4.8 Article

Imaging of Liver Tumors Using Surface-Enhanced Raman Scattering Nanoparticles

期刊

ACS NANO
卷 10, 期 5, 页码 5015-5026

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.5b07200

关键词

surface-enhanced Raman scattering; nanoparticles; hepatocellular carcinoma; sarcoma; intraoperative imaging; image-guided tumor resection

资金

  1. NIH [R01 EB017748, K08 CA16396, 5P01 CA013106, 5U01 CA168409]
  2. Damon Runyon Cancer Research Foundation [DRR-29-14]
  3. Pershing Square Sohn Prize
  4. Dana Foundation Brain and Immuno-Imaging Grant
  5. Dana Neuroscience Scholar Award
  6. Geoffrey Beene Cancer Research Center at MSKCC Grant Award
  7. Shared Resources Award
  8. Bayer HealthCare Pharmaceuticals/RSNA Research Scholar Grant
  9. Center for Molecular Imaging & Nanotechnology (CMINT) Grant
  10. Center for Experimental Therapeutics of Memorial Sloan Kettering Cancer Center
  11. Molecularly Targeted Intra-Operative Imaging Grants
  12. Mr. William H. and Mrs. Alice Goodwin and the Commonwealth Foundation for Cancer Research
  13. MSKCC Office of Technology TDF Grant
  14. Society of MSKCC Research Grant
  15. Deutsche Forschungsgemeinschaft (DFG) [NE 1922/2-1]
  16. NIH/NCI Cancer Center Support Grant [P30 CA008748]

向作者/读者索取更多资源

Complete surgical resection is the ideal first line treatment for most liver malignancies. This goal would be facilitated by an intraoperative imaging method that enables more precise-visualization of tumor margins and detection of otherwise in-visible microscopic lesions. To this end, we synthesized silica-encapsulated surface-enhanced Raman scattering (SERS) nanoparticles (NPs) that act as a molecular imaging agent for liver malignancies. We hypothesized that, after intravenous administration, SERS NPs would avidly home to healthy liver tissue but not to intrahepatic malignancies. We tested these SERS NPs in genetically engineered mouse models of hepatocellular carcinoma and histiocytic sarcoma. After intravenous injection, liver tumors in both models were readily identifiable with Raman imaging. In addition, Raman imaging using SERS NPs enabled detection of microscopic lesions in liver and spleen. We compared the performance of SERS NPs to fluorescence imaging using indocyanine green (ICG). We found that SERS NPs delineate tumors more accurately and are less susceptible to photobleaching. Given the known advantages of SERS imaging, namely, high sensitivity and specific spectroscopic detection, these findings hold promise for improved resection of liver cancer.

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