TY - JOUR
T1 - Plasmonic interferometer array biochip as a new mobile medical device for cancer detection
AU - Zeng, Xie
AU - Yang, Yunchen
AU - Zhang, Nan
AU - Ji, Dengxin
AU - Gu, Xiaodong
AU - Jornet, Josep Miquel
AU - Wu, Yun
AU - Gan, Qiaoqiang
N1 - Publisher Copyright:
© 2018 IEEE.
PY - 2018/1/1
Y1 - 2018/1/1
N2 - We report a plasmonic interferometer array (PIA) sensor and demonstrate its ability to detect circulating exosomal proteins in real-time with high sensitivity and low cost to enable the early detection of cancer. Specifically, a surface plasmon wave launched by the nano-groove rings interferes with the free-space light at the output of central nano-aperture and results in an intensity interference pattern. Under the single-wavelength illumination, when the target exosomal proteins are captured by antibodies bound on the surface, the biomediated change in the refractive index between the central aperture and groove rings causes the intensity change in a transmitted light. By recording the intensity changes in real-time, one can effectively screen biomolecular binding events and analyze the binding kinetics. By integrating signals from multiple sensor pairs to enhance the signal-to-noise ratio, the superior sensing resolutions of 1.63 × 10-6 refractive index unit in a refractive index change and 3.86 × 108 exosomes/mL in exosome detection were realized, respectively. Importantly, this PIA sensor can be imaged by a miniaturized microscope system coupled with a smartphone to realize a portable and highly sensitive healthcare device. The sensing resolution of 9.72 × 109 exosomes/mL in exosome detection was realized using the portable sensing system building upon a commercial smartphone.
AB - We report a plasmonic interferometer array (PIA) sensor and demonstrate its ability to detect circulating exosomal proteins in real-time with high sensitivity and low cost to enable the early detection of cancer. Specifically, a surface plasmon wave launched by the nano-groove rings interferes with the free-space light at the output of central nano-aperture and results in an intensity interference pattern. Under the single-wavelength illumination, when the target exosomal proteins are captured by antibodies bound on the surface, the biomediated change in the refractive index between the central aperture and groove rings causes the intensity change in a transmitted light. By recording the intensity changes in real-time, one can effectively screen biomolecular binding events and analyze the binding kinetics. By integrating signals from multiple sensor pairs to enhance the signal-to-noise ratio, the superior sensing resolutions of 1.63 × 10-6 refractive index unit in a refractive index change and 3.86 × 108 exosomes/mL in exosome detection were realized, respectively. Importantly, this PIA sensor can be imaged by a miniaturized microscope system coupled with a smartphone to realize a portable and highly sensitive healthcare device. The sensing resolution of 9.72 × 109 exosomes/mL in exosome detection was realized using the portable sensing system building upon a commercial smartphone.
KW - Plasmonic interferometer
KW - cancer diagnosis
KW - exosome
KW - optical biosensor
UR - http://www.scopus.com/inward/record.url?scp=85051789359&partnerID=8YFLogxK
U2 - 10.1109/JSTQE.2018.2865418
DO - 10.1109/JSTQE.2018.2865418
M3 - Article
AN - SCOPUS:85051789359
SN - 1077-260X
VL - 25
JO - IEEE Journal of Selected Topics in Quantum Electronics
JF - IEEE Journal of Selected Topics in Quantum Electronics
IS - 1
M1 - 8439005
ER -