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Pre-Clinical Investigations of the Pharmacodynamics of Immunogenic Smart Radiotherapy Biomaterials (iSRB).
Moreau, Michele; Acter, Shahinur; Ngema, Lindokuhle M; Bih, Noella; Sy, Gnagna; Keno, Lensa S; Chow, Kwok Fan; Sajo, Erno; Nebangwa, Oscar; Walker, Jacques; Oh, Philmo; Broyles, Eric; Ngwa, Wilfred; Yasmin-Karim, Sayeda.
Afiliación
  • Moreau M; Department of Radiation Oncology, Brigham and Women's Hospital, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA 02115, USA.
  • Acter S; Department of Radiation Oncology & Molecular Radiation Sciences, Johns' Hopkins Hospital, Baltimore, MD 21287, USA.
  • Ngema LM; Department of Chemistry and Department of Physics (Medical Physics), University of Massachusetts Lowell, Lowell, MA 01854, USA.
  • Bih N; Department of Radiation Oncology & Molecular Radiation Sciences, Johns' Hopkins Hospital, Baltimore, MD 21287, USA.
  • Sy G; Department of Radiation Oncology & Molecular Radiation Sciences, Johns' Hopkins Hospital, Baltimore, MD 21287, USA.
  • Keno LS; Department of Pharmacy & Pharmacology, WITS Advanced Drug Delivery Platform Research Unit, University of the Witwatersrand, Johannesburg 2050, South Africa.
  • Chow KF; Department of Radiation Oncology, Brigham and Women's Hospital, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA 02115, USA.
  • Sajo E; Department of Radiation Oncology & Molecular Radiation Sciences, Johns' Hopkins Hospital, Baltimore, MD 21287, USA.
  • Nebangwa O; Department of Health Administration and Human Resources, The University of Scranton, Scranton, PA 18510, USA.
  • Walker J; Department of Chemistry and Department of Physics (Medical Physics), University of Massachusetts Lowell, Lowell, MA 01854, USA.
  • Oh P; Department of Chemistry and Department of Physics (Medical Physics), University of Massachusetts Lowell, Lowell, MA 01854, USA.
  • Broyles E; Nanocan Therapeutics Corporation, Princeton, NJ 08540, USA.
  • Ngwa W; Nanocan Therapeutics Corporation, Princeton, NJ 08540, USA.
  • Yasmin-Karim S; Nanocan Therapeutics Corporation, Princeton, NJ 08540, USA.
Pharmaceutics ; 15(12)2023 Dec 14.
Article en En | MEDLINE | ID: mdl-38140118
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.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Pharmaceutics Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Pharmaceutics Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos