光动力疗法
铕
纳米颗粒
材料科学
辐照
卟啉
闪烁体
核化学
发光
光化学
纳米技术
光电子学
化学
光学
物理
有机化学
核物理学
探测器
作者
Natasha Policei Marques,Mileni Isikawa,Zeinaf Muradova,Toby Morris,Ross Berbeco,Éder José Guidelli
标识
DOI:10.1002/adhm.202400372
摘要
Abstract Successful 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 SrF 2 :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 ( 1 O 2 ) generation upon X‐ray irradiation for nanoparticles with 6TMPyP depositions (SrF@6TMPyP). The 1 O 2 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 SrF 2 :Eu ScNPs and their conjugates stand out as tunable nanoplatforms for X‐PDT due to the efficient blue emission from the SrF 2 :Eu cores; the ability to adjust the scintillation emission in terms of color and intensity by controlling the nanoparticle size; the efficient 1 O 2 production when conjugated to a PS and the efficacy of killing cancer cells.
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