4.8 Article

Surface Plasmon-Enhanced NIR-II Fluorescence in a Multilayer Nanoprobe for Through-Skull Mouse Brain Imaging

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 14, Issue 34, Pages 38575-38583

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.2c11218

Keywords

NIR-II fluorescence; surface plasmon; fluorescent imaging; gold nanorods; polymer dots

Funding

  1. National Key R&D Program of China [2020YFA0909000]
  2. Shenzhen Science and Technology Program [KQTD20170810111314625, JCYJ20210324115807021]
  3. Shenzhen Bay Laboratory [SZBL2021080601002]
  4. Guangdong Provincial Key Laboratory of Advanced Bio-materials [2022B1212010003]

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This study describes a surface plasmon-enhanced NIR-II fluorescence strategy, incorporating silica-coated gold nanorods and polymer dots into a multilayer nanostructure, achieving fluorescence enhancement in the NIR-II imaging window. This approach demonstrates superior signal-to-background ratio and penetration depth in mouse brain imaging.
Fluorescence imaging in the second near-infrared window (NIR-II, 10001700 nm) holds great potential for the accurate visualization of deeply located biological structures in vivo. However, the weak fluorescence of current NIR-II fluorophores remains a long-standing challenge for the ever-growing imaging demand. Here, we describe a surface plasmon-enhanced NIR-II fluorescence strategy by incorporating silica-coated gold nanorods (GNRs) and polymer dots (Pdots) into a multilayer nanostructure. Precise manipulation of the silica spacing layer thickness signifies an optimum distance of 8.6 nm, where an enhancement factor of up to 6.4 is achieved in the NIR-II imaging window. The surface plasmon enhancement approach is successfully extended to several types of Pdots fluorophores with NIR-II emission. We finally perform outer-layer encapsulation and PEGylation for the multilayer probes and demonstrate surface plasmon-enhanced NIR-II fluorescence for mouse brain imaging through the skull, which exhibits a refined signal-to-background ratio and penetration depth as compared to the clinically approved ICG dye.

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