4.8 Article

Ternary Z-Scheme Ag-Embedded TiO2-Ag2S Nanojunction as a Novel Photoelectrochemical Converter for CD44 Detection

Journal

ANALYTICAL CHEMISTRY
Volume 94, Issue 33, Pages 11713-11720

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.2c03046

Keywords

-

Funding

  1. National Natural Science Foundation of China [51904114]
  2. Special Foundation for Taishan Scholar Professorship of Shandong Province [ts201712052]
  3. Shandong Provincial Natural Science Foundation [ZR2020QB097]

Ask authors/readers for more resources

A biosensor utilizing TiO2-Ag-Ag2S nanostructure as a signal converter for the efficient detection of CD44 protein was developed, showing stable photocurrent output and highly specific identification of CD44. This approach provides a new alternative solution for breast cancer diagnosis.
Nanoarrays (NAs) with stable signal output have become the most promising photoelectrochemical (PEC) biosensing substrate. However, a general issue is that interfacial charge-carrier recombination in a single-component semiconductor cannot be easily prevented, resulting in a low photocurrent density. Herein, a biosensor utilizing a Ag-embedded TiO2-Ag2S nanojunction (TiO2-Ag- Ag2S) as a signal converter was developed for the detection of CD44 protein -a transmembrane glycoprotein highly expressed in breast cancer cells. The ternary Z-scheme heterojunction was prepared by a distinctive scheme in which the Ag layer is introduced onto the surface of rutile TiO2 NAs by magnetron sputtering, whereas the Ag2S is rooted in the local sulfuration of Ag. With a sufficient density of oriented nanorods, TiO2-Ag-Ag2S exhibits a smooth photocurrent output and minimal variation among different batches; it is undoubtedly a satisfactory PEC sensing carrier, which enables highly specific identification of target CD44 on the surface of MDA-MB-231 cells due to DNA strand displacement reactions (SDRs) and host-guest recognition between hyaluronic acid (HA) and CD44. The biosensor shows a sensitive PEC response to CD44 over a wide range of 37 to 5.0 x 10(5) cells/mL. We can conclude that this approach will provide an alternative solution to breast cancer diagnosis.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available