Abstract

A label-free and array-based optical liquid-crystal (LC) immunodetection technique for the detection of CA125 antigen, a protein biomarker most frequently used for ovarian cancer detection, was demonstrated with a nematic LC with larger birefringence (Δn) to promote sensitivity in detecting biomolecules. The LC-based immunodetection offers an alternative and sensitive approach for the detection of biomarker proteins, with the potential of replacing conventional immunoassays used in biochemical studies and clinical laboratories.

Highlights

  • Immunodetection of cancer biomarkers is an essential procedure in cancer detection and diagnosis

  • It is clear from the quantified data (Fig. 3) that, for a given bovine serum albumin (BSA) concentration, HDN gives rise to a more pronounced dark-to-bright optical response than does 5CB, indicating that the higher sensitivity can be achieved by using HDN in LC-based biosensing

  • It is necessary to choose a suitable anti-CA125 antibody concentration to ensure that the CA125 antigen is sufficiently bound to the antibody, and the optical texture of LCs is not affected by the CA125 antibodies in the absence of the CA125 antigen

Read more

Summary

Introduction

Immunodetection of cancer biomarkers is an essential procedure in cancer detection and diagnosis. The commercially available CA125 immunoassay has a detection limit of 15 U∕ml, which is sufficient to detect the generally accepted threshold level of CA125 when the disease is present (35 U∕ml).[2] Due to the importance of early diagnosis of cancer, various immunoassays for the detection of CA125 cancer biomarker have been reported, including enzyme-linked immunosorbent assay,[3] electrochemical immunoassay,[4,5,6,7] and colorimetric immunoassay.[8] These traditional label-based immunoassays are often complicated, timeconsuming, with the high cost of labeling antibodies. Development of label-free immunodetection techniques is highly desired to reduce the cost of detection systems as well as to simplify cancer screening procedures

Methods
Results
Discussion
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.