球体
纳米颗粒
材料科学
激发
纳米技术
分辨率(逻辑)
散射
激发波长
贝塞尔光束
激光器
光学
显微镜
光电子学
波长
梁(结构)
化学
计算机科学
物理
体外
人工智能
量子力学
生物化学
作者
Yongtao Liu,Fan Wang,Hongxu Lu,Guocheng Fang,Shihui Wen,Chaohao Chen,Xuchen Shan,Xiaoxue Xu,Lin Zhang,Martina M. Stenzel,Dayong Jin
出处
期刊:Small
[Wiley]
日期:2020-01-14
卷期号:16 (6)
被引量:37
标识
DOI:10.1002/smll.201905572
摘要
Abstract Cancer spheroids have structural, functional, and physiological similarities to the tumor, and have become a low‐cost in vitro model to study the physiological responses of single cells and therapeutic efficacy of drugs. However, the tiny spheroid, made of a cluster of high‐density cells, is highly scattering and absorptive, which prevents light microscopy techniques to reach the depth inside spheroids with high resolution. Here, a method is reported for super‐resolution mapping of single nanoparticles inside a spheroid. It first takes advantage of the self‐healing property of a “nondiffractive” doughnut‐shaped Bessel beam from a 980 nm diode laser as the excitation, and further employs the nonlinear response of the 800 nm emission from upconversion nanoparticles, so that both excitation and emission at the near‐infrared can experience minimal loss through the spheroid. These strategies lead to the development of a new nanoscopy modality with a resolution of 37 nm, 1/26th of the excitation wavelength. This method enables mapping of single nanoparticles located 55 µm inside a spheroid, with a resolution of 98 nm. It suggests a solution to track single nanoparticles and monitor their release of drugs in 3D multicellar environments.
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