Molecular Imaging Program at Stanford (MIPS), Department of Radiology, Bio-X Program and Stanford Cancer Center, Stanford University School of Medicine, Stanford, CA 94305, USA.
Wiley Interdiscip Rev Nanomed Nanobiotechnol. 2010 Jul-Aug;2(4):349-66. doi: 10.1002/wnan.85.
The use of in vivo near-infrared fluorescence (NIRF) imaging techniques for sensitive cancer early detection is highly desirable, because biological tissues show very low absorption and autofluorescence in the NIR spectrum window. Cancer NIRF molecular imaging relies greatly on stable, highly specific and sensitive molecular probes. Nanoparticle-based NIRF probes have overcome some of the limitations of the conventional NIRF organic dyes, such as poor hydrophilicity and photostability, low quantum yield, insufficient stability in biological system, low detection sensitivity, etc. Therefore, a lot of efforts have been made to actively develop novel NIRF nanoparticles for in vivo cancer molecular imaging. The main focus of this article is to provide a brief overview of the synthesis, surface modification, and in vivo cancer imaging applications of nanoparticle-based NIRF probes, including dye-containing nanoparticles, NIRF quantum dots, and upconversion nanoparticles.
体内近红外荧光(NIRF)成像技术在敏感的癌症早期检测中非常理想,因为生物组织在近红外光谱窗口显示出非常低的吸收和自发荧光。癌症 NIRF 分子成像在很大程度上依赖于稳定、高度特异性和敏感的分子探针。基于纳米粒子的 NIRF 探针克服了传统 NIRF 有机染料的一些局限性,例如亲水性差和光稳定性差、量子产率低、在生物系统中稳定性不足、检测灵敏度低等。因此,人们积极开发新型 NIRF 纳米粒子用于体内癌症分子成像。本文的主要重点是简要概述基于纳米粒子的 NIRF 探针的合成、表面修饰以及体内癌症成像应用,包括含染料的纳米粒子、NIRF 量子点和上转换纳米粒子。