4.8 Article

Gold Nanorod-Melanin Hybrids for Enhanced and Prolonged Photoacoustic Imaging in the Near-Infrared-II Window

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 13, Issue 13, Pages 14974-14984

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c00993

Keywords

gold nanorods; melanin; photoacoustic imaging; polydopamine coating; second near-infrared window

Funding

  1. National Science Foundation [1845683, 1937674]
  2. National Institutes of Health [DP2 HL 137187, R21 DE029917, R21 AI157957, S10 OD023527]
  3. NIH [T32 CA153915]
  4. NSF [DGE-1650112]
  5. [S10 OD021821]
  6. [S10 OD023555]
  7. Division Of Materials Research
  8. Direct For Mathematical & Physical Scien [1845683] Funding Source: National Science Foundation
  9. Division Of Materials Research
  10. Direct For Mathematical & Physical Scien [1937674] Funding Source: National Science Foundation

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This study presents monodisperse GNR-melanin nanohybrids with a tunable polydopamine (PDA) coating that significantly enhances the photoacoustic (PA) signal compared to pristine GNRs. The PA signal of GNR@PDAs only decreased by 29% during 5 minutes of laser illumination in the NIR-II window, while significant attenuation (77%) was observed for GNRs. The PDA-coating provides a rational design for robust PA imaging probes and offers opportunities for other photomediated biomedicines.
Photoacoustic (PA) imaging holds great promise as a noninvasive imaging modality. Gold nanorods (GNRs) with absorption in the second near-infrared (NIR-II) window have emerged as excellent PA probes because of their tunable optical absorption, surface modifiability, and low toxicity. However, pristine GNRs often undergo shape transition upon laser illumination due to thermodynamic instability, leading to a reduced PA signal after a few seconds of imaging. Here, we report monodisperse GNR-melanin nanohybrids where a tunable polydopamine (PDA) coating was conformally coated on GNRs. GNR@PDAs showed a threefold higher PA signal than pristine GNRs due to the increased optical absorption, cross-sectional area, and thermal confinement. More importantly, the PA signal of GNR@PDAs only decreased by 29% during the 5 min of laser illumination in the NIR-II window, while significant attenuation (77%) was observed for GNRs. The GNR@PDAs maintained 87% of its original PA signal in vivo even after 10 min of laser illumination. This PDA-enabled strategy affords a rational design for robust PA imaging probes and provides more opportunities for other types of photomediated biomedicines, such as photothermal and photodynamic regimens.

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