Detection of Glioma-Derived Exosomes with the Biotinylated Antibody-Functionalized Titanium Nitride Plasmonic Biosensor

Research output: Journal Publications and Reviews (RGC: 21, 22, 62)21_Publication in refereed journalNot applicablepeer-review

3 Scopus Citations
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Detail(s)

Original languageEnglish
Article number1806761
Journal / PublicationAdvanced Functional Materials
Volume29
Issue number9
Early online date20 Dec 2018
Publication statusPublished - 28 Feb 2019

Abstract

Titanium nitride (TiN), as an excellent alternative plasmonic supporting material compared to gold and silver, exhibits tunable plasmonic properties in the visible and near‐infrared spectra. However, label‐free surface plasmon resonance biosensing with TiN is seldom reported due to lack of proper surface functionalization protocols. Herein, this study reports biotinylated antibody functionalized TiN (BAF‐TiN) for high‐performance label‐free biosensing applications. The BAF‐TiN biosensor can quantitatively detect exosomes of 30–200 nm extracellular vesicles, isolated from a human glioma cell line. The limit of detection for an exosomal membrane protein with the BAF‐TiN biosensor is found to be 4.29 × 10−3 µg mL−1 for CD63, an exosome marker, and 2.75 × 10−3 µg mL−1 for epidermal growth factor receptor variant‐III, a glioma specific mutant protein, respectively. In conclusion, combining the biocompatibility, high stability, and excellent label‐free sensing performance of TiN, the BAF‐TiN biosensor could have great potential for the detection of cancer biomarkers, including exosomal surface proteins.

Research Area(s)

  • biotinylation, exosomes, glioma, surface plasmon resonance, titanium nitride

Citation Format(s)

Detection of Glioma-Derived Exosomes with the Biotinylated Antibody-Functionalized Titanium Nitride Plasmonic Biosensor. / Qiu, Guangyu; Thakur, Abhimanyu; Xu, Chen; Ng, Siu-Pang; Lee, Youngjin; Wu, Chi-Man Lawrence.

In: Advanced Functional Materials, Vol. 29, No. 9, 1806761, 28.02.2019.

Research output: Journal Publications and Reviews (RGC: 21, 22, 62)21_Publication in refereed journalNot applicablepeer-review