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上转换纳米粒子的生物缀合物用于癌症生物标志物的检测和成像。

Bioconjugates of photon-upconversion nanoparticles for cancer biomarker detection and imaging.

机构信息

Institute of Analytical Chemistry of the Czech Academy of Sciences, Brno, Czech Republic.

Department of Biochemistry, Faculty of Science, Masaryk University, Brno, Czech Republic.

出版信息

Nat Protoc. 2022 Apr;17(4):1028-1072. doi: 10.1038/s41596-021-00670-7. Epub 2022 Feb 18.

Abstract

The detection of cancer biomarkers in histological samples and blood is of paramount importance for clinical diagnosis. Current methods are limited in terms of sensitivity, hindering early detection of disease. We have overcome the shortcomings of currently available staining and fluorescence labeling methods by taking an integrative approach to establish photon-upconversion nanoparticles (UCNP) as a powerful platform for cancer detection. These nanoparticles are readily synthesized in different sizes to yield efficient and tunable short-wavelength light emission under near-infrared excitation, which eliminates optical background interference of the specimen. Here we present a protocol for the synthesis of UCNPs by high-temperature co-precipitation or seed-mediated growth by thermal decomposition, surface modification by silica or poly(ethylene glycol) that renders the particles resistant to nonspecific binding, and the conjugation of streptavidin or antibodies for biological detection. To detect blood-based biomarkers, we present an upconversion-linked immunosorbent assay for the analog and digital detection of the cancer marker prostate-specific antigen. When applied to immunocytochemistry analysis, UCNPs enable the detection of the breast cancer marker human epidermal growth factor receptor 2 with a signal-to-background ratio 50-fold higher than conventional fluorescent labels. UCNP synthesis takes 4.5 d, the preparation of the antibody-silica-UCNP conjugate takes 3 d, the streptavidin-poly(ethylene glycol)-UCNP conjugate takes 2-3 weeks, upconversion-linked immunosorbent assay takes 2-4 d and immunocytochemistry takes 8-10 h. The procedures can be performed after standard laboratory training in nanomaterials research.

摘要

在组织样本和血液中检测癌症生物标志物对于临床诊断至关重要。目前的方法在灵敏度方面存在局限性,阻碍了疾病的早期发现。我们通过综合方法克服了当前染色和荧光标记方法的缺点,建立了上转换纳米粒子(UCNP)作为癌症检测的强大平台。这些纳米粒子可以很容易地合成不同的尺寸,在近红外激发下产生高效和可调谐的短波长光发射,消除了标本的光学背景干扰。在这里,我们提出了一种通过高温共沉淀或热分解的种子介导生长来合成 UCNP 的方案,通过硅或聚(乙二醇)进行表面修饰,使颗粒不易发生非特异性结合,并通过链霉亲和素或抗体进行生物检测。为了检测基于血液的生物标志物,我们提出了一种上转换免疫吸附测定法,用于模拟和数字检测癌症标志物前列腺特异性抗原。当应用于免疫细胞化学分析时,UCNP 能够以比传统荧光标记物高 50 倍的信号背景比检测乳腺癌标志物人表皮生长因子受体 2。UCNP 的合成需要 4.5 天,抗体-硅-UCNP 缀合物的制备需要 3 天,链霉亲和素-聚(乙二醇)-UCNP 缀合物的制备需要 2-3 周,上转换免疫吸附测定法需要 2-4 天,免疫细胞化学需要 8-10 小时。这些程序可以在标准的纳米材料研究实验室培训后进行。

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