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Nanoscale Detection of Subcellular Nanoparticles by X-Ray Diffraction Imaging for Precise Quantitative Analysis of Whole Cancer Cells.
Guo, Amin; Zhang, Jianhua; Wang, Yufei; Fan, Jiadong; He, Bo; Wang, Jian; Tai, Renzhong; Liang, Xing-Jie; Jiang, Huaidong.
Afiliación
  • Guo A; School of Physical Science and Technology, ShanghaiTech University, Shanghai 201210, China.
  • Zhang J; School of Physical Science and Technology, ShanghaiTech University, Shanghai 201210, China.
  • Wang Y; CAS Key Laboratory for Biological Effects of Nanomaterials and Nanosafety, CAS Center for Excellence in Nanoscience, National Center for Nanoscience and Technology of China, Beijing 100190, China.
  • Fan J; University of Chinese Academy of Sciences, Beijing 100049, China.
  • He B; School of Physical Science and Technology, ShanghaiTech University, Shanghai 201210, China.
  • Wang J; School of Physical Science and Technology, ShanghaiTech University, Shanghai 201210, China.
  • Tai R; Canadian Light Source Inc., University of Saskatchewan, 44 Innovation Boulevard, Saskatoon, Saskatchewan S7N 2V3, Canada.
  • Liang XJ; Shanghai Synchrotron Radiation Facility, Shanghai Advanced Research Institute, Chinese Academy of Science, Shanghai 201204, China.
  • Jiang H; CAS Key Laboratory for Biological Effects of Nanomaterials and Nanosafety, CAS Center for Excellence in Nanoscience, National Center for Nanoscience and Technology of China, Beijing 100190, China.
Anal Chem ; 93(12): 5201-5210, 2021 03 30.
Article en En | MEDLINE | ID: mdl-33687204
Nanoparticles show great potential for drug delivery systems in cancer treatment and diagnosis, which mainly rely on the interaction between nanoparticles and living cells. However, there is still a lack of accurate and large field-of-view imaging techniques to reveal the aggregation and distribution behavior of nanoparticles in whole cancer cells without being destroyed. Here, we demonstrated quantitative imaging of unstained and intact mouse breast cancer cells (4T1) containing 50 nm gold nanoparticles (Au@citrate NPs) using an X-ray scanning coherent diffraction imaging (ptychography) technique in a large field-of-view. A two-dimensional spatial resolution of 17 nm was achieved on the 4T1 cell. We combine X-ray ptychography and equally sloped tomography (EST) to perform three-dimensional structural mapping, distribution, and aggregation behavior of Au@citrate NPs in cancer cells. By taking full advantage of the large field-of-view, high-resolution, and quantitative imaging technique, the single intracellular Au@citrate NPs are observed and the amount of Au@citrate NPs in aggregations can be accurately quantified. In addition, the morphological changes of lysosomes containing Au@citrate NPs can be observed in the high-contrast mass density images. This study provides an approach for exploring quantitative analysis and physiological delivery of nanomaterials in intact cancer cells at nanoscale resolution, which may greatly benefit the interdisciplinary research of material science, nanomedicine, and nanotoxicology.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Nanopartículas del Metal / Neoplasias Tipo de estudio: Diagnostic_studies Límite: Animals Idioma: En Revista: Anal Chem Año: 2021 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Nanopartículas del Metal / Neoplasias Tipo de estudio: Diagnostic_studies Límite: Animals Idioma: En Revista: Anal Chem Año: 2021 Tipo del documento: Article País de afiliación: China