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通过原位生物合成的荧光金纳米簇进行肿瘤的体内自生物成像。

In vivo self-bio-imaging of tumors through in situ biosynthesized fluorescent gold nanoclusters.

机构信息

State Key Laboratory of Bioelectronics-Chien-Shiung Wu Lab, School of Biological Science and Medical Engineering, Southeast University, Nanjing 210096, China.

出版信息

Sci Rep. 2013;3:1157. doi: 10.1038/srep01157. Epub 2013 Jan 29.

Abstract

Fluorescence imaging in vivo allows non-invasive tumor diagnostic thus permitting a direct monitoring of cancer therapies progresses. It is established herein that fluorescent gold nanoclusters are spontaneously biosynthesized by cancerous cell (i.e., HepG2, human hepatocarcinoma cell line; K562, leukemia cell line) incubated with micromolar chloroauric acid solutions, a biocompatible molecular Au(III) species. Gold nanoparticles form by Au(III) reduction inside cells cytoplasms and ultimately concentrate around their nucleoli, thus affording precise cell imaging. Importantly, this does not occur in non-cancerous cells, as evidenced with human embryo liver cells (L02) used as controls. This dichotomy is exploited for a new strategy for in vivo self-bio-imaging of tumors. Subcutaneous injections of millimolar chloroauric acid solution near xenograft tumors of the nude mouse model of hepatocellular carcinoma or chronic myeloid leukemia led to efficient biosynthesis of fluorescent gold nanoclusters without significant dissemination to the surrounding normal tissues, hence allowing specific fluorescent self-bio-marking of the tumors.

摘要

荧光体内成像是一种非侵入性的肿瘤诊断方法,可直接监测癌症治疗的进展。本文证明,荧光金纳米簇可以通过癌细胞(即 HepG2,人肝癌细胞系;K562,白血病细胞系)与毫摩尔氯金酸溶液孵育而自发生物合成,氯金酸溶液是一种生物相容性的分子 Au(III) 物种。金纳米颗粒通过细胞细胞质内的 Au(III) 还原形成,并最终集中在其核仁周围,从而实现精确的细胞成像。重要的是,这种情况不会在非癌细胞中发生,这可以用人胚胎肝细胞(L02)作为对照来证明。这种二分法被用于开发一种新的肿瘤体内自生物成像策略。在肝癌或慢性髓性白血病裸鼠模型的移植瘤附近皮下注射毫摩尔氯金酸溶液,可有效地生物合成荧光金纳米簇,而不会显著扩散到周围正常组织,从而可以特异性地荧光自标记肿瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c00/3557452/26b833032c75/srep01157-f1.jpg

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