4.8 Article

Quantitative Assessment of Copper(II) in Wilson's Disease Based on Photoacoustic Imaging and Ratiometric Surface-Enhanced Raman Scattering

Journal

ACS NANO
Volume 15, Issue 2, Pages 3402-3414

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.0c10407

Keywords

NIR-II; photoacoustic imaging; biosensing; SERS; Wilson's disease

Funding

  1. National Natural Science Foundation of China [21874024, 21635002]
  2. Natural Science Foundation of Fujian Province [2020J02012]
  3. joint research projects of Health and Education Commission of Fujian Province [2019-WJ-20]

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A Cu2+-activated nanoprobe was developed to quantify liver Cu2+ and urinary Cu2+ in Wilson's disease patients using photoacoustic (PA) imaging and ratiometric surface-enhanced Raman scattering (SERS). The nanoprobe showed promising results for in vivo quantitative detection of WD, potentially improving early and accurate diagnosis in clinical settings.
Cu2+ is closely related to the occurrence and development of Wilson's disease (WD), and quantitative detection of various copper indicators (especially liver Cu-2 and urinary Cu2+) is the key step for the early diagnosis of WD in the clinic. However, the clinic Cu2+ detection approach was mainly based on testing the liver tissue through combined invasive liver biopsy and the ICP-MS method, which is painful for the patient and limited in determining WD status in real-time. Herein, we rationally designed a type of Cu2+-activated nanoprobe based on nanogapped gold nanoparticles (AuNNP) and poly(N-isopropylacrylamide) (PNIPAM) to simultaneously quantify the liver Cu2+ content and urinary Cu2+ in WD by photoacoustic (PA) imaging and ratiometric surface-enhanced Raman scattering (SERS), respectively. In the nanoprobe, one Raman molecule of 2-naphthylthiol (NAT) was placed in the nanogap of AuNNP. PNIPAM and the other Raman molecule mercaptobenzonitrile (MBN) were coated on the AuNNP surface, named AuNNP-NAT@MBN/PNIPAM. Cu2+ can efficiently coordinate with the chelator PNIPAM and lead to aggregation of the nanoprobe, resulting in the absorption red-shift and increased PA performance of the nanoprobe in the NIR-II window. Meanwhile, the SERS signal at 2223 cm(-1) of MBN is amplified, while the SERS signal at 1378 cm(-1) of NAT remains stable, generating a ratiometric SERS I-2223/I-1378 signal. Both NIR-II PA(1250 nm) and SERS I-2223/I-1378 signals of the nanoprobe show a linear relationship with the concentration of Cu2+. The nanoprobe was successfully applied for in vivo quantitative detection of liver Cu2+ of WD mice through NIR-II PA imaging and accurate quantification of urinary Cu2+ of WD patients by ratiometric SERS. We anticipate that the activatable nanoprobe might be applied for assisting an early, precise diagnosis of WD in the clinic in the future.

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