Preclinical safety assessment of photoluminescent metal quantum clusters stabilized with autologous serum proteins for host specific theranostics.

Q1 Pharmacology, Toxicology and Pharmaceutics Nanotheranostics Pub Date : 2023-01-01 DOI:10.7150/ntno.82978
Kritika Sood, Pranjali Yadav, Manu Jamwal, Reena Das, Asifkhan Shanavas
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Abstract

Host derived serum proteome stabilised red-emitting gold quantum clusters (or Au-QC-NanoSera or QCNS) of size range ~2 nm have been synthesised in a first reported study. The host serum was taken from bovine, murine and human origins to establish the proof of concept. In-vitro biocompatibility with normal murine L929 fibroblast cells and radiosensitisation ability against PLC/PRF/5 hepatoma cells was established. A concentration dependant radiosensitisation effect of QCNS at differential γ-radiation doses was observed with almost 90% killing of cancer cells at a radiation dose of 5Gy. Acute and subacute safety, and non-immunogenicity of autologously derived QCNS was established in in-bred C57BL/6 mice. The biodistribution analysis revealed that the QCNS were effectively cleared from the body over a course of 28 days and were found to pose no major threat to the proper functioning and morphology of the mice.

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自体血清蛋白稳定的光致发光金属量子团簇用于宿主特异性治疗的临床前安全性评估。
在一项首次报道的研究中,我们合成了尺寸范围约为2nm的宿主来源的血清蛋白质组稳定的红发光金量子团簇(或Au-QC-NanoSera或QCNS)。宿主血清取自牛、鼠和人类,以建立概念证明。建立了与正常小鼠L929成纤维细胞的体外生物相容性和对PLC/PRF/5肝癌细胞的放射增敏能力。在不同γ-辐射剂量下,QCNS具有浓度依赖性的放射增敏效应,在5Gy的辐射剂量下,癌细胞的杀伤率几乎达到90%。在近交C57BL/6小鼠中建立了自源性QCNS的急性和亚急性安全性和非免疫原性。生物分布分析显示,在28天的过程中,QCNS被有效地从体内清除,并且发现对小鼠的正常功能和形态没有构成重大威胁。
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来源期刊
Nanotheranostics
Nanotheranostics Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (miscellaneous)
CiteScore
10.40
自引率
0.00%
发文量
37
审稿时长
12 weeks
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