Optical detection of CA 15.3 breast cancer antigen using CdS quantum dot. Issue 3 (28th July 2016)

• Record Type: Journal Article
• Authors: Elakkiya, Venugopal; Menon, Mridula Prakash; Nataraj, Devaraj; Biji, Pullithadathil; Selvakumar, Rajendran
• Is Part Of: IET nanobiotechnology. Volume 11:Issue 3(2017)
• Page Start: 268
• Page End: 276
• Publication Date: 2016-07-28
• Subjects: semiconductor quantum dots -- cadmium compounds -- II‐VI semiconductors -- wide band gap semiconductors -- cancer -- tumours -- optical sensors -- biosensors -- biomedical equipment -- visible spectra -- ultraviolet spectra -- Fourier transform infrared spectra -- transmission electron microscopy -- X‐ray chemical analysis -- fluorescence -- optical microscopy -- photoluminescence -- proteins -- molecular biophysics -- nanosensors -- nanomedicine -- nanoparticles; optical detection -- CA 15.3 breast cancer antigen -- optical sensing -- cadmium sulphide quantum dot -- saline samples -- serum samples -- cysteamine capping -- CA 15.3 antibody -- UV‐visible absorption spectroscopy -- Fourier transform infrared spectroscopy -- high‐resolution transmission electron microscopy -- energy dispersive X‐ray spectroscopy -- phase contrast inverted epifluorescence microscopy -- photoluminescence spectrophotometry -- antigen‐antibody interaction -- fluorescence intensity -- optical intensity -- CA 15.3 tumour marker -- surface modified CdS QD -- biosensor development -- time 15 min -- CdS; Biotechnology -- Periodicals; Nanotechnology -- Periodicals; 660.6
• DOI: 10.1049/iet-nbt.2016.0012
• Languages: English
• ISSNs: 1751-8741

Abstract

Abstract : The present study focus on optical sensing of breast cancer antigen 15.3 (CA 15.3) using cadmium sulphide quantum dot (CdS‐QD) in saline and serum samples spiked with antigen. The surface of CdS‐QD was modified by cysteamine capping followed by tagging of CA 15.3 antibody. The samples were characterised using UV‐visible absorption spectroscopy (UV‐VIS Spectroscopy), Fourier transform infrared spectroscopy (FTIR), high‐resolution transmission electron microscopy (HRTEM) attached with energy‐dispersive X‐ray spectroscopy, phase contrast inverted epi‐fluorescence microscopy and photoluminescence (PL) spectrophotometry (EDS). The CdS‐QD showed a mean diameter of 3.02 ± 0.6 nm. The complex formed after antigen‐antibody interaction resulted in distinguishable optical and fluorescence intensity with respect to varying concentration of antigen. The PL study revealed that CA 15.3 antibody labelled CdS QD can detect CA 15.3 tumour marker even at very low concentration of 0.002 KU/L with a constant response time of 15 min. This study clearly indicates that detection of CA 15.3 at low concentration is possible using surface modified CdS QD in serum samples and can find immense applications in biosensor development for detection of breast cancer marker similar to various automated detection kits available in market.