Atomically-precise Au22(Lys-Cys-Lys)16 nanoclusters for radiation sensitization

Radiotherapy is a leading method for cancer treatment, effectively eliminating cancer cells but often causing collateral damage to surrounding healthy tissue. Radiosensitizers aim to enhance the therapeutic effects of radiotherapy while minimizing harm to normal cells. We recently reported atomically-precise gold nanoclusters, Au<sub>22</sub>(Lys-Cys-Lys)<sub>16</sub>, synthesized via a photochemical method coupled with a novel accelerated size-focusing procedure. These nanoclusters exhibit a distinct luminescence emission profile, reflecting exceptional optical purity and the absence of contamination from other nanocluster species. They demonstrate efficient oxygen radicals generation under light irradiation. In this study, we comprehensively evaluated the radiosensitization potential of Au<sub>22</sub>(Lys-Cys-Lys)<sub>16</sub> nanoclusters in vitro and in vivo, alongside their pharmacokinetics, biodistribution and toxicity. The nanoclusters demonstrated high stability under physiological conditions and efficient internalization in tumor cells, achieving dose enhancement factors of 2.0 and 1.6 in KB and 4T1 tumor cells, respectively, under 225 kVp X-ray irradiation. Mechanistic investigations revealed enhanced radiation-induced DNA damage and disruption of DNA repair pathways. The radiosensitizing effects were further validated in radioresistant pancreatic ductal adenocarcinoma cells using the clonogenic assay and γH2AX analysis of double-strand breaks, as well as in a duck chorioallantoic membrane model. With ultra small size (~ 1.7 nm) and favorable surface framework, the nanoclusters exhibited relevant pharmacokinetics (circulation half-life, t₁<sub>/</sub>₂ = 10.4 h) and renal clearance. In a KB tumor-bearing mouse model, Au<sub>22</sub>(Lys-Cys-Lys)<sub>16</sub> significantly delayed tumor progression and prolonged survival under 8 Gy irradiation without observed side-effects. These findings establish Au<sub>22</sub>(Lys-Cys-Lys)<sub>16</sub> nanoclusters as a potentially translatable radiosensitizer, advancing cancer radiotherapy strategies.

Authors

Institutions

Publication Details

Journal
Journal of Nanobiotechnology
Published
2025-03-07
DOI
https://doi.org/10.1186/s12951-025-03256-7
Citations
4
Primary Topic
Nanocluster Synthesis and Applications
Type
article
Field-Weighted Citation Impact
2.07

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Atomically-precise Au22(Lys-Cys-Lys)16 nanoclusters for radiation sensitization

Lucie Malbeteau, Kristen Harrington, Lili Ding, Marianne Koritzinsky et al.
4 citations
Journal of Nanobiotechnology
Nanocluster Synthesis and Applications
2.07
article

Atomically-precise Au22(Lys-Cys-Lys)16 nanoclusters for radiation sensitization

Lucie Malbeteau, Kristen Harrington, Lili Ding, Marianne Koritzinsky, Kevin G. Stamplecoskie, Marcus A. Horn, Parimah Aminfar, Gang Zheng, Carla Calçada, Brian C. Wilson, Layla Pires, Juan Chen, Alina Jaglanian, Elham Zeinizade, Mohamad Dukuray, Goonay Yousefalizideh
article en
4 citations

Abstract

Radiotherapy is a leading method for cancer treatment, effectively eliminating cancer cells but often causing collateral damage to surrounding healthy tissue. Radiosensitizers aim to enhance the therapeutic effects of radiotherapy while minimizing harm to normal cells. We recently reported atomically-precise gold nanoclusters, Au<sub>22</sub>(Lys-Cys-Lys)<sub>16</sub>, synthesized via a photochemical method coupled with a novel accelerated size-focusing procedure. These nanoclusters exhibit a distinct luminescence emission profile, reflecting exceptional optical purity and the absence of contamination from other nanocluster species. They demonstrate efficient oxygen radicals generation under light irradiation. In this study, we comprehensively evaluated the radiosensitization potential of Au<sub>22</sub>(Lys-Cys-Lys)<sub>16</sub> nanoclusters in vitro and in vivo, alongside their pharmacokinetics, biodistribution and toxicity. The nanoclusters demonstrated high stability under physiological conditions and efficient internalization in tumor cells, achieving dose enhancement factors of 2.0 and 1.6 in KB and 4T1 tumor cells, respectively, under 225 kVp X-ray irradiation. Mechanistic investigations revealed enhanced radiation-induced DNA damage and disruption of DNA repair pathways. The radiosensitizing effects were further validated in radioresistant pancreatic ductal adenocarcinoma cells using the clonogenic assay and γH2AX analysis of double-strand breaks, as well as in a duck chorioallantoic membrane model. With ultra small size (~ 1.7 nm) and favorable surface framework, the nanoclusters exhibited relevant pharmacokinetics (circulation half-life, t₁<sub>/</sub>₂ = 10.4 h) and renal clearance. In a KB tumor-bearing mouse model, Au<sub>22</sub>(Lys-Cys-Lys)<sub>16</sub> significantly delayed tumor progression and prolonged survival under 8 Gy irradiation without observed side-effects. These findings establish Au<sub>22</sub>(Lys-Cys-Lys)<sub>16</sub> nanoclusters as a potentially translatable radiosensitizer, advancing cancer radiotherapy strategies.

Journal of NanobiotechnologyVol. 23(1)
University Health Network (CA), University of Toronto (CA), Queen's University (CA), Princess Margaret Cancer Centre (CA)
Princess Margaret Cancer Foundation
Openalex Percentile: Top 14%
Nanocluster Synthesis and Applications
2.07
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.