Dang Xiangnan, Gu Li, Qi Jifa, Correa Santiago, Zhang Geran, Belcher Angela M, Hammond Paula T
Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA 02139; Department of Materials Science and Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139;
Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA 02139; Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139;
Proc Natl Acad Sci U S A. 2016 May 10;113(19):5179-84. doi: 10.1073/pnas.1521175113. Epub 2016 Apr 25.
Fluorescence imaging in the second near-infrared window (NIR-II, 1,000-1,700 nm) features deep tissue penetration, reduced tissue scattering, and diminishing tissue autofluorescence. Here, NIR-II fluorescent probes, including down-conversion nanoparticles, quantum dots, single-walled carbon nanotubes, and organic dyes, are constructed into biocompatible nanoparticles using the layer-by-layer (LbL) platform due to its modular and versatile nature. The LbL platform has previously been demonstrated to enable incorporation of diagnostic agents, drugs, and nucleic acids such as siRNA while providing enhanced blood plasma half-life and tumor targeting. This work carries out head-to-head comparisons of currently available NIR-II probes with identical LbL coatings with regard to their biodistribution, pharmacokinetics, and toxicities. Overall, rare-earth-based down-conversion nanoparticles demonstrate optimal biological and optical performance and are evaluated as a diagnostic probe for high-grade serous ovarian cancer, typically diagnosed at late stage. Successful detection of orthotopic ovarian tumors is achieved by in vivo NIR-II imaging and confirmed by ex vivo microscopic imaging. Collectively, these results indicate that LbL-based NIR-II probes can serve as a promising theranostic platform to effectively and noninvasively monitor the progression and treatment of serous ovarian cancer.
在第二近红外窗口(NIR-II,1000 - 1700纳米)进行荧光成像具有组织穿透深、组织散射减少以及组织自发荧光减弱的特点。在此,包括下转换纳米颗粒、量子点、单壁碳纳米管和有机染料在内的NIR-II荧光探针,因其模块化和多功能的特性,利用层层(LbL)平台构建成生物相容性纳米颗粒。LbL平台先前已被证明能够掺入诊断剂、药物和核酸如小干扰RNA,同时延长血浆半衰期并实现肿瘤靶向。这项工作对目前具有相同LbL涂层的NIR-II探针在生物分布、药代动力学和毒性方面进行了直接比较。总体而言,基于稀土的下转换纳米颗粒表现出最佳的生物学和光学性能,并被评估为高级别浆液性卵巢癌(通常在晚期被诊断)的诊断探针。通过体内NIR-II成像成功检测到原位卵巢肿瘤,并通过体外显微镜成像得到证实。这些结果共同表明,基于LbL的NIR-II探针可作为一个有前景的诊疗平台,以有效且无创地监测浆液性卵巢癌的进展和治疗情况。