1. Academic Validation
  2. Indocyanine green modified silica shells for colon tumor marking

Indocyanine green modified silica shells for colon tumor marking

  • Appl Surf Sci. 2020 Jan 1;499:143885. doi: 10.1016/j.apsusc.2019.143885.
Adrian Garcia Badaracco 1 Erin Ward 2 Christopher Barback 3 Jian Yang 4 James Wang 1 Ching-Hsin Huang 1 Moon Kim 5 Qingxiao Wang 5 Seungjin Nam 5 Jonathan Delong 2 Sarah Blair 2 William C Trogler 4 Andrew Kummel 4
Affiliations

Affiliations

  • 1 Department of Nanoengineering, University of California, San Diego, 9500 Gilman Drive, La Jolla, California 92093, United States.
  • 2 Department of Surgery, University of California, San Diego, 9500 Gilman Drive, La Jolla, California 92093, United States.
  • 3 Department of Radiology, University of California, San Diego, 9500 Gilman Drive, La Jolla, California 92093, United States.
  • 4 Department of Chemistry and Biochemistry, University of California, San Diego, 9500 Gilman Drive, La Jolla, California 92093, United States.
  • 5 Department of Materials Science and Engineering, The University of Texas at Dallas, 800 West Campbell Road, Richardson, Texas 75080, USA.
Abstract

Marking colon tumors for surgery is normally done with the use of India ink. However, non-fluorescent dyes such as India ink cannot be imaged below the tissue surface and there is evidence for physiological complications such as abscess, intestinal perforation and inconsistency of dye injection. A novel infrared marker was developed using FDA approved indocyanine green (ICG) dye and ultrathin hollow silica nanoshells (ICG/HSS). Using a positively charged amine linker, ICG was non-covalently adsorbed onto the nanoparticle surface. For ultra-thin wall 100 nm diameter silica shells, a bimodal ICG layer of < 3 nm is was formed. Conversely, for thicker walls on 2 μm diameter silica shells, the ICG layer was only bound to the outer surface and was 6 nm thick. In vitro testing of fluorescent emission showed the particles with the thinner coating were considerably more efficient, which is consistent with self-quenching reducing emission shown in the thicker ICG coatings. Ex-vivo testing showed that ICG bound to the 100 nm hollow silica shells was visible even under 1.5 cm of tissue. In vivo experiments showed that there was no diffusion of the ICG/nanoparticle marker in tissue and it remained imageable for as long as 12 days.

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