo, Y. Kim, X. Wang, M.W. Kilpatrick, P. Tsipouras, T. Tafas, W.F. Bodmer, Br. J. Cancer 99, 789 (2008)
H. Ben Hsieh, D. Marrinucci, K. Bethel, D.N. Curry, M. Humphrey, R.T. Krivacic, J. Kroener, L. Kroener, A. Ladanyi, N. Lazarus, P. Kuhn, R.H. Bruce, J. Nieva, Biosens. Bioelectron. 21(10), 1893 (2006)
B. Fuchs, A. Romani, D. Freida, G. Medoro, M. Abonnenc, L. Altomare, I. Chartier, D. Guergour, C. Villiers, P.N. Marche, Lab Chip 6(1), 121 (2005)
L. Wang, P. Balasubramanian, A. Chen, S. Kummar, Y.A. Evrard, R. Kinders, Semin. Oncol. 43(4), 464 (2016)
K.C. Andree, G.V. Dalum, L.W.M.M. Terstappen, Mol. Oncol. 10(3), 395 (2016)
J. Lorincik, D. Marton, R.L. King, J. Fine, J. Vac. Sc. Technol. B 14(4), 2417 (1996)
D.D. Nolte, M. Zhao, X. Wang, J. Opt. Commun. 5(4), 456 (2009)
L. Peng, Diss. Abstr. Int. 66–10(B), 5471 (2005)
R. Königsberg, E. Obermayr, G. Bises, G. Pfeiler, M. Gneist, F. Wrba, M.D. Santis, R. Zeillinger, M. Hudec, C. Dittrich, Acta Oncol. 50, 700 (2011)
M. Borgatti, N. Bianchi, I. Mancini, G. Feriotto, R. Gambari, Int. J. Mol. Med. 21(1), 3 (2008)
L. Zabaglo, M.G. Ormerod, M. Parton, A. Ring, I.E. Smith, M. Dowsett, Cytom. A 55A(2), 102–108 (2010)
S.J. Hao, Y. Wan, Y.Q. Xia, X. Zou, S.Y. Zheng, Adv. Drug Deliv. Rev. 125, 3–20 (2018)
H. Busch, Y. Daskal, F. Gyorkey, K. Smetana, Can. Res. 39(3), 857–863 (1979)
P.V. Asharani, G.L.K. Mun, M.P. Hande, S. Valiyaveettil, Arch. Toxicol. 85, 743 (2011)
F. Vari, K. Bell, Electrophoresis 17, 20 (1996)
M. Gong, Z. Zhou, J. Ma, IEEE Trans. Image Process. Publ. IEEE Signal Process. Soc. 21, 2141 (2012)
A. Rodriguez, A. Laio, Science 344, 1492 (2014)
Y.J. Cha, W. Choi, O. Büyüköztürk, Comput. Aided Civ. Infrastruct. Eng. 32, 361 (2017)
Acknowledgements
This work is supported by the Project of Natural Science Foundation of Anhui Province of China (no. 1808085MF207). The fabrication work was partially carried out at the USTC Center for Micro and Nanoscale Research and Fabrication.
Author information
Authors and Affiliations
Corresponding authors
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
About this article
Cite this article
Li, C., Xu, K., Qin, J. et al. Ellipsoidal mirror dark-field scanning for detection of circulating tumor cells. Appl. Phys. B 125, 38 (2019). https://doi.org/10.1007/s00340-019-7143-x
Received:
Accepted:
Published:
DOI: https://doi.org/10.1007/s00340-019-7143-x