Spectral Photon-Counting Molecular Imaging for Quantification of Monoclonal Antibody-Conjugated Gold Nanoparticles Targeted to Lymphoma and Breast Cancer: An In Vitro Study

Author:

Moghiseh Mahdieh1ORCID,Lowe Chiara1ORCID,Lewis John G.2ORCID,Kumar Dhiraj3ORCID,Butler Anthony1ORCID,Anderson Nigel1ORCID,Raja Aamir1ORCID

Affiliation:

1. Department of Radiology, University of Otago, Christchurch School of Medicine, 2 Riccarton Avenue, Christchurch 8011, New Zealand

2. Steroid & Immunobiochemistry Laboratory, Canterbury Health Laboratories, 524 Hagley Ave, Christchurch 8011, New Zealand

3. Department of Obstetrics and Gynecology, University of Otago, Christchurch School of Medicine, 2 Riccarton Avenue, Christchurch 8011, New Zealand

Abstract

The purpose of the present study was to demonstrate an in vitro proof of principle that spectral photon-counting CT can measure gold-labelled specific antibodies targeted to specific cancer cells. A crossover study was performed with Raji lymphoma cancer cells and HER2-positive SKBR3 breast cancer cells using a MARS spectral CT scanner. Raji cells were incubated with monoclonal antibody-labelled gold, rituximab (specific antibody to Raji cells), and trastuzumab (as a control); HER2-positive SKBR3 breast cancer cells were incubated with monoclonal antibody-labelled gold, trastuzumab (specific antibody to HER2-positive cancer cells), and rituximab (as a control). The calibration vials with multiple concentrations of nonfunctionalised gold nanoparticles were used to calibrate spectral CT. Spectral imaging results showed that the Raji cells-rituximab-gold and HER2-positive cells-trastuzumab-gold had a quantifiable amount of gold, 5.97 mg and 0.78 mg, respectively. In contrast, both cell lines incubated with control antibody-labelled gold nanoparticles had less gold attached (1.22 mg and 0.15 mg, respectively). These results demonstrate the proof of principle that spectral molecular CT imaging can identify and quantify specific monoclonal antibody-labelled gold nanoparticles taken up by Raji cells and HER2-positive SKBR3 breast cancer cells. The present study reports the future potential of spectral molecular imaging in detecting tumour heterogeneity so that treatment can be tuned accordingly, leading to more effective personalised medicine.

Funder

Ministry of Business, Innovation and Employment

Publisher

Hindawi Limited

Subject

Radiology Nuclear Medicine and imaging

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