Affiliation:
1. Departamento de Física—Faculdade de Filosofia Ciências e Letras de Ribeirão Preto Universidade de São Paulo Ribeirão Preto São Paulo 14040‐901 Brazil
2. Department of Radiation Oncology Brigham and Women's Hospital Dana‐Farber Cancer Institute Harvard Medical School Boston MA 02115 USA
3. Department of Physics and Applied Physics University of Massachusetts Lowell Lowell MA 01854 USA
Abstract
AbstractSuccessful implementation of X‐ray‐activated photodynamic therapy (X‐PDT) is challenging because most photosensitizers (PSs) absorb light in the blue region, but few nanoscintillators produce efficient blue scintillation. Here, efficient blue‐emitting SrF2:Eu scintillating nanoparticles (ScNPs) are developed. The optimized synthesis conditions result in cubic nanoparticles with ≈32 nm diameter and blue emission at 416 nm. Coating them with the meso‐tetra(n‐methyl‐4‐pyridyl) porphyrin (TMPyP) in a core–shell structure (SrF@TMPyP) results in maximum singlet oxygen (1O2) generation upon X‐ray irradiation for nanoparticles with 6TMPyP depositions (SrF@6TMPyP). The 1O2 generation is directly proportional to the dose, does not vary in the low‐energy X‐ray range (48–160 kVp), but is 21% higher when irradiated with low‐energy X‐rays than irradiations with higher energy gamma rays. In the clonogenic assay, cancer cells treated with SrF@6TMPyP and exposed to X‐rays present a significantly reduced survival fraction compared to the controls. The SrF2:Eu ScNPs and their conjugates stand out as tunable nanoplatforms for X‐PDT due to the efficient blue emission from the SrF2:Eu cores; the ability to adjust the scintillation emission in terms of color and intensity by controlling the nanoparticle size; the efficient 1O2 production when conjugated to a PS and the efficacy of killing cancer cells.
Funder
Fulbright U.S. Scholar Program
Conselho Nacional de Desenvolvimento Científico e Tecnológico