[ 90 Y]Yttria Alumino Silicate Glass Microspheres: A Biosimilar Formulation to "TheraSphere" for Cost-Effective Treatment of Liver Cancer.
K V VimalnathArdhi RajeswariAnupam DixitRubel ChakravartyHaldhar D SarmaSuyash KulkarniAshish JhaAmeya PuranikVenkatesh RangarajanMadhumita GoswamiSudipta ChakrabortyPublished in: Cancer biotherapy & radiopharmaceuticals (2024)
Background: Selective internal radiation therapy (SIRT) using a suitable β - -emitting radionuclide is a promising treatment modality for unresectable liver carcinoma. Yttrium-90 ( 90 Y) [ T 1/2 = 64.2 h, E β (max) = 2.28 MeV, no detectable γ-photon] is the most preferred radioisotope for SIRT owing to its favorable decay characteristics. Objective: The present study describes indigenous development and evaluation of intrinsically radiolabeled [ 90 Y]yttria alumino silicate ([ 90 Y]YAS) glass microsphere, a formulation biosimilar to "TheraSphere" (commercially available, U.S. FDA-approved formulation), for SIRT of unresectable liver carcinoma in human patients. Methods: YAS glass microspheres of composition 40Y 2 O 3 -20Al 2 O 3 -40SiO 2 (w/w) and diameter ranging between 20 and 36 μm were synthesized with almost 100% conversion efficiency and >99% sphericity. Intrinsically labeled [ 90 Y]YAS glass microspheres were produced by thermal neutron irradiation of cold YAS glass microspheres in a research reactor. Subsequent to in vitro evaluations and in vivo studies in healthy Wistar rats, customized doses of [ 90 Y]YAS glass microspheres were administered in human patients. Results: [ 90 Y]YAS glass microspheres were produced with 137.7 ± 8.6 MBq/mg YAS glass (∼6800 Bq per microsphere) specific activity and 99.94% ± 0.02% radionuclidic purity at the end of irradiation. The formulation exhibited excellent in vitro stability in human serum and showed >97% retention in the liver up to 7 d post-administration when biodistribution studies were carried out in healthy Wistar rats. Yttrium-90 positron emission tomography scans recorded at different time points post-administration of customized dose of [ 90 Y]YAS glass microspheres in human patients showed near-quantitative retention of the formulation in the injected lobe. Conclusions: The study confirmed the suitability of indigenously prepared [ 90 Y]YAS glass microspheres for clinical use in the treatment of unresectable hepatocellular carcinoma.
Keyphrases
- end stage renal disease
- endothelial cells
- radiation therapy
- ejection fraction
- drug delivery
- positron emission tomography
- computed tomography
- chronic kidney disease
- prognostic factors
- molecularly imprinted
- combination therapy
- induced pluripotent stem cells
- wastewater treatment
- mass spectrometry
- quantum dots
- pluripotent stem cells
- pet ct
- optical coherence tomography
- rectal cancer
- magnetic nanoparticles
- fluorescent probe