On-chip screening for prostate cancer: an EIS microfluidic platform for contemporary detection of free and total PSA
Prostate cancer affects a large part of the western male population. The need for an early and accurate detection is thus a great challenge in common clinical practice, but the lack of specificity of the serum marker PSA (Prostate Specific Antigen) is a serious problem since its increased concentrat...
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Published in | Analyst (London) Vol. 138; no. 18; pp. 544 - 541 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
21.09.2013
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Subjects | |
Online Access | Get full text |
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Summary: | Prostate cancer affects a large part of the western male population. The need for an early and accurate detection is thus a great challenge in common clinical practice, but the lack of specificity of the serum marker PSA (Prostate Specific Antigen) is a serious problem since its increased concentration can be related to several abnormalities. PSA, however, is found in serum in both a free and a complexed form with other proteins and the percentage amount of unbound PSA (the free-to-total PSA ratio) can be employed to distinguish prostate cancer from benign prostatic conditions, and also to predict the future risk of prostate cancer. To improve the operating characteristics of current PSA tests and to provide a clinical tool able to run label-free and sensitive analysis, we thus developed a biosensing platform based on Electrochemical Impedance Spectroscopy (EIS), which allows the contemporary detection of free and total PSA on a single biochip, enabling a quick screening for the risk of prostate cancer thanks to the presence of two different immobilized antibodies specific for the different antigens researched.
A low-cost impedimetric platform for on-chip early detection of prostate cancer has been developed, able to perform a label-free and time-saving test for free-to-total PSA ratio. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 ObjectType-Article-2 ObjectType-Feature-1 |
ISSN: | 0003-2654 1364-5528 |
DOI: | 10.1039/c3an00911d |