TY - JOUR
T1 - Liquid phase immunoassays utilizing magnetic markers and SQUID magnetometer
AU - Kuma, Hiroyuki
AU - Oyamada, Hiroko
AU - Tsukamoto, Akira
AU - Mizoguchi, Takako
AU - Kandori, Akihiko
AU - Sugiura, Yoshinori
AU - Yoshinaga, Kohji
AU - Enpuku, Keiji
AU - Hamasaki, Naotaka
N1 - Funding Information:
We would like to thank Dr. Sheshadri Narayanan for critical reading of the manuscript, Dr. Hidemitsu Kobayashi and Dr. Yukiko Ogawa for technical advice about bacterial cultures and antigens for Candida albicans. This work was supported by a Grant-in-Aid for Young Scientists (Start-up) and for Young Scientists (A) from the Japan Society of the Promotion of Science, and a Charitable Trust Laboratory Medicine Foundation of Japan.
PY - 2010/9/1
Y1 - 2010/9/1
N2 - Background: Immunoassays are one main detection system used in the field of clinical chemistry. Recent developments of a new detection method utilizing a magnetic marker and magnetic sensor have enabled rapid and sensitive immunoassay without the need for bound/free (BF) separation. Methods: Newly-synthesized conjugated avidin was used as the magnetic marker for quantitative analysis of human interleukin-8 (hIL-8) and immunoglobulin E (hIgE) in several media. A superconducting quantum interference device sensor detected the magnetic fields from markers fixed to antigens by the sandwich method. Magnetic signals from unbound markers were nearly zero due to Brownian rotation. Results: Our magnetic immunoassay could detect four attomoles of model proteins (hIL-8, hIgE) in phosphate buffer without BF separation. Using our standard curve, the range of protein detected ranged from 40 femtomoles to 4 attomoles, and we observed a strong association between protein amounts and magnetic signals from the bound markers. The homogeneous immunoassay could also quantify three hundred cells from the fungus Candida albicans in phosphate buffer. Conclusions: The present study demonstrates the ability of magnetic markers for measuring biological targets without BF separation. This detection system has great potential for use as the next generation's analytical system.
AB - Background: Immunoassays are one main detection system used in the field of clinical chemistry. Recent developments of a new detection method utilizing a magnetic marker and magnetic sensor have enabled rapid and sensitive immunoassay without the need for bound/free (BF) separation. Methods: Newly-synthesized conjugated avidin was used as the magnetic marker for quantitative analysis of human interleukin-8 (hIL-8) and immunoglobulin E (hIgE) in several media. A superconducting quantum interference device sensor detected the magnetic fields from markers fixed to antigens by the sandwich method. Magnetic signals from unbound markers were nearly zero due to Brownian rotation. Results: Our magnetic immunoassay could detect four attomoles of model proteins (hIL-8, hIgE) in phosphate buffer without BF separation. Using our standard curve, the range of protein detected ranged from 40 femtomoles to 4 attomoles, and we observed a strong association between protein amounts and magnetic signals from the bound markers. The homogeneous immunoassay could also quantify three hundred cells from the fungus Candida albicans in phosphate buffer. Conclusions: The present study demonstrates the ability of magnetic markers for measuring biological targets without BF separation. This detection system has great potential for use as the next generation's analytical system.
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U2 - 10.1515/CCLM.2010.259
DO - 10.1515/CCLM.2010.259
M3 - Article
C2 - 20678032
AN - SCOPUS:77957320982
SN - 1434-6621
VL - 48
SP - 1263
EP - 1269
JO - Clinical Chemistry and Laboratory Medicine
JF - Clinical Chemistry and Laboratory Medicine
IS - 9
ER -