Pre-Clinical Investigations of the Pharmacodynamics of Immunogenic Smart Radiotherapy Biomaterials (iSRB)

Author:

Moreau Michele123ORCID,Acter Shahinur2ORCID,Ngema Lindokuhle M.24ORCID,Bih Noella1,Sy Gnagna2ORCID,Keno Lensa S.5,Chow Kwok Fan3,Sajo Erno3ORCID,Nebangwa Oscar6,Walker Jacques6,Oh Philmo6,Broyles Eric6,Ngwa Wilfred123,Yasmin-Karim Sayeda1

Affiliation:

1. Department of Radiation Oncology, Brigham and Women’s Hospital, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA 02115, USA

2. Department of Radiation Oncology & Molecular Radiation Sciences, Johns’ Hopkins Hospital, Baltimore, MD 21287, USA

3. Department of Chemistry and Department of Physics (Medical Physics), University of Massachusetts Lowell, Lowell, MA 01854, USA

4. Department of Pharmacy & Pharmacology, WITS Advanced Drug Delivery Platform Research Unit, University of the Witwatersrand, Johannesburg 2050, South Africa

5. Department of Health Administration and Human Resources, The University of Scranton, Scranton, PA 18510, USA

6. Nanocan Therapeutics Corporation, Princeton, NJ 08540, USA

Abstract

The use of an immunogenic smart radiotherapy biomaterial (iSRB) for the delivery of anti-CD40 is effective in treating different cancers in animal models. This study further characterizes the use of iSRBs to evaluate any associated toxicity in healthy C57BL6 mice. iSRBs were fabricated using a poly-lactic-co-glycolic-acid (PLGA) polymer mixed with titanium dioxide (TiO2) nanoparticles incorporated into its matrix. Animal studies included investigations of freely injected anti-CD40, anti-CD40-loaded iSRBs, unloaded iSRBs and control (healthy) animal cohorts. Mice were euthanized at pre-determined time points post-treatment to evaluate the serum chemistry pertaining to kidney and liver toxicity and cell blood count parameters, as well as pathology reports on organs of interest. Results showed comparable liver and kidney function in all cohorts. The results indicate that using iSRBs with or without anti-CD40 does not result in any significant toxicity compared to healthy untreated animals. The findings provide a useful reference for further studies aimed at optimizing the therapeutic efficacy and safety of iSRBs and further clinical translation work.

Funder

National Institutes of Health

Publisher

MDPI AG

Subject

Pharmaceutical Science

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