Abstract

Radiotherapy is often the most straightforward first line cancer treatment for solid tumors. While it is highly effective against tumors, there is also collateral damage to healthy proximal tissues especially with high doses. The use of radiosensitizers is an effective way to boost the killing efficacy of radiotherapy against the tumor while drastically limiting the received dose and reducing the possible damage to normal tissues. Here, we report the design and application of a good radiosensitizer by using ultrasmall Au29–43(SG)27–37 nanoclusters (<2 nm) with a naturally-occurring peptide (e.g., glutathione or GSH) as the protecting shell. The GSH-coated Au29–43(SG)27–37 nanoclusters can escape the RES absorption, leading to a good tumor uptake (~8.1% ID/g at 24 h post injection). As a result, the as-designed Au nanoclusters led to a strong enhancement for radiotherapy, as well as a negligible damage to normal tissues. After the treatment, the ultrasmall Au29–43(SG)27–37 nanoclusters can be efficiently cleared by the kidney, thereby avoiding potential long-term side-effects caused by the accumulation of gold atoms in the body. Our data suggest that the ultrasmall peptide-protected Au nanoclusters are a promising radiosensitizer for cancer radiotherapy.

Highlights

  • Radiotherapy is often the most straightforward first line cancer treatment for solid tumors

  • The as-designed Au nanoclusters led to a strong enhancement for radiotherapy, as well as a negligible damage to normal tissues

  • It is very important to strike the right balance between eradicating tumor and saving normal tissues by controlling the target and the dose of radiation administered to the patient

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Summary

Tumor Uptake and High Renal Clearance

Xiao-Dong Zhang[1], Zhentao Luo[2], Jie Chen[1], Shasha Song[1], Xun Yuan[2], Xiu Shen[1], Hao Wang[1], Yuanming Sun[1], Kai Gao[3], Lianfeng Zhang[3], Saijun Fan[1], David Tai Leong[2], Meili Guo4 & Jianping Xie[2]. Taken together of the two key attributes (size and surface) for NPsbased radiosensitizers, we hypothesized that: 1) small naturallyoccurring peptides, such as glutathione or GSH, could be a good surface ligand for Au NPs by helping them escape the RES absorption and improving their deposition in tumors; and 2) ultrasmall Au NPs with core sizes below 2 nm (hereafter referred to as nanoclusters, NCs) in combination with the GSH ligands can ensure a small hydrodynamic diameter (HD), which could provide good interface with the biological system, improve their in vivo pharmacokinetics, and enhance their deposition in tumors[39] We demonstrate such concept by using sub-2-nm GSH-protected Au NCs with a welldefined molecular formula of Au29–43(SG)27–3740. This study has enriched the family of Au NPs and NCs that could show good performance for cancer radiotherapy[33,37]

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