4.6 Article

Biofunctionalization of Large Gold Nanorods Realizes Ultrahigh-Sensitivity Optical Imaging Agents

期刊

LANGMUIR
卷 31, 期 45, 页码 12339-12347

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.langmuir.5b02902

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资金

  1. Stanford Biophysics Program training grant [T32 GM-08294]
  2. Pew Charitable Trusts
  3. Alexander and Margaret Stewart Trust
  4. United States Air Force [FA9550-15-1-0007]
  5. National Institute of Health [NIH DP50D012179]
  6. National Science Foundation [NSF 1172802-100-QAANU]
  7. Damon Runyon Cancer Research Center (DFS) [06-13]
  8. Susan G. Komen Breast Cancer Foundation [SAB15-00003]
  9. Mary Kay Foundation
  10. Donald E. and Delia B. Baxter Foundation
  11. Claire Giannini Fund
  12. Skippy Frank Foundation from the Center for Cancer Nanotechnology Excellence and Translation [CCNE-T U54CA151459]
  13. Stanford Nano Center (SNC) and Stanford Nano-characterization Lab (SNL) for GNR characterization, and a Stanford Bio-X Interdisciplinary Initiative Seed Grant
  14. Div Of Chem, Bioeng, Env, & Transp Sys
  15. Directorate For Engineering [1434465] Funding Source: National Science Foundation

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Gold nanorods (GNRs, similar to 50 x 15 nm) have been used ubiquitously in biomedicine for their optical properties, and many methods of GNR biofunctionalization have been described. Recently, the synthesis of larger-than-usual GNRs (LGNRs, similar to 100 x 30 nm) has been demonstrated. However, LGNRs have not been biofunctionalized and therefore remain absent from biomedical literature to date. Here we report the successful biofunctionalization of LGNRs, which produces highly stable particles that exhibit a narrow spectral peak (FWHM similar to 100 nm). We further demonstrated that functionalized LGNRs can be used as highly sensitive scattering contrast agents by detecting individual LGNRs in clear liquids. Owing to their increased optical cross sections, we found that LGNRs exhibited up to 32-fold greater backscattering than conventional GNRs. We leveraged these enhanced optical properties to detect LGNRs in the vasculature of live tumor-bearing mice. With LGNR contrast enhancement, we were able to visualize tumor blood vessels at depths that were otherwise undetectable. We expect that the particles reported herein will enable immediate sensitivity improvements in a wide array of biomedical imaging and sensing techniques that rely on conventional GNRs.

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