4.7 Article

Calcium Alginate Gel Beads Containing Gold Nanobipyramids for Surface-Enhanced Raman Scattering Detection in Aqueous Samples

Journal

ACS APPLIED NANO MATERIALS
Volume 4, Issue 10, Pages 10287-10295

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsanm.1c01789

Keywords

SERS; gel bead; gold nanobipyramids; ready-to-use; uric acid

Funding

  1. National Natural Science Foundation of China [21775026, 81371902, 81772287]
  2. Natural Science Foundation of Fujian Province [2018J01682, 2020J011241]
  3. China Postdoctoral Science Foundation [2019M662250]
  4. Xiamen foundation for Scientific and technological plan projects [3502Z20214ZD3003]

Ask authors/readers for more resources

A plasmonic gel bead was developed for rapid and effective detection of aqueous samples with high sensitivity and reproducibility. The gel bead contains gold nanobipyramids and an aqueous sample, forming a three-dimensional SERS-active gel network for trapping analytes and offering a uniform hotspot region, resulting in reproducible and uniform signal generation. The method shows excellent reproducibility and detection limit, and has potential for monitoring disease-related biomarkers and point-of-care testing.
The application of surface-enhanced Raman scattering (SERS) in aqueous sample detection is normally limited by the low affinity between analytes and SERS-active nanoparticles. Furthermore, a tendency of uncontrollable aggregation of solute (nanoparticles or analytes) can cause poor reproducibility of the detected SERS signal. Herein, a ready-to-use plasmonic gel bead was developed for rapid and effective detection of aqueous samples with high sensitivity and reproducibility. The SERS gel bead is made of calcium alginate gel beads (CAGBs) that contain gold nanobipyramids (Au NBPs) and an aqueous sample, which can be prepared and detected within only 1 min. Au NBPs/CAGBs can generate an in-depth three-dimensional SERS-active gel network for trapping analytes and offering a uniform hotspot region, which produces a reproducible and uniform signal. Using rhodamine 6G as a model target, the proposed method exhibits excellent reproducibility with a relative standard deviation of 6.57% and a detection limit of 0.4 nM. Then, Au NBPs/CAGBs were applied to quantitatively detect serum uric acid in the range of 10-1000 mu M and a limit of detection of 0.18 mu M, and the results were strongly consistent with those of the commercial ELISA method. This work offers a low-cost and easy route for the fabrication of a versatile SERS substrate for monitoring disease-related biomarkers and point-of-care testing.

Authors

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

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available