Gold Nanostars Obviate Limitations to Laser Interstitial Thermal Therapy (LITT) for the Treatment of Intracranial Tumors

Author:

Srinivasan Ethan S.1ORCID,Liu Yang234ORCID,Odion Ren A.24ORCID,Chongsathidkiet Pakawat15ORCID,Wachsmuth Lucas P.1ORCID,Haskell-Mendoza Aden P.1ORCID,Edwards Ryan M.1ORCID,Canning Aidan J.24ORCID,Willoughby Gavin15ORCID,Hinton Joseph15ORCID,Norton Stephen J.24ORCID,Lascola Christopher D.67ORCID,Maccarini Paolo F.24ORCID,Mariani Christopher L.8ORCID,Vo-Dinh Tuan234ORCID,Fecci Peter E.15ORCID

Affiliation:

1. 1Department of Neurosurgery, Duke University Medical Center, Durham, North Carolina.

2. 2Department of Biomedical Engineering, Duke University, Durham, North Carolina.

3. 3Department of Chemistry, Duke University, Durham, North Carolina.

4. 4Fitzpatrick Institute of Photonics, Duke University, Durham, North Carolina.

5. 5Department of Pathology, Duke University Medical Center, Durham, North Carolina.

6. 6Department of Radiology, Duke University Medical Center, Durham, North Carolina.

7. 7Department of Neurobiology, Duke University Medical Center, Durham, North Carolina.

8. 8Department of Clinical Sciences, NC State College of Veterinary Medicine, Raleigh, North Carolina.

Abstract

Abstract Purpose: Laser interstitial thermal therapy (LITT) is an effective minimally invasive treatment option for intracranial tumors. Our group produced plasmonics-active gold nanostars (GNS) designed to preferentially accumulate within intracranial tumors and amplify the ablative capacity of LITT. Experimental Design: The impact of GNS on LITT coverage capacity was tested in ex vivo models using clinical LITT equipment and agarose gel–based phantoms of control and GNS-infused central “tumors.” In vivo accumulation of GNS and amplification of ablation were tested in murine intracranial and extracranial tumor models followed by intravenous GNS injection, PET/CT, two-photon photoluminescence, inductively coupled plasma mass spectrometry (ICP-MS), histopathology, and laser ablation. Results: Monte Carlo simulations demonstrated the potential of GNS to accelerate and specify thermal distributions. In ex vivo cuboid tumor phantoms, the GNS-infused phantom heated 5.5× faster than the control. In a split-cylinder tumor phantom, the GNS-infused border heated 2× faster and the surrounding area was exposed to 30% lower temperatures, with margin conformation observed in a model of irregular GNS distribution. In vivo, GNS preferentially accumulated within intracranial tumors on PET/CT, two-photon photoluminescence, and ICP-MS at 24 and 72 hours and significantly expedited and increased the maximal temperature achieved in laser ablation compared with control. Conclusions: Our results provide evidence for use of GNS to improve the efficiency and potentially safety of LITT. The in vivo data support selective accumulation within intracranial tumors and amplification of laser ablation, and the GNS-infused phantom experiments demonstrate increased rates of heating, heat contouring to tumor borders, and decreased heating of surrounding regions representing normal structures.

Funder

N/A

Publisher

American Association for Cancer Research (AACR)

Subject

Cancer Research,Oncology

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